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School of Law
MEDICAL
LAW
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Module Tutor:
Michelle RobsonTel: 0191 2273965e-mail:[email protected]
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CONTENTS
CHAPTER CONTENTS PAGE
Study Materials 1
1 Introduction 42 The NHS 83 Contract Law 134 Judicial review 195 Clinical Negligence 306 Duty of care 397 Standard of care 558 Causation 739 Damages 10110 Litigation 12211 Consent to Treatment 14112 Medical Confidentiality 17413 Access to Medical records 20414 Beginning of Life 21015 Ending of Life 23416 Human rights 255
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Study Materials
WHO TO CONTACT ABOUT THIS MODULE
Your tutor is Michelle Robson. She is the joint LLM Medical Law Programme Leader, M Law
Medical Law Module Tutor, Open Learning Medical Law Module Tutor and is a Senior Lecturer
in Law in the School of Law at the University of Northumbria specialising in medical law. If you
have any queries about the module then contact her on 0191 227 3965. Her e-mail address is:
AIMS OF THE MODULE
The overall purpose of this module is to provide students with a knowledge and appreciation of
the underpinning theory, law and practice of medical law in England and Wales.
LEARNING OUTCOMES
The learning outcomes for this module are:
To have an appreciation of the distinction between legal rules and ethical rules and the
consequences of not observing either.
To have an appreciation of Medical Law as a discrete subject of study
To have a general knowledge of: the application of contract to medical negligence;
judicial review and complaints.
To have a detailed knowledge of the substantive and procedural rules associated with a
claim in clinical negligence
To understand and speculate on how the Human Rights legislation will impact on
various areas of the syllabus
To know (where appropriate) how other jurisdictions deal with the issues that we will be
focusing on
To be able to comment upon the legal and ethical issues arising from the latest topical
issues
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To know, understand and analyse the latest relevant case law, statute, articles in
relation to the areas covered.
2. ASSESSMENT
The module is assessed by way of a three hour exam. Further details regarding the assessment
will be given once the module has begun.
3 METHOD OF STUDY
All materials for this module can be located on the E-learning Portal (ELP). On the ELP you will
find the teaching materials which provide an overview of the law. Other materials are available
through hyperlinks within the module materials.
The hyperlinks from the electronic workbook to case law are designed to link you directly to the
Westlaw database to which the university subscribes. This database may require you to
provide your database password each time you link to the database. This will mean that you
can only link to the home page for the database, and will then need to provide the case
reference detailed in the workbook before you can access the case itself. Having logged in
once, Westlaw should allow you to link directly to subsequent cases provided you remain
logged on. Hyperlinks for other documents are provided to sites which are freely available
through the internet. Since internet links do frequently change or move, if you have difficulties
accessing any of these hyperlinked materials then please let the module tutor know. Equally, if
you do have difficulties logging into the ELP please do let us know. Students should note that
when accessing sites through the hyperlinks, students will be responsible for abiding by any
copyright or other restrictions imposed on such sites.
Each chapter of the workbook will have a learning outcome(s) which you should be able to
satisfy at the conclusion of your reading of the relevant chapter, the self-test questions and the
recommended reading. Where there is no reference to specific pages of a textbook, it is
intended that the material in the workbook should be enough to enable you to complete the self-
test questions; however, if at all possible you should try and do some additional reading.
The material in this module workbook is only an introduction to the area(s) of law under
consideration. Consequently the workbook will focus on the main legal issues/principles; but on
its own the workbook will not suffice: you must read more widely from both the recommended
textbooks and the other sources as indicated. In addition under Teaching Materials on the ELP
you will find all medical lecture slides used on the M Law Medical Law module. This module
follows broadly the same syllabus as the open learning.
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The recommended textbook for this module is:
Text, Cases and Materials on Medical Law and Ethics: Stauch & Wheat (Routledge, 5th ed)
If you wish to use a revision book then the recommended text is:Robson, Swift et al: Q & A Law Express Medical Law (Pearson) 1
st ed
Other Recommended Reading
Medical Law, Cases and Materials by Emily Jackson 3rd
ed (OUP)
Jonathon Herring Medical Law and Ethics 4th ed (OUP).
Margaret Brazier and Emma Cave: Medicine, Patients and the Law (Penguin Books) (5th
edition)
Pattinson, Shaun: Medical Law and Ethics, 4th ed, (Sweet and Maxwell)
Khan, Robson & Swift: Clinical Negligence (Cavendish Publishing) 2nd edition
Herring, Jonathan, Medical Law and Ethics, 4th ed (OUP)
Mason, McCall Smith & Laurie: Law and Medical Ethics 9th edition (OUP)
Kennedy and Grubb: Principles of Medical Law (Butterworths)
Journals
Professional Negligence
British Medical Journal
Solicitors JournalNew Law Journal
Medical Law Review
Clinical Risk
Reports
The majority of cases cited in this text are located in either LS Law Med (formerly Lloyds
Reports (Medical also known as the Medical Law Reports) or the All England Law Reports;
GMC –http://www.gmc-uk.org/; DOH –http://www.dh.gov.uk; BMA –http://www.bma.org.uk/;
MDU –http://www.the-mdu.com/;NHA –http://www.nhs.uk/
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CHAPTER 1
INTRODUCTION
1.1 SCENARIO
Consider the following scenario:
X, a patient, who has been involved in a motor cycle accident, is treated at the A&E unit
of his local hospital. Unfortunately, because of a misunderstanding in the instructions
given by the casualty doctor over the telephone to the nurse, the wrong injection for a leg
wound is given to X. The result is that seven days later X has to have an operation on his
leg which in turn has caused him to have to stay off work for six months. Advise X.
Whether as a student or a practitioner the advice you will offer to X will very much depend
on certain key basic questions, such as:
Was X treated as an NHS patient?
What does X want? An explanation? An apology? Compensation?
What exactly caused the damage? Human error? The faulty contents of the
injection?
1.2 NHS v PRIVATE
The reader needs to distinguish between patient/claimants who receive their medical
treatment on the NHS as opposed to privately. The distinction is important because the
private patient may, if/when things go wrong, sue in contract and/or tort, whereas the
NHS patient can only sue in tort. The law has consistently said that there is no contract
between an NHS patient and the NHS on the ground that the requirements of a contract,
such as voluntariness and consideration, are missing. (See Pfizer v Ministry of Health
[1965] AC 512 and Reynolds v Health First Medical Group 2000).
1.3 EXPLANATION v COMPENSATION
It is important, when things go wrong and lawyers are asked for advice that they should
try and find out what the patient/claimant wants. For example, if an explanation is needed
for the patient’s family to be able to draw a line under the episode , then litigation is not
the most appropriate route; instead, using the NHS resolution procedure may provide the
patient with both the explanation being sought and a reassurance that something similar
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might not happen in the future to another patient. But if compensation is required then the
right approach will be to consider the courts and litigation.
1.4 OTHER LAW OPTIONS
Based on the facts in front of him a lawyer will know that there are other legal options
open to him and the patient/claimant. For example, if the medical misadventure was
caused by a medicinal product he would do well to consider the possibility of a remedy
under the product liability legislation in the form of the Consumer Protection Act; again if it
is a “policy” decision which might have a future adverse effect, for example a decision not
to fund a certain medical procedure (see Rogers v Swindon NHS PCT & Secretary of
State for Health [2006] EWCA Civ 392 one might want to think about judicial review as a
remedy.
1.5 SOURCES OF ENGLISH MEDICAL LAW
* Statute Law – Primary and delegated legislation.
* Common Law – (Judicial Precedent).
* International Conventions, such as the European Convention on Human Rights
(ECHR).
* Professional Disciplinary Rules - health carers will belong to a particular
professional body which will ensure that professional standards are maintained. * Circulars, Protocols, Guidance Notices, Guidelines, Executive Letters. In general
these “laws” are not legally binding, but a failure to follow them will be closely
looked at by both courts and professional bodies.
* European Rules.
* Patients Charter.
READING:
Stauch Text, Cases and Materials on Medical Law and
Ethics (Routledge, Chapters 1 & 2
Pattinson Medical Law and Ethics 4th ed (Sweet &
Maxwell Chapter 2 (overview only)
Jackson Medical Law Text, Cases and Materials 3rd
ed
(OUP) Chapter 3 introduction only
Brazier & Cave: Medicine, Patients and the Law (5th
ed)
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(Penguin Books), Chapter 1
Herring Medical Law & Ethics (4th ed) Chapters 1 & 2
SUMMARY
At the end of this chapter you should be able to:
* appreciate some of the different branches of law making up the study of medical
law
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NOTES
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CHAPTER 2
THE NHS AND PROFESSIONAL BODIES
2.1 INTRODUCTION
The purpose of this chapter is to introduce you briefly to the structure of the NHS and to
act as a brief guide to some of the governing bodies of the medical profession. The NHS
however is still in a period of transition following the enactment of the Health and Social
Care Act 2012 (HCSA) on 27 March 2012. An outline only of the structure of the NHS
follows below but frequent reference should be made both to the NHS and DOH websites
for the latest guidance. Much of the material in this chapter is taken from the saidwebsites.
However by way of reference the following paragraphs give an overview of the NHS and
the regulatory bodies governing the medical professions. They also serve as a glossary
of the more common terms you will come across.
Please also refer however to the supplementary material on the eLP under teaching
materials.
2.2 THE NATIONAL HEALTH SERVICE
The NHS was established in 1948 “to provide healthcare for all citizens, based on need,
not the ability to pay.” It is funded by the taxpayer and is therefore accountable to
Parliament. The NHS employs more than 1.7m people, just under half of which are
clinically qualified, including nearly 40,000 general practitioners (GPs), over 400,000
nurses and 18,450 ambulance staff. When the NHS was launched in 1948 it had a
budget of £437million (roughly £9billion at today’s value). In 2015/6 the NHS budget
£115.4 billion.
2.3 DEPARTMENT OF HEALTH
The Department of Health controls the NHS. The Secretary of State for Health (currently
Jeremy Hunt) is the head of the Department of Health and reports to the Prime Minister.
Under HCSA the new Act the Department of Health (DH) will be responsible for strategic
leadership of both the health and social care systems, but will no longer be the
headquarters of the NHS, nor will it directly manage any NHS organisations.
2.4 THE NHS ACT AND THE SECRETARY OF STATE
The National Health Service Act 1977 is the seminal piece of legislation and empowers
the Secretary of State and the Department of Health to make provision for health care.
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It is worthwhile remembering that care may be provided outside the NHS. This is often
funded by insurance policies. Treatment may also be provided by an independent
hospital, where the care has been commissioned (paid for) by the NHS.
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2.7 REGULATORY BODIES
2.7.1 The Care Quality Commission (CQC)
The Care Quality Commission is the health and social care regulator for England
established in 2009 to regulate and inspect health and adult social care services in
England. These services may be provided by the NHS, local authorities, private
companies or voluntary organisations. The Commission is also responsible for
protecting the rights of people detained under the Mental Health Act. The Health and
Social Care Act 2008 empowers the Commission to carry out its role.
2.7.2 National Institute of Clinical Excellence (NICE)
Set up in 1999 it seeks to promote the highest quality in treatment and technology in the
NHS and looks at the cost-effectiveness of the NHS services for example see NICE’s
decision restricting the use of certain drugs for the treatment of Alzheimer’s disease
considered further in Chapter 2. NICE also advises on the best clinical practice and
issues guidelines in order to provide uniform quality of treatment across the country.
2.7.3 Professional Bodies
All doctors must be registered with their governing body, the General Medical Council(GMC). The equivalent body for nurses is the Nursing and Midwifery Council, for
dentists, the General Dental Council These bodies set the standard of best professional
practice which their members are required to adhere to and have the power to discipline.
Additionally the Medical (Professional Performance) Act 1995 gives the GMC power to
act where the doctor’s conduct is found to be seriously deficient in performance of his
professional duties. The GMC have a number of publications one of which is entitled
“Good Medical Practice”. Although these guidelines have no legal basis it is suggested
that any departure from them could be used as evidence to show that the doctor is in
breach of his standard of care.
2.8 COMPLAINTS PROCEDURE
If medical treatment goes wrong what can the patient do? If he wants the matter
investigated and followed up (possibly) by an explanation and/or an apology and/or a
reassurance that a similar thing will not happen in the future, then using NHS resolution
procedure may be the way forward.
2.9 LEGAL ACTION
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NOTES
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CHAPTER 3
CONTRACT
3.1 INTRODUCTION
The major distinction between any patient who is treated privately and one who is treated
on the NHS is that the private patient, if dissatisfied with the treatment, can seriously
contemplate a claim for breach of contract. Such a claim is not open to the NHS patient
on the ground that there is no equality of bargaining between the parties – health care
has to be provided, see Pfizer Corp v MOH [1965] AC 512 . In Pfizer the House of Lords
ruled that where services are provided pursuant to a statutory obligation there is nocontractual relationship for the element of compulsion is inconsistent with the consensual
basis of contract; the fact that the patient makes some payment is irrelevant. The NHS
patient can only sue in tort because there is no freedom of bargaining power; the parties
must enter into the relationship in order to fulfil their obligations.
The private patient however can pursue a claim for breach of contract as well as a tort
claim. As contracting parties the patient and the health carer are free to determine their
own obligations and responsibilities, except that the health carer is unable to exclude
himself from liability for injury to the patient caused by his negligence (see the Unfair
Contract Terms Act 1977, section 2).
3.2 WHEN IS A CONTRACTUAL CLAIM AVAILABLE?
As regards contract, unless there is clear evidence that the defendant, by words,
gestures etc., was guaranteeing a successful outcome, then the courts would only imply
into the contract that the defendant was agreeing to carry out the contractual treatment
with reasonable care and skill. For example, a husband contracts to undergo a
vasectomy operation. Two years later, his wife becomes pregnant. The husband
decides to sue the defendant consultant on the ground that the latter broke his agreement
in that he had contracted to render the husband sterile which has clearly not happened.
Did the defendant contract to make the husband sterile? If there is evidence that he did
then he is in breach of the agreement. But if the agreement is silent on a guaranteed
outcome then the courts will not read such an outcome into the contract; instead they
would simply assert that the agreement was to carry out a vasectomy operation with
reasonable skill and care. If that was, in the eyes of the court, achieved then no breach
of contract claim is possible. In this area see Thake v Maurice [1986] 1 QB 644 and Eyre
v Measday [1986] 1 ALL ER 488. It is possible that some courts may hold, more as a
matter of policy, that certain types of elective treatment e.g. cosmetic surgery, lend
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themselves more easily to an argument founded in contract, given that the arrangement
resembles a business agreement. In La Fleur v Cornelis (1980) 63 APR 569 (Canadian)
a plastic surgeon was held liable in contract for scarring consequent on surgery to reduce
the size of the claimant’s nose.
Contract may continue to assume greater significance in the future as more and more
elective surgery e.g. cosmetic surgery is done privately. In these cases the courts will
more readily imply into the contract that the health carer guaranteed a specific outcome
e.g. a nose of a specific length, breast reduction to a certain size etc. In Thompson v
Sheffield Fertility Clinic [2000] MLC 0282 £20,000 was paid by Sheffield Fertility Clinic to
the claimants in an out of court settlement for breach of contract. The claimants had been
receiving IVF treatment at the Sheffield Fertility Clinic. The defendants had transferred
three embryos back to Mrs Thompson who claimed that she had agreed with the
defendants that they would only transfer two embryos back. No signed consent form had
been obtained from the claimants. The Clinic’s actions were held to be a breach of
contract.
In Jane Dove v Andrew Jarvis (6 February 2013) the court concluded that an assurance
given by the defendant private consultant orthopaedic surgeon that the operation would be
“well done” did not create a contractual duty of skill and care higher that the tortuous
(Bolam) duty of skill of care (see further Chapter 6). Whilst in Silverstone v Mortensen &
Oxford University Hospital NHS Trust [2012] EWHC 2706 one of the terms pleaded was
that the surgeon would exercise the skill and care of a world authority. There was no
dispute that he was a world authority but the judge held the term did not add anything to
the ordinary duty in contract and tort that the surgery would be performed to the standard
expected of a consultant surgeon. Moreover the judge continued and held that although it
was a private contract, the standard of care expected was the same as that required in the
sur geon’s NHS practice.
Finally if the contract is one to provide medicinal products such as a wheelchair or a heart
pacemaker, then certain provisions under the Supply of Goods and Services Act 1982,
such as the product being fit for its particular purpose or the goods matching their
description, will become relevant and applicable.
3.3 CONTRACT OR TORT
The contractual duty of reasonable care and skill is similar to the tort duty of reasonable
care. Consequently there is, at first sight, no obvious advantage in suing in contract
instead of tort and the courts have been at pains to confirm that one type of patient
should not be seen to have an advantage over the other. It was Lord Donaldson who said
in Hotson v E. Berkshire A.H.A. [1987] 1 AC 750,
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“…I am…unable to detect any rational basis for a state of the law…whereby
in identical circumstances, Dr A who treats a patient under the national
health service, and whose liability…falls to be determined in accordance with
the law of tort, should be in a different position from Dr B who treats a patientoutside the service and whose liability…falls to be determined in accordance
with the law of contract…”
But having said that, there are indeed differences between a tort claim and a contract
claim; these include:
Different limitation periods;
Loss of a chance claims are possible in contract but doubtful in the tort of clinical
negligence ( see Hotson v E. Berkshire A.H.A. [1987] 1 AC 750, Gregg v Scott
[2005] UKHL 2 and
Measure of damages is different.
Further reading
Brazier & Cave: Medicine, Patients and the Law (5th
edition) (Penguin Books),
Chapter 11 pages 307 et seq & Chapter 10
Khan, Robson & Swift: Clinical Negligence (Cavendish Publishing) 2nd
edition, pages
71, 87
Jackson: Medical Law Text Cases and Materials (Oxford University Press)
Chapter 3 pp 102-104
Pattinson Medical Law and Ethics (4th
ed) Chapter 3 (opening pages only)
Herring: Medical Law and Ethics 4th ed (OUP) Chapter 3
Stauch Text, Cases and Materials on Medical Law and Ethics
(Routledge, Chapter 6 (introduction only)
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SUMMARY
At the end of this chapter you should be able to:
* identify some of the advantages/disadvantages of bringing a claim in contract.
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SELF-TEST QUESTIONS – CHAPTER 3
1. In what circumstances (if any) will the private patient succeed in an action for
clinical negligence whereas an NHS patient will fail?
2. What is the legal standard of care that a private patient may expect from his health
carer? Does it differ in any way from his NHS contemporary?
3. Annie has recently undergone an operation to reduce the size of her breasts.
Unfortunately she is very unhappy with the result and wishes to sue her private
consultant Dr Corgy. What further information would you require in order to advise
Annie as to her chances of success?
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NOTES
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CHAPTER 4
JUDICIAL REVIEW
4.1 INTRODUCTION
It is possible to argue that, since the Secretary of State for Health has overall political
responsibility for the nation’s health, policy decisions that impact directly or indirectly on a
patient can be challenged in a court of law. Normally the way to do this is by judicial
review in the High Court. A patient who applies for judicial review asks the court to rule
that a decision by a health authority/trust not to provide treatment is unreasonable and
that decision has been made irrationally, illegally or is undermined as there are several
procedural irregularities. If the decision is viewed as unreasonable then the court may
quash the decision. In R v Secretary of State for Social services, West Midlands RHA
and Birmingham AHA (Teaching) ex p. Hincks & Others (1980) 1 BMLR 93 the court
looked at the meaning of section 3(1) of the National Health Service Act 1977 (see now
NHS Act 2006, s.1) and in particular whether the Secretary of State was under an
absolute duty to provide services regardless of available funding. Unsurprisingly the
court refused to grant a declaration in those terms ruling that the Secretary of State must
have regard to available funding.
4.2 RESOURCES AND OTHER ARGUMENTS
In general, arguments concerning the use of resources are likely to fail simply because it
is difficult to satisfy the court that the decision taken has been that unreasonable.
An illustration of this point is the case of R v Cambridge District Health Authority ex parte
B [1995] 2 All ER 129. B, a ten year old girl, suffering from myeloid leukaemia had
previously undergone a bone marrow transplant which was unsuccessful. The healthauthority refused to fund further treatment. B’s father challenged their decision. The
Court of Appeal held that where there was conflicting medical opinion it was not for the
court to decide how the health authority should spend its budget where there were
competing claims on its resources.
4.3 WHEN SHOULD THE APPLICATION BE MADE?
Ordinarily any application for judicial review should be made within three months from
when the grounds of the application first arose. In St George’s Healthcare Trust v S
(Application for Judicial Review) [1998] 3 All ER 673 a case which was widely reported in
the press, the applicant had been detained under section 2 of the Mental Health Act 1983
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and subjected to a caesarean operation without her consent. She sought judicial review
of both decisions but the application was made four months after the expiry of the time
limit for such applications. The Court of Appeal held that although in most cases a delay
of this kind would be a complete bar to granting leave where the case raised genuine
matters of public importance that might as a matter of public policy constitute a goodreason to extend time.
Note that the application for judicial review is very much a last resort. In R v Portsmouth
Hospital NHS Trust [1999] Lloyds Rep Med 367 (see www.lawtel.co.uk) (another case
that was widely reported in the press concerning the dispute over the treatment of David
Glass a 12 1/2 year old child suffering from cerebral palsy) the court denied the mother’s
application for judicial review and held the more appropriate application was for a best
interests declaration with the assistance of the Official Solicitor. This case was then heard
by the European Court of Human Rights where it was held that the decision by the Trust
that it could take no active steps to prolong David Glass’s life was in breach of Article 8 o f
the European Convention on Human Rights in the absence of express authorisation by
the courts; see Glass v United Kingdom MLC 1095 [2004] Lloyds Rep Med 76 .
4.4 EXAMPLES OF SUCCESSES AND FAILURES
From reading the cases listed below it is evident that no-one has an indisputable right to
health care treatment and/ or facilities. Where the complaint is that the health carer is
failing to provide treatment, the courts have repeatedly demonstrated that they will not
intervene in hospital policy and matters of resources.
Consider:
(i) R v Central Birmingham Health Authority ex parte Walker (1987) 3 BMLR 32
(ii) R v Central Birmingham Health Authority ex parte Collier (1988) Lexis transcript 6
January
Both cases concerned “hole in the heart” babies where the respective parents brought an
application for judicial review that the decision to postpone their babies operations had
been arrived at unlawfully and unreasonably and they sought an order for mandamus to
compel the health authorities to carry out the operations. The court refused to intervene
ruling that the case was not justiciable.
(iii) R v St Mary’s Ethical Committee ex parte Harriott [1988] 1 FLR 512 . Refusal of
IVF treatment on the grounds that Mrs Harriott had been a prostitute; the court
refused to intervene.
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But there have been some successes. In R v North Derbyshire HA ex parte Fisher [1997]
8 Med LR 327 Mr Fisher, a multiple sclerosis sufferer, applied for judicial review of North
Derbyshire Health Authority’s decision not to fund his treatment with the drug beta
interferon on the grounds of insufficient resources. Previously the NHS Executive had
issued a circular requesting that all NHS hospitals should continue prescribing this drug.The respondent, however, stated that its policy was to fund the drug only as part of
clinical trials and then stated that it would not be participating in any trials. The
respondent also cancelled a £50,000 budget for the drug when it found that it had
overspent in its overall budget.
The court allowed Mr Fisher’s application finding that the respondent had failed to give
serious consideration to the advice given in the NHS circular and that its policy was not in
conformity with the circular. Hence the blanket ban on the drug was unlawful and the
decision to refuse to fund Mr Fisher’s further treatment would be quashed.
Two further cases which again caught the attention of the public were R v North West
Lancashire Health Authority, ex parte A, D&G [2000] 1 WLR 977 and R v NE Devon HA
ex p Coughlan [1999] 8 Lloyd’s Rep Med 306 see www.lawtel.com. In Coughlan, Ms
Pamela Coughlan successfully challenged the decision of her health authority to close
Mardon House as being unfair and an abuse of process after previously promising her a
home for life. In reaching the decision per curiam the court held that s.1 (1) of the NHS
Act 1977 does not place on the Secretary of State a duty to provide a comprehensive
health service but to promote such a service. Relying on the decision in Hincks see
Chapter 2 paragraph 2.1 the court held that the Secretary of State is required to take into
account the resources available and the demands on those resources. Notably the court
also found that the decision to close Mardon House was in breach of Article 8 of the
European Convention of Human Rights.
In R v North West Lancashire Health Authority, ex parte A, D&G the defendant authority
had formulated a policy which, although recognising that gender identity dysphoria
('trans-sexualism') is a medical illness, had allocated virtually no funding for its treatment.
The policy had specified that gender 'reassignment' would not be offered, subject to an
exception of overriding need in order to avoid 'serious mental illness'. The applicants'
requests for reassignment surgery were refused and they sought judicial review. Auld LJ,
discussing the decision-making process stated:
“[I]n establishing priorities-comparing the respective needs of patients suffering from
different illnesses and determining the respective strengths of their claims to treatment-it
is vital for an authority: (1) accurately to assess the nature and seriousness of each type
of illness; (2) to determine the effectiveness of various forms of treatment for it; and (3) to
give proper effect to that assessment and that determination in the formulation and
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individual application of its policy.”
Despite acknowledging that trans-sexualism is an illness, the health authority had
grouped gender reassignment alongside conditions such as minor cosmetic surgery,
tattoo removal, homeopathy and 'alternative medicine' in a list of priorities. The courtfinding for the applicants ruled that the health authority had failed to give sufficient weight
to the facts. In AC v Berkshire West Primary Care Trust [2010] EWHC 1162, a recent
case again concerning gender dysphoria treatment, the court ruled that the health
authority’s policy to refuse funding for breast augmentation was not irrational or in
contravention of the Sexual Discrimination Act 1975.
A case which made the headlines was Rogers v Swindon NHS PCT & Secretary of State
for Health [2006] EWCA Civ 392. Ann Marie Rogers, (R) appealed against a decision
refusing her application for judicial review of a decision of the respondent PCT (S) to
reject her application for funding for treatment with Herceptin, an unlicensed drug. R had
breast cancer. Her consultant stated that she had a 25% chance of remaining free of the
disease after 10 years, and a 57% chance of dying within that time. Clinical trials of
Herceptin, which had been licensed for only late stage breast cancer, indicated that it
also produced considerable therapeutic benefit in the early stages of certain forms of
breast cancer. R’s consultant had already commenced treating her with Herceptin, and
she had been paying for the treatment privately. However, she could not afford to pay for
a full course of treatment.
S had funds available to provide the drug for all patients within the eligible group who
fulfilled the clinical requirements for Herceptin treatment, and whose clinician had
prescribed it. However, its policy was to refuse funding for Herceptin unless a patient
could demonstrate “exceptional personal or clinical circumstances”. R argued that S’s
policy was irrational.
At first instance Bean J firstly held that the Secretary of States duties under the then s.3
NHS Act 1977 were not absolute, the judgments in Hincks and Coughlan applied (see
above). Bean J also ruled that the defendant’s policy requiring an applicant for Herceptin
to show exceptional circumstances among the eligible group for Herceptin was not
unlawful and arbitrary. In reaching this decision he stated that what other PCTs did could
not be determinative of the defendant’s policy nor of its lawfulness, “rationality in law is
not determined by counting heads” (para 67). Bean J firmly placed policy issues in the
political arena ruling that it was not a matter for a judge however at para 70 he did have
this to say:
“I emphasise, however, that in my view decision-makers in this difficult field
must continue to keep their policy under review in the light of the up-to-date
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evidence and any further guidance from the Secretary of State. If the
verdicts from the EMEA and NICE are unequivocally favourable the position
would plainly be transformed. Even in the meantime, if medical opinion in the
UK moves towards a consensus in favour of using Herceptin to treat early
stage HER2+ breast cancer sufferers that is something to which Trustsshould give careful consideration.”
Bean J perhaps emphasising that decisions must be constantly reviewed and the health
authorities must always be able to justify their decisions which would of course find
accord with Laws J in R v Cambridge District Health Authority ex parte B [1995] 2 All ER
129.
On appeal however Mrs Rogers was ultimately successful. The Court of Appeal held a
policy of withholding assistance save in “exceptional circumstances” would be rational
only if it was possible to envisage, and S did envisage what those exceptional
circumstances would be. However, if it were impossible to envisage such circumstances,
the policy would, in practice, amount to a complete refusal of assistance, and as such
would be irrational because it was sought to be justified not as a complete refusal but as
a policy of exceptionality. In deciding whether S’s policy was rational or not, the court had
to consider whether there were any relevant exceptional circumstances that could justify
granting funding to treat one patient, but refusing it to another within the same eligible
group. There could be no rational basis for distinguishing between patients within the
eligible group on the basis of exceptional clinical circumstances, nor on the basis of
exceptional personal circumstances. Once S had decided that it would fund Herceptin for
some patients, and that the question of cost was irrelevant, the only reasonable approach
was to focus on the patient’s clinical needs, and therefore to fund patients within the
eligible group who had been properly prescribed Herceptin by their physician. This would
not open the floodgates as only a few patients suffering from breast cancer satisfied the
criteria needed to qualify for the eligible group. Thus S’s policy was irrational and
consequently unlawful and R’s appeal was allowed.
Since the Court of Appeal decision, Herceptin has been cleared for use by the European
Medicines Evaluation Agency (EMEA), which has approved the drug for use in patients
with early stage breast cancer. This was the first time a drug had been given accelerated
assessment by the EMEA’s committee for human medicinal products. NICE has now
issued its final guidance to English and Welsh Trusts on the use of Herceptin for the
treatment of early stage breast cancer in women with HER2 disease who are free of heart
disease. Now it has NICE approval it will be very difficult for PCTs to refuse to fund it.
What this case does serve to illustrate is that decisions must be constantly reviewed and
the health authorities must always be able to justify their decisions which would of course
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find accord with Laws J in R v Cambridge District Health Authority ex parte B [1995] 2
All ER 129.
4.5 HUMAN RIGHTS?
The key question addressed in R (on the application of Condliff) v North Staffs PCT
[2011] EWCA Civ 910 was whether a policy that only considered clinical factors in
determining requests for funding unlawful in breach of Article 8? Mr Condliff had a BMI in
excess of 40kg/m2. North Staffordshire PCT would only provide laparoscopic gastric by-
pass surgery for those with BMI more than 50. It was not in dispute that Mr Condliff would
benefit from the surgery. Moreover Mr Condliff also fell within NICE guidelines which
recommended surgery. On this basis he applied for an Individual Funding Request. The
PCT had the following policy for deciding whether an individual’s circumstances were
exceptional: “non-clinical or social factors including social value judgments about the
underlying medical condition or the patient’s circumstances are never relevant”. Article
8(1) of the ECHR provides: “Everyone has the right to respect for his private and family
life, his home and his correspondence.” Thus Mr Condliff argued that Article 8 of ECHR
makes it unlawful for a PCT to adopt and individual funding request policy which
considers requests for individual funding solely by reference to clinical factors. The Court
of Appeal however were not persuaded by this argument stating that Article 8 cannot be
relied on as giving rise to a positive duty to take account of welfare considerations and
moreover even if Article 8 was applicable there were legitimate equality reasons for thePCT to adopt the policy that it did.
As a postscript Mr Condliff was however successful with his second individual funding
request (IFR) a month after the Appeal Court’s ruling, the PCT finding that the new
supporting medical evidence made his circumstances exceptional.
It is always worthwhile remembering in these often very difficult and arbitrary cases the
words of the PCT in their ethical framework, “Every decision we make to fund one
treatment means that we are effectively taking a decision not to fund another treatment…
as a result … effectiveness, equity and patient choice – must be carefully balanced .”
4.6 GOING ABROAD FOR TREATMENT - R (WATTS) V BEDFORD PCT
[2006] 3 WLR 213
Mrs Watts suffered from osteoarthritis in the hips and was in considerable pain. She was
placed on the waiting list for a hip replacement, the waiting time approximately 12
months. Her condition then deteriorated and she was placed on a higher waiting list; waittime approximately 4 months. Mrs Watts asked for an E112 certificate to pay for her
treatment abroad in another state. Her application was refused though she went and had
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the operation anyway. Mrs Watts then demanded that her costs in funding the treatment
should be refunded and she succeeded in her claim. And the likely impact? Arguably
cases of this nature will increase pressure on NHS to reduce the waiting times and
improve clinical priorities in The UK. However this decision of the ECJ which effectively
has said that if “normal” treatment cannot be obtained at home without “undue delay” itmay be purchased in the EU abroad on the basis that the cost will be met by the home
HA does have its drawbacks. Such a decision undermines the role of exceptional case
review committees. If such treatment considered normal in the EU is unavailable in the
NHS but may be obtained irrespective of NHS cash flow problems then those willing and
able to travel abroad will have greater access to expensive treatments than those who
are too old, ill or disabled to travel. As the cost of funding care in the EC increases the
funds remaining to those at home will diminish.
4.7 THE IMPACT OF THE CORPORATE MANSLAUGHTER AND
CORPORATE HOMICIDE ACT 2007
Under this Act where there is a death and that death was caused by gross negligence or
criminal negligence, or manslaughter, by the directors and managers, the organisation
may be liable. So for example potential liability would extend to the DOH, HA, health care
trusts, hospitals, LA, private providers (BUPA) and pharmaceutical companies. There is
no crown immunity. (s.11). The personal liability of doctors, nurses and health
professionals remains as before.
Under s.3 matters of public policy are excluded from the duty of care including the
allocation of public resources or the weighing of competing public interests. So it will not
be open to argue that the Secretary of State did not put sufficient resources into a
particular type of treatment or hospital. If the corporation has a proper policy for allocation
of resources then the case against them will be thin. The case may be different if the
drug, as recommended by NICE, was widely and successfully used and not very
expensive yet was denied to a patient. Note that the new law applies to partnership as
well as corporate bodies so a GP practice could be liable, in addition to an individual GP.
Generally the new law is aimed at the policies of any organisation and its administration
rather than the individual.
Further Reading
Pattinson Medical Law and Ethics 4th ed
(Sweet & Maxwell) Chapter 2
Jackson Medical Law Text, Cases and
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Materials 3r
ed (OUP)
Chapter 2
Brazier & Cave: Medicine, Patients and the Law (5th ed)
(Penguin Books), Chapter 2
Khan, Robson & Swift: Clinical Negligence(Cavendish Publishing) 2
nd edition,
pages 93,192
Mason, McCall Smith & Laurie: Law and Medical Ethics 9t ed (2011)
Oxford Chapter 11
Stauch Text, Cases and Materialson Medical Law and Ethics(Routledge, Chapters 1 & 2
For a case with local interest see:
R (on the application of Save our Surgery Ltd) v Joint Committee of Primary Care Trusts &Newcastle Upon Tyne Hospitals NHS Foundation Trust (interested party) [2013] EWHC 439.
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SUMMARY
At the end of this chapter you should be able to:
* Appreciate when a claim for judicial review may be available.
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SELF-TEST QUESTIONS - CHAPTER 4
1. In what circumstances will the courts intervene in respect of a resourceallocation decision by a health authority?
2. To what extent has the Human Rights Act 1998 affected, if at all, the above
answer?
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NOTES
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CHAPTER 5
CLINICAL NEGLIGENCE
5.1 INTRODUCTION
Suing your doctor is not a new phenomenon; there have been claims against doctors and
health authorities for many years. Everyone has an opinion on what they should be able
to expect from their health carers; combine that with the fact that as “consumers” we are
apparently more compensation minded today and one can appreciate why there is still so
much clinical negligence litigation and why strenuous efforts are being made to find viable
alternatives to the tort claim of negligence. (One question you may want to keep in mind
is this: is there a better way of dealing with clinical negligence than the tort action?).
5.2 WHY IS CLINICAL NEGLIGENCE LITIGATION DIFFERENT?
Practitioners and students should not assume that knowledge of tort law imports
knowledge of medical negligence. Tort is a most useful basis but consider the following
factors which are peculiar to clinical negligence litigation:
(i) The identity of the defendant. Who would have thought of suing their General
Practitioner fifteen or twenty years ago? Hardly anyone, considering the high
esteem in which they were (and are) held. Also there was the feeling you should
not sue people who were only doing their best for you.
(ii) The attitude of doctors. Will other doctors “tell tales” against their colleagues? Will
they be prepared to act for claimants?
(iii) The prevailing attitude of society. Are the doctors sued necessarily the “bad”
doctors? Will suing doctors necessarily make them “good” doctors?
(iv) The time the claim is brought may be several years after the incident. This may
cause problems with limitation periods and the fading memories of witnesses.
(v) Medical law is not an exact science: things can and do go wrong.
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5.2.1 Alternatives to litigation
Sometimes the client only wants to know what went wrong. In such a situation the
solicitor must explain to the client the alternatives to litigation. Note, however, the
one thing that the NHS complaints procedure will provide you with is a written
report may indicate that there is a possibility of a clinical negligence legal claim.
Additionally the Clinical Negligence Protocol now actively encourages the pursuit of
the complaints procedure before resorting to litigation (see Chapter 9).
With regard to private healthcare providers The Care Standards Act 2000
introduced a process of inspection and regulation. This Act has now been
amended by the Health and Social Care Act 2008 and the powers of inspection lie
with the Care Quality Commission. As the Care Quality Commission are now
responsible for the inspection and regulation of both NHS and private healthcare
providers and this could mean that The Local Authority Social Services and NHS
Complaints (England) Regulations 2009 (SI 2009/309) apply to non-NHS bodies as
well. The regulations state amongst other matters that all private hospitals that
provide care to NHS patients are to have complaints arrangements as if the
regulations applied to them.
Note also if the client wants disciplinary action against the person involved, then he
should contact the health carer’s professional body. Such bodies invariably have
the power to strike off or suspend the health carer.
However if the client wants financial compensation, then this will mean taking legal
action in the courts.
5.3 WHO TO SUE AND WHAT TO SUE IN?
From a practical view point if the patient decides to litigate, then the first task of the
lawyer is to decide who to sue and what to sue in.
Who are the possible defendants?
* The Trust - sue the Trust in its own name directly on the ground that it breached its
own legal duty to the client/patient or vicariously because a health care employee
of the Trust was negligent.
* The Health Authority – assuming it does not have Trust status.
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* The Private hospital - sue the hospital and / or the consultant who provided the
private treatment. Such a claim may be based in either contract or tort depending
on the circumstances.
* The Consultant - is he treating the patient privately or under the NHS? If the
former, the nature of any claim will depend on his agreement with the private
hospital; if the latter, then he will be an employee of the NHS hospital and as such
the hospital will be vicariously liable. Such an individual is always liable, if
negligent, whether financially it is worth suing him or her is doubtful.
* Health carers, such as nurses, physiotherapists etc. Either sue them personally in
tort or sue their employers vicariously in tort or, if the treatment was provided
privately, in contract.
General Practitioner – GPs – the action is against the GP in question (and he is
vicariously liable for his staff) and /or the partnership.
5.4 INGREDIENTS FOR A CLINICAL NEGLIGENCE CLAIM
Substantively there are four “hurdles” which the patient claimant has to overcome; failure
to get or over any of the hurdles will be fatal for the success of the claim. Also it should
be remembered that the onus of proof is always on the claimant and the standard ofproof is on the balance of probabilities.
The four substantive hurdles are:
a) duty of care;
b) breach of that duty of care (also referred to as standard of care);
c) causation i.e. the link between breach and damage;
d) foreseeable damage.
The major procedural “hurdle” is the issue of limitation.
Further Reading
Stauch Text, Cases and Materials on Medical Law and Ethics
(Routledge, Chapters 6, (Introduction only)
Brazier & Cave: Medicine, Patients and the Law (5th ed) (Penguin
Books), Chapter 8 pages 218-222
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Khan, Robson & Swift: Clinical Negligence (Cavendish Publishing) 2n
edition, Chapter 3 pps 86; 94-104
Pattinson Medical Law and Ethics 4t ed (Sweet & Maxwell)
Chapter 3
Jackson Medical Law Text Cases and Materials 3r
ed (OUP)
Chapter 3 (introduction only)
Herring: Medical Law and Ethics 4th
ed (OUP) Chapter 3
(introduction only)
SUMMARY
At the end of this chapter you should be able to:
* identify the problems associated with a clinical negligence claim;
* identify the potential defendants in a clinical negligence claim;
* understand when it is appropriate to bring an action in contract and when the
claim should be brought in negligence.
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SELF-TEST QUESTIONS – CHAPTER 5
1. In what circumstances could the patient have a contractual claim and a claim in
tort?
2. Why is it inappropriate to sue an employee of the health authority personally?
3. What must be shown to succeed in a clinical negligence claim?
.
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NOTES
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CHAPTER 6
THE DUTY OF CARE
6.1 INTRODUCTION
“In practice, within the NHS, the existence of a duty of care is seldom challenged ”(CMO
2003 51)
To bring a clinical negligence claim the claimant must first establish that a duty was owed
to him by the defendant. In doing this a number of questions will have to be answered
including:
(i) who owes the duty;
(ii) when exactly does the duty arise;
(iii) what is the extent of the duty;
(iv) is there one duty or a number of duties?
6.2 WHAT IS THE NATURE OF THE DUTY?
This will depend on whether the patient is being treated under the NHS or is receiving
private treatment. The NHS patient will be owed a duty in tort by the health carer(s) and /
or the health carer(s) employer(s) and this will commence as soon as treatment is
undertaken. The private patient will also be owed a duty in tort, however, alongside that
the private patient may rely on the contractual obligations that he is owed under the
contract he has with the health carer.
The scope of the duty owed by a Health Authority in relation to operational systems andprocedural arrangements for the provision of health care was considered in the case of
Hardaker v Newcastle HA & Chief Constable of Northumbria [2001] All ER (D) 157. The
claimant, who was an experienced diver developed decompression illness (DCI) while
diving off a sunken wreck one Sunday in 1994. There was a decompression chamber at
the RVI which was within a short flying time from the dive site but it was closed at
weekends. The Northumberland Police National Diving School at Sunderland also had a
chamber and there was an arrangement that the police chamber would be made
available as a back-up facility to emergency cases when the RVI was closed. Following a
medical assessment at the RVI as required by the arrangement, the claimant was taken
to the police chamber which there was some delay in opening. The claimant survived but
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sustained serious permanent disabilities. He alleged that, but for the delay caused by the
Health Authority’s arrangements for dealing with such cases, he would have made a full
or at least a better recovery.
It was held that the Health Authority owed the claimant a duty of care but that the dutywas qualified by the resources available. The Health Authority could not be held to be
negligent for failing to apply sufficient resources to the RVI chamber to keep it available at
all hours. Cases of DCI were relatively rare. It could not sensibly be suggested that
every coastal town should have a decompression chamber. Moreover, it was not
negligent of the Health Authority to make an arrangement requiring a suspected case of
DCI to attend the RVI for diagnosis because if the patient was not suffering from DCI he
could be admitted and dealt with there. Also, if the patient was suffering from an illness
such as pneumothorax which could be mistaken for DCI, it would have been dangerous
to have sent him to Sunderland. In any event the claim would have failed on the ground
of causation as there was no evidence to justify a finding that if the compression had
begun earlier the claimant would have made a full or better recovery.
6.3 IS THERE ONE DUTY OR SEVERAL DUTIES?
The English courts have answered this question by stating that there is only one duty, but
for simplicity, it is divided into separate components e.g. the duty to diagnose, the duty to
provide information (as defined by Bolam v Friern H.CC [1957] 2 All ER 118), the duty to
provide post-operative care etc. This means that the Bolam standard is applicable to all
forms of medical treatment.
In Chapter 6 you will see that the Bolam standard has been the source of constant
criticism as many academics and non-academics alike feel it allows the medical
profession to dictate what is the appropriate standard. The area where it has been
subjected to the strongest criticism is in relation to the disclosure of risks/information to
the patient. See for example the dissenting judgment of Lord Scarman in Sidaway vBoard of Governors of Bethlehem Hospital [1985] 2 WLR 480 ) where he attempted to
introduce the doctrine of informed consent and contrast this with the Australian case of
Rogers v Whittaker [1993] 4 Med LR 79 ) (these cases are considered in more detail in
Chapter 7).
6.4 WHEN DOES THE DUTY OF CARE BEGIN AND END?
The duty will begin when treatment begins and will end when the treatment is completed
or the patient or health carer dies. So, for example in the case of a GP treatmenteffectively begins when the patient attends the GP’s surgery or in the case of a consultant
when he sees the patient following a referral.
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the child whether there were any risks as a result of having chickenpox in pregnancy, that
it was incumbent upon the hospital doctor to discover what advice had been given by the
GP and to correct it. The Court of Appeal, however, held that the hospital doctor was
under no such duty and this argument went far beyond what was intended by Sidaway .
The mother had expressly asked the GP if her baby would be alright whereas no suchquestion had been put to the hospital doctor. After being told that the mother was aware
of the risks of chickenpox and was unconcerned the hospital doctor was entitled to
assume that she had been given the correct advice by a competent GP.
In contrast in the case of Deriche v Ealing Hospital NHS Trust [2003] MLC 1083, another
case in relation to severe damage sustained by a child after the claimant contracted
chickenpox whilst pregnant, the court held that a consultant should be satisfied that a
patient fully understood the risks involved. It was not enough to infer this from the
counselling of a previous doctor. The case ultimately failed on causation.
Once the duty has commenced it will extend to all forms of treatment whether or not the
patient is seen by the health carer e.g. the doctor who gives the nurse instructions for the
patient’s treatment, see Barnett v Chelsea and Kensington HMC [1968] 1 All ER 1068.
6.5 WHO OWES THE DUTY?
All those persons involved in the care of the patient, e.g. doctor, nurse, physiotherapist
etc. Inexperience has no bearing on the nature of the duty, see Wilsher v Essex A.H.A.
[1986] 3 All ER 801 where a junior doctor unsuccessfully argued that he did not have to
meet the same standard of care as his more experienced counterpart. The Court of
Appeal held that once the doctor had held himself out as competent to perform the
treatment then the claimant was entitled to assume that he had the necessary expertise.
This decision was obviously based on a sense of justice for claimants for whilst one could
have sympathy for the junior doctor who was “thrown in at the deep end”, a claimant
should not be penalised simply because he had the misfortune to be treated by someone
with limited experience. The Court of Appeal went on to say that the health authority
could be at fault for placing a junior doctor in a situation which he was ill equipped to deal
with. Thus a health authority could be directly liable for a failure in its organisational /
administration procedures in addition to being vicariously liable for the acts or omissions
of its employees. This does not mean that where the fault has arisen because of poor
resources that the court will impose direct liability, see Chapter 2 Judicial Review, rather
the court is looking at the operational set up, see for example Cassidy v Minister of
Health [1951] 2 KB 343 and Bull v Devon A.H.A. [1993] 4 Med LR 117). In the latter case
direct liability was imposed because the hospital should have had more staff involved to
deal with a difficult twin birth.
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The proximity test was again in issue in Farraj v King’s Healthcare Trust and Another
[2006] EWHC 1228. The question was whether there was sufficient relationship of
proximity between a laboratory (C) used by the trust to test samples of tissue, and the
claimants who were seeking damages for wrongful birth. F, the claimant, was seeking
damages for the wrongful birth of her son who had been born with a serious hereditaryblood disease which the family alleged should have been diagnosed during the
pregnancy. C had no direct connection with the family but had tested tissue for pre-natal
DNA analysis on behalf of the trust. F, the claimant, had provided a poor sample and the
laboratory argued that it offered only a limited service costing £80. The trial was of a
preliminary issue as to whether C owed a duty of care to F. The court held there was
sufficient proximity between the family and C for a duty of care to be established. It did
not matter that the parents and C did not communicate. The family would have expected
that there would be several processes involved in the testing of the samples and C would
be aware that family relying on the advice that it gave. As the hospital would be
vicariously liable for negligence on the part of staff no difference would be made between
a hospital and a private laboratory and hence C owed a duty of care to F. C was held
two-thirds liable and the trust one third liable as the court held the hospital should have
enquired of C whether the sample was a reliable source for genetic testing. This latter
finding however has been successfully appealed by the trust, see Farraj v (1) King’s
Healthcare NHS Trust (2) Cytogenetic DNA Services Ltd [2009] EWCA Civ 1203 . The
Court of Appeal held that the trust had entrusted the analysis and diagnosis of sampling
to an apparently competent laboratory and therefore there was no reason to impose a
non-delegable duty to P. Consequently C was held 100% liable.
Two other cases which are of interest on the scope and nature of the duty owed are West
Bromwich Albion Football Club Ltd v El-Safty [2006] EWCA Civ 1299 and St George v
Home Office [2008] EWCA Civ 1068. In West Bromich an independent orthopaedic
surgeon was held not to owe a duty of care to the football club either in contract or in tort
in respect of the negligent treatment he administered to P, one of the club’s players. As
the surgeon’s fees were settled by an insurance scheme taken out by the club it was heldthat the surgeon had not assumed any responsibility to the club in respect of foreseeable
economic loss. The St Georges case is of interest as it concerned the scope of duty owed
by a prison doctor. The prisoner, S was addicted to drugs and alcohol and had previously
suffered withdrawal seizures and epileptic fits. The prison were aware of this and yet
allocated S the top bunk in a prison cell. S subsequently fell and sustained brain damage.
The prison was found in breach of their duty of care and additionally the prison doctor
was found in breach for not arriving quickly enough.
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Finally in Woodland v Swimming Teachers Association [2013] UKSC 66 the Supreme
Court recognised that there might be in certain circumstances a non-delegable duty may
be owed by a defendant in respect of negligent care provided by a third party with whom
they sub-contract. In Woodland such a duty as owed by a local authority to a pupil
attending a swimming lesson conducted by an independent contractor
6.6 VICARIOUS LIABILITY
As mentioned in the preceding paragraph a health authority or trust will be vicariously
liable for the torts of its employees. In the case of an agency nurse whether or not the
hospital is vicariously liable will depend on the terms of the contract with the agency,
whether the hospital has chosen a reputable agency and whether the nurse was properly
instructed. Likewise in the case of private patients being treated in an NHS hospital,
ultimately where liability lies will depend on the nature of the agreement between the
private contractor and the NHS hospital.
Locums, however, pose a unique problem. A locum is not an employee of the GP;
however, a GP has an obligation to select a competent locum. The action should
therefore be brought against the locum as he is an independent contractor but if it is
established that the GP’s selection procedure was inadequate then he and/ or the
practice may also be directly liable, see the Canadian case of Rothwael v Rees (1988) 54DLR (4
th) 193 . Note that the GP or the medical practice will be vicariously liable for the
staff it employs.
6.7 DUTIES OWED BY SPECIFIC GROUPS
The following paragraphs examine the nature of the duty owed by certain identifiable
groups of health carers which have recently been the focus of judicial debate or are
subject to specific legislation.
6.7.1 OCCUPATIONAL HEALTH CARERS
Often the situation arises where an employer requests an employee to undergo a
medical examination. What is the nature of the duty owed, if any, by the health
carer who performs that examination and is also another employee? This matter
has been considered in two cases, Baker v Kaye [1997] overruled by Kapfunde v
Abbey National plc [1999] 2 Lloyds Rep Med 48 . In the latter case Kennedy LJ
said,
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“….the position of Dr Daniel is plainl y comparable with that of social
workers and the doctors in X v Bedforshire CC [1995] 2 AC 633 or
with that of a doctor examining for the purposes of life insurance….in
my judgment there was no special relationship between Dr Daniel and
the appellant to give rise to a duty of care. I prefer that formula from tosaying there was no sufficient proximity, but it amounts to the same
thing.”
In these cases the courts were at pains to point out that the doctor does not
undertake to treat the person as a patient and therefore his only duty will be not to
damage him in the course of the treatment.
Do you think this will always be the case?
6.7.2 THE AMBULANCE SERVICES
In Kent v Griffiths, Roberts & London Ambulance Services [1999] 2 Lloyds Rep
Med 58 it was held that ambulance services were under a duty to attend with
speed and care and are not in the position of a volunteer or bystander. An appeal
by the London Ambulance Services was then dismissed by the Court of Appeal,
see [2000] 3 Lloyd’s Law Rep Med 109. Lord Woolf said that it was wholly
inappropriate to regard the LAS and its employees as volunteers as the LAS were
under at least a public law duty. The LAS were simply providing a health service
and health services under the NHS Act attracted a duty of care. There was no
reason why the position of ambulance staff should be any different from that of a
doctor or nurse and once the LAS accepted the call a duty of care was established.
See also the case of Oakes v (1) Neininger (2) Brown (3) Greater Manchester
Ambulance Service [2008] EWHC 548 where an ambulance crew where found
negligent for not referring the claimant to hospital. In the more recent case of Taafe
v East England Ambulance Service NHS Trust [2012] EWHC 1335 paramedics
were found liable for failing to take a proper history and proper assessment of thepatient’s symptoms and for ignoring an abnormal ECG printout.
6.7.3 A GP’S DUTY TO AN ACCIDENT VICTIM
A GP’s terms of service will create a formal doctor/patient relationship between the
GP and an accident victim in two situations:
(i) if he is immediately required to attend the injured person and the accident is
in his practice area; or
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prescription was correct or whether there had been some error in this case. The
branch procedures manual covered such a situation and in failing to follow the
procedures set out in the manual and in not enquiring of E or H whether the
prescription was correct G had fallen below the standard of care which would
reasonably be expected of a competent pharmacist.
This case is also of interest from a causation perspective see paragraph 7.10.2.
6.8 DUTIES OWED TO PARTICULAR PARTIES OR IN PARTICULAR
SITUATIONS
The paragraphs below focus on two areas, (1) the duty owed to certain special groups
and (2) the duty owed in somewhat unusual situations. Both have been subject to judicial
debate hence there special treatment.
6.8.1 IS THERE A DUTY TO THE EMBRYO?
The answer to this question is yes but it is dependent on the child being born, see
Burton v Islington H.A. [1993] 4 Med LR 8. This means that only when the child is
born can he sue for injuries inflicted whilst in the womb. In some jurisdictions this
will extend to pre-conception negligence see for example X v Y & Pal and others
[1992] 3 Med LR 195 ).
Alongside the common law position is the statutory duty defined in the Congenital
Disabilities (Civil Liability) Act 1976 which defines the statutory duty to the embryo
and applies to all births after 22 July 1976. Under the Act a child may sue for any
act which affected either parent in his/her ability to have a normal child or any act
which affected a mother during pregnancy or a child during birth. The Act appears,
however to rule out “wrongful life” claims, see McKay v Essex AHA [1982] QB 1166
and Chapter 8 Damages paragraph 8.6.
6.8.2 CAN A DUTY BE OWED TO A THIRD PARTY?
In English law the proposition is still that A cannot be liable for harm caused by B to
C, see for example, Smith v Littlewoods [1987] 1 All ER 710). Only in very
exceptional circumstances will the court impose a duty; usually where one party is
capable of exacting some degree of control over another, see Home Office v
Dorset Yacht [1970] 2 All ER 294.
In Goodwill v British Pregnancy Advisory Service [1996] 2 All ER 161 the
defendants had performed a vasectomy for a married man. Some three years later
he began a relationship with the claimant. Thinking that the man was now sterile
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the claimant did not use any contraceptive measures; she later became pregnant.
The vasectomy had undergone a spontaneous reversal. The claimant sued the
defendants and on appeal her claim was dismissed. The Court of Appeal held that
the defendants were not in a sufficient or any special relationship with the claimant
to give rise to a duty of care. At the time the vasectomy was performed she waslike any other woman in the world: simply a potential future sexual partner of the
man and therefore the defendants had no responsibility to her. In addition, the
case of Palmer v Tees Health Authority and Hartlepool & East Durham NHS [1999]
9 Lloyd’s Rep Med 351 emphasised the need for proximity of relationship between
the defendant and the third party. In this case the court found that the health
authority was not liable for the death of a child murdered by a psychiatric outpatient
confirming the restrictive approach the courts have taken to this type of scenario as
illustrated by Hill v Chief Constable of West Yorkshire [1989] AC 53. Considering
this in mind then one wonders at the wisdom of the solicitors advising the claimant
in the case of Nunes v Agrawal (Re N) [1999] 7 Lloyd’s Rep Med 257 where a
victim of alleged rape and buggery asserted that the medical practitioner who
examined her owed her a duty to attend court and give evidence at the trial of her
alleged assailant. The court held that the patient / doctor relationship did not arise
the duty was simply to take care in the course of the examination not to make the
patient’s condition worse.
The American courts, however, have on more than one occasion held that a doctor
can owe a duty to a third party in respect of the activities of his patient.
In Tarasoff v Regents of the University of California (1976) 551 P 2d 334 the
defendant physician's patient had repeatedly threatened to kill a young woman.
These threats were uttered to the physician on several occasions. Unfortunately
the patient carried out his threat and the deceased woman's parents sued the
defendant for failing to warn the young woman or the parents. The claim
succeeded.
In Bradshaw v Daniel (1993) 854 S.W. 2d 865 the claimant's father had been the
patient of the defendant physician. He had died of Rocky Spotted Mountain Fever.
The claimant's mother, who was not a patient of the defendant, also contracted and
died of the same disease. The claimants brought an action on behalf of their
deceased mother arguing that the defendant should have warned their mother
notwithstanding the fact that she was not his patient. The court agreed with this
reasoning holding that in this instance the defendant did owe a duty of care to a
third party.
It should be emphasised that in both cases a duty was only imposed because there
was a degree of control exercised by the defendant over his patient and the third
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party was either identified or identifiable and it was foreseeable that harm would
result if the third party was not warned. These factors are also present in the GMC
guidance for dealing with HIV patients, which state that, where an HIV patient
refuses to give his consent to disclosure of his condition to a third party, then the
doctor may disclose where there is a specific risk to an identifiable individual, e.g. asexual partner or spouse. Note the strict limitation on disclosure to an identifiable
individual. Thus a patient who has a number of sexual partners may be safe in the
knowledge that a doctor would not be able to reveal his condition to any party for in
such a situation who would the doctor disclose to? In addition any disclosure
should only take place after all other options have been explored e.g. several
attempts to obtain the patient’s consent, counselling etc. Such is the social stigma
attached to someone who is HIV and the need to protect those affected by it that
any disclosure should never become a matter of routine but only take place within
the strict parameters outlined above.
In JD v East Berkshire Community Trust [2005] UKHL 23; [2005] 2 WLR 993 the
claim was brought by a mother whose son appeared to suffer from severe allergic
reactions. The son was referred to the defendant hospital and assessed. During
this assessment the clinicians concluded that the mother was exaggerating his
symptoms and alleged that she was suffering from Munchausen’s syndrome by
proxy. A referral was made to Social Services. However later investigations by a
different consultant showed that the claimant’s son symptoms were in fact genuine
and therefore it had been inappropriate to diagnose the claimant as suffering from
Munchausen by proxy. The claimant pursued a claim against the Trust alleging that
the diagnosis of Munchausen by proxy was negligent and that as a result she had
suffered psychiatric injury.
On appeal to the House of Lords the claims failed but perhaps more importantly
their Lordships held that the defendant health authority did not owe a duty of care
to a person suspected of child abuse to investigate the case without carelessness;
the only requirement is that the investigating person should have acted in good
faith. Further to find such a duty would not be fair just or reasonable because such
a duty involved conflicting interests and was not justified. Notably it would be also
be opposite to the policy of settled law which was opposed to the granting of
remedies to third parties for the effects of injuries to other people.
Clearly policy had a part to play in this decision. Health professionals have been
allowed to retain immunity from claims in negligence when detecting child abuse.Once of the reasons for this is that the parents could bring a human rights claim
that their convention rights have been infringed. Note however the dissenting
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judgment of Lord Bingham which does set out grounds for allowing the appeal and
also hints that the common law should evolve and create new remedies i.e.
perhaps breach of rights instead of breach of duties to form the basis of liability
rather than let all these claims be swept away by the Convention.
Although not a case of clinical negligence the decision in Selwood v Durham CC
[2012] EWCA Civ 979 is of interest. In Selwood the issue was whether two NHS
trusts owed a duty of care to a social worker who suffered injuries at the hands of
one of their patients. In brief the claimant was a social worker employed by
Durham CC. She was the designated social worker for a girl who father (GB)
attacker her with a knife causing serious injuries. Her claim was against her
employer (first defendant), the NHS Trust which ran the mental health services
team treating the daughter and GB (second defendant), and an NHS Trust which
ran a mental health admissions ward and whose employees treated GB (third
defendant). The three defendants had signed a protocol entitled “working together
in the delivery of services to adults and children.” During an outpatient assessment
with the second defendant GB had said that there was someone involved in the
family proceedings who he wished to harm but that he was trying to avoid her. He
then subsequently said he was having violent thoughts about certain individuals
involved in his family’s care. This information was passed to the CC and the third
defendant. There then followed other instances of GB having paranoid delusions
about specific individuals culminating with GB informing the third defendant that if
he saw the claimant he would kill her on the spot. This threat was communicated to
the second defendant but not the claimant or her employer. Not being aware GB
had left hospital the claimant attended GB home for a case conference where he
attacked her.
On appeal it was held that it was at least arguable that the defendants did owe a
duty to the claimant. The Court of Appeal made reference to the joint protocolbetween all three defendants and that it was reasonable to infer that there was a
responsibility to reduce or avoid any foreseeable risk of harm to which an
employee was exposed. Moreover there was a policy issue, namely social workers
who work in the field of child abuse, as this case was, should be protected as far
as possible.
The implications for practice of the Selwood decision may be significant. The
decision suggests that public bodies engaged in joint-working activities may owe
more onerous obligations to the employees of partner organisations than might
previously have been assumed. Moreover it would suggest that where one of the
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care partners obtains information that suggests another’s employee may be at risk
the case for disclosure of that information may be compelling.
6.8.3 NERVOUS SHOCK AND THIRD PARTIES
This is dealt with in chapter 9.
Further Reading
Stauch Text, Cases and Materials on Medical Law and Ethics
(Routledge, Chapter 6 pp 256-270
Brazier & Cave: Medicine, Patients and the Law (5t ed) (Penguin
Books), Chapter 7
Khan, Robson & Swift: Clinical Negligence 2n
ed (Cavendish Press) Chapter 3
Khan & Robson: Personal Injury Law and Medical Review [1995] Vol 2
No1 page 44
Jackson Medical Law Text Cases and Materials Oxford University
Press Chapter 3 pp 104-112
Pattinson Medical Law and Ethics 4th ed (Sweet & Maxwell)
Chapter 3
Herring: Medical Law and Ethics 4th ed (OUP) Chapter 3 pp 105-129
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SUMMARY
At the end of this chapter you should be able to:
* identify when the duty begins and ends;
* explain what is the nature of this duty;
* identify who can owe a duty;
* explain the difference between direct and vicarious liability.
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SELF-TEST QUESTIONS – CHAPTER 6
1. Who owes the duty of care in a clinical negligence claim?
2. In what circumstances will the contractual obligations owed to a private patient
differ to the obligations owed in tort to his NHS contemporary?
3. If a GP refers a patient to a consultant does his duty of care end there? If not
where does it end?
4. In what circumstances might a health authority be found directly liable as
opposed to vicariously liable for the act / omissions of its employees?
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NOTES
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CHAPTER 7
THE STANDARD OF CARE
7.1 INTRODUCTION
Once the claimant has established that the defendant owed him a duty of care he must
then go on and show that the defendant has failed to reach the standard of care expected
of him. In determining this question the courts apply what has become known as the
"Bolam test" which originates from the case of Bolam v Friern H.C.C. [1957] 2 All ER 118
. In that case McNair J said:
“The test is the standard of the ordinary skilled man exercising and
professing to have that special skill. A man need not possess the highest
expert skill; it is well established law that it is sufficient if he exercises the
ordinary skill of an ordinary man exercising that particular art.”
In Bolam the claimant had argued that the defendant was negligent in his administration
of electro-convulsive therapy and he alleged, inter alia, that the defendant should have
warned him of the risks involved in the treatment and that he should have been restrained
manually. The claimant's case failed because the defendant was able to demonstratethat he had acted in accordance with a practice adopted by his colleagues.
7.2 What is the required standard of care?
7.2.1 Objectivity
It is an objective test – it is what a reasonable and responsible group of health
carers with similar skills to the defendant would or would not have done - seeBrooks v Home Office (1999) The Times 17 Feb 1999 . It was argued by the
defendant in this case that the claimant was not entitled to receive the same
standard of care by a prison doctor as she would expect to receive outside prison
but thankfully this argument failed. But is it a legal standard or a medical
standard? Generally like is compared with like, for example a specialist must meet
the standard of care of a specialist practising in his particular field of medicine,
likewise a GP must meet the standards expected of a reasonably competent GP.
The standard remains constant no matter what the treatment - Bolam is applicable;
though there have been attempts to introduce a different standard in the area of
advice and disclosure of risks though there have been attempts to introduce a
different standard in the area of advice and disclosure of risks (see later). In the
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recent case of Meiklejohn v St George’s Healthcare Trust and Homerton University
Hospital NHS Foundation Trust [2014] EWCA Civ 120 the Court of Appeal rejected
an argument that a consultant haematologist should have to reach a higher
professional standard of care because she happened to be internationally
renowned. The appropriate standard of care was that of a tertiary specialist inaplastic anaemia.
Inexperience is no defence; a junior doctor cannot excuse himself because of his
lack of experience in the job. See for example Wilsher v Essex A.H.A. [1986] 3 All
ER 801 . Once the health carer has held himself out as able to meet the task in
hand then the patient is entitled to assume that the doctor has the competence to
fulfil that task. In some ways this is nothing new; see for instance the position of
learner drivers and refer to previous notes on tort. To escape liability the junior
(inexperienced) doctor should seek the advice of a more senior colleague (as was
the case in Wilsher ). The liability will then fall upon the more senior colleague
should he fail to give the requisite level of supervision. In the case of a nurse he is
usually acting on the doctor's instructions but it must be emphasised that the nurse
cannot follow those instructions blindly if he believes them to be erroneous or
illegal.
7.2.2 Accepted medical practice
Bolam – “ A doctor is not guilty of negligence if he has acted in
accordance with a practice accepted as proper by a responsible body
of medical men skilled in that particular art... Putting it the other way
round a doctor is not negligent, if he is acting in accordance with such
a practice, merely because there is a body of opinion that takes a
contrary view”
The Bolam test demands that the doctor comply with an accepted medical practice.It then goes on to say is that it does not matter if there is more than one body of
medical opinion on the issue in question, the defendant simply has to show that he
acted in accordance with the practice of one particular and responsible group of
doctors. The rationale behind this approach is the view that the courts are not the
forum for the medical profession to squabble over what is the right practice. In any
event since medicine is an imprecise science there must be and will be more than
one way of treating a patient. Why should the courts – a non-medical body – say
which is the more preferable form of treatment in any given situation? They should
not.
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Having stated that there can be more than one practice does it matter how many
medical practitioners follow that practice? Apparently not, if the case of DeFreitas
v O'Brien & Connolly [1995] 6 Med LR 108 is to be followed. There the claimant
argued that the practice had to be followed by a “substantial body” of medical
practitioners. The Court of Appeal held that this approach was erroneous. Whetheror not a practice was accepted could not be determined by "counting heads". Thus
it could follow that the views of two could outweigh the views of fifty. Can this be
right? Can it not be argued that if fifty people support a practice it is more arguable
that there is an accepted practice? In Walsh v Gwynedd HA it was said that only
one doctor could not constitute a body of medical opinion.
7.2.3 Current practice
The practice itself must be current. This means that at all times the health carer
must endeavour to keep up to date. Like any other profession the doctor will be
judged by the prevailing English standard at the time. (See Roe v Minister of
Health [1954] 2 QB 66 and Crawford v Charing Cross Hospital The Times Dec
1953 and Boustead v North West SHA [2008] LS Law Med p 471.
One obvious problem caused by this rule is in determining when a health carer
should have adopted a new practice; this will depend to a large extent on the
length of time the knowledge has been available but there is no absolute rule.
In Kent v Griffiths, Roberts and London Ambulance Service [1999] 10 Lloyd’s Rep
Med 424 the claimant’s claim against her general practitioners failed despite the
fact that the defendant general practitioner had failed to follow the latest BMA
guidelines for the treatment of asthma, the court ruling that if the failure to follow
guidelines were the only deciding factor as to whether negligence was proven then
that would mean rejecting clinical judgment of the treating practitioner. Guidelines
are no substitute for clinical judgment. Whilst agreeing with this ruling one
wonders in what situations the court will find that clinical judgment has erred given
their reluctance to challenge medical opinion, see paragraphs 6.3 onwards.
7.3 WHEN WILL THE DEFENDANT BE IN BREACH OF THE STANDARD OF
CARE?
7.3.1 When he departs from accepted practice
This is not an absolute rule; each case will turn on its facts.
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One area where Bolam has caused the most consternation is in relation to the
disclosure of risks. It has been argued that the patient should be told all the risks
associated with the procedure and not just what the medical profession thinks the
patient should know. There is certainly something to be said for this view; the
Australian courts, for example, have resoundly rejected Bolam in this area and heldthat the patient should be told everything when he needs to make an informed
choice about his treatment. In Rogers v Whittaker [1993] 4 Med LR 79 the
Australian High Court said that a doctor’s duty was not decided “solely or even
primarily by reference to the practice followed by or supported by a responsible
body of opinion in the relevant profession.” To see the injustice that Bolam may
cause contrast this case with the English case of Sidaway v Board of Governors of
Bethlehem Hospital [1984] 1 All ER 1018. Whereas the Australian courts were
prepared to find that the defendants’ were in breach of their duty of care for failing
to disclose a 1/14,000 risk to the claimant, the English courts were not prepared to
do the same in the Sidaway case where the risk was 1-2%. There were some
attempts to be more innovative in the lower courts, see for example the judgments
in Smith v Tunbridge Wells [1994] 5 Med LR 344 and Joyce v Merton, Sutton &
Wandsworth H.A. [1996] 7 Med LR 1 where at first instance Overend J said that
the defendant would not be negligent if he acted in accordance with accepted
practice, “provided that clinical practice stood up to analysis.” In the Court of
Appeal Roch LJ commented on this direction and said,
“.... the decision of negligence or no negligence....must at the end of
the day be one for the courts.”
Moreover in Fallows v Randle [1997] 8 Med LR 160); www.lawtel.co.uk (a failed
sterilisation case) the Court of Appeal held that where there was a conflict of
medical evidence then the Bolam principle had no application, it was simply a
question of fact which had to be determined on a balance of probabilities, (see
further Penney, Palmer and Cannon v E Kent H.A. [2000] Lloyd’s Rep Med 41
discussed below).
Note however following the Montgomery decision the application of Bolam to cases
of risk disclosure has been firmly rejected by the Supreme Court (see below).
7.3.3 When the Practice does not have a Logical Basis
The House of Lords seized the opportunity to re-explain the Bolam rule in Bolitho v
City and Hackney H.A. [1997] 4 All ER 771); and made some interesting
observations on the status of the Bolam test. It was not enough to glibly rely on
medical opinion, the opinion itself must, commented the Lords’, have a “logical
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basis”. The court therefore must be satisfied that the experts in question had
weighed up the risks and advantages associated with a particular procedure and
had reached, in Lord Browne-Wilkinson’s words, “a defensible conclusion”.
Whether this was a new approach was debatable as the Lords’ acknowledged that
it would only be “a rare case” where the court would find that the opinion did notmeet these requirements. But just how many of these “rare” cases would there be
warranting the new approach?
In Penney, Palmer and Cannon v E Kent H.A. [2000] Lloyd’s Rep Med 41); the
Court of Appeal found that the defendant Health Authority was liable to the
claimants in respect of the negligent assessment of their cervical smear tests.
Expert opinion differed yet the Appeal Court held that that did not necessarily
provide the solution to the dispute on liability. The court relied on the judgment in
Bolitho and further held that the Bolam test had no application when the judge was
required to make findings of fact even where the findings of fact were the subject of
conflicting expert opinion. Bolam did not apply where there was no question of
acceptable practice. In this case the court had to decide as a question of fact “what
was to be seen on the slide” and the court found that the cytoscreener should have
at least been aware that Mrs Penney’s slide was difficult to interpret and referred
the slide for further examination. Applying the risk benefit approach canvassed in
Bolitho the judge balanced the need not to give a false negative result against the
need not to give a false positive. The Court of Appeal preferred the expert
evidence of the claimant and found that the abnormalities could be seen but
stressed that it was not rejecting the general approach of the defendant. The
approach taken in Penney was endorsed in Conway v Cardiff and the Val NHS
Trust [2004] EWHC 1841.
In Marriott v W Midlands HA (and SE Staffs AHA) and Patel [1999] 1 Lloyds Rep
Med 23 [1999] the Court of Appeal applied Bolitho in a non-disclosure case.
Beldam LJ held that the judge at first instance had been correct in carrying out her
assessment of the risk. At (at p 28):
“ It was open to the judge to hold that, in the circumstances as she
found them …. it could not be a reasonable exercise of a general
practitioner’s discretion to leave a patient at home and not refer him
back to hospital.”
Pill LJ whilst agreeing that the appeal should be dismissed held that Bolitho was
not really applicable in this instance as the expert evidence only pointed one way.
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See also Zinzuwadia v Home Secretary (2000) and Calver v Westwood Veterinary
Group [2001] 1 Lloyd’s Rep Med 20, MLC 0350.
7.3.4 Bolitho and Risk Disclosure
Lord Browne-Wilkinson had notably omitted the area of risk disclosure from his
judgment in Bolitho, some would say because Bolitho was not intended to be of
general application to all areas of clinical negligence, another view being that his
Lordship already perceived a different test being applied to what is in reality a non-
clinical area. In Pearce v United Bristol Healthcare NHS Trust [1999] 48 BMLR
118; MLC 0086; see www.medneg.com the health carer had failed to point out to a
pregnant woman that there would be an increased risk of stillbirth as a result in the
delay in delivery of her 6th
child. The claim in negligence was dismissed but Lord
Woolf said
“Obviously the doctor, in determining what to tell a patient, has to take into
account all the relevant considerations, which include the ability of the
patient to comprehend what he has to say to him or her and the state of the
patient at the particular time, both from the physical point of view and an
emotional point of view. There can often be situations where a course
different from the normal has to be employed. However, where there is what
can realistically be called a "significant risk", then, in the ordinary event, as I
all have already indicated, the patient is entitled to be informed of that risk.”
The courts continued to refine the extent of a doctor’s duty and the appropriate
standard of care in the area of risk disclosure.
In Birch v University College London Hospital NHS Foundation Trust [2008] EWHC
2237; although the neurosurgeons and neuro-radiologists had not been negligent
they were held liable for not properly obtaining the claimant’s consent because
they should have discussed the alternative treatments with the claimant and the
comparative risks. Had they done so the claimant would have declined the catheter
angiography and so avoided the stroke.
In Nathanson v Barnet & Chase Farm Hospitals NHS Trust [2008] EWHC 460 N,
who suffered from a series of psychiatric illnesses, fell down some stairs whilst
visiting her son from Australia. She was taken to hospital and examined by a
doctor who made no enquiries regarding her psychiatric condition as she appeared
lucid. The doctor told N of the necessity for deep breathing to avoid bronchial
infection and also prescribed her pain killers. Thereafter her physical health
deteriorated and she had symptoms of her psychiatric illness. Her son was
unaware of the doctor’s advice of the necessity of deep breathing and decided not
to force N to take her analgesics. N died and her son brought a claim arguing that
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the advice given to N was inappropriate and insufficient and that the treating doctor
should have taken a full medical history. However the court opined that this was
going too far and that unless there was something to suggest that a patient had a
psychiatric or medical history that might be relevant to her treatment or
understanding there was no general requirement to ask about her medical orpsychiatric history.
However in Meiklejohn v St George’s Healthcare Trust and Homerton University
Hospital NHS Foundation Trust [2014] EWCA Civ 120 (considered above) the
Court of Appeal reiterated that the duty to advise and warn about diagnosis and
treatment and possible side-effects was to be assessed in accordance with Bolam
and Sidaway. There was no duty to warn of possible diagnoses that were not
reasonably suspected. The court distinguished Sidaway and Chester (considered
below) both of which had concerned the failure to warn of serious side-effects of
surgery, and also Birch where although the risk had been explained a less risky
alternative had not.
However following the decision in Montgomery v Lanarkshire Health Board [2015]
UKSC 11 the courts have at long last caught up with professional guidance and
firmly shut the door on Bolam in cases of risk disclosure.
7.3.5 Montgomery v Lanarkshire Health Board [2015] UKSC 11
Nadine Montgomery suffered from diabetes, was of small stature and was carrying
a large baby. It was commonly accepted that diabetic mothers are likely to have
larger babies and are at increased risk of problems during delivery. During the
delivery of her son, Sam shoulder dystocia occurred resulting in Sam being born
with severe disabilities. The risk of this happening was 9-10%. Nadine Montgomery
argued that she should have been informed of this risk and of the alternative
means of delivery by caesarean section. In an earlier hearing in the Scottish courts
(see M’s Guardian v Lanarkshire Health Board [2010] CSOH 104) Lord
Bannatyne at para 207
“I am unable to conclude that the defender’s experts’ views o n the interpretation of
the CTG trace cannot be supported at all……Their position that there was no need
to intervene at any of the points identified by the pursuer’s experts was overall in
my view clearly defensible. Their views may be wrong. I am, however, unable to
identify any basis for wholly rejecting them as illogical.”
In trying to argue the defendant’s practice was illogical the claimant failed to
convince the Scottish courts in spite of her reliance on Bolitho.
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By the time the case reached the Supreme Court the issue was solely confined to
what was the appropriate standard of care in negligent pre-operative disclosure. In
other words did Bolam or Sidaway still apply in risk disclosure cases. The answer
is a resounding no.
Lords Kerr and Reed pr onounced that a doctor’s duty is to take reasonable care to
ensure that the patient is aware of any material risks involved in any recommended
treatment, and of any reasonable alternative. Significantly the test as to whether a
risk is material is whether in the present circumstances a reasonable person in the
patient’s position would likely think the risk was significant or whether the doctor is
aware that the patient would think the risk is significant. Here the risk of shoulder
dystocia was significant and it should have been disclosed. The risk of a caesarean
section was in contrast very small to both mother and baby. Furthermore Nadine
Montgomery herself had expressed concerns about a vaginal delivery and this
further emphasized the need to advise her fully about the risks and the alternatives
available.
In reality this decision simply brings the court more into line with the approach
taken by the GMC which states that the doctor must always counsel a patient as to
the options available to the patient and the benefits,risks,burdens and side effects
associated with each option. The GMC state it is the patient who “decides whether
to accept any of the options and, if so, which one” (GMC, Consent: Patients and
Doctors Making Decisions Together 2008).
7.3.6 Bolam, Bolitho and Breach
Set out below are a few of the many decisions reviewing the Bolam / Bolitho
approach which you may find of interest. More recent decisions on clinical
negligence and standard of care are listed under the Further Reading section.
(i) McDonnell v Holwerda [2005] EWHC 1081. This case is of interest for the
comments made warning against judging breach of the standard of care with
the benefit of hindsight and that when considering whether a referral was
appropriate a GP should look at the aggregate of symptoms. In McDonnell a
GP was found negligent for failing to refer a child with meningococcal
septicaemia. The doctor in this case was required to refer “without waiting
for the illness to develop to the point where specific symptoms and signs
have developed.” (para 53). The concern here is that the judge’s comments
seem to suggest that in every case where a child presents with symptoms
which could be explained in accordance with more common ailments the
doctor should still refer based on an “aggregate of those symptoms”. Could
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this result in huge increase of referrals if GPs are compelled to take the
aggregate of symptoms approach?
(ii) Kingsberry v Greater Manchester Strategic Health Authority [2005] EWHC
2253. In Kingsberry an obstetric registrar was found negligent for deliveringa baby (the claimant) by manual rotation and forceps delivery on the ward. It
was held that the registrar should have set in motion trial of forceps in
theatre with a senior registrar in attendance. If this had occurred it was
accepted that the claimant would have been delivered within ten minutes by
caesarean section and consequently not have suffered from cerebral palsy.
What is interesting about this decision is the apparent use of hindsight to
judge whether the defendant was in breach or not (this is alluded to in an
article by Andrew Farkas, see www.medneg.com). McKinnon J held that a
trial by forceps in 1985 was an accepted obstetric management technique
and that it should have been employed where there was uncertainty of
outcome. He however continues by stating that that is what would have
happened in 2005. Is this not bringing hindsight into the equation? At
paragraph 45 McKinnon J said;
“Trial of forceps was an accepted obstetric management
technique by 1985 and was to be employed when the operator
recognised or ought to have recognised that the prospects of
successful forceps delivery were uncertain. As there was
undoubtedly such uncertainty as to outcome, a trial of forceps
was mandatory. That is what would have happened in 2005.
Accepting the evidence of the claimant’s experts, for all
practical purposes, there was no difference between 1985 and
2005 in their experience……..Even if there was a practice in
1985 not to perform a trial of forceps in the circumstances of
this case in certain hospitals then such a practice was not in
accordance with any responsible body of obstetric opinion in
1985. Further it did not withstand logical analysis…..The proper
risk benefit analysis applied in 2005 did require trial of forceps
and, indeed, a trial of forceps would have resulted in this case.
That being so there was no sensible reason why such an
approach should not apply equally in 1985.”
Did the registrar’s conduct really fail the logical analysis test as per Bolitho?
To what extent was the judgment made with the benefit of hindsight? See
further Boustead v NWSHA [2008] LS Law Med p 471.
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(iii) Burne v A [2006] EWCA Civ 24
This case is worthy of a read as an illustration of how and when the Bolitho
judgment should be applied in standard of care cases. The Court of Appeal
held that although the trial judge’s approach was correct in applying Bolithohe should have given the defendant’s expert witness (and the claimant’s too)
a proper opportunity to explain the practice, or at least one acceptable
school of thought within it.
(iv) Smith v Southampton University Hospital NHS Trust [2007] EWCA Civ 387
This was an appeal brought by the claimant S against the defendant for
clinical negligence during a hysterectomy operation. The Court of Appeal
held that the approach of the trial judge was incorrect in her assessment of
expert evidence. It was insufficient to rely exclusively on the Bolam test
where there was a clear conflict of medical opinion. The court was under a
duty to not only say which expert view it preferred but to explain why it
preferred one to the other. In essence the court had to do more than simply
say that the defence expert was representative of a responsible body of
medical opinion and consequently the defendant was not negligent.
(v) Holt v Edge [2007] EWCA Civ 602
This was an appeal from a High Court decision. H had fallen in the shower
and her husband had contacted the GP and was told to contact the out of
hours GP service. An emergency doctor visited H that evening and told her
to see her GP the following morning. The next day E confirmed the
diagnosis of a minor neck injury. Two days later H was still feeling unwell
and was admitted to hospital and diagnosed with subarachnoid
haemorrhage and subsequently suffered a stroke. Surgery was carried out
three days later. E admitted breach of duty by failing to ensure that H spoke
to a doctor at an earlier time on the day of her accident but denied liability for
the injury.
H argued that had there been competent telephone triaging after the first
phone call to E surgery, this would have meant there would have been an
earlier diagnosis and surgery would have been carried out sooner. She also
contended that E was in breach of duty by failing to ask her about her history
of vomiting and had he done so she would have been referred to hospital
earlier.
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The Court of Appeal held that telephone system would have made no
difference as the GP would have learned nothing through that process which
would have led him as a competent GP to refer H without delay. The vital
symptoms of pounding headache and vomiting had not been present when
the initial call was made and not when the emergency doctor visited thehouse. Even though E should have made enquiry there was no evidence
that H answer would have precipitated an immediate referral to hospital.
A GP cannot be expected to have the detailed knowledge of an expert in
every field of medicine.
(vi) Stephen Atwood v Health Service Commissioner (2008) EWHC 231
(Admin)
The Bolam test is not just confined to the courts. Although the Health
Service Commissioners Act 1993 s.3 (1) did not dictate that the Bolam test
should be applied by the Health Service Commissioner to questions of
clinical negligence; in Attwood it was clear from the documents produced by
the commissioner that when considering whether to stigmatise a clinical
judgment as "unreasonable" she and her predecessor had stated that they
would apply a test that was indistinguishable from the Bolam test.
7.4 Res ipsa loquitur
As with all tort cases the burden of proof is on the claimant, however, he may additionally
rely on the principle of res ipsa loquitor. In the clinical negligence field the courts have on
several occasions indicated their disapproval of the application of res ipsa to clinical
negligence cases. See for example Bouchta v Swindon H.A. [1996] 7 Med LR 62 where
the court held that the claimant had established that lack of care had resulted in damage
to her ureter during a routine hysterectomy though the doctrine of res ipsa was
inappropriate. Refer also to Fallows v Randle [1997] 8 Med LR 160 (see above at
paragraph 6.3.2).
However, where for example, the patient was unconscious in the operating theatre and
consequently had no idea of what events took place, then the doctrine may be
appropriate, see Cassidy v Minister of Health [1951] 2 KB 343; claimant went into the
operating theatre with two stiff fingers and emerged after the operation with four stiff
fingers; Denning LJ held that res ipsa was appropriate because the result of the operation
was highly indicative of negligence and the defendant had control of the situation); and
Glass v Cambridge H.A. [1995] 6 Med LR 91 (Lawtel logon). In the latter case the court
held that the onus was on the defendant to explain why the claimant suffered a heart
attack whilst under general anaesthetic as this would not normally happen in such
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circumstances. If the defendant had given a reasonable explanation then the inference of
res ipsa would have been rebutted, see also Saunders v Leeds Western H.A. (1984) 129
S.J. 225 where a child suffered a cardiac arrest during an operation the defendant
contended that the child’s heart had suddenly stopped – this explanation was held to be
implausible.
In Jacobs v Great Yarmouth and Waveney HA [2002] MLC 0710; www.medneg.com
(date of judgment March 1984) the claimant sought damages for the alleged negligent
administration of anaesthetic when she underwent a hysterectomy at Lowestoft Hospital.
She contended that the anaesthetic must have missed her vein with the result that the
anaesthetic had no appreciable effect. The claimant alleged that she remained conscious
and aware of the operative procedures right up to the moment of the first surgical
incision. She alleged that as a result she underwent the terrifying experience of believing
that the surgeon intended to operate on her and remove her womb while she was
conscious but, because of the paralysing effect of the second injection, was unable to
communicate with those carrying out the operation. This, it was claimed, had gravely
affected her nervous system.
The Court of Appeal upheld the finding of the judge that after having received pre-
operative drugs the claimant’s memory, would be unreliable and, although a prima facie
case had been raised by proving that the claimant had pre-operative awareness that had
been fully answered by the evidence. The alternative submission that, if the court
concluded that the claimant’s recollection was pre-operational, negligence had been
established by the doctrine of res ipsa loquitor, was not accepted. Although a prima facie
case had been raised, that case had been fully answered by the evidence. It was
concluded that on the balance of probabilities, the claimant was one of those well
documented people, who do have a degree of awareness, whereas the ordinary patient is
entirely unconscious.
In Lillywhite v University College London Hospitals’ NHS Trust [2005] EWCA Civ 1466 the
Court of Appeal once again revisited the application of res ipsa loquitor in a clinical
negligence case. The case concerned the alleged negligence on the part of an eminent
consultant, who was a leader in his field, for failing to detect a condition called
holoprosencephaly by obstetric ultrasonography which the defendant’s experts said went
undetected on scans in between 40-60% of cases at the time in question. What is of
interest in this case is the very marked differences between the judiciary, the defendant
had succeeded at first instance; however the claimant succeeded in front of a very
divided Court of Appeal. Although concluding that this case was not one in which res ipsa
could or should be applied Lord Justice Latham commented that in some cases the
evidence produced by the claimant “may be such as to require the court to focus with
some care on the explanation given by a defendant to displace that which would
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otherwise be the inevitable inference from the claimant’s case that negligence has been
established.” (page 280). Latham LJ had no doubt that the ultrasound was performed with
due care however he went on to say that there a heavy burden on the defendant
consultant to produce an explanation as to why he mistakenly thought the structures in
the ultrasound were present and what could have led him to this incorrect assumption.The dissenting judgment of Arden LJ is particularly erudite recognising that what was
being asked by Latham LJ was much too onerous commenting that it was sufficient that
the defendant’s explanation be plausible only and not probable. She added, “The
claimants could not show what the doctor had done, the judge was satisfied that doctor
had acted carefully and there was evidence that one possible explanation involved no
negligence on his part. If, in an area of medicine where there are no clear answers, the
court were to require the doctor, who is said to have been negligent, to provide a full
clinical explanation of what might have happened in order to rebut a prima facie case of
negligence, the court would be requiring the doctor to go beyond the bounds of known
medical science.” (para 60-62). Clearly the lack of an explanation as to what was seen
on the scan is an important factor but it seems as this was considered to the exclusion of
the factors that the scan was performed competently, the consultant was the eminent
expert in his field and that this was a developing area of medicine. Perhaps a case where
we have some sympathy with the medical profession and a preference for the dissenting
judgment.
See also Ratcliffe v Plymouth and Torbay Health Authority [1998] Lloyd’s Rep Med 162
and Pithers v Leeds Teaching Hospital NHS Trust [2004] EWHC 1392, Aintree Hospitals
NHS Trust v Sutcliffe [2008] EWCA Civ 179. More recently in the private medicine case of
Hussain v King Edward VII Hospital [2012] EWHC 3441 the claimant pleaded res ipsa
loquitor alleging that one or more members of staff must have done something during the
period when he was anaesthetised which damaged his shoulder. It was apparent from
the facts of the case that something had happened to the claimant’s shoulder during the
anaesthetic but it was also apparent from the evidence that the claimant’s shoulder
already had asymptomatic degenerative changes and this was sufficient to rebut the
inference. Moreover it was apparent that the defendant had taken reasonable care.
Commenting on the application of res ipsa Mr Justice Eady sai d, “Res ipsa loquitor does
not give rise to a presumption of any kind. It is simply a conventional way of saying that
the facts, as known to the claimant at the time he pleads his case, give rise themselves to
a prima facie case of negligence.”
Finally in Thomas v Curley [2013] EWCA Civ 117 the Court of Appeal summarised res
ipsa as, “The term res ipsa loquitor describes a situation in which it is possible for the
court to draw an inference of negligence where a Claimant has proved a result without
proving any specific act or omission on the part of the Defendant which has produced the
result.”
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7.5 Clinical Guidelines
As more and more national bodies, e.g. NICE, produce national guidelines then it
is arguable that the Bolam defence will become less acceptable – how can the
defendant argue that he was following accepted practice when it was contrary to
national standards. Teff in Law and Medicine (pp 67-80 at p 77) writes “Yet as they
do become more “authorative” the perceived epitome of “best practice” they could,
even without displacing Bolam, create pressure to reverse the onus of proof,
requiring the doctor to establish that failure to adhere to guidelines was not
negligent.”
In Martin Adshead v Dr Sarah Tottle (Unreported) (2008) Gray J held that a
newly qualified locum GP was negligent for failing to act in accordance with DOH
guidelines. The defendant had examined the claimant’s deceased wife’s breast
lump in 2000 and concluded that it was benign and consequently had chosen not
to refer the deceased to a breast cancer specialist. This was contrary to DOH
guidelines which stipulated that there should have been an immediate referral and
moreover a follow-up appointment made within a month of the referral. Such an
earlier referral would have allowed the deceased (aged 35 when she died in 2003)
to have survived for another 10 years.
Further reading
Stauch Text, Cases and Materials on Medical Law and /Ethics
(Routledge, Chapter 3 126-142, Chapter 6 pp 270-288;
Jackson Medical Law Text, Cases and Materials Oxford
University Press
Pattinson Medical law and Ethics (Sweet & Maxwell)
Chapter
Brazier & Cave Medicine, Patients and the Law (5th ed) (Penguin
Books), Chapter 8 pages 181-200
Khan, Robson & Swift Clinical Negligence, 2nd
ed (Cavendish Press) Chapter
5
Mason, McCall Smith & Laurie Law and Medical Ethics 2011 Butterworths chapter 5
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Khan & Robson What is a responsible group of medical opinion”,
Professional Negligence (1995) Vol 11 No 4 page 121-
123
Harpwood Viv “Bolitho, Expert Evidence and the Role of Judges”
Health Law Nov 2001 Vol 6 Issue 10 Brazier & Miola Bye-Bye Bolam: A Medical Litigation Revolution
Medical Law Review Spring 2000 pp 85-114
Kirby “Patients’ rights – why the Australian courts have
rejected “Bolam”” Journal of Medical Ethics 1995 pp 5-
8
Mulheron Cambridge Law Journal 2010 p 609
Heywood “R.I.P Sidaway: Patient – Oriented Disclosure – A
Standard Worth Waiting For?” Med Law Review Vol 23
pp 455-466
GIlbar and Miola “One Size Fits All? On Patient Autonomy, Medical
Decision-Making, and the Impact of Culture” Medical
Law Review Vol 23 No 3 pp375-399
Geoff Clarke “The differing treatments of judgment by professionals
at work and when they are driving home” Journal of
Personal Injury Law 2011 p1-5
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SUMMARY
At the end of this chapter you should be able to:
* understand the Bolam test and how it is applied;
* identify the limitations the court places on Bolam (if any) and when the
defendant may be found negligent.
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SELF-TEST QUESTIONS – CHAPTER 6
1. What are the essential ingredients of the Bolam test?
2. What is the major criticism levelled at the Bolam decision?
3. What is the ratio decidendi of the Bolitho decision?
4. What is the legal status of guidelines?
5. Does Bolam afford protection for the innovative or for the minority of opinion?
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NOTES
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CHAPTER 8
CAUSATION
8.1 INTRODUCTION
The claimant must prove on a balance of probabilities that the defendant’s lack of care
caused his injuries. It cannot be assumed that the claimant's injuries resulted from the
defendant's breach of duty.
In cases where there is only one cause of the injury, namely the defendant's breach, the
claimant should have no problem in pursuing his claim. However, where there is more
than one possible cause for the claimant’s injury, and only one results from thedefendant's breach of duty, then the issue is not quite so simple. For an illustration of the
complexities that causation attracts see Garcia v East Lancashire Hospitals NHS Trust
[2006] EWHC 2062. In cases of birth injuries it can be difficult to establish that the cause
was clinical negligence and not some other factor.
8.2 THE “BUT FOR” TEST
The claimant is saying that but for the defendant's negligence he would not have suffered
damage. It will be rare for this test to be sufficient in a clinical negligence case as more
often than not there will be more than one possible cause of the damage. For an
illustration of this principle see Barnett v Chelsea & Kensington Hospital Management
Committee [1969] 1 QB 428.
8.3 DID THE NEGLIGENT ACT MATERIALLY CONTRIBUTE TO THE
DAMAGE?
Where there is more than one possible cause of the damage but only one of which is the
defendant's negligence then it is sufficient if the claimant can show that the defendant's
conduct materially contributed to the damage. This test originates from Bonnington
Castings Ltd v Wardlaw [1956] 1 All ER 615. In Bonnington the court held that if the
claimant could prove, on a balance of probabilities that the defendant's breach materially
contributed to the damage then he should recover all of the loss. Lord Reid said “What is
a material contribution is a question of degree”. Generally it will be anything that does not
fall within the de minimus rule.
8.4 DID THE NEGLIGENT ACT MATERIALLY INCREASE THE RISK?
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At first instance the judge held that the defendant was liable only to the extent of the
damage it had caused and consequently reduced damages by some 25%. The evidence
indicated that had the claimant only been exposed to asbestos whilst working for the
defendant that his condition would not have been as severe. This decision was upheld on
appeal.
This decision therefore is in stark contrast to Bonnington which held that if the claimant
can demonstrate that the defendant’s breach of duty materially contributed to the injury
then the claimant could recover in full subject to the de minimus rule (see above at
paragraph 7.3). Only where the defendant’s contribution is known is the defendant liable
to that extent and no more.
Whilst the Court of Appeal were in agreement about the outcome of the appeal there was
a divergence of reasoning. Stuart Smith LJ relied on the fact that in Bonnington and
McGhee it was never argued that the defendant was only liable to the extent of the
material contribution. He stated that if the defendant fails to argue that their liability should
be only to the extent of their material contribution then the claimant should succeed in full.
Clarke LJ, however, said the defendant bears a burden to show that others have
contributed to the claimant’s disease and the defendant must plead the point if they wish
to rely upon it.
Prior to Holtby claimants have been entitled to the full award of damages unless
apportionment has been clear cut or where it was known that only part of the damage
was due to the defendant’s fault as in Thompson v Smiths Shiprepairers (North Shields)
Ltd [1984] ICR 236.
8.6 THE RE-EMERGENCE OF MCGHEE - Fairchild v Glenhaven Funeral
Services Ltd and Others; Matthews v Associated Portland Manufacturers
Ltd; Fox v Spousal (Midland) Ltd [2002] 8 Lloyd’s Rep Med 361
In Fairchild v Glenhaven Funeral Services Ltd and Others; Matthews v Associated
Portland Manufacturers Ltd; Fox v Spousal (Midland) Ltd ) the Court of Appeal had
reluctantly held that where there is more than one employer who has exposed an
employee to asbestos and consequently the claimant is unable to prove which employer
is responsible for the fibre that created the mutation in the mesothelial cell that develops
into the cancer, mesothelioma, then the claimant’s claim fails as no single defendant is
responsible for over 50% exposure. Mesothelioma unlike asbestosis or pneumonconiosis
can be caused by a single fibre of asbestosis and the condition is not made worse by
further exposure. The last two mentioned diseases in stark contrast are made worse by
the cumulative inhalation of increased quantities of dust. In Fairchild the claimant could
not establish on a balance of probabilities when it was that he inhaled the asbestos fibre
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or fibres which caused a mesthelial cell in his pleura to become malignant and
consequently which employer was responsible. What is apparent is that the extent and
severity of the injury is not increased by further exposure but the risk of contracting the
condition increases. In unanimously overturning the Court of Appeal decision the Law
Lords commented that to find for the defendants would “reflect no credit on the law” (LordBingham); and be “morally wrong.” In his summing up Lord Rodger commented;
“The men did nothing wrong, whereas all the defendants wrongly exposed
them to the risk of developing a fatal cancer, a risk that has eventuated in
these cases. At best it was only good luck if any particular defendant’s
negligence did not trigger mesothelioma.”
The claimants’ argument that, applying McGhee, an increase in the risk should equate to
a material contribution to the injury and should result in a 100% finding against a single
employer was accepted by the Law Lords in circumstances where it is impossible to
prove a material contribution to the injury. Further the House of Lords ruled that Lord
Bridge’s opinion in Wilsher that Lord Reid’s view in McGhee “lays down no new principle
of law” was incorrect.
A favourable outcome for the claimant but the new rule was not of a general ambit and
would only work within fairly defined circumstances – it would not help in a Wilsher type
situation where there are a number of factors that could have caused the damage and the
negligent act complained of is simply one of those factors. In the leading judgment Lord
Bingham identified the six conditions for a material increase in the risk to be a sufficient
causal requirement each of which were present in the three cases which were the subject
of the appeal.
1. The claimant was employed at different times by A and B.
2. A and B were both under a duty to take reasonable care to prevent C inhaling
asbestos dust because of the known risk that such dust, if inhaled, might cause
mesothelioma.
3. Both A and B were in breach of that duty to C during C’s employment by each of
them with the result that C inhaled excessive quantities of asbestos dust.
4. C is suffering from mesothelioma.
5. Any cause of C’s mesothelioma other than inhalation of asbestos dust at work can
effectively be discounted.
6. C cannot because of the current limits of science prove, on the balance of
probabilities, that his mesothelioma was the result of his inhaling dust during his
employment by A or B or both taken together.
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On the basis of the above Lord Bingham considered that it was both just and in
accordance with common sense to treat the conduct of each of the defendants as making
a material contribution to the risk of an employee contracting the disease.
The House of Lords seem to have reverted to the position that existed following thedecision of the Lords in McGhee that proof that a defendant’s wrongdoing had materially
increased the risk is to be treated as proof that it had materially contributed to it. Yet are
these one and the same? In terms of the applicability of the McGhee principle to clinical
negligence claims Lord Hoffman acknowledged that such cases do give rise to difficulties
in causation. He concluded, however, that the duty to take reasonable care in treating
patients would not be virtually drained of content by the failure to accept a material
increase of injury as sufficient to satisfy the causal requirements for liability. However it
seems that a material increase in the risk will be sufficient to establish causation only for
those cases falling within the parameters laid down in Fairchild and it for the claimant to
establish that these conditions are satisfied.
For an interesting read on the scope of the Fairchild exception see Sienkiewicz v Grief
(UK) Ltd [2011] UKSC 10.
And then the decision in Barker and the rest……
Barker v Corus (UK)PLC:Murray (Widow & Executrix of the Estate of John Lawrence
Murray, Deceased) v British Shipbuilders (Hydrodynamics) Ltd & Ors: Patterson (Son &
Executor of the Estate of J Patterson, Deceased) v Smiths Dock Ltd & Ors [2006] UKHL
20
There were perhaps two issues still to be resolved after following Fairchild: (1) need all of
the claimant’s exposure to asbestos fibres be tortious and (2) in cases where the
exposure was from more than one source should damages be apportioned between the
negligent parties. These issues were considered in Barker v Corus UK plc and others
[2006] UKHL 20. In respect of the first issue their Lordships found that non-tortious
exposure did not remove a case from the Fairchild exception. It is their Lordships ruling
on the second issue that has been seen as somewhat controversial and some
commentators would say has effectively rewritten Fairchild. Mesothelioma may be
caused by single fibre of asbestosis; hence each exposure increases the risk of
contracting this condition but the condition itself is not made worse by further exposure.
Mesothelioma should therefore be contrasted to asbestosis and pneumoconiosis both of
which conditions are aggravated by the cumulative inhalation of increased quantities of
dust. Fairchild had ruled that where there was more than one negligent party then an
injured party may pursue an action against a single defendant and recover damages in
full. However by a majority of 4:1 the House of Lords have now introduced apportionment
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in respect of indivisible injury. Lord Hoffmann giving the leading judgment found that
because liability had been exceptionally imposed to assist the injured party fairness
dictated that if more than one party was responsible then damages should be
apportioned between them. He further interpreted that the decisions in McGhee and
Fairchild did not suggest that materially increasing the injury equated with a materialcontribution to the injury. At paragraph 43 he states;
“The defendant was a wrongdoer, it is true, and should not be allowed to
escape liability altogether, but he should not be liable for more than the
damage which he caused and, since this is a case in which science can
deal only in probabilities, the law should accept that position and attribute
liability according to probabilities.”
The strong dissenting judgment of Lord Rodger is worthy of a read. He cited Lord
Bingham in Fairchild as clearly stating that materially increasing the risk did equate to
materially contributing to the injury. At paragraph 84 he comments;
”…But the reasoning in McGhee [1973] 1WLR 1 and Fairchild [2003] 1 AC
32 indicates that the House was primarily concerned to maintain a
consistency of approach with the main body of law on personal injuries.
Under that law victims recover damages because the defendant’s wrongful
act has materially contributed to them becoming ill, not because it has
created a risk that they will become ill.”
He saw the practicalities of the decision which meant that where exposure had taken
place over a lengthy period of time then many of the potential defendants would be
insolvent or difficult to trace. Moreover given that claimants will now have the burden of
trying to trace all of the potential tortfeasors this will inevitably increase the costs of the
litigation and significantly the time taken to conduct these cases which is a luxury many of
these terminally ill claimants do not have.
The Government recognising the injustice of this decision rushed through the
Compensation Act 2006 within three months of the Barker decision. Under this Act,
negligent employers are jointly and severally liable, enabling the claimant to recover full
compensation from any relevant employer. That employer could then seek a contribution
to the damages awarded from other negligent employers or from the Treasury, if it thinks
fit, out of public funds. Notably the Act has retrospective effect.
APIL praised the speed with which the government had addressed the “devastating blow”
dealt by the ruling in Barker. Charles Lewis, however, took a different view labelling the
Act as a “knee jerk reaction” and commented that the speed in which the legislation was
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introduced did not bode well for any future judicial decision which the Government
happened to disagree with.
In Brett v Reading University [2007] EWCA Civ 88 the Court of Appeal once again
revisited breach of the duty of care and mesothelioma. The personal representatives ofthe deceased claimant were able to prove that the deceased was likely to have come into
contact with asbestos during his period of employment with the defendant. Unfortunately
it could not be established that the defendant was in breach of duty and the fact that the
deceased had developed mesothelioma could not fill the evidential gap as he had been
employed in other jobs that could equally have brought him into contact with airborne
asbestos.
In Bailey v MOD [2008] LS Law Med 481 the courts revisited the meaning of the phrase
“material contribution”. The facts of Bailey are somewhat detailed but are necessary to
understand the relevance to the material contribution test. B was admitted to a hospital
run by MOD for bile duct surgery (the first procedure). The procedure was complicated by
bleeding and consequently B developed renal failure and acute pancreatitis and the onset
of respiratory failure. She was admitted to intensive care unit and then eventually
transferred to another hospital where she had additional procedures for bleeding to the
liver. She was then transferred from intensive care after making a slow recovery to a
renal ward where her condition again deteriorated culminating in her aspirating her vomit
and subsequent cardiac arrest that caused brain damage. B alleged that the lack of post-operative care and resuscitation after the first procedure ultimately led to her cardiac
arrest. On appeal it was held that if she had properly been resuscitated and cared for
after the original (first) procedure then B would have been subjected to further
intervention. Moreover the judge at first instance had been entitled to conclude that B’s
weakened and debilitated condition caused her not to be able to respond effectively when
she vomited.
The important point here however is what may be termed as a “gloss” on the material
contribution test. The Court of Appeal said in a cumulative cause case where the
evidence demonstrated that the injury would not have occurred as a result of a non
tortious cause (pancreatitis) in any event, but neither could the evidence prove that the
injury would not have happened but for the negligent cause (her weakened condition), the
but for test is slightly watered down and the claimant may establish causation if it can be
proven that the contribution of the negligent cause was more than negligible (i.e. a
material contribution). Putting it more simply the claimant succeeded on the basis that
she could establish that here the risk of injury (cardiac arrest) was enhanced by
negligence (the lack of care), which had a significant albeit unquantifiable effect on her
general condition although she could not definitively show that but for the negligence,
injury would have been avoided. Has this case weakened the balance of probabilities
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test? See further Gregg v Scott below and Boustead v North West SHA [2008] 8 LS Law
Med 471.
For a discussion of the application of Bailey see Conan Ingram v Williams [2010] EWHC
758. More recently in Nathan Popple v Birmingham Women’s NHS Foundation T rust[2011] EWHC 2320 the claimant relying on Bailey successfully argued that not delivering
the claimant five minutes earlier was a material contribution to the damage. Although
medical science was not able to identify when the damage precisely occurred due to the
failure of midwives to monitor the CTG trace the court accepted the claimant case on
causation. The defendant was unsuccessful on appeal, see [2012] EWCA Civ 1628.
8.7 MORE THAN ONE TORTFEASOR?
In Wright v Cambridge Medical Group (a Partnership) [2011] EWCA Civ 669 the
Court of Appeal was asked to consider whether the defendants could escape liability
by establishing the negligence of a second wrongdoer. The claimant (W), then aged
11 months, was admitted to hospital with chickenpox on April 9 1998. She
unfortunately developed a super-infection and was discharged without this being
diagnosed on 12th April. The claimant’s mother then contacted the defendant who
failed to see W; it was established that had she been seen she would have been
referred back to hospital on the 15th April. Eventually another GP referred W on an
urgent basis 17th April but due to the negligence of South Cleveland Hospital her
condition was not diagnosed until 21st April and consequently she was left with an
unstable hip and mobility problems. The Court of Appeal held that a defendant who
had negligently failed to refer his patient to hospital and, as a result, she had lost the
opportunity to receive the treatment she would have had, could not escape liability by
establishing that the hospital would have negligently failed to treat the patient
appropriately, even if he had made the referral promptly.
8.8 LOSS OF CHANCE
The claimant alleges that because of the defendant's negligence he lost the chance of a
successful recovery, for example by failing to make a prompt diagnosis of cancer the
claimant did not receive treatment as early as he could and consequently is denied his
chance of a complete recovery. In Hotson v East Berkshire H.A. [1987] 2 All ER
909; the claimant alleged that had the defendant made a prompt diagnosis he would
have had a 25% chance of a complete recovery. The Court of Appeal chose to award
him 25% of the damages in line with the 25% chance he had lost. The House of Lords,
however, held that this approach was incorrect, the claimant should either be awarded all
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of the damages or nothing at all. To succeed the claimant had to show that there was at
least a 51 /49 likelihood that without the defendant's negligence he would have made a
complete recovery. The claimant in Hotson could not show this, there was still a 75%
chance he would have suffered the damage notwithstanding the defendant’s negligence,
hence the claim failed.
It has been said Hotson may have signalled the end of a loss of chance claim in medical
negligence. Certainly such a claim may be brought in contract successfully but the same
cannot be said of the equivalent tortious claim. There have, however, been cases in the
non-medical field where the court have recognised such a claim in tort. In Allied Maples
Group Ltd v Simmons & Simmons [1995] 1 WLR 1602 the Court of Appeal held that the
claimant must prove that he has lost a real or substantial chance as opposed to a
speculative one. The claimant (a retailing company) had wanted to acquire certain
businesses and properties belonging to its rival company, G. Four of the properties
however could not be conveyed directly to the claimant because of restrictive covenants
that were personal to K, a subsidiary of G, in which the properties were vested. The
defendant solicitors advised the claimant to acquire all the shares in K and then pass on
the unwanted properties and liabilities to another company thereby retaining the
properties they wanted. However, after completion of the sale the claimant found that K
had liabilities for which it was responsible and could not reclaim from G. The trial judge
found that the defendant had negligently failed to warn the claimant of this potentially
open-ended liability and if they had warned the claimant then it would have tried to
protect itself by obtaining some form of warranty from G. The judge also held that on the
balance of probability, if asked G would have given that warranty or some other form of
protection and that if K’s properties had not been included in the sale the deal would not
have proceeded. In the Court of Appeal the court ruled that where the claimant’s loss
depended on the acts of an independent third party the claimant need only show that he
had a substantial chance as opposed to a speculative one of avoiding the liability - a
substantial chance may be less than 50%.
Allied Maples was applied in Stovold v Barlows [1996] 1 PNLR 91 and First Interstate
Bank of California v Cohen Arnold & Co [1996] 1 PNLR 17 . In Stovold which concerned
the loss of the sale of the claimant’s property because of his solicitor’s negligence, the
Court of Appeal held that it must evaluate the claimant’s chance that but for the
defendant’s negligence the sale would have gone ahead. If the claimant proved that he
had lost a real chance as opposed to a speculative one then the court would go on to
evaluate that chance.
Also see Harrison & another v Bloom Camillin (1999) The Times Law Reports 12
November and Smith v National Health Litigation Authority [2001] 2 Lloyd’s Rep Med 90
and the Australian decision of Gavalas v Singh MLC 0388 (see Medical Litigation October
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2001) which comments that it would be unwise to lay down a general rule about whether
a loss of chance / loss of opportunity claim should be made available in medical
negligence cases.
What may be the final word on the subject has probably been uttered with the House ofLords decision in Gregg v Scott [2005] UKHL 2. In 1994 the claimant developed non-
Hodgkins Lymphoma. He saw his GP in the November of that year who negligently
diagnosed it as a benign lymphoma and failed to refer him to a specialist. In August 1995
a GP did refer the claimant on a non-urgent basis for investigation. The surgeon
suspected lymphoma and this was confirmed by a biopsy. The claimant was then treated
with high dose chemotherapy and radiotherapy. In 1998 the claimant suffered a relapse
and received further chemotherapy as a palliative measure since the prognosis was that
he could not be cured.
It was accepted that the failure to refer the claimant to a specialist in 1994 was negligent
and that it delayed treatment by some nine months. The Judge ruled that the delay in
treatment had reduced the claimant’s chance of surviving for five years from mid 2001
from 42% to 25%. However the Judge also accepted the defendant’s evidence that with
this disease the prospects of a cure had always been less than 50%. Therefore the claim
was dismissed because, applying Hotson, the claimant would not in any event have been
cured i.e. his chance of a cure was less than 50% and therefore he would still be in his
present position whether or not treatment had been begun earlier.
The claimant appealed on the grounds that the evidence indicated that if had been
treated in April 1995 he would have been cured and that the statistical chances of
survival were relevant to quantification of damages not causation. The claimant argued
that the court was able to reconsider the question as to whether or not loss of a chance in
the diminution of an adverse outcome as a result of medical advice or intervention should
itself be recognised as damage that could give rise to claim in negligence. By a 2-1
majority the Court of Appeal dismissed the claim. The Appeal Court found that the Judge
had not erred in his assessment of the evidence. The claimant would be allowed to
recover damages for diminution of life expectancy if he could show, on a balance of
probabilities, that the defendant’s negligence caused it. The reasoning in Hotson
indicated that loss of a less than even chance was not an actionable injury. The claim
failed since the claimant could not show on the balance of probabilities that the negligent
failure to refer had a material effect on the outcome of the disease because the prospects
of a cure were in any event less than 50%.
The House of Lords also favoured the defendant and by a majority of 3-2 dismissed the
appeal. Their Lordships all had differing opinions about the merits (or not) of a loss of a
chance claim. Ultimately the majority found that the claimant had not shown on a balance
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of probabilities that the delay in commencing his treatment that was attributable to the
defendant’s negligence had affected the course of his illness or his prospects of survival.
Further that loss of a chance of a more favourable outcome should not be introduced into
a personal injury claim. Why was this decision reached – well it seems to the writer more
on grounds of policy than anything else and a judicial reluctance to “rock the boat”(something which did not hold them back in Chester v Asfhar considered below). At
paragraph 79 Lord Hoffmann (notably in the minority in Chester) comments:
“The law regards the world as, in principle, bound by the laws of causality.
Everything has a determinate cause, even if we do not know what it
is…..The fact that proof is rendered difficult or impossible because no
examination was made at the time, as in Hotson, or because medical
science cannot provide the answer, as in Wilsher, makes no difference.
….Everything is determined by causality. What we lack is knowledge, and
the law deals with the lack of knowledge by the concept of the burden of
proof.”
And at paragraph 85 Hoffman LJ states that to compensate all those claimants that
where a defendant may have caused injury and increased the likelihood of injury would
“involve abandoning a good deal of authority” (Wilsher and Hotson are cited) and in Lord
Hoffman’s opinion there are “no new arguments or change of circumstances which could
justify such a radical departure from precedent.”
Contrast this approach with that of Lord Nicholls who reasons that the difference between
good and poor prospects is a matter going to the amount of compensation payable and
not to liability. He cites Dore J in Herskovitis v Group Health Cooperative of Puget Sound
(1983) 664 P 2d 474,477:
“To decide otherwise would be a blanket release from liability for doctors and
hospitals any time there was less than a 50% per cent chance of survival,
regardless of how flagrant the negligence.”
He goes on to say that a change of approach would represent a development of the law
and the present law “generates continuing instinctive judicial unease.”(para 45)
Consider also the use of and perhaps one could say the over reliance by the judiciary on
statistical evidence, see Lord Nicholls at paragraph 28 an approach which has been
seemingly readily endorsed in subsequent cases, for example Carter v Basildon &
Thurrock NHS Trust [2007] 10 LS Law Med 657 (see below).
As so often is the case the Australian courts have chosen not to follow their English
brethren in Rufo v Hosking [2004] NSWCA 391 in ruling that it was sufficient for the
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plaintiff to prove on the balance of probabilities “that he or she had been deprived of a
valuable chance” (para 9) and per Hodgson JA at para 10 “That chance must be inherent
in the circumstances, not merely an artefact of the way evidence is presented in the
case….if it appears that the best medical science can do is to say that the treatment had
a quantifiable chance of success, then in my opinion that can be treated as a valuablechance for the loss of which a plaintiff can be compensated.”
But the outcome of this sorry tale for the English claimant is to ensure that your lawyer
deletes the words “loss of a chance” from any prospective clinical claims.
Read the House of Lords judgment in Gregg v Scott which can be found at
www.parliament.the-stationery-office.co.uk and contrast the approach taken in this case
with that of Chester v Afshar considered at 7.13 below.
In Johnston v NEI International Combustion Ltd: Rothwell v Chemical & Insulating Co Ltd
& Ors: Topping v Benchtown Ltd (Formerly Jones Bros Preston Ltd): Grieves v FT
Everard & Sons &Ors [2007] UKHL 39 the House of Lords faced a different question. The
claimant was suffering from pleural plaques in his lungs. The pleural plaques themselves
did not cause asbestos disease but signalled the presence in the lungs of asbestos fibres
that might independently cause life threatening or fatal diseases. The risk of asbestos
related diseases was entirely independent of the presence of pleural plaques. The issue
the court had to resolve was whether if the pleural plaques are not in themselves damage
could they become damage when aggregated with the risk which they evidence or the
anxiety which that risk causes. The court held that the risk of itself is not actionable. In
essence the House of Lords ruled that neither the risk of future injury nor anxiety at the
prospect of future injury is actionable endorsing the approach taken in Gregg v Scott and
Hicks v Chief Constable of South Yorks.
See also Carter v Basildon & Thurrock University Hospitals NHS Foundation Trust [2007]
10 LS Law Med 657; [2007] EWHC 1882 the court affirming the burden is always on the
claimant to show that had the treatment been administered earlier then the claimant was
more likely to survive than not, (Gregg applied) and Bailey v MOD considered above at
paragraph 7.6.
8.9 A DIFFERENT APPROACH? JD v Melanie Mather [2012] EWHC 3063
(QB)
In JD v Mather the defendant admitted breach of duty of care to the claimant by failing to
diagnose a malignant melanoma but made no admissions about causative damage. The
claimant alleged that had his testicular cancer been diagnosed earlier he would have in
all likelihood have survived. In the alternative, which was not initially pleaded but which
was allowed, he claimed that earlier treatment would have given him longer life
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expectancy. The first of these two claims was dismissed by Bean J, who acknowledged
that “There is a difficulty about applying such statistics to show an individual cancer
patient’s prognosis for the purposes of a trial of causation: see Gregg v Scott [2005] 2 AC
176 ”. However the claimant succeeded in his alternative claim, Bean J referring again to
Gregg v Scott and the judgment of Baroness Hale at paragraphs [206]-[207]:
“The defendant is liable for any extra pain, suffering, loss of amenity, financial loss and
loss of expectation of life which may have resulted from the delay. If, without the delay,
the claimant would have achieved a longer gap before more radical treatment became
necessary, then he should be entitled to damages to reflect the acceleration in his
suffering. If the pain and suffering he would have suffered anyway was made worse by
the anguish of knowing that his disease could have been detected earlier, then he should
be compensated for that. There is also the distinct possibility that the delay reduced his
life expectancy in the following sense. It is possible that had he been treated when heshould have been treated, his median life expectancy then would have been x years,
whereas given the delay in treatment his median life expectancy from then is x minus y.
This argument requires that the assessment of loss of life expectancy be based on
median survival rates: i e those to be expected of half the relevant population at
the particular time. If half the men with Mr Gregg's condition would have
survived for x years or over with prompt treatment, and half would have survived
for less than x years, then x is the median life expectancy of the group. If the
same calculation of life expectancy from when he should have been treated is
done in the light of the delay in treatment, the median life expectancy may have
fallen. There might theref ore be a modest claim in respect of the “lost years‟”.
The court found that had the claimant’s cancer been diagnosed earlier the median life
expectancy of a cohort of 100 patients with the same cancer diagnosed at the same time
would have been three years longer than the median life expectancy given the actual
date of diagnosis and progression of the tumour.
8.11 REMOTENESSThe rules for remoteness are no different in this area to any other area of tort. The
defendant will only be liable for that harm which was foreseeable. In the medical context
it will be rare for the court to find that the claimant’s injury was unforeseeable. See for
example Loraine v Wirral University Teaching Hospital NHS Foundation Trust [2008] 10
LS Law Med 573 where Mr Justice Plender found the defendant liable for exposing the
claimant to cerebral palsy “although the route by which the claimant came to suffer that
outcome was not the same as the route that was to be foreseen at the time of the
breach.” (paragraph 71).
Likewise the eggshell skull rule is equally applicable.
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8.12 BREAK IN THE CHAIN OF CAUSATION
8.12.1 By the claimant
In Emeh v Kensington A.H.A. [1985] QB 1012 the defendant argued that the
claimant’s failure to have an abortion was a novus actus (for a discussion of the
general principles and meaning of this term refer to the preliminary material on
Blackboard). This argument was rejected, the Court of Appeal holding that it would
only be in the most exceptional circumstances that such a decision could amount
to a novus actus. Obviously the question that then occurs is what would amount to
“exceptional circumstances”? One scenario where the defendant may try and rely
on a novus actus is where the claimant has been specifically warned to come back
to his GP if his symptoms deteriorate or reappear, and he fails to do so, though this
argument will probably only succeed in the minority of cases. In any event thecourt will then probably critically examine the instructions / advice given by the
defendant to the claimant. See however Sabri – Tabrizi v Lothian Health Board
(1998) SC 373.
In Corr v IBC Vehicles Ltd [2008] UKHL 13 a claim was brought by a widow on
behalf of her late husband. Thomas Corr had suffered an accident at work,
severing part of his ear and head. Despite extensive surgery he was left
permanently disfigured. Mr Corr’s employers admitted their negligence caused the
accident but before the claim was settled Thomas Corr committed suicide. Mrs
Corr then brought a claim for the financial losses attributable to his suicide. The
House of Lords were asked to determine whether Mr Corr’s suicide was a novus
actus or whether it could be construed as being a reasonably foreseeable
consequence of his depression. Their Lordships held that Mr Corr’s employer could
reasonably foresee that he might commit suicide some years later as a response to
a severely depressive illness although the court held that some reduction for
contributory negligence may be appropriate.
In the interesting decision in Maher v Pennine Acute Hospitals NHS Trust [2012]
JPI law 25 (Blackpool County Court 23/6/11) the court were faced with the dilemma
of who should take responsibility for the claimant’s religious beliefs. The defendant
trust admitted there had been unacceptable delay in returning the claimant to
theatre to investigate her blood loss following an emergency caesarean section.
The claimant unfortunately died but the trust argued that even if she had been
taken to theatre earlier she would have refused blood as she was a Jehovah’s
Witness and this refusal of blood broke the chain of causation. The court found that
as the claimant was simply following her religious beliefs and that the trust were
fully aware of her religious beliefs and had a protocol to deal with this situation it
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could not be said that the claimant was acting unreasonably and consequently her
actions could not amount to a break in the chain of causation.
8.11.2 By a third party
In Prendergast v Sam & Dee [1989] 1 Med LR 36 a doctor’s handwriting was so
bad it was misread by a pharmacist with the result that the claimant was given the
wrong tablets and consequently suffered brain damage. The doctor tried to rely on
the pharmacist’s conduct being a novus actus, however, this argument was
dismissed the court holding that it was foreseeable that if the prescription was not
clearly written mistakes could happen. The doctor was consequently held liable as
was the pharmacist for failing to make further enquiries.
See also Panther v Wharton (2001) MLC 0358; and Horton v Evans; Lloyds
Pharmacy Ltd [2006] EWHC 2808 considered at paragraph 5.7.4. During June the
claimant had gone to the USA and had been prescribed the tablets by an American
doctor, a Dr Ewell who, surprisingly, did not question the high dosage. The
causation point was whether Dr Evans should be held liable for Dr Ewell’s
prescription or was it an independent act thus breaking the chain of causation.
Keith J reasoned that the chain was not broken and it was fair, just and reasonable
and foreseeable that a doctor later down the line would rely on or be influenced by
the label on the pill bottle and hence prescribe the same strength. There is
however a strong possibility that the American doctor, Dr Ewell, acted negligently.
The case is an interesting read – why not try it!
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8.12 CONTRIBUTORY NEGLIGENCE?
As with other areas of tort the Law Reform (Contributory Negligence) Act 1945 will apply
to all claims whether brought by a NHS or private patient. Until fairly recently this
defence did not feature in clinical negligence cases brought in the English courts and the
only case entertaining this defence was the Canadian case of Crossman v Stewart (1977)
82 DLR (3d) 677. Here the claimant was left almost blind as a result of drugs which had
been prescribed for a skin disorder. Her damages were, however, reduced by two thirds
as it transpired that she had failed to consult her treating physician and had obtained
some of the drugs from an unknown source.
There have however been more recently two cases that have embraced the idea of a
patient being partly responsible for their eventual condition. In Pidgeon v Doncaster HA
(2002) Lloyd’s Rep Med 130 the claimant sought damages in respect of a cervical smear
which was wrongly reported as normal by the Defendant in 1988. In 1997 she wasdiagnosed with cervical cancer. The defendant argued that by failing to undergo a routine
cervical smear test, despite repeated requests to do so, the claimant’s actions had
broken the chain of causation or alternatively amounted to contributory negligence. The
evidence indicated that the claimant had been spoken to on seven occasions about the
need to have a smear between 1988 and 1997 and furthermore she had received two
letters from the cervical cancer screening programme in 1991 and 1994 requesting her to
have a smear test. Judge Bullimore found the claimant’s conduct not so unreasonable to
break the chain of causation however she was contributory negligent for repeatedly failing
to attend and her damages were reduced by two-thirds.
In P (Deceased) v Sedar [2011] EWHC 1266 P had attended her GP in 1999 with a mass
in her breast. She was subsequently referred to the breast clinic and told that no
abnormality had been detected. She visited her GP again in 2000 as the breast lump was
now bigger and she was again referred to a breast clinic. She was sent two
appointments, one in January and one in February both of which she failed to attend. The
hospital sent a letter to the GP stating that as she had not attended the two appointments
they would not be sending any more. The GP admitted negligence in failing to chase up
P. It transpired that P did not attend either of those appointments as they had been sent
to the wrong address. P moved and was seen by a new doctor in 2001 and immediately
referred to hospital where it was found that she had primary breast cancer and bone
metastases. P died in 2003. The issue was whether P should bear some fault for what
eventually happened as a result of not chasing up her missed appointments. The court
distinguished P’s case from Pidgeon as being a case where the P had simply failed to
chase up her missed appointment and not as extreme as the facts in Pidgeon and hence
there was no finding of contributory negligence.
An interesting decision on contributory negligence albeit not in the clinical negligence
domain is Badger v Ministry of Defence [2005] EWHC 2941; MLC 1318. The claimant,
Beryl Badger, was the widow of Reginald Badger who had been employed by the
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defendant. During his employment he was exposed to asbestos dust which was
causative of the lung cancer that killed him. He also began smoking at the age of 16,
about the same time he commenced working for the defendant. There was nothing to
suggest that his smoking had caused any ill health until Mr Badger was nearly 30. His
smoking was also causative of his cancer. Although the defendant admitted liability it was contended that the claimant’s claim
should be reduced on the grounds that Mr Badger continued to smoke when he knew or
should have known that by doing so he was having an adverse affect on his health. In
finding that the claimant’s damages would be reduced by 20% Stanley Burton J applying
the Law Reform (Contributory Negligence) Act 1945 s.1 (1) held that the appropriate
question the court had to ask was not whether Mr Badger’s conduct fell below the
standard reasonably expected of him but whether it fell below the standard reasonably
expected of a person in his position: did his conduct fall below that to be expected of a
person with ordinary prudence? In answering this question it was not necessary to show
that Mr Badger foresaw harm. It was inferred that Mr Badger must have repeatedly been
advised of the dangers of smoking by health professionals that his symptoms may have
been caused by his smoking. This together with the fact that from 1971 a health warning
appeared on cigarette packets warning of the dangers of smoking led the court to
conclude that he should have given up smoking as a reasonably prudent person in his
position would have done so in the mid 1970’s which would have substantially affected
his risk of contracting lung cancer.
As a society we are continually encouraged to take more responsibility for our health, to
lead healthier lifestyles and make responsible health choices. It will be interesting to see
whether the defence of contributory negligence will become more prevalent if a patient
has not attended an appointment or followed specific instructions, or made inappropriate
lifestyle choices such as smoking or over-eating. See http://www.bbc.co.uk/news/uk-
politics-20508405 “”Lifestyle Patients” may have to pay for their drugs in future says MP”.
8.13 OMISSIONS AND CAUSATION – THE EFFECT OF THE
BOLITHO CASE
8.13.1 Where the defendant's breach of duty consists of an omission the courts
have introduced the Bolam test into the area of causation. In Bolitho v City and
Hackney H.A. [1998] AC 232) a paediatric registrar had failed to attend a patient
when summoned by a sister. The defendant argued, however, that even if she had
attended she would not have given the treatment the patient required to avoid the
injury and further, that other experts would have acted likewise. The claimant
argued the opposite, namely that the defendant would have given the treatment
had she attended and this argument was endorsed by expert opinion. The Court of
Appeal held that where the defendant's breach was an omission then the question
to be resolved was what would have happened had the breach not occurred. The
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court was therefore bound to rely on expert advice and as the claimant had failed
to show that a failure to give treatment was contrary to Bolam then the claim failed.
The Court of Appeal therefore abandoned the tests previously employed in
Bonnington, McGhee and the like and held that the Bolam test was now equally
applicable at the standard of care and causation stages. There was, however, astrong dissenting judgment by Simon Brown LJ who adopted McGhee and held
that it was up to the court to infer what would have happened.
Bolitho finally reached the House of Lords in late 1997. Unfortunately for the
claimant the Lords held that causation had not been proven. In claims of
hypothetical causation the Lords identified two questions (1) what would have
happened in the absence of the breach of duty? (a simple application of the but for
test) and (2) whether the defendant’s actions would be endorsed by a responsible
body of medical opinion (the Bolam test) - that if no responsible doctor would
endorse the defendant’s actions the claimant would establish causation.
The dissenting judgment of Simon Brown LJ in the Court of Appeal was strongly
criticised by Lord Browne-Wilkinson. He stressed that it was not for the judge to
infer what would have happened as being the most effective thing for the claimant
but rather to assess the truth of the evidence.
The Lords’ also took the opportunity to comment on the Bolam test see Chapter 6.
Many writers have criticised the encroachment of the Bolam rule into causation and
have argued that the courts should resort back to the tests canvassed in McGhee
and the like.
What do you think? Is the appropriate question: (1) whether the doctor was not
negligent in not intubating, or should it be: (2) would on a balance of probabilities a
doctor normally intubate in such circumstances? Does the Bolitho majority
decision confuse what should have been done (is the defendant’s account plainly
illogical) with what would have probably been done (is this the normal way in which
doctors respond)? In the Court of Appeal Simon Brown LJ said:
“No doctor in this case ever took a decision whether or not to intubate
the plain fact here is that no doctor ever arrived at Patrick’s bedside. It
is that want of attention that constitutes the undoubted negligence in
this case.”
Now does a claimant have to prove two negligent acts? What for the balance of
probabilities. Can the evidence of the defendant be relied on? In Bolitho is there
not in the very least an argument to say that the evidence of Dr Horn was self
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serving – did Simon Brown LJ recognise that fact and find that although the
evidence of the defendant was honestly given it could not be relied on? Charles
Foster comments that Simon Brown’s LJ approach was dominated by a practical
consideration that a profession whose negligent failure to attend leads to
catastrophic results will be under great pressure to give evidence that he would notin any event have taken the action necessary to avert the catastrophe (see
Solicitors Journal 1997 p 1151). Do you agree with this statement?
See also Wisniewski v Central Manchester HA [1998] Lloyds Law Rep Med 223
for an example of a post-Bolitho case and more recently Kingsberry v Greater
Manchester Strategic Health Authority MLC 1290, (see chapter 5) and Bright v
Barnsley District Hospital [2005] 10 Med LR 449 (Lawtel login)
In Gouldsmith v Mid Staffordshire General Hospital NHS Trust [2007] EWCA Civ
397 the Court of Appeal revisited the correct interpretation of Bolitho as applied to
causation. The claimant had a lesion on her hand, which she had been advised,
was responsible for the deterioration in the condition of her dominant left hand. She
had received treatment at the defendant hospital but her left finger ultimately was
amputated. She was re-admitted to hospital and there was a further deterioration in
her condition resulting in the amputation of her remaining digits. The claimant
contended that her lesion should have been dealt with by surgery on referral to a
specialist tertiary hospital, rather than by drugs and this would have avoided the
amputations. The Trust denied that this was the appropriate measure and surgery
at that time would have served no purpose.
At first instance the trial judge found that the trust had been in breach of duty by
not referring the claimant to a specialist hospital but on causation on the balance of
probabilities every specialist exercising the appropriate standard of care would not
have operated so it followed that the breach of duty had not caused the claimant’s
injuries.
On appeal the claimant argued that the trial judge had applied the wrong test and
should not have asked whether in accordance with Bolam the specialist hospital
would have been bound to operate but should have asked what on the balance of
probabilities would have happened if she had been referred to a specialist hospital
for treatment.
The Court of Appeal agreed that the judge had applied the wrong test and went on
to clarify the correct application of Bolitho to matters of causation. The trust was in
breach of its duty of care in not referring the claimant to the specialist hospital (the
omission). The judge should then have first considered what would have happened
had the claimant been referred to a specialist hospital and then whether on the
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balance of probabilities the specialist would have conducted surgery or not.
Secondly if there had not been an affirmative answer to the first question, the court,
applying Bolitho, should have considered whether the specialist would have been
negligent in not conducting the surgery. Bolam only became relevant in deciding
the second question but the trial judge had allowed the first question to besubsumed within the second. In this instance the answer to the first question was
in the affirmative, i.e. had the claimant been properly referred as she should have
been then, on the balance of probabilities, the surgery would have taken place.
Hence the breach of duty caused the claimant’s injuries.
See also Nasir Hussain v Bradford Teaching Hospital NHS Foundation Trust
[2011] EWHC 2914
8.14 CAUSATION AND NON-DISCLOSURE
Where the claimant alleges that he was not warned about an inherent risk in a procedure
and he successfully proves that the risk should have been disclosed then his battle is
only half complete. He must then go on and establish that had the risk been disclosed
then he would not have accepted the treatment. It is for this reason that wherever
possible where the case is for non-disclosure of risks then the solicitor would be well
advised to frame it as a case in trespass to avoid the problems of causation. The
majority of cases will undoubtedly fall at this hurdle as the courts will infer that even if all
the risks had been disclosed then the claimant would still have had the treatment. The
courts apply a subjective test – would this claimant have acted so, in contrast with other
jurisdictions where an objective test is applied, i.e. the reasonable man.
See Reibl v Hughes (1980) 114 DLR (3d) 1; Smith v Barking, Havering & Brentwood H.A.
[1994] 5 Med LR 285. In Smith Hutchinson J urged caution in considering the claimant’s
evidence in what was a wholly artificial situation. The court should look at the evidence
objectively and only if there were some other extraneous or additional factors e.g.
religious or some other firmly held convictions or social convictions and these assertions
were made immediately following the operation should the court be persuaded by this
evidence. Contrast this approach with Reibl v Hughes where the Canadian court asked
what would a reasonable person in the claimant’s position have done. Here as the risk
was great (10%) and the claimant was only about a year and a half away from retirement
on a full pension then the court held that the claimant would probably have declined the
operation.
The difficulties of proving that medical procedures would not have been consented to if
an adequate warning of the risks had been given is illustrated by the case of Chapman v
Mid-Essex Hospital Services [2002] MLC 0774. The claimant had a successful
hysterectomy operation, however she suffered a deep vein thrombosis in her left thigh
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having previously suffered the same condition some years previously following a
miscarriage. She claimed damages from the hospital alleging that the medical staff had
given her an assurance that she would not suffer a DVT as a result of the hysterectomy.
Alternatively she contended that the hospital staff had failed to warn her of the extent to
which she was at risk of such a complication. She alleged that if she had been given sucha warning, she would not have undergone the operation at all.
The claim failed on the basis that she had been given an assurance that she would not
suffer DVT; the doctors had reassured her by indicating that the risk was reducible to a
low level by prophylactics. The court also concluded that her willingness to undergo the
operation was the fact that her ever increasing menstrual problems had become
intolerable to her, and she ultimately decided to undergo the operation, even though, as
she was aware, there was a low risk of a further DVT.
In Chester v Afshar [2004] UKHL 41 the claimant alleged that the defendant had
negligently failed to inform her of the risks of having three intra-vertebral discs removed.
The claimant had asked a series of lengthy questions but at no time did the defendant
inform her of the risk of 0.9-2% nerve root damage. The Court of Appeal found that a
proper warning had not been given to the claimant. The Appeal Court was clearly
influenced by the amount of detailed recollection that the claimant was able to produce in
stark contrast to the defendant who had made no note about what he had told the
claimant. Given her aversion to surgery and the concerns she expressed about being
crippled, the judge found that the very least she would have done would have been to
seek a second or third opinion. This would inevitably have meant that the proposed
operation would not have gone ahead on the day the operation took place. Although it
was impossible to determine when she would have been seen, what advice would have
been given and how she would have reacted to it, it was improbable that any surgery she
might undergo would be identical to the operation she underwent. Hence this was
sufficient to prove a causal link between the failure to warn and the damage.
Surprisingly the House of Lords also decided in favour of the claimant by a 3-2 majority.
Their Lordships accepted that, according to accepted principles of causation, the claimant
had to fail. However the majority felt that there was a clear wrong here: the duty of care
owed by the defendant to the claimant was such a special duty that it demanded that the
claimant should have a remedy even if the strict rules on causation would indicate
otherwise. Lord Hope’s view was,
“To leave the patient who would find the decision [about whether or not to
have the surgery] difficult without a remedy, as the normal approach to
causation would indicate, would render the duty useless in the cases where
it is needed most…”….”The injury was intimately involved with the duty to
warn. The duty was owed by the doctor who performed the surgery that [the
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claimant] consented to. It was the product of the very risk that should have
been warned about when she gave consent.” (paragraph 87).
In contrast Lord Hoffmann likened the claimant’s argument to winning in a casino. For
Lord Hoffmann the question is “whether one would have taken the opportunity to avoid orreduce the risk, not whether one would have changed the scenario in some irrelevant
detail.” (paragraph 31).
What are the consequences of this decision? The majority in Chester has decided that
the duty of care to warn is such an important duty that a “narrow and modest departure
from traditional causation principles” (per Lord Steyn, para 24) is justified. Why? Why is
this duty any more important than the duty to diagnose, duty to treat etc? Their Lordships
seemed to have adopted the position that justice demanded that this claimant be afforded
a remedy, see for example para 25 per Lord Steyn “This result is in accord with one of
the most basic aspirations of the law, namely to right wrongs”, and per Lord Hope at para
88 “I would hold that justice requires Miss Chester be afforded the remedy which she
seeks…”. The decision certainly set alarm bells ringing for practitioners. The NHSLA
issued a risk alert on informed consent, warning that clinicians’ liabilities would be
extended in cases where less than full consent was obtained, see further
www.nhsla.com. Also compare this case with Gregg v Scott above – which of the
claimants do you think was the more deserving of a novel and radical approach?
See also the Australian case of Chappel v Hart (1999) Lloyd’s Law Rep 223 where it was
sufficient for the claimant to prove that had she known of the risks she would not have
undergone that operation that day if properly advised. In that case although the patient
would still have had the operation some time in the future the situation would have been
different and the risk not necessarily identical, thus it could not be said that she would
have suffered the same injury.
Case law since Chester?
White v Paul Davidson & Taylor [2005] PNLR 15 (solicitors)
Beary v Pall Mall Investments [2005] EWCA Civ 415 (financial advisors)
Moy Pettman Smith [2005] UKHL 7 (barristers)
Smith v Lothian University Hospitals NHS Trust [2007] CSOH O8; MLC 1164
All these cases have seen the court stress that Chester did not establish a general
causation rule. In White per Arden LJ at para 40:
“I would like to add a few observations on Mr White’s supplementary written
submissions in which he places reliance on the recent decision of the House
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of Lords in Chester v Afshar [2004] WLR 927. In my judgment, this case
does not establish a general rule in causation. It is an application of the
principle established in Fairchild v Glenhaven Funeral Services [2003] 1 AC
32 that, in exceptional circumstances, rules as to causation may be modified
on policy grounds.” See also Birch v University College London Hospital NHS Foundation Trust
[2008] EWHC 2237 at para 6.3.4.
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Further Reading
Brazier & Cave, Medicine, Patients and the Law 5th ed) (Penguin Books), Chapter 7, pp 200-206
Khan, Robson & Swift, Clinical Negligence (2nd
ed) Cavendish Press Chapter 6
Mason, McCall Smith & Laurie, Law and Medical Ethics 2002 Butterworths chapter 9 pages
297-302
Healey, Medical Negligence: Common Law Perspectives (Sweet & Maxwell) Chapter 7 pages
191-231
Harpwood, “Bolitho, Expert Evidence and the Role of Judges” Health Law November 2001 Vol 6
Issue 10
Charles Lewis, “Fairchild and the Rehabilitation of McGhee” Medical Litigation August 2002
page 14
Michael Jones, “Another lost opportunity” Professional Negligence PN (2003) Vol 19 No 4
pages 542-559
William Edis, “Gregg v Scott” Solicitors Journal 11/2/05 page 166
Charles Foster, “Last chance for lost chances” New Law Journal 18/2/05
Mark Shaw, “Sick Pay” Solicitors Journal 29/10/04 page 1228
Charles Foster, “It should be, therefore it is” New Law Journal 5/11/04 page 1644
Charles Lewis, See www.medneg.com The Compensation Act 2006
Gemma Turton, A care for clarity in causation? Medical Law Review 2009(17)1:140-147
Jose Miola, On the Materiality of Risk: Paper Tigers and Panaceas Medical Law Review 2009
(17) 76SH Bailey: “Causation in Negligence: what is a material contribution?” Legal Studies Vol 30,
Issue 2 pp167-185
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SUMMARY
At the end of this chapter you should be able to:
* identify and apply the various tests for causation;
* distinguish between the test in Bonnington and that in McGhee;
* understand the application of Bolam to causation and omissions;
* identify any possible problems with establishing causation and any defences
the defendant may have.
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NOTES
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CHAPTER 9
DAMAGES
9.1 INTRODUCTION
These notes assume that you are already familiar with the general principles of damages
for personal injuries and rather serves to highlight the recent developments in this area
and to act as a reminder of the more important issues. As such there are no special rules
for compensation in the area of clinical negligence; the claimant is entitled, amongst other
things, to be compensated for pain and suffering, the cost of nursing care, and past and
future loss of earnings.
9.2 GENERAL DAMAGES
9.2.1 Pain and suffering
Inevitably there will be a certain amount of pain and suffering associated with the
injury; damages awarded under this head include compensation for any
embarrassment caused by the injury e.g. a disfiguring scar, and any shock suffered
by the claimant. The damages will also take into account the characteristics
peculiar to the claimant, an unconscious claimant, for example, suffers no pain.
See for example Hicks and others v Chief Constable of the South Yorkshire Police
[1992] 2 All ER 65.
9.2.2 Loss of Amenity
Damages under this head are to compensate the claimant for what he can no
longer do as a result of the injury. This can range from compensation for not being
able to participate in a hobby or play a sport to loss of sex drive and not being able
to enjoy any facet of life. Note that the claimant need not be aware of the loss of
amenity e.g. an unconscious claimant, what matters is that the amenity is lost.
In Heil v Rankin [2000] 5 Lloyds Law Rep 203 the Court of Appeal heard eight
appeals which were selected as test cases to allow the court to issue guidelines
following the Law Commission Report 257 which recommended an increase in the
level of damages for non-pecuniary loss for personal injuries. However, the court
stated that not all awards were deserving of an increase and there should be no
increase for those awards of less than £10,000 notwithstanding that the Law
Commission had recommended an increase for awards over £3,000 by a factor of
1.5-2. The most serious injuries were those where damages were in the region of
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£150,000-£200,000, attracted the highest increase of about a third. As a general
rule the awards would increase in line with the Retail Price Index although the court
would also taken into account other changes in society. The courts therefore would
periodically review the awards if they appeared out of line with the standards set. In
doing so, the court could take account of other economic factors such as higherinsurance premiums for the defendant and less resources available for the NHS;
the court reasoning that the needs of the defendant and society must be
considered as a whole.
9.2.3 Loss of Future Earnings
Normally any pecuniary losses fall within special damages but compensation under
this head is an exception to the general rule. This is because such damages are
speculative, i.e. what would the claimant have earned had he not been injured?
These sums can be very difficult to calculate see for example Appleton v El Safty
[2007] EWHC 631. The court will take into account the claimant’s future car eer
prospects, e.g. was he due a promotion, would his salary have
increased/decreased, was he likely to have been made redundant, the age of the
claimant - was he likely to retire soon, etc. See for example Collett v Smith and
Middlesborough Football Club [2008].
Damages for future loss of earnings are assessed at the date of the trial. To
calculate such damages the court first takes the claimant’s net annual salary (themultiplicand) and then multiplies this by the multiplier. The multiplier is not
necessarily the number of years the claimant still had to work as this could lead to
over compensation, the figure will be arrived at by the court taking into
consideration the factors discussed above. The court’s aim is that the
compensation awarded to the claimant will be exhausted at the time when the
claimant no longer has a need for it. For an illustration of how the court select an
appropriate multiplier see the case of Worrell v Powergen plc [1999] 5 Lloyds
Rep Med 177.
In deciding what is an appropriate award the court also assumes that the claimant
will act prudently and invest the money and discount the award to cater for this and
the fact that the claimant is receiving the compensation as a lump sum. Following
the decision in Wells v Wells, Thomas v Brighton HA and Page v Sheerness Steel
Co Ltd [1998] 3 All ER 481, the House of Lords held that the discount rate should
be based on investment in Index Linked Government Securities which would
currently yield a return on income and capital of 3%. Previously awards had been
discounted by up to 4.5% as the court assumed that the claimant could invest the
money in the best long-term investment i.e. the stock market. However in these
cases the House of Lords at long last recognised that the claimants were not in the
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same position as the ordinary investor who could simply wait for the stock market
to recover if it fell – they had to secure their long term needs and therefore choose
a safe investment.
Section 1 of the Damages Act 1996 empowers the Lord Chancellor to prescribe
the rates of return on damages and in so doing affect the multiplier to be used inpersonal injury cases. From 25 June 2001 the discount rate was lowered to 2.5%,
see further www.lcd.gov.uk/civil/discount.htm. Note that the courts may by
virtue of section 1(2) adopt a different rate in any particular case if there are
exceptional circumstances that may justify it doing so.
See also Cooke v United Bristol Health Care [2003] EWCA Civ 1370 where the
Court of Appeal reaffirmed that the conventional method of assessing damages,
(see Wells v Wells) should be used. However in Peter Crouch v King’s Healthcare
NHS Trust [2004] EWCA Civ 1332 the Court of Appeal endorsed the approach of
the trial judge who had not used the standard multiplier/multiplicand approach in an
assessment of damages for loss of earning capacity. There was evidence that the
claimant had reassessed his life and priorities prior to the accident and was not as
committed to his profession (dentistry) and hence the judge was entitled not to
assess damages on the basis of past earnings in his practice.
9.2.4 Handicap in the labour market
This is known as the Smith v Manchester award following the decision in the caseof the same name, see (1974) Knights Industrial Reports 1 and is designed to
compensate the claimant who, although can return to his job, because of his
injuries is at more of a risk of either loosing his job or being made redundant.
9.3 SPECIAL DAMAGES
Many of the items discussed below can equally fall into the general damages category
depending whether or not they have accrued to date, e.g. the claimant may have already
incurred medical expenses which will fall within special damages as they are capable of
precise calculation but may also need future nursing care which will come within the
general damages sphere.
9.3.1 Accommodation
This may either be the cost of new housing or the cost of the claimant’s present
accommodation being adapted /altered to cater for his disabilities. See Robert v
Johnstone [1988] 3 WLR 1247 for how the court calculate this head of damage.
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9.3.2 Nursing Care
This may be provided by an institution or an individual carer where the claimant is
being cared for at home by a relative. If it is an individual and he is a relative of the
claimant he will be allowed to claim for any earnings lost as a result of caring for
the claimant, see for example Donnelly v Joyce [1974] QB 454 and Hardwick v
Hudson & Another [1999] 3 All ER 426. In the latter cases the Court of Appeal held
that damages could not be awarded to compensate the victim’s wife for giving her
unpaid services to her husband’s business. A distinction was made between
voluntary services provided in a commercial as distinct from a domestic
environment.
9.3.3 Medical Expenses
These may be any expenses caused by the claimant’s injuries. Note, further, that
the claimant may claim for the cost of private medical treatment notwithstanding
that the same is available on the NHS pursuant to s.2 (4) Law Reform (Personal
Injuries) Act 1948. In Parkhouse v North Devon Healthcare NHS Trust [2002] 3
Lloyd’s Rep Med 100 the defendant argued, on appeal, that the award associated
with wheelchair funding should be disregarded as the equipment was supplied by
the state and/or charitable institutions. Mr Justice Gage found on the evidence that
the state would probably continue to provide the equipment free of charge but only
on occasions and therefore only discounted the award to reflect this. In the more
recent case of A v B Hospitals NHS Trust [2006] EWHC 1178 the court awardeddamages for the cost of having two carers. The claimant suffered from dystonic
athetoid quadriplegic cerebral palsy and dyskinetic tetraplegic cerebral palsy. The
Trust admitted liability for clinical negligence and all parties agreed that the
claimant was incapable of carrying out any activities of daily living without
assistance and that he required 24 hour care. He was entirely dependent on other
people for all his routine needs. As it was very difficult to transfer the claimant into
positions in which his care could be properly administered it was apparent that it
was unsafe for both the claimant and the carer for that transfer to be attempted by
a carer working alone. The combination of the claimant’s size and weight together
with his capacity for involuntary movements made it essential for two carers to be
present. When one of the claimant’s parents were on hand to provide the care it
would not be reasonable to have two commercial carers present, but it was not
sensible just to award damages for only one professional carer as the claimant’s
parents could not always be relied on as available to assist. As his parents also
preferred his care to be provided by professional carers hence it the court inferred
it was reasonable to take this approach in awarding damages.
For a more recent example see Smith v East & North Herts Hospitals NHS Trust
[2008].
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9.3.4 Loss of Earnings
The claimant’s employer will be contacted to calculate what earnings the claimant
has lost as a result of being absent from his employment. The claimant will be
allowed to recover his loss of earnings net of tax. If the claimant is self-employed
an accountant will need to be instructed. The claimant’s solicitor is required to
prepare a schedule of special damages that must be served with the proceedings.
Note that the claimant must give credit for any benefits received.
9.3.5 Other Expenses
These can be anything as a result of the accident, e.g. the costs of a specially
adapted car, special clothing or food etc.
9.3.6 Interest
The claimant is entitled to interest at 2% on general damages for pain, suffering
and loss of amenity. Interest on special damages will usually run from the date of
the cause of action to trial or earlier settlement at half the court’s special account
rate (currently 7%). There can be no interest claim for future losses.
9.4 BENEFITS
The claimant is not permitted to recover twice. The recoupment provisions under the
Social Security (Recovery of Benefits) Act 1997 will apply if the claimant has been
receiving benefits as a result of the accident and the defendant (compensator) makes a
payment in respect of damages for personal injury to the claimant. The benefit that is
r ecoverable is that which has been paid “in consequence of any accident, injury or
disease” and the relevant period over which benefit is paid begins the day after the injury
or accident, or in the case of disease the first day benefit is claimed. The period ends five
years later or whenever the last compensation payment is made whichever is the sooner.
Note that the clawback provisions do not apply to compensation awarded for pain and
suffering and future loss of earnings.
9.5 LOSS OF A CHANCE
This has already been noted in Causation, see for example Hotson v East Berkshire HA
[1987] 2 All ER 909, Gregg v Scott [2005] UKHL 2, and Stovold v Barlows [1996] 1 PNLR
91. Note that the claimant will either recover all of the damages or nothing at all; the
courts do not favour the proportionality approach as endorsed by cases such as Bagley v
North Herts HA (1986) 136 NLJ 1014 and Clark v McClennan [1983] 1 All ER 416.
Where the claim is that but for the defendant’s negligence the claimant would haveenjoyed a better quality of life for a longer time the courts will compensate that loss, see
Sutton v Population Services Family Planning Programme Ltd (1981) The Times 7
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November . In Sutton if the claimant had been diagnosed earlier it would have delayed the
onset of cancer by up to 4 years therefore the claimant was compensated for those four
years when she would have led a normal life.
9.6 WRONGFUL LIFE / BIRTH / CONCEPTION
A wrongful life claim is brought by the parents of a disabled child who has been born as a
result of the defendant’s negligence, e.g. a failed abortion attempt. The claimant’s claim
is that had the defendant not been negligent then he would not have been born, i.e. that
non-existence is preferable to the existence he now has. In McKay v Essex AHA [1982]
QB 1166 the court held that damages could not be awarded against a doctor for failing to
advise a mother to have an abortion. The court gave a variety of reasons for disallowing
the claim but one of the more significant was that to award damages here would mean
that the court would have to compare non-existence with existence and that would mean
assessing the value of the life of a handicapped child as less worthy than that of a normal
child. This approach has recently been followed by the Australian courts, see Harriton v
Stephen MLC 1104 where a wrongful life claim was disallowed as the claim did not
reflect values generally or widely held in the community.
Wrongful birth is the equivalent of a wrongful life claim save that the claim is brought by
the parents following the birth of a handicapped child, claiming for pain, suffering,
physical injury and financial loss. In McKay this part of the claim was successful.
Damages for wrongful conception are claimed for the upkeep of a healthy child which has
been born as a result of a failed vasectomy/sterilisation operation. The mother may also
claim the compensation for the pain and suffering associated with pregnancy and
childbirth. Up until 1993 compensation was also awarded notwithstanding the child is a
healthy child, (a wrongful conception claim), see Allen v Bloomsbury HA [1993] 1 All ER
651. However the House of Lords took the opposite view in the Scottish case of
McFarlane v Tayside Health Board [1999] 4 All ER 961. The Health Board successfully
appealed against the Court of Session’s decision to award damages for the birth of a
healthy child following a negligently performed vasectomy. The House of Lords accepted
that the loss (that is the cost of bringing up the child) was foreseeable but saw the
question as a wider issue – what was the extent of the duty of care owed to the husband
and wife and what was the liability of the defendant in what was viewed as a claim for
economic loss. Lord Slynn asked was it “fair, just and reasonable for the law to impose a
duty” and that the doctor’s duty was only to avoid a pregnancy and that did not extend to
the costs of rearing a child if born and accepted into the family. Lord Steyn however saw
the decision as being one of corrective justice versus distributive justice and sometimes a
decision had to be made between the two approaches. In this instance the principle of
distributive justice dictated that the law of tort did not permit parents of a healthy
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unwanted child to claim the costs of bringing up the child from the health authority or
doctor. The claim did not satisfy the requirements of being fair, just and reasonable. Note
however that the parents were allowed to recover the costs of the solatium and costs
attendant on the pregnancy.
In the recent case of Denise Less and Michael Carter v Sarah Hussain [2012] EWHC3513 the court once again considered what was the scope of the duty of care owed to the
claimants in matters of conception. The claimants’ alleged that the defendant had not
given proper advice about the risks of pregnancy, namely the presence of a known
thromboembolic condition, and had such risks been explained Ms Less would not have
fallen pregnant. The claimant’s child was stillborn. The judge accepted the argument on
breach of duty however the claimants’ case failed on causation as the court found that
even if proper advice had been given the claimants would have proceeded with
conception. Commenting obiter on the scope of the duty owed the judge concluded that
to satisfy the duty of care the doctor must give the patient sufficient information to enable
the patient to make a balanced decision. Applying Walkin the judge ruled that the starting
point for the injury was conception and given that the advice was about conception, the
judge considered that the loss of the baby during term was a kind of loss in respect of
which a duty was owed, it made no difference that the precise manner of the loss was not
foreseen. Moreover it would have been fair, just and reasonable to compensate Ms Less
for her injuries applying the same principles that a mother of a disabled child can and as
such she would have been entitled to damages for pain, suffering and loss of amenity
and some special damages. She would not be entitled however to the Rees award (see
below) as there was no loss of autonomy.
The first wrongful birth case to come before the courts after the McFarlane decision was
Rand v East Dorset HA [2000] 4 Lloyd’s Rep Med 181. The parents claimed damages for
the defendant’s negligent omission to advise Mrs Rand that she may give birth to a
disabled child and consequently her loss of opportunity to terminate the pregnancy. The
child was subsequently born with Down’s Syndrome. The Court of Appeal held that the
parents were entitled to recover for those losses relating to their child’s disability and not
for the full cost of bringing up the child. This ruling was followed in the Scottish case of
McLelland & Another v Greater Glasgow Health Board March 7, 2001, MLC 0364.
Both Rand and McClelland are distinguishable from McFarlane not just on the basis that
the resulting child was born disabled as opposed to healthy but also on the nature of the
respective claims. Rand and McClelland were both cases concerning a failure to
diagnose rather than a failed sterilisation / vasectomy claim. However in Parkinson v St
James and Seacroft University Hospital NHS Trust [2001] 6 Lloyd’s Rep Med 309 the
Court of Appeal considered what costs are recoverable for the birth of an unplanned
disabled child. Brooke LJ held that the parents’ award should be limited to those extra
expenses associated with the child’s disabilities. Parkinson was then applied in Roberts v
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Bro Taf Health Authority [2002] 4 Lloyd’s Rep Med 182 where the High Court ruled that
damages are not to be limited by the economic circumstances of the family as, the court
reasoned, this would be inconsistent with Parkinson and, in any event, the agreed
general damages would alter the claimant’s status.
In Rees v Darlington Memorial Hospital NHS Trust [2003] UKHL 52 the Court of Appeal
had previously awarded damages to a blind woman for the costs of bringing up a healthy
child following a failed sterilisation. Katrina Rees who was born with a genetic disorder
was blind in her left eye and had only one sixth of normal vision in her right. She had
wanted to be sterilised because of her visual handicap which made her doubt her ability
to look after a baby. The Trust admitted that the operation was negligently performed but
disputed quantum. At first instance the court albeit reluctantly refused her claim for the
costs of bringing up her son to his 18th birthday. The Court of Appeal ruled that Miss Rees
was entitled to cover the extra costs of bringing up her son attributable to her disability.
Lady Justice Hale commented that this case raised “novel and important” issues and told
the court that “we can only imagine the difficulties facing them both.” A factor influencing
this decision was that Ms Rees disability was known to the surgeon – it was pre-existing
and the surgeon knew that was the reason why she was being sterilised.
The decision was appealed to the House of Lords who decided:
A disabled mother who gave birth to a healthy child after a negligently performed
sterilisation operation was not entitled to recover the extra costs of child care
occasioned by her disability. Instead a conventional award of £15,000 would be
made to mark her injury and loss of the benefit she was entitled to expect.
Unusually there were 7 Law Lords sitting and it was a 4-3 majority. Their Lordships
declined to reconsider their views on the McFarlane decision. There is however little
consistency in their reasoning. Three of their Lordships (LJ Hope, LJ Millet and LJ Steyn)
had been three of the judges in the McFarlane case. In McFarlane Lord Justice Millet had
alone proposed that all the mother should be awarded was £5,000 for the loss of the right
to control the size of her family (“the Millet award”). In Rees however four of the judges
(Bingham, Nicholls, Millet and Scott LJ) allowed pregnancy damages plus the “Millet
award” which they increased to £15,000. Lord Steyn and Lord Hope dissented arguing
that this ran counter to the view of the majority in McFarlane.
Clearly the McFarlane decision was reached on two grounds. First that a child is a god-
given gift and his birth should not be the subject of a claim (Lord Justice Millet per
McFarlane “morally offensive to regard a normal healthy baby as more trouble and
expense than it is worth.”). Secondly that the benefit the cla imant receives from having a
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child must be set against the economic loss claimed and as that benefit is incalculable, no
damages may be awarded for economic loss. Are these arguments sustainable?
Their Lordships could also not come with a universal answer to the question does the
McFarlane rule apply to all negligent birth cases?
The three dissenting Law Lords were LJ Steyn, LJ Hope and LJ Hutton. Lord Steyn
agreed with Parkinson, and contended that McFarlane did not apply to the seriously
disabled child. The case of a disabled mother as in Rees was an exception to the
McFarlane rule. Lord Hope was of a similar mind and Lord Hutton simply stated that it
was fair, just and reasonable to award extra damages for the extra costs of bringing up a
disabled child and that there was a clear distinction between a healthy mother and a
disabled one.
So to summarise what seems to be the current position:
Cases where the child is born healthy – an award of £15,000 plus costs arising directly
out of the pregnancy (McFarlane)
Cases where the child is born disabled – difficult to say as all their Lordships gave
differing opinions but damages for the additional costs of upbringing arising from the
handicap (Parkinson) still seem recoverable
Cases where the parent is disabled parent – damages as for the birth of a healthy child –
no extra award for the parent’s disability.
And The Australian View is…..
The Australian courts however rejected McFarlane in Cattanach v Melchior [2003] 9
Lloyds Rep Med 447; [2003] HCA 38; MLC 410 ( textbook page 390). This was again
a failed sterilisation case and a claim for the upkeep of a healthy child. On further appeal
to the High Court by a majority of 4-3 it was held that the defendant was in breach of duty
to the claimant and that had been the cause of her pregnancy. Although the claim was for
pure economic loss it involved in Mrs Melchior’s pregnancy an element of personal injury
and therefore the court would more readily impose a duty of care. It was reasonably
foreseeable that if Dr Cattanch was negligent the result would be a pregnancy the very
consequence Mrs Melchior had sought to avoid. The Australian courts reasoned that as a
matter of public policy it was in society’s interests to encourage the nurturing of children
within the family unit and the award of such damages would encourage this. It was
unseemingly and against public policy to litigate the potential benefit or otherwise of the
birth of a child. At paragraph 68 per McHugh and Gummow JJ:
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“The unplanned child is not the harm for which recompense is sought in this
action; it is the burden of legal and moral responsibilities which arise by
reason of the birth of the child that is in contention.”
The idea of any notional set-off between any damages for the costs of rearing a child andthe joys of raising a child was also rejected. At paragraph 90 Kirby J commented:
“But the head of damages that is relevant in the present case is the financial
damage that the parents will suffer as the result of their legal responsibility to
raise the child. The benefits to be enjoyed as a result of having the child are
not related to that head of damage. The coal miner, forced to retire because
of injury does not get less damages for loss of earning capacity because he
is now free to set in the sun each day reading his favourite newspaper.
Likewise, the award of damages to the parents for their future financial
expenditure is not to be reduced by the enjoyment that they will or may
obtain from the birth of the child.”
And at paragraph 179 Kirby J said:
“Ordinary principles of tort liability would entitle the victim of the appellants’
wrong to recover from the appellants all aspects of their harm that are
reasonably foreseeable and not too remote. By the application of that test
the inclusion in the parents’ damages of a component for the costs of child -
rearing involved no legal or factual error.”
The High Court refused to draw any distinction between the birth of a healthy or disabled
child ruling that it would be discriminatory and was irrelevant to the award of damages.
Further Reading
Emeh v Kensington & Chelsea & Westminster A.H.A [1985] QB 1012
Thake v Maurice [1986] QB 644
Goodwill v BPAS [1996] WLR 1397
Walkin v South Manchester H.A. [1996] 7 Med LR 211
Lovelace Medical v Mendez (1991) 805 P 2d 603
CES Superclinics (Australia) Pty Ltd [1996] Med L Rev 102
Provenzano v Integrated Genetics (1998) 22 F Supp 2d 406.
Roberts v Bro Taff Health Authority [2002] 4 Lloyd’s Rep Med 182
Groom v Selby [2002] Lloyd’s Rep Med 1
AD v East Kent Community NHS Trust [2002] 9 Lloyd’s Rep Med 424
“Return of the burden of blessing” Dr J Ellis Cameron-Perry, (1999) NLJ December 17 pp1887-
1888
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“Wrongful birth. New light from the North” Charles Foster Solicitors Journal 21 January 2000
Booth Penny “A child is a blessing heavily in disguise, right?” New Law Journal Nov 23 2001
page 1738
“Failed Sterilisations And Child Costs Revisited” Roderick Denyer, Family Law Feb 2004 Vol 34
page 123.Brazier & Cave, “Medicine, Patients and the Law” 5
th ed (Penguin) Chapter 12
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9.7 DAMAGES FOR NERVOUS SHOCK CAUSED TO A RELATIVE
There have been a number of claims where a relative alleges that he has suffered
nervous shock after seeing a loved one suffer/die as a result of medical negligence. See
Sion v Hampstead H A [1994] 5 Med LR 170 and in contrast in Tredget & Tredget v
Bexley H A [1994] 5 Med LR 178. In Tan v East London & City H.A. [1999] 9 Lloyd’s Rep
Med 389 a father who was informed by telephone of the death in utero of his daughter
and who then spent several hours comforting his wife, watching the caesarean delivery of
his dead child, and then keeping an overnight vigil claimed damages for psychiatric injury
from the defendant health authority. The health authority admitted that the stillbirth was
the result of their negligence. The claimant’s claim failed however for several reasons.
First it was held that the claimant did not witness the immediate aftermath (i.e. death of
the child in utero); secondly the death, still birth and vigil were not all one event and
therefore did not satisfy the aftermath test; and finally the psychiatric illness was not
induced by shock, e.g. the caesarean operation was planned etc.
Is this a good decision? The Law Commission Report No 249, Liability for Psychiatric
Illness stated that the “aftermath” principle was unjust. It recommended that where the
claimant is the secondary victim that the only restriction that should be imposed on a
claimant is that he should be able to demonstrate a close tie of love and affection with the
victim.
In Walters v North Glamorgan NHS Trust [2003] Lloyd’s Rep Med 49 the Appeal Court
took a rather more lenient view as to what events may constitute a shock and thus come
within the aftermath principle. The claimant was a mother who had suffered pathological
grief reaction as a result of the death of her baby son aged 10 months. The defendant
had failed to diagnose acute hepatitis in the claimant’s son and, it was accepted that, if
properly diagnosed and treated the child would have been given a liver transplant. The
claimant who was staying at hospital with her son awoke to find him choking and large
amounts of blood. A CAT scan was then carried out and the claimant was told that her
son had suffered no brain damage and that he should be transferred to another hospital
for a liver transplant. On transfer the claimant was informed that he had suffered severe
brain damage and eventually agreed to his life support machine being disconnected.
It was not in dispute that the claimant had suffered a pathological grief reaction but on
appeal the defendant argued that the claimant’s illness was not induced by shock. The
Court of Appeal found that the law permitted a realistic view to be taken in each case as
to what constituted the necessary event and found that the claimant’s appreciation was
sudden rather than an accumulation of gradual assaults on her mind. The Appeal Court
held that being woken by the convulsion; the unexpected news on arrival at the second
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hospital and the switching off of the life support machine all had a sudden impact there
and then.
In the interesting case of Froggatt v Chesterfield & North Derbyshire Royal Hospital MLC
0887 not only was the claimant awarded damages for psychiatric trauma caused by thenegligent diagnosis of breast cancer and an unnecessary mastectomy but the claimant’s
husband and son were also awarded damages for the psychiatric illness they had
suffered as a result of these events. The claimant’s husband and son had established
that they were both secondary victims. The claimant’s husband illness had begun when
he first saw his wife undressed for the first time following the mastectomy and was quite
unprepared for what he saw. In the case of the son his sudden appreciation of a
horrifying event came when the claimant, as a result of the negligent advice she had
been given, felt compelled to tell him that she had cancer and was likely to die.
In Atkinson v Seghal [2003] Lloyd’s Rep Med 285 Mrs Atkinson; had refused to give her
daughter (Livia) a lift to her ballet class which resulted in her daughter walking to the
class. Tragically on her way there Livia was knocked down and killed by a motor cycle.
The accident happened at 7.05pm and Livia was pronounced dead at 7.40pm. When
Livia had not arrived home by 8.05pm her father decided to drive to the ballet class. He
was diverted by a police cordon, arriving at the class to find that she was not there. He
was informed of Livia's death by the police officers at the scene. Ms Atkinson had
travelled down the scene independently and had been told by a police officer that Livia
was dead. The parents were then driven in a police car to the mortuary, arriving at
9.15pm where Livia's body was seen by her parents including disfiguring facial and head
injuries. Ms Atkinson cradled her daughter. After Livia's death Ms Atkinson was a regular
visitor to the graveyard and made her home a shrine to her daughter. Mr Justice Wilson
referred to the "seamless activity" that had taken place using the phrasing that had been
adopted in Walters and upheld Ms Atkinson's claim for psychiatric damage. However it is
debatable whether in Atkinson there was a seamless activity - the three events that Ms
Atkinson experienced namely arriving on the scene, being informed of her daughter's
death and attending at the mortuary are clearly more discrete events than those
experienced by Ms Walters who was with her child from his first fit to his final diagnosis of
brain damage. Further it was some two hours and ten minutes after the accident that Ms
Atkinson saw her daughter. This is a considerably longer period than the one hour before
Mrs McLoughlin saw her children in McLoughlin v O'Brien and arguably not within the
"immediate aftermath" of the accident. Ms Atkinson had experienced a shocking event
but were the courts stretching the boundaries of what constitutes immediacy and
aftermath to rule in her favour?
Finally see (1) JD (2) MAK & RK (3) RK & ANOR v (1) East Berkshire Community Health
NHS Trust & Ors & Two Other Actions [2005] UKHL 23 where the appellant parents
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argued that their claims for damages for psychiatric injury against doctors or social
workers who had wrongly determined that they had abused or harmed their children
should not have been dismissed on public policy grounds. The appellants submitted that
the health care professionals’ duty to exercise skill and care when investigating child
abuse extended to the child’s parents as primary carers as well as to the child. TheHouse of Lords (Lord Bingham dissenting) held that health professionals responsible for
investigating suspected child abuse did not owe a parent suspected of having committed
the abuse a duty sounding in damages if they carried out that investigation in good faith
but carelessly. Furthermore the respondents did not owe substantially the same duty of
care to the parents as to the children as the parents were not deemed to be in sufficient
proximity to give rise to a duty of care. The House of Lords agreed with the Court of
Appeal that there were cogent reasons of public policy not to impose a duty of this nature
and furthermore it could place the health professional in a position where he owed
conflicting duties.
At present there does not seem to be any hard and fast rule for these claims and the
courts’ approach is rather inconsistent. If damages are awarded under this head they will
extend to all foreseeable damages in line with the decision in Smith v Leech Brain & Co
Ltd [1962] 2 QB 405, Page v Smith [1995] 2 WLR 644 and the egg shell skull rule, see
paragraph 8.7.
There have been a number of recent decision on psychiatric damage see Less and
Carter v Hussain [2012] EWHC 3513 and Crystal Taylor v A Novo (UK) Ltd [2013] EWCA
Civ 194. In the first of these cases (see para 8.8 for facts) although the judge held that Mr
Carter was a secondary victim he ruled that his bereavement reaction was not caused by
the result of “shock” so his claim had not been made out. In Taylor the daughter of a
woman who died unexpectedly three weeks after an accident at work failed in her claim
for damages against her mother’s employer because she had not witnessed the accident
or its immediate aftermath. The Court of Appeal thus allowed the defendant’s appeal
ruling that it was the mother’s accident and not her subsequent death that was relevant
for purposes of proximity. In Liverpool Women's Hospital NHS Foundation Trust v
Ronayne | Westlaw UK a husband claim for damages for psychiatric injury he suffered
following his wife’s hysterectomy failed as the court ruled the necessary “shock” element
was not present and secondly his wife’s appearance was not exceptional for a person in
hospital.
See also Shorter v Surrey and Sussex Healthcare NHS Trust; Wild v Southend University
Hospital NHS Foundation Trust [2014]; Brock v Northampton General Hospital NHS Trust
[2014].
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Further Reading:
Taylor v Somerset H.A. [1993] 4 Med LR 34
Taylorson v Shieldness [1994] PIQR 329
AB v Tameside & Glossop H.A. [1997] PNLR 140
Allin v City & Hackney H.A. [1996] 7 Med. L.R. 167
Reilly & Reilly v Merseyside R.H.A. [1995] 6 Med LR 246
Jones v Royal Devon & Exeter NHS Trust [2008] EWHC 558.
9.8 MITIGATION
As with any other area of tort the claimant has a duty to mitigate his damages. This may
mean that the claimant should undergo further medical treatment, but that treatment
should be reasonable in all the circumstances. A failure to have an abortion after a failed
sterilisation is not considered unreasonable, se Emeh v Kensington and Chelsea AHA
[1985] QB 1012. In Geest plc v Lansiquot [2002] Lloyd’s Rep Med 482 a claimant’s
refusal to undergo surgery on a prolapsed disc which she had sustained during an
accident at work was not unreasonable in the absence of any guarantee from her doctor
that such surgery would be successful and therefore she had not failed to mitigate her
loss.
9.9 METHODS OF AWARDING DAMAGES
9.9.1 Lump Sum
Traditionally damages are awarded in a lump sum on a once and for all basis.
9.9.2 Structured Settlements – the end of
As of 1 April 2005 periodical payments may now be imposed by the court for all
personal injury claims involving future pecuniary loss. Section 100 of the Courts
Act 2003 substitutes a new s 2 of the Damages Act 1996. Under section 2(1) of the
Damages Act 1996 the court may order that the whole or part of the award should
take the form of periodical payments. Additionally under s 2(2) of the Damages Act
the court may order that other damages be paid by periodical payments but only if
the parties consent. The court will also have the power to award an interim
payment through periodical payments. Section 2B of the Damages Act will enable
the Lord Chancellor by order to empower the courts to vary periodical payments in
specified circumstances.
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Previously structured settlements could only imposed where the parties consent. It
seems under the new system that periodical payments will be imposed whenever
the courts consider them suitable.
For examples of structured settlements see A v B Hospitals NHS Trust [2006]EWHC 2833 and Thompstone v Tameside and Glossop Acute Services NHS Trust
EWHC 29904
9.9.3 Provisional Damages
This is an exception to the general rule that damages are awarded once and for all.
Where the claimant’s condition is uncertain then the claimant’s may be awarded
damages for his present condition and then be awarded further damages at a later
date should his condition deteriorate. See Willson v Ministry of Defence [1991] 1
All ER 638 where the court laid down guidelines for when an award of provisional
damages will be appropriate. An application for provisional damages should be
made under Civil Procedure Rules Part 41.
9.9.4 Interim Payment
In certain circumstances the claimant may be awarded a payment on account of
the eventual damages he may be awarded at trial. This will only occur where it
seems apparent that the claimant will win at trial or the defendant has already
admitted liability. An application for an interim payment may be necessary whenthe claimant requires immediate nursing care or has other immediate medical
expenses. Any application for an interim payment should be made under Civil
Procedure Rules Part 25, r 6. Note that for any case involving an infant the award
of an interim payment, provisional damages or structured settlement will first
require court approval. For ant example decision on the appropriateness of interim
payments see Isla Richmond v East & North Hertfordshire NHS Trust [2007]
EWHC 1999.
9.10 DAMAGES WHICH ARE NOT ENTIRELY COMPENSATORY
9.10.1 Exemplary Damages
Essentially these damages are awarded against the defendant to “teach him a
lesson”. See Rookes v Barnard [1964] 1 All ER 367.
Although damages of this nature are awarded in other jurisdictions in the area of
clinical negligence and product liability they are not as yet favoured by the English
courts. The Law Commission in Report No 147 “Aggravated, Exemplary andRestitutionary Damages” recommended that exemplary damages should be
renamed as punitive damages and should be very much awarded as a last resort.
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Further Reading:
Stauch & Wheat: Text, Cases and Materials on Medical Law (5th
ed) (Routledge)
Jackson: Medical Law Text Cases and Materials (Oxford University
Press 3rd
ed) Chapter 3,14
Pattinson: Medical Law and Ethics (Sweet & Maxwell) Chapter 3
Brazier & Cave: Medicine, Patients and the Law (5th ed)
Penguin Books), Chapters 8, 11
Khan, Robson & Swift: Clinical Negligence (2nd
ed) Cavendish Press Limited Chapter 7
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SUMMARY
At the end of this chapter you should be able to:
* explain the difference between general and special damages;
* identify the various ways that compensation may be awarded;
* identify any factors which may reduce the award.
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SELF-TEST QUESTIONS – CHAPTER 9
1. How is loss of future earnings assessed?
2. In what situations will a claim for psychiatric injury as a result of the negligence
of a doctor or hospital succeed?
3. Distinguish between “wrongful life”, “wrongful birth” and “wrongful conception”.
4. Distinguish between exemplary and aggravated damages
5. What are provisional damages?
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CHAPTER 10
CLINICAL NEGLIGENCE LITIGATION
10.1 INTRODUCTION
Following the Woolf Report “Access to Justice” civil procedure has undergone a drastic
review. There is now one set of rules - The Civil Procedure Rules that govern procedure
in both the High and County Court. Every part of the rules has a corresponding practice
direction that must be followed. Additionally a number of pre-action protocols have been
introduced, for our purposes the most relevant being the protocols for personal injury
claims and for clinical negligence actions. Great emphasis has been placed on the
overriding objective of the new civil regime as being to enable the court to deal with cases
justly. One of the ways the court will seek to do this is by active case management, that
is the courts will take a very much more pro-active approach. Before we look at the rules
and protocols in more detail there are a number of preliminary matters the solicitor must
deal with.
10.2 THE FIRST INTERVIEW
The solicitor will take a detailed statement from the client and sometimes also a close
relative (known as a proof of evidence). The first question that should be addressed is
what does the client want - an apology or compensation? Has the client contacted any
other agencies such as the Citizens Advice Bureau or lodged a complaint with the Health
Authority? If yes the solicitor should obtain any papers from these organisations. It will
need to be made clear to the client that ultimately court action will often result in only the
objective of monetary compensation being achieved and not an apology or any other
remedy (although it may be possible to use Alternative Dispute Resolution). The solicitor
should also be alive to the fact that the client has already placed his trust in the hands of
one group of professionals, namely his health carers, only to be let down and he may find
it difficult to place his trust in yet another professional. The statement should cover all
matters of liability and quantum and will be updated frequently as new evidence comes to
light. Clients have notoriously poor memories and will often remember events long after
the first statement.
The First Interview -Examples of questions to ask
The names of all medical staff involved in the client’s treatment if known to include
GPs and hospital doctors/staff;
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What was said by the client to the doctor and vice versa at each consultation and
what treatment was given and how did the client respond;
Were any witnesses present at any of the appointments or procedures?
Any relevant medical history to include what was the client’s condition prior to the
clinical treatment he complains of; Who administered the treatment, where was it administered and when?
What was the outcome of the treatment?
The reason why the client thinks his care was negligent;
Whether a formal complaint has been made if yes to whom, with what result and
when?
What made the client think that treatment had gone wrong? Did anyone say
anything to the client that made him realise that the treatment had gone wrong? If
yes, what was said and when and when did he first think of going to a solicitor?
Following the interview the solicitor will draft the client’s proof of evidence and send
it to him for checking. Additionally the solicitor will:
* ask the client to complete a form of authority for the release of his medical
records;
* send a client care letter in accordance with Solicitors Practice Rule 15;
* identify the expiry of the limitation period;
* consider any other special considerations e.g. in the case of a minor the
appointment of someone to act on his behalf known as a litigation friend, or
in the case of a fatality whether to attend an inquest.
Note that the solicitor will have discussed how the case is to be funded at the first
interview and funding is dealt with in the paragraphs immediately below.
10.3 FUNDING
At the first interview the matter of how the case is to be funded must be addressed.
10.3.1 The privately funded action
The privately paying client must be aware of how the costs are calculated and how
much the case is likely to cost in accordance with r 15 Solicitors Practice Rules and
also the Solicitors’ Costs Information and Client Care Code 1999. The privately
funded action is now relatively rare as clinical negligence claims are generally
complex and expensive involving consideration of often lengthy medical records
and instructing several independent experts.
10.3.2 Legal Aid, Sentencing and Punishment of Offenders Act
2012 - The End of Legal Aid
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1 April 2013 marked the coming into force of the Legal Aid, Sentencing and Punishment
of Offenders Act (LASPO) 2012. Under its provisions, legal aid for medical negligence
claims will very restricted. This passing of LASPO has not been without controversy, the
President of the UK Supreme Court, Lord Neuberger, commented, “My worry is the
removal of legal aid for people to get advice about law and get representation in court willstart to undermine the rule of law because people will feel like the government isn’t giving
them access to justice in all sorts of cases.” Lord Bach, the former Labour justice
secretary, has also commented: “Has there ever been an Act that so picks on the poor
and attacks access to justice?”
Legal Aid is now restricted to claims involving children who have been seriously injured
during pregnancy, childbirth or within the first 8 weeks of life. There as yet seems to be
no explanation as to why the “cut off” point of 8 weeks of life was chosen. There remains
however for most medical negligence cases the opportunity to bring a claim under a
conditional fee agreement, which is discussed in the paragraphs below.
10.3.2 Conditional Fee Agreements
There is also the possibility of a conditional fee arrangement under s.58, 59 of the
Courts and Legal Services Act 1990 whereby the solicitor agrees with his client
that he will charge an enhanced fee, if he is successful, together with his basic
charges and disbursements (such as fees for medical reports etc.) A success fee
becomes payable because the solicitor has taken a risk when agreeing to enterinto a conditional fee agreement with the client. There is no guarantee the case will
be won and even if it is the solicitor will only receive payment at the end of the case
(in contrast to a case which is privately funded where the client is often requested
to make payment on account). However, if he should fail then the client will only
be responsible for his opponent’s costs and his own solicitor’s disbursements.
Before agreeing to take the case on that basis the solicitor must make an accurate
risk analysis of the situation, i.e. with reference to the facts, the law and the
evidence what is the client’s pr ospect of success. If the solicitor is incorrect with his
assessment of the risk then the client loses and he will forfeit his fees. The risk
assessment is also vital in deciding the appropriate success fee, see below.
10.3.4 Conditional Fee Agreements and LASPO
Now under LASPO, although a successful claimant may still recover his legal costs
from the defendant, the success fee element of the case is not recoverable and
can be deducted from his damages. There is however a cap to any success fee
that can be deducted from the claimant’s damages of 25% of general damages
(damages awarded to compensate for pain and suffering) and past losses (i.e.,
losses already incurred: no deduction can be made from future losses). To mitigate
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the effect of this the level of damages awarded for pain and suffering will be
increased by 10%.
10.4 LIMITATION
Please refer to ss 11,14,28,33 Limitation Act 1980. Note all references are to the
Limitation Act 1980 unless otherwise stated.
10.4.1 Trespass Claims
If the claimant’s claim is for purely financial losses, e.g. damage to his business
reputation or the claimant’s claim is brought in trespass then the limitation period
may be six years, s.2. In Stubbings v Webb [1993] AC 498 the court held that in
the case of a deliberate assault then this fell within the six year rule. This case
arguably implied that where the claim is that the patient did not consent to the
medical procedure then the claim should be brought in trespass and so fall within
the six year rule. However recently the House of Lords in A v Hoare and others
[2008] UKHL 6 held that Stubbings had been wrongly decided and the correct
approach was set out in Letang v Cooper (1965) 1 QB 232 and that an action for
damages for personal injuries for intentional trespass did not fall outside the three
year limit and hence the claimant could rely on s.33 of the Limitation Act and
request the court to exercise their discretion and extend the limitation period.
10.4.2 Claims for personal injury
In most cases, however, the claim will be for personal injuries and should be
brought within three years of either the accrual of the action or when the claimant
has knowledge, see ss11, 14(1), (3). Personal injuries is defined in s.38(1) and
includes “any disease and any impairment of a person’s physical or mental
condition”. Following the decision in Walkin v S Manchester H.A. [1996] 7 Med LR
211 a claim which was confined to the merely financial losses, the costs of rearing
a child following a negligent sterilisation, may still be held as a claim for personal
injuries and consequently within the three year rule.
See also Godfrey v Gloucestershire Royal Infirmary NHS Trust [2003] Lloyd’s Rep
Med 398 which considered the effect of Walkin.
In clinical negligence cases the crucial date from when the three year period will
run will be when the claimant has knowledge that he has a claim i.e. that his injury
was significant. The majority of claimants, however, do not realise they have a
claim until sometime later.
Knowledge can either be actual (s.14(1)) or constructive (s.14 (3)).
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[Note: a claim brought under the Human Rights Act 1998 must be begun within a
period of one year of the date on which the act complained of took place unless
there is a prescribed shorter time limit for the proceedings, s.7 (5) HRA 1998.]
10.4.3 Actual knowledge
See s.14 (1). It is not necessary for the claimant to know of the specific act or
omission which caused his injury or that he has a claim as a matter of law, i.e. that
the defendant was negligent, what he must have is some broad knowledge that
something has gone wrong. See for example Briggs v Pitt Payne & Lias [1999] 1
Lloyds Rep Med 1; Dobbie v Medway HA [1994] 5 Med LR 160 and Hallam-Eames
and others v Merrett [1996] 7 Med LR 122 (a non-medical case).
The courts have constantly sought to refine this concept of what constitutes
knowledge. In North Essex District H A v Spargo [1997] 8 Med LR 125 the Court
of Appeal held that the claimant should have “a broad knowledge of the essence of
the causally relevant act or omission to which the injury is attributable, that is in the
sense of being a real possibility”. The Court of Appeal to a certain extent qualified
this approach and added that if a claimant is mistaken in her belief and in fact is
“barking up the wrong tree” she will not have knowledge, nor will she have
knowledge if the defendant’s conduct is so vague or general that she cannot be
expected to know what to investigate. In determining what she should be expectedto know her state of mind will be relevant.
See also the cases of Roberts v Winbow [1999] 2 Lloyd’s Rep Med 31 and Ali v
Courtaulds Textiles Ltd [1999] 8 Lloyd’s Rep Med 301. In Roberts v Winbow the
claimant was held to have knowledge despite medical assurances that her
condition was of unknown aetiology. Do you think it is reasonable that a claimant is
deemed to have knowledge even when his belief is contradicted by the full weight
of the legal and/or medical profession? Roberts was then applied in Rowbottom v
Royal Masonic Hospital [2002] 4 Lloyd’s Rep Med 173 where the Court of Appeal
held that time did not begin to run against a claimant until expert evidence was
obtained that informed him of the negligent omission that may have caused his
injury. After a total hip replacement in 1991 the claimant developed an infection
which eventually resulted in the amputation of his left leg. The claimant believed
this to have been caused by the failure of a drain inserted into the leg. He
consulted solicitors in 1991 who obtained an expert report in 1993. That report said
that there was only two things which may have lessened the likelihood of infection;
(1) inadequate suction (and in the expert’s view it would be difficult to make this
allegation stick); or (2) the failure to administer antibiotics, and the expert indicated
that there was nothing in the records to indicate that antibiotics were given.
However it was only after the solicitor raised further queries of the expert and when
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the expert responded that one could assume that no antibiotics were given that the
claimant, applying Spargo, was held to have knowledge. The Court of Appeal said
that this was very much a borderline case and indeed the judgment was on a 2-1
majority basis. Certainly the dissenting judgment of Gibson LJ is very persuasive.
Finally in Haward v Fawcetts [2006] UKHL 9, a professional negligence caseagainst a firm of accountants, the House of Lords looked at the degree of
knowledge required under s.14A(8) (a) of the Act (a claim for latent damage).
Although Haward is not a clinical negligence case it is of interest for the comments
their Lordships made on what constitutes knowledge and also the mere fact that it
is a House of Lords judgment. In Haward it was held that the degree of knowledge
required for the purposes of the Act was knowledge of the facts constituting the
essence of the complaint of negligence (Hallam-Eames v Merrett approved). The
relevant date was not when the claimant first knew that he might have a claim for
damages but rather an earlier date when he first knew enough to justify setting
about investigating the possibility that the defendant’s advice was defective. The
claimant did not have to have a detailed knowledge of how and why the defendant
had failed in their duty of care.
Haward has recently been applied in the arm vibration case, Kew v Bettamix Ltd
[2006] EWCA Civ 1535 referred to below.
After reading the judgments what do you think?
10.4.4 What is meant by constructive knowledge?
Under s.14 (3) the claimant’s knowledge inc ludes knowledge that he might
reasonable have been expected to acquire:
(a) from facts observable or ascertainable by him; or
(b) from facts ascertainable by him with the help of medical or other appropriate
expert advice which it is reasonable for him to seek but a person shall not be
fixed under this subsection with knowledge of a fact ascertainable only with
the help of expert advice so long as he has taken all reasonable steps to
obtain (and, where appropriate, to act on) that advice.
If the claimant is deemed not to have actual knowledge then the courts will look to
see if there was some point at which the claimant should have made further
enquiry. There has raged a debate whether or not the character and intelligence of
the claimant should be taken into account in determining the reasonableness of a
further enquiry, see Nash v Eli Lilly [1992] 3 Med LR 353, Forbes v Wandsworth
HA [1996] 4 All ER 881, Smith v Leicester H A [1998] 3 Lloyd’s Rep Med 77 and
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Fenech v East London City HA [2000] . The final word though has perhaps been
spoken on the subject in the recent House of Lords decision in Adams v Bracknell
Forest Borough Council [2004] UKHL 29 their Lordships held that first a claim for
damages for dyslexia was a claim for damages in respect of personal injuries and
more importantly that the test for constructive knowledge under the LA 1980 – section 14(3)(b) is objective not subjective. With regard to the test for constructive
knowledge their Lordships were faced with the question do you factor in all the
personal characteristics of the claimant or do you ask what the average sufferer
reasonably have done. Overall the judgement favoured the objective test with the
caveat that each case will still be decided on its own facts.
Lord Hoffmann stated that the particular characteristics or intelligence of the
particular claimant was not relevant “in the absence of some special inhibiting
factor.” The normal expectation is that a person suffering from a significant injury
will be curious about its origins. Lord Scott also felt that the test should be mainly
objective “it is the norms of behaviour of the person in the situation of the claimant
that should be the test”. In any event he said that the court could always exercise
its s.33 discretion. Baroness Hale queried whether there was much difference
between the two tests but she agreed that strictly personal characteristics such as
shyness or embarrassment are not relevant.
The overall outcome of all this is the test for constructive knowledge now is what
would you expect the average man or woman with this injury and in possession of
these facts to have done about making further enquiries – if the answer is more
than he did, is there any compelling reason, (supported by medical evidence where
relevant), for making this claimant a special case.
In Catholic Care (Diocese of Leeds) and another v Young [2006] EWCA 1534 a
child abuse case, the Court of Appeal held that the test for reasonableness under
s.14(3) was common to s.14(3) and s.14(2) following Adams v Bracknell (see
above). The more serious the claimant realised the injury was, the less likely the
court would be to conclude that any feelings of inhibition or other factors were
reasonable grounds for not instituting proceedings. The Court of Appeal reasoned
that as the court had a wide discretion to extend the limitation period the provisions
of the Limitation Act could be given their ordinary meaning.
Finally in Kew v Bettamix Ltd [2006] EWCA Civ 1535 the claimant brought a claim
in respect of his exposure to vibrating equipment during the course of his
employment with the defendant. In the early 1990’s the claimant had experienced
numbness in his fingers but had attributed that to his age. It was not until the late
1990’s that the claimant considered that his age might not have been the only
cause. Following a routine occupational health care assessment in March 2000,
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the claimant’s doctor informed him that his condition may be attributable to
exposure to vibration at work and confirmed later in that year that the claimant was
suffering from hand arm vibration syndrome. The claimant was not subsequently
called for review. The claimant issued proceedings in July 2004 and the judge at
first instance found that the primary limitation period had expired but chose toexercise her discretion under s.33.
On appeal with regard to what constitutes knowledge, Haward v Fawcetts (see
above) was applied, and it was found that the claimant did not have knowledge in
the early or late 1990’s as there was no evidence that the claimant had any idea of
the link between the injury he was suffering and his working conditions. However,
applying Adams v Bracknell the claimant was deemed to have constructive
knowledge from March 2000. Although he was not told of the causative link, the
doctor’s findings demonstrated that there was a real possibility that his working
conditions had caused the symptoms and a reasonable man would have made
further investigation.
More recently in Johnson v MOD, Hobourn Eaton Ltd [2012] EWCA Civ 1505 in a
case concerning industrial deafness, the Court of Appeal confirmed that s.14(3)
provides for an objective test as provided for in Adams. Dame Janet Smith
however commenting obiter sought to refine this rule by adding to the factors that
may be taken account as part of the objective “reasonable man” standard. Until
Johnson it was accepted that youth, mental capacity and the extent to which the
injury would reasonably inhibit the claimant but not the claimant’s particular
intelligence or character may be considered. Dame Janet Smith has sought to add
a further category; namely the seriousness of the condition and the way in which it
manifested itself. Thus a reasonable man might not have sought medical advice as
to a condition acquired at birth during childhood whereas it may have been
reasonable for him to have done so having sustained an operation following an
operation whilst in adulthood. It remains to be seen how this new caveat on the
objective test is worked out.
As a final example of the intricacies of s. 14(1) and s. 14(3) see Whiston v London
Strategic H.A. [2010] EWCA Civ 195. The claimant (W) suffered from cerebral
palsy caused by brain damage sustained at his birth in the defendant's hospital in
1974. W did not commence proceedings until 2006 alleging that there had been
negligence by a junior doctor who had who tried for over half an hour to deliver him
using forceps before seeking assistance from a more experienced registrar, who
went on to deliver W within five minutes using different forceps. W’s mother was a
nurse and had been trained as a midwife, and was concerned about her treatment
however she did not inform W of her concerns until 2005 when his health
deteriorated. This led to W commencing proceedings. Until that point W with the
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support of his family had decided to get on with life and make the best of it. He was
highly intelligent and went to Eton and then Cambridge and achieved a 2:1. Then
he obtained a PhD in maths. His disability did not affect him until he was 24 when
his mobility decreased; he had to use a wheelchair, his speech became slurred
and he had to take increasing amounts of time off work.
W stated that he had known that he had been delivered by forceps and that his
condition was caused by a lack of oxygen at birth, but as he had been able to live a
relatively normal life he had never investigated further.
The Court of Appeal held that the fact that W knew he was delivered by forceps did
not capture the essence of the claim; the essence of the claim was the junior
doctor’s delay in seeking assistance, his persistence in trying to deliver W and
using the wrong forceps. With regards to s.14(3) as W knew his injury wassignificant there would come a time when a reasonable person in W's
circumstances would ask his mother, particularly since she was a nurse and a
midwife. Moreover he would have known that as she was a trained midwife she,
would be able to answer his questions. Therefore W would have constructive
knowledge in his early 20s, and the claim was statute-barred.
The Appeal Court however exercised its s.33 discretion (see below) and allowed W
to bring a claim reasoning that otherwise W would lose all prospect of his future
needs being provided for. The court held that under s.33 the claimant’s reasons for
delay should be considered and not his family.
10.4.5 Exception to the basic rule
Finally, two exceptions to the three year rule. For claimants under a disability the
limitation period will not start to run until that disability ceases, s.28. For minors
(persons under the age of 18, s.1 (1) Family Law Reform Act 1969) time does not
begin to run until the child reaches the age of 18, hence they have until the age of21 to commence an action. For patients who are incapable of managing or
administering property affairs, (s.1 (2) Mental Health Act 1983) time will run when a
patient is sane and he will have three years from that date. Note that a child
claimant on reaching the age of majority will not be fixed with the knowledge of his
parent, see Appleby v Walsall H A [1999] 5 Lloyds Rep Med 154.
Secondly, the court has the ultimate discretion to extend the limitation period under
s.33 of the Limitation Act 1980 if it is just and equitable to do so. The court will
weigh up the prejudice cause to the claimant and the defendant should the action
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not proceed. S.33 (3) lists some of the factors that the court will consider though
the court will look at the claim as a whole. These include:
(a) the length of the delay and the claimant’s reasons for the delay;
(b) the cogency of the evidence;
(c) the response of the defendant;(d) whether the claimant was under a disability;
(e) the steps that the claimant took to progress his claim.
For an illustration of what facts the court may take into account in exercising this
discretion see, for example Davis v Jacobs & Camden & Islington H A & Novaritis
[1999] 3 Lloyds Rep Med 72 and Briggs v Pitt Payne & Lias [1999] 1 Lloyds Rep
Med 1 . In Das v Ganju [1999] 6 Lloyds Rep Med 198 the Court of Appeal
exercised their discretion under s.33 in favour of the claimant ruling that the delay
was due mainly to misleading and wrong advice given by her lawyers, Lord Justice
Buxton at page 205 stating that the failings of the claimant’s lawyers were not “to
be visited upon her”. This decision has been criticised on the grounds that
previous decisions have held that the claimant’s actions cannot be divorced from
his lawyers and further in Das part of the delay seems to have been caused by the
claimant’s lack of funding. See more recently Leeson v Marsden and United Bristol
Healthcare Trust [2008] LS Law Med 393 a case commenting on abuse of process
and the factors relevant to s.33 discretion and Cain v Francis [2009] LS Law Med
82 a recent case commenting on whether the defendant suffered prejudice with the
loss of the limitation defence
10.5 THE PRE-ACTION PROTOCOL FOR THE RESOLUTION OF CLINICAL
DISPUTES
Following the Woolf reforms there is now a pre-action protocol for clinical negligence
claims. The protocol is the work of the Clinical Disputes Forum, a multi disciplinary body
which was formed in 1997 as a result of Lord Woolf’s “Access to Justice” inquiry.
Why the Protocol?
Lord Woolf perceived in his Access to Justice Report in July 1996 that the major causes
of costs and delay in medical litigation occur at the pre-action stage. He recommended
that patients and their legal advisors should try and work more closely with health care
providers to resolve disputes without recourse to litigation.
10.5.1 General aims of the Protocol
These are:
to maintain/restore the patient/healthcare provider relationship; and
to resolve as many disputes as possible without recourse to litigation.
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10.6.1 Records
Requests for patients’ records should be made using the Law Society and
Department of Health approved standard forms and they should be provided within
40 days of the request for a maximum cost £10. If they cannot be provided within
this timescale then the healthcare provider should give an explanation quickly. If
the healthcare provider fails to disclose the records then the patient or their advisor
may apply for pre-action disclosure against a party or non-party under the Civil
Procedure Rules Part 31.16, 31.17.
The defendant may refuse disclosure on the grounds that the records are subject
to lawyer/client privilege and should therefore remain confidential, i.e.
communications between a solicitor and his client or communications between a
lawyer and a third party for the purposes of the litigation, see Waugh v British
Railways Board [1980] AC 521, Lask v Gloucester HA The Times 13 Dec 1985,
Lee v South West Thames RHA [1985] 1 WLR 845.
Disclosure may be refused on the grounds that it is embarrassing to the defendant
or damaging to the public interest, see Re HIV Haemophiliac Litigation (1990) 140
NLJ 1349.
10.6.2 Letter of claim
See annex to the protocol at C1. The letter should contain a clear summary of the
facts and the main allegations of negligence. It should also describe the patient’sinjuries and prognosis and an indication of the heads of damage to be claimed. A
chronology should be provided in more complex cases together with any relevant
documents.
Enough information must be given for the healthcare provider to begin investigating
the claim and to put an initial value. Proceedings should not be issued until three
months after the letter of claim unless there is a limitation problem.
The claimant can make an offer to settle at this or any other stage. An offer should
be accompanied by a copy of the medical report and schedule of special damages.
10.6.3 The response
This should be within 14 days of receipt of the letter and identify who is dealing
with the matter. A reasoned answer should be provided within 3 months and either
admit the claim or say why:
if only part of the claim is admitted say which and why the remainder is denied;
if the claim is denied comment on the specific allegation of negligence and whichparts, if any, of the chronology are disputed.
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Experts
The use of joint experts is increasing. Experts may be needed to provide an
opinion on:
(i) breach of duty and causation;(ii) patient’s condition and prognosis;
(iii) to assist in valuing aspects of the claim.
However the protocol does not attempt to be prescriptive on whether a joint expert
should be instructed nor on the manner in which the reports should be disclosed.
See further paragraph 1.6.5 for further details re choosing and instructing your
expert.
The protocol finally goes on to encourage the use of Alternative Dispute
Resolution, see para 4.4(3) “starting proceedings should usually be a step of last
resort.” The courts will expect parties to try and settle their differences without
resorting to litigation if at all possible. Mention is made of the NHS Complaints
Procedure which although will not provide compensation can be used where an
explanation is the only goal or to find out more information to decide what to do.
10.6.4 Failing to follow the Protocol
The Practice Direction provides that the court may make an order that the party atfault be penalised in costs or if the party at fault is a claimant that he be deprived of
interest on his damages or awarded interest at a lower rate for such a period as the
court deems appropriate or if the party at fault is the defendant that he be ordered
to pay interest at a higher rate not exceeding 10 % above the base rate.
10.7 DISCLOSURE OF MEDICAL RECORDS
Initially this is covered by the protocol, see above and the protocol paras 3.7-3.13 and
Annex B. Where disclosure is sought from a third party then again initially that is dealt
with by the protocol, see para 3.13. However from 24th October 2001 if the third party is a
health care provider then access will be under the Data Protection Act 1998. This and
other measures available to parties to obtain the disclosure of their records is discussed
in the paragraphs below.
10.7.1 Access to Health Records 1991
This Act allowed patients access to all their health records post November 1991,
subject to certain exceptions e.g. access was denied where there was a genuine
risk to the physical or mental health of either the applicant or a third party or if
access would reveal information about any individual other than the patient. This
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Act now has been partly repealed (except in relation to dead patients) and replaced
by the Data Protection Act 1998 (see below).
10.7.2 The Data Protection Act 1998
The most significant change introduced by the 1998 Act is that manual records that
are held in “relevant filing systems” now fall within the definition of data in the 1998
Act. The Act derives from a European Directive which states its object as “to
protect the fundamental rights and freedoms of natural persons, and in particular
their right to privacy with respect to the processing of personal data.” Note,
however, that some of the 1998 Act’s provisions will not be fully appreciated until
2001, others by the year 2007.
The Act sets out eight Data Protection principles which, subject to certain specified
exceptions, all information relating to or capable of identifying a living individual
must be processed fairly, lawfully, accurately and securely. The Act introduces a
new category of ‘sensitive information’ which is subject to stricter controls than
other personal data. Patient records come within the definition of sensitive
personal data. Examples of when disclosure of patient records may be permitted
include:
Where the patient gives consent;
Where processing or disclosure is required by law or in legal proceedings; For medical purposes’
For insurance or pension purposes;
For research purpose.
The Act establishes the right of every individual (subject to stated exceptions), to
require the relevant data controller to confirm the nature and extent of the data
being held and the recipients to whom they are or may be disclosed.
Any person may also be entitled to a copy of the information in an intelligible form.
The data controller is required to supply the information within 40 days of a written
request. Note that the disclosure of personal data for the purpose of or in
connection with legal proceedings is allowed; see Mensah v Jones 19.11.04.
Two cases which are of interest in this area for the implications of the Human
Rights legislation are R v DoH ex parte Source Informatics [2000] 2 WLR 940 and
A Health Authority v X [2001] 7 Lloyd’s Rep Med 349. In the Informatics case the
Court of Appeal held that the European Directive from which the DPA derived did
not have any applicability to anonymised data. In A Health Authority v X the
disclosure of medical records was challenged as being in violation of Article 8 of
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the ECHR 1950. Munby J held that disclosure of the records could be made but
only subject to a bonding and transmissible duty of confidentiality being imposed
on the recipients (and any subsequent recipients). This goes further than the
requirements under the DPA which are essentially concerned with the internal
controls within an organisation
10.8 EXPERT EVIDENCE
The court has the power to restrict expert evidence to that which is reasonably necessary
to resolve the proceedings, CPR r 35.1. The use of joint experts is increasing. However
the protocol does not attempt to be prescriptive on whether a joint expert should be
instructed nor on the manner in which the reports should be disclosed, see para 4.2 and
see also Oxley v Penwarden [2001] 7 Lloyd’s Rep Med 347.
The solicitor should always choose the independent expert and not someone who is
involved with the incident or works in the same area as the defendant. There are a
number of sources that may assist in the choice of an expert:
(i) AvMA;
(ii) APIL (The Association of Personal Injury Lawyers);
(iii) Law Society’s Directory of Expert Witnesses;
(iv) Professional journals e.g. The Lancet;
(v) Experts you have seen in other case reports.
The solicitor should ensure that an expert from the appropriate speciality is chosen, and
that a fee and a time limit for the report is agreed. Another consideration is whether more
than one expert is required and whether separate reports on causation and prognosis are
required. Assuming that the expert is not a joint expert then rules concerning their
instruction are to be found at CPR r 35.8.
10.8.1 The report
Once the solicitor receives the report he should check to see if it is favourable or
not and if it is to his satisfaction. If it is unfavourable then he should only instruct a
second expert if he suspects that there is a case to answer. If there is anything in
the report which is unclear the solicitor should go back to the expert and seek
clarification. An expert’s report must comply in its form with the requirements of
CPR r 35.10 and paragraph 1 to PD 35. Under CPR r 35.12 the court can direct
experts to meet in an attempt to narrow down the issues in dispute.
It is also at this stage that the solicitor will choose counsel and should instruct
someone who has specialist knowledge in this field. Many of the organisations
discussed above in the choice of a medical expert will be valuable sources for
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choices of counsel. Counsel should be provided with a comprehensive set of
instructions together with the medical records. There will then usually be a
conference with counsel where the solicitor, client and expert will attend and
identify the issues in dispute and test the evidence. If counsel is reasonably
satisfied he will then usually go on to prepare the particulars of claim (see below).
10.9 WHO TO SUE?
See earlier notes.
10.10 THE ACTION
10.10.1 Which Court
The County Court has unlimited jurisdiction. For a clinical negligence claim to be
issued in the High Court it must have a value of £50,000 or more.
10.10.2 The Claim
The claimant will complete a claim form N1 which will be accompanied by a
particulars of claim which may be either stated on the claim form or contained
within a separate document. The particulars of claim must contain a concise
statement of facts on which the claimant relies. When the particulars of claim are
served a medical report and a schedule of special damages must accompany it. If
the defendant wishes to defend the claim he must acknowledge service within 14
days of service of the claim and file a defence 14 days thereafter. It is at this stage
that the court will send the parties an allocation questionnaire with the aim of
allocating the case to one of the three tracks. Should the parties fail to respond to
this questionnaire then the claim could ultimately be struck out. The three tracks
are the small claims track for personal injury cases where the value of damages
claimed for pain and suffering does not exceed £1,000; the fast track for monetary
claims where the amount of the claim does not exceed £15,000; and the multi track
for claims where neither of the aforementioned tracks are appropriate and
generally for claims where the amount claimed exceeds £15,000. Note that any
claim that is complex either with regard to the facts or the evidence will be
allocated to the multi-track, hence the majority of clinical negligence claims will be
allocated to this track. The court will then proceed to hold a case management
conference where it will proceed to give directions on the steps that the parties
must take. At all times the court will try and keep cost and delay to a minimum and
will try and set a trial date as soon as possible.
Further Reading:
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Brazier & Cave: Medicine, Patients and the Law (5th ed) (Penguin Books), Chapters 8 &
9
The Kennedy Report www.bristol-inquiry.org.uk/final_report/index.htm
Report of the Mid Staffordshire NHS Foundation Trust Public Inquiry published 6th February
2013 (“The Francis Report”) (although not directly relevant to clinical negligence claims the
summary is a worthwhile read)
SUMMARY
At the end of this chapter you should be able to:
* understand the basic procedural steps in a clinical negligence claim and
identify any problems you could face;
* explain the important provisions of the Limitation Act 1980 and, in particular,
with reference to case law, what is meant by knowledge.
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SELF-TEST QUESTIONS – CHAPTER 10
1. What are the various ways in which a claimant may see his medical records? What
are the advantages and disadvantages of each?
2. What constitutes actual knowledge and constructive knowledge within the meaning
of the Limitation Act 1980?
3. What factors will the court take into consideration in deciding whether or not to apply
section 33 of the Limitation Act?
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NOTES
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CHAPTER 11
CONSENT TO TREATMENT
11. INTRODUCTION
Working Definition of Consent
“Consent is the voluntary and continuing permission of a patient to be given
a particular treatment, based on a sufficient knowledge of the purpose,
nature, likely effects and risks of that treatment, including the likelihood of its
success and any alternatives to it. Permission given under any unfair or
undue pressure is not consent” . (Mental Health Act 1983 Code of Practice
(revised 2008)).
Consent to medical treatment is at the heart of the relationship between the patient and
the health carer.
11.1 Purpose of Consent to Medical Treatment.
“There seems to be some confusion in the minds of some as to the purpose
of seeking consent from a patient (whether adult or child) or from someone
with authority to give that consent on behalf of the patient. It has two
purposes, the one clinical and the other legal. The clinical purpose stems
from the fact that in many instances the co-operation of the patient and the
patient’s faith or at least confidence in the eff iciency of the treatment is a
major factor contributing to the treatment’s success. Failure to obtain suchconsent will not only deprive the patient and the medical staff of the
advantage, but will usually make it much more difficult to administer the
treatment…The legal purpose is…to provide those concerned in the
treatment with a defence to a criminal charge of assault or battery or a civil
claim for damages for trespass to the person. It does not … provide them
with any defence to a claim that they negligently advised a particular
treatment or negligently carried it out.” (Per Lord Donaldson MR in Re W
[1993] Fam. 64 at P. 76).
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Much of the clinical treatment which a patient receives will invariably involve some degree
of touching of the patient by the health carer; invasive treatment, such as surgical
operations, certainly will whereas counselling of a patient need not. Since any
unauthorised touching of a person is a battery which is a trespass to the person and
actionable per se (no hostile intent needed, see Lord Goff in Re F [1990] 2 AC 1 at 73B),then the health carer will need to ensure that his touching of the patient is indeed
authorised. The actionable touching need only be slight and it is no defence to argue, as
some health carers may be tempted to do, that the touching was and is in the
complainant’s best interests. Not only will the patient’s consent provide a defence to a
possible trespass claim but it also flags up clearly that, in medical law, patient autonomy
(or self-determination) is a fundamental concept which, if ignored, could have serious
repercussions for the health carer.
It has often been said that a patient has complete autonomy over his own body; what this
means is that the patient can decide for himself /herself whether he wants treatment or
not, whether he wants a particular treatment or not, whether he wants to be touched or
not etc. As Cardozo J said in 1914 in Scholendorff v Society of New York Hospital (1914)
211 NY 125.
“Every human being of adult years and sound mind has a right to determine what shall be
done with his own body; and a surgeon who per forms an operation without the patient’s
consent commits an assault.” Mr Justice Wall also expressed the same idea this way,
“The law, in my judgment, is very clear. It is in general terms a criminal and
tortious assault to perform physically invasive tr eatment without a patient’s
consent, and that a mentally competent patient has an absolute right to
refuse to consent to medical treatment for any reason, rational or irrational,
or for no reason at all, even where that decision will lead to his or her own
death.”
(Re J T (Adult: Refusal of Medical Treatment) [1998] 1 FLR 48 at p 51)
It could be argued that the upholding of patient autonomy is very much in keeping with
human rights law ever since the Human Rights Act 1998 became operative in England on
October 2nd
2000. Given that NHS organisations are “public authorities“ they must act in
accordance with the European Convention on Human Rights and Fundamental
Freedoms 1950; consequently, it may be possible to argue that to treat someone without
his consent is a breach of, say, Article 3 of the European Convention on Human Rights
1950 (incorporated into English law as a result of the Human Rights Act). Article 3 says,
“No one shall be subjected to torture or to inhuman or degrading treatment
or punishment”.
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The crucial question for the English Courts will be to decide whether invasive medical
treatment without the patient’s consent is ‘inhuman’ or ‘degrading’ to that patient.
Following the decision in Herczegfavly v Austria (1993) 15 EHRR 437 where force-
feeding of a patient and intolerable detention conditions were not regarded as a breach of Article 3, then perhaps non-consensual invasive medical treatment will not be seen as a
breach of Article 3. Again, non-consensual treatment may be questioned under Article 8
(1) which says that, “Everyone has the right to respect for his private and family life, his
home and his correspondence”; but then Article 8(2) does allow some interference of this
right in, for example, the public interest. All of this discussion probably only serves to
demonstrate that the 1998 Act and the Convention have had to date only limited influence
in the health care field, with perhaps two notable exceptions (1) in the field of mental
health (notably Article 5; deprivation of liberty) and (2) confidentiality (see above).
Since most forms of health treatment will involve some degree of touching, then any
health carer touching a patient without the latter’s consent will be committing trespass
(civil and/or criminal) (see Malette v Shulman 1991 and B v An NHS Hospital Trust
2002).
Students should refer to GMC guidance effective from June 2008, in relation to consent-
‘Consent: patients and doctors making decisions together’ (which can be accessed via
the GMC website.
11.2 CONSENT AND AUTONOMY
Patient autonomy (or the right to self-determination) is so fundamental in English medical
law that a health carer who treats a patient without the latter’s consent but in the firm
belief that the patient will die without the treatment, (in other words in the patient’s best
interests) will still be held liable in trespass. In Malette v Shulman [1991] 2 Med LR 162
the claimant who was seriously injured in a road accident was taken to a hospital for
treatment. As her condition worsened and she lapsed into unconsciousness it was
decided that a blood transfusion was needed. However, among her personal belongings
the hospital had discovered a Jehovah’s Witness card which expressly indicated that no
blood transfusion should be administered. The claimant’s daughter, who had been
summoned to the hospital, also confirmed her mother’s wish not to have a blood
transfusion; the daughter even signed a form indicating that she would absolve the
defendant and the hospital from any blame should her mother die as a result of not
receiving a blood transfusion. Despite this, but clearly convinced that a transfusion would
save the mother’s life, a blood transfusion was administered. The Ontario Court of
Appeal held that the defendant health carer was liable in trespass. As Robins J A said at
p 165,
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“The principles of self -determination and individual autonomy compel the
conclusion that the patient may reject blood transfusions even if harmful
consequences may result and even if the decision is generally regarded as
foolhardy… To transfuse a Jehovah’s Witness in the face of her explicitinstructions to the contrary would, in my opinion, violate her right to control
her own body…” (See also B v An NHS Hospital Trust [2002] EWHC 429
(Fam.))
Not only must the health carer accede to the patient’s request even though the latter may
seriously harm himself by his choice but he must also accede if the patient’s choice is likely
to injure a third party. In St George’s Healthcare NHS Trust v S [1998] 3 All ER 673. In that
case a pregnant woman, diagnosed with pre-eclampsia, opted for natural childbirth rather
than the safer caesarean section. The evidence was clear that not only did she appreciate
that her choice had serious consequences for both herself and her unborn child but also
the defendants’ decision to ignore her choice and subject her to a caesarean section was
done in her interests and in the interests of her unborn child; yet the court upheld her right
to decide even though that choice had the potential to kill her unborn child
For recent case law concerning a Jehovah’s Witness patient and the refusal of medical
treatment see Newcastle upon Tyne Hospitals Foundation Trust v LM 26th Feb 2014 and
Nottinghamshire Healthcare NHS Trust v RC [2014] EWHC 1317.
11.3 THE ONUS OF PROOF
This lies with the patient/claimant and the standard of proof is on a balance of probabilities.
It is for the claimant to show that no consent, express or implied, has been given to the
“touching”. Trespass will be committed even though there was no malice or ill-will involved
in the touching.
11.4 WHAT IS MEANT BY CONSENT?
For the patient’s consent to amount to a valid legal defence to a trespass (or negligence)
claim, the consent can be express or implied, oral or written or part oral, part written.
From the defendant health carer’s perspective it is always safer to obtain express written
consent, and this is certainly the norm where invasive treatment is involved.; that is why
as a general rule a consent form will have to be signed prior to undergoing surgery in a
hospital. In their guidance “Consent: patients and doctors making decisions together ” the
GMC give some specific examples of when express consent should be sought (see paras
44-49). For the majority of other treatments, for example a general practitioner checking
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your ears or throat etc. implied consent by agreeing to what is asked of you, as the
patient, is sufficient. Silence on its own may not be sufficient.
11.4.1 Express Consent
Express written consent usually involves the patient signing a consent form. But the
signing of that form is not conclusive evidence that legal consent has been obtained; it is,
however, very good evidence that it has been obtained. Consequently, it would be
possible for a claimant to later argue that his signature on a consent form had been
improperly obtained e.g. as a result of a misrepresentation of the circumstances in which
the consent was sought or fraud on the part of the health carer (see R v Tabassum [2000]
9 Lloyds L.Reps. 404). Again, if a claimant has expressly consented to procedure A and,
in the course of that procedure, something else was done which was not immediately
necessary, then the written consent to procedure A may be no defence to a trespass
claim in respect of the further procedure.
See DoH standard consent forms & DoH guidance (‘Reference Guide to Consent for
Examination or treatment’, 2009)
11.4.2 Implied Consent
The actions of a patient may imply that consent has been given. For example, the patientwho holds her arm out for an injection will have inferred her consent “whatever her
unexpressed feelings may have been” (see O’Brien v Cunard SS Co [1891] 28 N.E. 266
(Supreme Judicial Court of Massachusetts. Consent will not be implied where the patient
is incompetent although treatment may be given in the patient’s best interests (see
Chapter 9 and the Mental Capacity Act 2005, s.4). See again, “Consent: patients and
doctors making decisions together ” (GMC paras 44-49).
As stated earlier, consent given which is then exceeded by the health carer may result in
a successful claim in trespass (or negligence) against the health carer unless the latter
can show that the further procedure was immediately necessary (and not merely
convenient) to save the patient’s life or prevent a serious deterioration in the patient’s
condition. The consent form puts it this way, “[I understand] that any procedure in
addition to those described on this form will only be carried out if it is necessary to save
my life or to prevent serious harm to my health.”
It cannot be over-emphasised that the onus of showing the common law principle of
necessity here is on the defendant health carer. In the Devi case the defendants could
not show it was necessary to sterilise a woman who had consented to an operation on
her womb; their fear that, should she become pregnant again – she already had four
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children and wanted more – the womb might rupture, was not, in the opinion of the court,
so immediately necessary that the defendants could not wait and discuss sterilisation and
other options such as a vasectomy for the male partner (Devi v W Midlands AHA [1980]
C.L.Y. 687).
Now the Mental Capacity Act 2005 puts the common law principles of necessity
and definition of and assessment of lack of capacity on a statutory footing. Finally
note the GMC guidance: Consent: patients and doctors making decisions together
reiterates that a doctor must not exceed the scope of the authority given by a
patient, except in an emergency (para 39). Even in cases of emergency treatment
the guidance stresses that the treatment provided “must be the least restrictive of
the patient’s future choices.” (para 79)
11.5 TRUE CONSENT/ INFORMED CONSENT
Many adjectives are suggested in the text books in an attempt to explain the nature of the
consent needed to negative a tr espass claim, for example, “real”, “true”, “genuine”,
“informed” etc. It is suggested that the only valid distinction is the one between “true” and
“informed consent,” the latter phrase denoting the amount of information which is to be
given to the patient prior to getting his consent. In the normal course of events true
consent will be required in English law. This can be given by a capable, conscious adult,who has received a certain amount of information and has understood that information;
also the consent must have been obtained voluntarily.
Breaking the above statement down, the following become the essential ingredients of a
true consent:
a) Capacity (& competence) to consent
b) Based on sufficient information.
c) Given voluntarily.
11.5.1 Capacity & Competence
Guidance from the GMC on capacity in this context is at Part 3 of the GMC
guidance, -‘Consent: patients and doctors making decisions together’.
a) Adults
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In English medical law general reference to a patient consenting invariably
means a patient who is an adult, and an adult is defined as someone who is
aged 18 and over (see the Family Law Reform Act 1969). The common law
and statutory rule is that there is a rebuttable presumption that if you are
over the age of 18 you have the capacity (competence) to consent (or refuseconsent) to medical treatment. (see Re T (adult: refusal of Treatment)
[1992] 4 All ER 649; Re B (Adult: Refusal of Medical Treatment) (2002)) and
section 1(2) of the Mental Capacity Act 2005 which says that a person must
be assumed to have capacity unless it is established that he lacks capacity.
Further, and this is to reinforce what has already been said, a patient aged
18 and over is in law able to both consent to and refuse all forms of medical
treatment. In Paton v B.P.A.S. 1979 a husband sought an injunction to
prevent his pregnant wife from obtaining a legal abortion. The court refused,
arguing that the wife had autonomy over her own body.
11.5.2 Assessing Capacity
a) Adults
Although, as we have seen, an adult is presumed to have capacity, what
about the situation, however, where that person lacks capacity, e.g. because
they are unconscious, or due to mental disorder or otherwise? In these
circumstances a valid consent can not be given (by that person- though note
he possibility of a ‘proxy decision maker’ under the MCA- see below).
First it must be stressed that the Mental Capacity Act 2005 will only apply to
those adults who lack capacity the common law will continue to have effect
for all those adults who have capacity. Common law is still of some
importance as it is likely that many common law decisions will continue to be
influential, and referred to by the Court of Protection, in relation to its powers
under the MCA. Additionally you will see that many of the common law tests
have all but been replicated within the body of the Act.
In addition to the Act students should have regard to the Mental Capacity Act
Code of Practice (the Code) which was formally issued by the Lord
Chancellor on 23 April 2007. The Code provides guidance and explains how
the Act will work on a day to day basis for practitioners and carers
Finally note that this section will also very briefly look at the Mental Health
Act. This Act (currently) provides a statutory regime for the treatment and
care for mental disorder, containing provisions allowing for compulsory
admission and detention in a hospital, and compulsory treatment under what
are commonly known as the Part IV provisions.
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11.5.3 Presumption and Definition of Capacity
Section 1(2) of the Mental Capacity Act 2005 states
(“A person must be assumed to have capacity unless it is established that he
lacks capac ity”.)
Section 1 of the MCA sets out 5 key principles which should be followed by anyone
exercising any power, or carrying out any act under the MCA. All of the key
principles in s.1 of the Mental Capacity Act 2005, mirror the common law position
and are set out below. The five key principles under s.1 are:
A person is assumed to have capacity unless prove otherwise;
A person is not to be treated as unable to make a decision unless all practicable
steps to help him to do so have been taken without success.
A person is not to be treated as incapable to make a decision merely because he
makes an unwise decision;
Any act or decision made, under the Act on behalf of a person who lacks capacity
must be in his best interests;
Before any act / decision regard should be given to whether the purpose could be
achieved by taking an option that is less restrictive of the person's rights/ freedom.
11.5.4 Definition of Incapacity
S.2(1) of the Act defines a person (“P”) as lacking capacity when” he is unable to make a
decision for himself in relation to the matter because of an impairment of, or a
disturbance in the functioning of, the mind or brain.” The section goes on and adds that “it
does not matter whether the impairment or disturbance is permanent or temporary.”
(s.2(2)). (See for example the Code chapter 4)
In assessing capacity the Act borrows a negligence test and stipulates that any decision
is to be made on “the balance of probabilities” (s.2 (4)). However incapacity cannot be
established simply by reference to a person’s age or appearance or “a condition of his, or
an aspect of his behaviour, which might lead others to make unjustified assumptions
about his capacity.” (s.2 (3)).
Hence when assessing capacity a person must consider:-
o
Is there an impairment/ disturbance of functioning mind/brain?o If so
o Is it sufficient that the person lacks capacity to make the particular decision?
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What is now made clear, as was the case under common law, is that the person’s mental
capacity is to be judged (a) in relation to a specific issue/matter, and (b) at a specific time;
therefore incapacity as regards, say, paying bills does not mean that the person is also
incapable of consenting to medical treatment and vice-versa and incapacity to consent totreatment in the year 2010 does not mean that the person is to assumed incapable of
consenting in 2013. Hence it is particularly important that capacity is properly assessed
(and the Code guidance taken into account as appropriate).
11.5.5 The assessment of incapacity
S.3 of the Act deals with the assessment of capacity
Section 3
“A person is unable to make a decision for himself if he is unable-
a. To understand the information relevant to the decision
b. To retain that information
c. To use or weigh that information as part of the process of making the
decision or
d. To communicate his decision (whether by talking, using sign language or
any other means)”
If a person (P) understands the information if it is given in a way that is “appropriate to his
circumstances” then he will not be deemed to lack capacity (s.3 (2)). Moreover the fact
that any person may only be able to retain such information for a limited period, again
does not render a person incapable (s.3 (3)). Relevant information includes information
about the reasonably foreseeable consequences of deciding one way or another or failing
to make a decision (3(4)).
At common law the test for capacity was the one given by Thorpe J in Re C (adult: refusal
of medical treatments) [1994] 1 All ER 819. In Re C a 68 year old schizophrenic, detainedin Broadmoor refused to have his gangrenous leg amputated. Thorpe J held that for the
patient to possess decision making capacity he must be able to:
understand information relevant to the decision about treatment;
believe in that information; and
weigh that information, balancing risks and needs, when arriving at a choice.
This test was reinforced by Butler-Sloss L J in Re MB [1997] 2 FLR 426 when she said,
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“(4) A person lacks capacity if some impairment or disturbance of mental
functioning renders the person unable to make a decision whether to
consent to or to refuse treatment; that inability to make a decision will
occur when:
a) the patient is unable to comprehend and retain the information
which is material to the decision, especially as to the likely
consequences of having or not having the treatment in
question;
b) the patient is unable to use the information and weigh it in the
balance as part of the process of arriving at the decision….”
This test has been closely followed in the new MCA at section 3 which sets out a
functional test for determining capacity. The Act adds a further element to the Re MB
test at (d) that a person may be treated as incapable if they are unable communicate a
decision in any way. Section 3 of the new 2005 Act may be thought of as not all that
different from the common law rules above. It is therefore highly probable that many of
the common law principles will continue to be highly influential, and referred to/ relied
upon by the new Court of Protection, in relation to its powers under the MCA.
11.5.6 Best interests
Once a decision has been made that a person lacks capacity then care and
treatment must be in his best interests, (s.4). This applies to any decisions made
on behalf of a person under the MCA. Once again it is reiterated that no decision
should be made purely on the basis of a person’s age, appearance or peculiarity in
his behaviour. Reference must be made to a checklist and the person making the
decision must reasonably believe that his actions are in the best interests of the
person.
Providing any decision is reached in this way then s.4 will have been complied with
notwithstanding that the court may subsequently come to a different decision.
In assessing capacity the assessor therefore must consider:
whether it is likely that the person will regain capacity to deal with the issue in
question and when that is likely to be (s.4(3);
so far as reasonably practicable try and encourage P’s participation or to improve
his ability to participate in the decision making process, (s.4 (4)).
The effect of the MCA will be that such applications will now be made to the new Court of
Protection and not the High Court as before. If there is a valid advance directive (see
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para 9.8) in place in the correct format then the healthcarer must follow that and
treatment must not continue to be administered. Where P has appointed a LPA (see
further paragraph 9.7) to deal with consenting to or refusing life saving treatment and it
clear that the LPA is acting in P’s best interests then the authority of the LPA will suffice.
(See further COP paragraph 7).
Section 4(6) then goes to provide a rather comprehensive list of what must be taken into
account in assessing capacity. The assessor must, so far as is reasonably ascertainable,
consider:
(a) P's past and present wishes and feelings, (in particular any written statement made
by him when he was capable
b) the beliefs and values that would influence his decision if he was capable capacity;
and
(c) any other factors that P would consider if he was able to do so.
Section 4(7) also stipulates that if at all practicable and appropriate to consult them, the
views of the following in determining what would be in P’s best interests:
(a) anyone named by P as someone to be consulted;
(b) anyone caring for P or having an interest in P’s welfare;
(c) any donee of a lasting power of attorney
(d) any deputy appointed for P by the court,
So is this new test be any different to the common law test for “best interests”? By way of
comparison Dame Butler-Sloss in An Hospital NHS Trust v S [2003] EWHC 365 said, “the
assessment of best interests is not a narrow one. I said in Re A (Male Sterilisation)
[2000] 1 FLR 549 at 555, in my judgement best interests encompasses medical,
emotional and all other welfare issues”. Likewise this view had been endorsed by the
BMA. In their consent tool kit (card 8) lists below the following (minimum?) matters which
should be considered in any given situation:
“the patient’s own wishes and values (where these can be ascertained),
including any advance decision;
clinical judgment about the effectiveness of the proposed treatment,
particularly in relation to other options;
where there is more than one option, which option is least restrictive of the
patient’s futur e choices;
the likelihood and extent of any degree of improvement in the patient’s
condition if treatment is provided;
the views of the parents, if the patient is a child;
the views of people close to the patient, especially close relatives, partners,carers, welfare attorneys, court-appointed deputies or guardians about whatthe patient is likely to see as beneficial; and
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any knowledge of the patient’s religions, cultural and other non-medicalviews that might have an impact on the patient’s wishes”.
For further guidance see the Code (chapter 5). What seems clear is that any doctor must
adhere to the checklist at section 4 to demonstrate that he has carried out as full an
assessment as possible. However the practice itself does not seem so far removed from
the common law test and provided that there was a “reasonable belief” that the decision
was in P’s best interests then the assessor will be protected.
Perhaps the main difference is the importance attached to P’s own views (s.4 (6)). P’s
views form only one part of the assessment process, they are by no means
determinative. However this approach is markedly different to the common law test where
the test was much more objective and perhaps clinical?
Remember that the test for “best interests” has no relevance where P has (or there is no
reasonable belief that P does not have) capacity to make the particular decision for
himself. Moreover the section also has no bearing where a where a valid advance
decision applies (this will be considered further below).
Finally any discussion of “best interests” must now have regard to the decision in Aintree
University Hospitals NHSFT v James [2013] UKSC 67 the first Supreme Court decision
on the approach to be taken in assessing best interests. The words of Baroness Hale set
out below at para 39 emphasised that a much more
A more subjective (patient-driven
approach) must be taken.
“The most that can be said, therefore, is that in considering the best interests of this
particular patient at this particular time, decision-makers must look at his welfare in the
widest sense, not just medical but social and psychological; they must consider the nature
of the medical treatment in question, what it involves and its prospects of success; they
must consider what the outcome of that treatment for the patient is likely to be; they must try
and put themselves in the place of the individual patient and ask what his attitude to the
treatment is or would be likely to be; and they must consult others who are looking after him
or interested in his welfare, in particular for their view of what his attitude would be.”
And on the meaning of “no prospect of recovery” and the concept of “futility” Baroness Hale
at para 44 said “Resuming a quality of life which the patient would regard as worthwhile is
more readily applicable, particularly in the case of a patient with permanent disabilities. As
was emphasised in Re J (1991), it is not for others to say that a life which the patient would
regard as worthwhile is not worth living.”
There has been numerous decisions on best interests and there is not space within this
workbook to consider them all but some of the more interesting are listed below.
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A NHS Hospital Trust v M and K [2013] EWHC 2402 (pre Aintree)
Re M (Best Interests: DOL) [2013] EWHC 3456 (COP)
An NHS Trust v VT and A [2013] EWHC B26 (Fam)
Sheffield Teaching Hospitals NHS Foundation Trust v TH & Anor [2014] EWCOP 4
Reference should also be made to the Prolonged disorders of consciousness National
Clinical Guidelines” (RCP Dec 2013)
11.5.7 Acts in connection with care and treatment, Section 5
Section 5 of the Act provides protects healthcarers from legal liability when treatment is
carried out on incapacitated adults without their consent provided such treatment is in
their “best interests”. Under section 5 the healthcarer will have to refer to sections 2, 3
(above) in first assessing capacity, and then to section 4 (best interests) and the Code
where relevant. Section 5 requires only a reasonable belief that P lacks capacity and that
P further lacks capacity to the matter in question and that it is in P’s best interests.
Note that this section will not afford protection if any act is performed negligently, ss (5(2),
5(4)).
Section 5 only applies where the care is in connection with care/ treatment. “Care” is notdefined in the Act, though “treatment” is defined as including a ‘diagnostic or other
procedure.” (s.64). This wide definition encompasses a wide range of health care, and
will include other care provided by carers, e.g. help with eating, drinking, mobility,
dressing, washing, shopping etc, see further the Code, chapter 6.
Section 5 will also extend protection to anyone carrying out life-sustaining treatment; and
treatment/ any act ‘necessary to prevent a serious deterioration’ in P’s condition, provided
that there is a reasonable belief that treatment/ the act is necessary (s.6(7)), pending a
decision from the Court.
Section 5 will not apply “if a person (D) does an act that is intended to restrain P” unless
two conditions are satisfied (s.6 (1)). These are:
that D reasonably believes that it is necessary to do the act in order to prevent
harm to P; and
the measures taken are a proportionate response to the likelihood and the
seriousness of the harm P would suffer if no steps were taken. (ss.6 (2) (3).
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An act of restraint is defined as one which “uses, or threatens to use, force to secure the
doing of an act which P resists, or restricts P's liberty of movement, whether or not P
resists” (s. 6(4)).
Finally s.5 will not authorise any care/treatment in conflict with a decision made by adonee of an LPA, or deputy appointed by the court (s.6 (6)).
The importance of sections 5 and 6 are they provide a healthcarer with protection in
certain defined circumstances, similar in many ways to the common law doctrine of
necessity (not to be confused with the common law doctrine of best interests). Section 5
however does not provide authority to anyone else to make decisions on behalf of P;
unlike LPAs, which do introduce new powers which can actually enable someone to
make decisions on behalf of P in certain circumstances. These are considered at
paragraph 9.7.
11.6 LASTING POWERS OF ATTORNEY (LPA)
Sections 5 and 6 above empowered healthcarers to make certain decisions about P, they
did not give any right however to third parties. However as a result of sections 9 -14 of
the Mental Capacity Act 2005, lasting powers of attorney (LPA’s) may now be created by
patients at a time when they are conscious and mentally capable (s.9 (2)). The general
implications of this section is that in relation to welfare decisions, a capable adult canauthorise others to make decisions about his care and treatment should he become
incapable. The LPA powers in relation to welfare issues will only be effective where P
lacks capacity to make the decision his/her self (s.11(7)(a)). Any act done by a donee is
subject to the principles set out in s.1 and best interests and s. 4 (s.9 (4)).
Note however the donee can not override a valid advance decision (s.11 (7)).
So for the first time ever a third party may give consent to a healthcarer to treat an
incapable adult. But if there is a disagreement between healthcarer and donee and the
donee refuses to consent to such treatment? Then the healthcarer will need to challenge
the donee’s decision via the Court of Protection (s.6 (6)).
11.7 ADVANCE DECISIONS
Prior to the Mental Capacity Act 2005 a patient may have made it known that, should he
become incapable through an accident or an illness of consenting or not consenting to his
medical treatment, then he does not want any life-supporting medical treatment to beadministered to him. If made formally such prior statements are referred to as advance
decisions (or to use the American terminology, living wills). The legal status of such
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statements at common law is that, provided certain conditions exist, then the statement
must be obeyed; to treat a patient in defiance of such a declaration is unlawful and will
render the health carer liable to a criminal charge or a civil claim for assault and battery.
As Lord Goff said in the Bland case:
“…the same principle applies where the patient’s refusal to give his consent
has been expressed at an earlier date, before he became unconscious or
otherwise incapable of communicating it; though in such circumstances
special care may be necessary to ensure that the prior refusal of consent is
still properly to be regarded as applicable in the circumstances which have
subsequently occurred…” (p 864).
An advance decision is most useful in knowing what treatment the patient does not want;
it should have little effect were it to stipulate that the patient wanted a particular form of
treatment since such matters are generally left legally to the clinical judgement of the
health carers and the courts would (invariably) support their decisions. But in the High
Court in R (Burke) v General Medical Council (Official Solicitor intervening) [2005] 2 WLR
431 this latter point was successfully questioned. There the patient, Leslie Burke, who
was suffering from the degenerative brain disease cerebellar ataxia, sought judicial
review of the G.M.C’s guidance to doctors that artificial feeding and hydration could be
withdrawn from him against his wishes , after he lost the ability to speak. Holding for the
patient the judge, Munby J., declared that the guidance was indeed unlawful since it
failed to observe, “the heavy presumption in favour of life-prolonging treatment….” Mr.
Burke had clearly expressed his wishes that, should he lose the ability to speak
(consent), he wanted his medical treatment to continue; the judge’s decision took away
from the health carers the decision to treat or not to treat in the patient’s best interests: a
clear victory for patient autonomy. But such an approach was effectively stifled by the
ruling of the Court of Appeal ((2005) 3 WLR 1132 and leave to appeal to the House of
Lords was refused).
Advance decisions can now be found in sections 24, 25 and 26 of the MCA and the first
thing that strikes the reader about these sections is that they are headed up “advance
decisions to refuse treatment” thereby reinforcing the Appeal Court’s decision in Burke.
Second, some of the common law criteria have now been given statutory force, such as
the age of the maker, (18), his mental capacity, and the relevant medical circumstances
etc.
Note that as the advance decision was made when P had capacity, the best interests
tests has no bearing on P’s wishes even if those wishes are contrary to the opinions of
health professionals or moreover a donee of an LPA.
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Mental Health Act 1983 (MHA) as amended by the Mental Health Act 2007) and requires
treatment for their mental disorder, the application of the MHA must also be considered.
A patient may be admitted to hospital for treatment for mental disorder in two ways, either
as (i) voluntary/informal patients, or (ii) compulsorily detained under the Mental Health Act
1983. For informal patients the common law rule of treating out of necessity in thepatient’s best interests was the applicable rule of law. This was the broad result of the
House of Lords’ decision in the Bournewood case where at pp 297-8 Lord Goff had this to
say,
“…the basis upon which a hospital was entitled to treat and to care for
persons who were admitted as informal patients… but lacked the capacity to
consent to such treatment….was the common law doctrine of necessity.”
(See also Re F (Adult Patient: Jurisdiction) [2000] 9 Lloyds Rep. Med. 381, Re W (a
Minor) (Medical Treatment: Courts Jurisdiction), [1992] 4 All ER 627 and A National
Health Service Trust v D [2000] Lloyds Rep. Med. 411.
The position has now changed with the implementation of the MCA. So any patient who
lacks capacity who is admitted to hospital informally for treatment for mental disorder will
be provided with any treatment or care under the authority of the MCA (see s.5). This
does, however, cause difficulties where the care provided in hospital is said to amount to
a deprivation of liberty. In the Bournewood case it was argued in the European Court that
an admission to hospital and care there that amounted to a deprivation of liberty was a
breach of Article 5 of the European Convention (see HL v UK). This argument
succeeded, and, on the facts of the case, it was held that Mr L (the patient in the case)
had been deprived of his liberty. Therefore up until April 09 the MCA did not authorise the
deprivation of liberty of a patient without an order from the Court of Protection (s.16). Post
April 09 a new DoLs authorisation procedure was introduced by the MHA 07 into the
MCA, and set out in schedule A1 of the MCA. It enables responsible bodies (known as
the managing authority of the relevant hospital or care home where a person is being
deprived of their liberty) to apply to a ‘supervisory body (the relevant PCT or Local
Authority) for an authorisation of any such deprivation. Once the responsible body
receives the said authorisation they then must be able to justify the necessity of the
treatment under s.5 of the MCA. It is important to note that the deprivation of liberty
decision is entirely separate from the decision to treat.
For a decision on deprivation of liberty and best interests see DH NHS Foundation Trust
v PS (By her litigation friend, The Official Solicitor) (2010) EWHC 1217 . In this case the
court thought it simpler for the court to authorise the deprivation of liberty as the
deprivation would be for a limited duration, rather than invoke the DOL safeguards.
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[Note that the House of Lords Select Committee concluded in their recent review of the
MCA that the DOL safeguards were “not fit for purpose” and they should be repealed and
replaced. The Government is yet to respond. Furthermore in P v Cheshire West and
Chester Council and another [2014] UKSC 19 the Supreme Court has substantially re-
defined what amounts to a deprivation of liberty. Further detail can be found in theoptional module Mental Health and Capacity.]
As regards patients who are compulsorily detained under the MHA, the law on consent
can be found in Part IV of the Act, key sections being 57, 58, 62 and 63.
Briefly the effect of sections 57, 58, 58A, 62 and 63 may be summed up as follows:
for s 57 treatments e.g. psycho-surgery, the patient’s capable consent and a
second opinion are needed;
for s 58 treatments –this covers the administration of medicine once three months
have passed since the medication was initially given during the period of detention,
either the patient can consent or a second opinion will be required;
for section 58A treatments e.g. ECT, this may not be given without the consent of a
capable patient, if the patient is incapable then ECT can not be given if there is an
advance refusal in place or where a proxy decision maker refuses consent. This
section is subject to provisions in section 62 below.
if urgent treatment is needed the safeguards laid down in sections 57,58, 58A can
be disapplied (s.62); otherwise treatment for the mental disorder can be administered under S63 without
the detained patient’s consent.
Detention under the Act does not, per se, mean that the detained person lacks the
capacity to consent. The provisions noted above provide for compulsory treatment of
those who have, and for those who lack, capacity.
Of all the above provisions, the one which seems to fly in the face of the patient’s human
rights and also cause the greatest problems is section 63. That section stipulates that,
“the consent of person is not required for any medical treatment given … for the
mental disorder from which he/she is suffering, not being treatment falling within
section 57 or 58 […], if the treatment is given under the direction of the approved
clinician in charge of the treatment.”
The problem is that the court’s interpretation of the kind of treatment which can be
administered under this section without the patient’s consent and without the safeguards
of sections 57 and 58 is that it is treatment which is not necessarily linked to the patient’s
particular mental disorder. Thus, caesarean sections and force-feeding have been held
to come within section 63. This is questionable since at first sight it seems doubtful
whether such treatments could be connected to the patient’s mental condition, a
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connection which section 63 clearly requires. In B v Croydon Health Authority [1995] 1All
ER 683 the patient had been compulsorily detained under section 3 of the 1983 Act
suffering from borderline personality disorder coupled with post traumatic stress disorder.
She was force-fed as part of her treatment and the question for the courts was whether
that treatment was, “treatment …for the mental disorder”. It was held that it was, NeillL.J. laying down the principle that section .63 includes “treatments given to alleviate the
symptoms of the disorder as well as treatments to remedy its underlying cause:” (See
also Tameside & Glossop Acute Services Trust v CH [1996] 1 FLR 762,R v Collins and
Ashworth HA ex p Brady [2000] 8 Lloyds Rep. Med. 355. In R (on the application of B) v
Ashworth HA [2005] UKHL 20 the court went even further and said that the section was
not confined to the mental disorder specified in the application justifying detention: it
applied to any mental disorder from which the person was suffering).
11.9 CHILDREN
11.9.1 16/17 yr olds
The Children Act 1989 s.105(1) and the United Nations Convention on Rights of the
Child, Article 1 both consider any person within England and Wales who is under
eighteen, to be a child. For patients between the ages of 16 and 18, a special rule
applies and that is to be found in section 8 of the Family Law Reform Act 1969. That
section allows people between the ages of 16 and 18 to consent to surgical, medical or
dental treatment as if they were adults.
That section says:
“(1) The consent of a minor who has attained the age of sixteen years to any
surgical, medical or dental treatment which, in the absence of consent,
would constitute a trespass to his person, shall be as effective as it would be
if he were of full age; and where a minor has by virtue of this section given
an effective consent to any treatment it shall not be necessary to obtain
consent for it from his parents or guardian.”
From a practical standpoint this means that administering medical treatment to a 16 or 17
year old with the latter’s consent as opposed to their parents’ or guardians’ consent will
not incur any civil or criminal liability. Note the FLRA does not apply in cases of all
“treatment”; for example organ donation, procedures which are not therapeutic or
research does not fall within the ambit of the Act.
As Lord Donaldson put it in Re W (a Minor) (Medical Treatment: Courts Jurisdiction),
[1992] 4 All ER 627,
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“The section [S8]… does not… ex tend to the donation of organs or blood
since, so far as the donor is concerned, these do not constitute either
treatment or diagnosis.” (p 635).
In such cases the consent will have to come from the parents/guardians but the consentwill have to be exercised in the best interests of the child; therefore the consent can and
will be ignored if, in the court’s view, the procedure is not in the child’s interests (see Re B
(A Minor: Wardship –Sterilisation)[1988] AC 199; Re J (A Minor : Muslim Upbringing and
Circumcision [2000] 1 FLR 571; Re C & F (Children: Immunisation) [2003] 2 FLR 1095;
Royal Alexandra Hospital for Children v J (2005) NSWSC 465) For an interesting
consideration of the position where parents/ carers and professionals conflict see the
case of Glass, where the European court held that providing treatment to David Glass
against his parents’ wishes was a breach of Article 8 of the HRA ( David Glass & Carol
Glass v UK (2004) application No 00061827/00, (20040 39 EHRR 15 ).
The Mental Capacity Act confirms that those children aged between 16-18 years (defined
in the COP as “young persons”) will be treated as adults for the purposes of the Act,
subject to two key exceptions - 16-18 year olds are not able to make a Lasting Power of
Attorney (LPA) (s.9(2)(c) or an Advance Decision (s.24). For these “young persons”,
there will be an overlap between various legal schemes- see chapter 12 of the Code
11.9.2 Under 16
If the patient is someone under the age of 16 but considered by the courts to be “ Gillick
mature” then the patient, and not the parents or the guardians, may consent to the
medical treatment. In Gillick v West Norfolk and Wisbech AHA [1985] 3 All ER 402, a
circular issued by the DHSS which advised that, in certain circumstances, contraceptive
counselling and advice could be sought and given to under 16 year olds without parental
consent, was challenged by a mother with five daughters who argued that it was unlawful
(ultra vires) and contrary to a doctor’s legal obligations. The majority of the Law Lords
held that, in exceptional circumstances, contraceptive advice and guidance could be
legally provided to under 16 year olds without their parents’ involvement or consent. The
exceptional circumstance would be where the girl, in the Court’s opinion, was competent
in that she had already achieved “a significant understanding and intelligence to enable
…her to understand fully what [was] proposed”. (per Lord Scarman at p 423). As to
whether any particular under 16 year old would be regarded as sufficiently mature,
reference has to be made to the more detailed criteria laid down by Lord Fraser
guidelines at p 413 where he indicated that the doctor had to be:
(i) satisfied that the child understood his advice;
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(ii) prepared to try and persuade the child to tell his parents or let him [the doctor] do
so; only if the child refused would he [the doctor] then be entitled to proceed with
the treatment;
(iii) of the opinion that the child was very likely to have sexual intercourse with or
without contraceptive advice or treatment;(iv) of the opinion that, unless the child got the advice, his physical or mental health or
both would suffer; and
(v) sure that the child’s best interests required the advice.
What seems to be required here is knowledge on the part of the health carer making the
assessment that the under 16 year old really does understand and appreciate the
consequences of consenting to the particular medical procedure, such as the risks
involved, the benefits to be gained, the short-term and long-term disadvantages of the
treatment, etc. (“….what is involved is not merely an ability to understand the nature of
the proposed treatment… but a full understanding and appreciation of the consequences
both of the treatment in terms of intended and possible side effects and… the anticipated
consequences of a failure to treat” (per Lord Donaldson in Re R (A Minor; Wardship;
Medical Treatment) [1992] 3 Med. L.R 342 at p348.))
In their guidance “0-18 years” the GMC state that only if a young person can
“understand, retain, use and weigh this informa tion, and communicate their
decision to others can they consent to that investigation or treatment.” (para 24)
Two comments should be made on the Gillick rule. First, although the case itself arose
against the background of contraceptive advice and counselling, it is submitted that the
court’s ruling on the capacity of such a person is not restricted to contraceptive issues; it
is applicable to most forms of clinical treatment. Second, the converse of the Gillick rule,
namely that if you are Gillick mature to consent you are Gillick mature to withhold your
consent, does not hold good. As Lord Donaldson MR pointed out in Re R (A Minor)
(Wardship: Medical Treatment [1991] 4 All ER 177 at p 186:
“Both in this case and in Re E the judges treated Gillick’s case as deciding
that a ‘Gillick competent’ chi ld has a right to refuse treatment. In this I
consider that they were in error. Such a child can consent, but if he or she
declines to do so or refuses, consent can be given by someone else who
has parental rights or responsibilities.”
See also Re W (a minor) (medical Treatment) [1992], where the court held that the
health professionals only required one valid consent and where others, in this case the
parent/ court can lawfully consent, then this is sufficient despite the child’s refusal).
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It would therefore appear that, as the law currently stands, a Gillick mature minor’s refusal
to be treated may be over-ridden by either the parents or guardians or the Court on the
grounds that, (a) either the parents or the guardians have a concurrent legal capacity to
consent, and (b) such a refusal might conceivably lead to death or serious injury and the
mature under 16 may not be able to fully comprehend the consequences of a refusal.
It has to be said that this reasoning is highly questionable and a somewhat illogical
situation for English law to hold. Why should there be a concurrent capacity in refusal
cases but not in consent cases? Why is it assumed that a mature under 16 cannot
appreciate the serious consequences of a refusal? Further, in the light of the Human
Rights Act, 1998, (Articles 14 and 8) can such apparent discrimination on the grounds of
age be upheld?
More recently the courts have returned to the Gillick case, in considering whether abortion/
other treatments could lawfully be provided to an under 16 year old without the parent
being informed- see Axon (R (on the application of Sue Axon) v The Secretary of State for
Health and others [2006] EWHC 372. )
Note: The MCA does not generally apply to under 16s, for the purpose for this module.
This means that the issue of whether the child is ‘Gillick competent’ will still arise.
11.9.2 Patients under the age of 16 but not Gillick competent.
If the patient is under 16 years of age but is not Gillick competent then legal consent to
the medical treatment rests with the patient’s parents or guardians. Section 3 (1) of the
1989 Act defines parental responsibility as “all the rights, duties, powers, responsibilities
and authority of which by law a parent of a child has in relation to the child and his
property.” Consent need only be given by one such person but it is both legally advisable
and good medical practice to involve both parents. The persons who have parental
responsibility are set out in the Children Act 1989 (section 2) and listed in the DOH‘s
guidance, “Consent: Working with Children”. But this parental control has never been
regarded as unfettered. Parental responsibility exists for the benefit of the child. For
example, if Jehovah’s Witness parents were to refuse a blood transfusion for their child, it
is almost certain that an application will be made to the courts for the child to be dealt
with pursuant to the Children Act 1989, in which case it will be for the court to decide
whether the treatment should be given or not, and this it will do on the basis of what is in
the minor’s best interests. This could mean that in certain circumstances parents’ wishes
will be ignored; in other cases those wishes may be followed by the courts. Much will
depend on what the court sees as the minor’s “best interests” in any particular situation.
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The GMC in “0-18 years: guidance for all doctors” specifically single out medical
procedures that are undertaken for religious, cultural, social or emotional reasons stating
that such procedures that are not undertaken for therapeutic benefit may be carried out
providing they are in the best interests of the child. In assessing the child’s best interests
the doctor should amongst other factors consider the religious and cultural beliefs of thechild and their parents together with any social and emotional benefits (see paras 34-35).
In Re R (a minor) (Blood Transfusion) [1993] 2 FLR 757 , the parents, both Jehovah
Witnesses, refused to allow their 10 month old daughter to receive blood transfusions. A
specific issue order was sought by the local authority under S8 of the Children Act 1989
for the treatment to be administered against the parents’ wishes. Granting it, Booth J
said:
“In the present case, I am in no doubt that the application is well -
founded…The welfare of the little girl is the court’s paramount
consideration…. so overwhelming is her need for blood and so much is it in
her best interests to have it in the light of current medical knowledge that, for
her welfare, I am bound to override the parents’ wishes …” (p 760)
But in Re T (a minor) (Wardship: Medical Treatment) [1997] 1 All E.R. 906 where the
child was born with a life-threatening liver defect, the Appeal Court upheld the parents’
decision not to subject the child to a liver transplant, although the unanimous medical
view was that a transplant would have been in the child’s best interests. It is clear that
the courts have to indulge in a delicate balancing exercise in determining whether
something is or is not in a patient’s best interests; as such each case will have to be
decided on its merits.
A striking example of parents not having an unfettered control over their child’s medical
treatment is the Siamese twins case at the beginning of this century. (Re A (minors)
(conjoined twins: separation) [2000] Lloyds Rep. Med. 425.). This was the case where
Jodie and Mary were Siamese twins who shared a common aorta. Mary was the weaker
twin and she was dependent on Jodie for her blood supply and on Jodie’s heart to keep
her alive. With a separation operation Jodie stood a very good chance of living a
relatively normal life, but Mary would certainly die; without a separation operation the
prognosis was that both twins would ultimately die within six months. The parents,
deeply religious as they were, refused to give consent to the separation operation
believing that it should be left to God to decide what should happen to the twins. On the
other hand the hospital wanted to separate them. Should the surgery be carried out?
And if so, on what basis? In the twins’ best interests? Possibly yes, if you consider the
interest of the stronger twin; but what about Mary’s best interests? Was it in her best
interests to die, as she certainly would if the operation went ahead?
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At first instance Johnson J held that the operation should go ahead. The parents
appealed. The Court of Appeal (Ward, Brooke and Robert Walker LJJ) unanimously
agreed with the trial judge but arrived at their conclusions by different processes of
reasoning. Yet the entire court seemed to be clear on one thing: that the parents’ wishes,in the circumstances, were not in the children’s best interests; significantly the court also
decided that Mary’s human rights were not infringed. Was the Appeal Court morally and
legally right in this case?
If the basic test which the Court was going to apply and did apply was the ‘best interests’
test and if Mary had no interests or no best interests , then attention had to be focussed
on Jodie’s best interests; consequently if the parents’ wishes were not in Jodie’s best
interests then rightly they should have been, and were, ignored. As Ward LJ put it , “The
best interests of the twins is to give the chance of life to the child whose actual bodily
condition is capable of accepting the chance to her advantage even if that has to be at
the cost of … the life which is so unnaturally supported”. That said the parents’ views
were listened to and considered but as Andrew Pack writing in the Family Law periodical
for November 2000, noted:
“They [the parents] seemed to be very much at the sidelines in the case, lost
amongst the complex medical issues and the theoretical discussions about the
sanctity or otherwise of life” (p 783).
See also Wyatt v Portsmouth NHS Trust [2005] EWHC 693 and Re OT (A Baby)
Unreported March 20 2009.
Withdrawing life sustaining treatment from young children will always be an emotive
and controversial topic particularly where the views of the clinicians and the parents
conflict. For two further cases see NHS Trust v Baby X & Others [2012] EWHC 2188
(Fam) (withdrawal of life support from a baby against the wishes of parents) and KH
[2012] EWHC B18 (Fam) (Trust seeking Court approval of an Advanced Care Plan
which includes withholding life sustaining treatment.)
A case which hit the headlines albeit involving an older child was that of Neon
Roberts (NHS Trust v SR [2012] EWHC 3842 (Fam)). Here a trust sought a
declaration that it was in a 7 year old boy’s best interests to have radiation treatment
for a brain tumour. Neon’s father was in agreement, however Neon’s mother. Sally
Roberts objected and wanted to explore alternative therapies. The court ruled in
favour of the trust and was rather critical of Mrs Roberts limited argument against the
treatment proceeding.
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Further Reading
See “Mental Capacity: One Standard for All Ages” [2011] Family Law which examines Gillick
competence in the light of the subsequent developments of the UNCRC, Human Rights Act
1998 and the Mental Capacity Act 2005.
11.9.3 Reminder - MCA
16/17 year olds
The MCA also applies (though with some important limitations) to 16/17 year olds. This
means that, as above, (for the purposes of the MCA) there will be a presumption of
capacity, and assessment of capacity and best interests will fall within s.s2-4 of the MCA.
Under s.5, acts can be carried out in connection with care and treatment (as an alternative
to seeking consent from someone with parental responsibility).
Under 16s
Because the MCA is of (almost) no application in this context, the common law provisions
will continue to apply, as seen above.
11.10 INFORMATION
The health professional must impart a certain amount of information to the patient to
enable the decision to be made. The information must be relevant and must be such as
would be imparted by a similarly qualified health carer faced with a similar factual scenario.
As regards the nature and volume of the information to be given to the patient, there is a
difference of opinion between English law and American/Canadian law. English law
seems to prefer the rule which says that the “broad terms” of the treatment etc. should be
volunteered to the patient as laid down in Chatterton v Gerson [1981] 1 All ER 265,
whereas American and Canadian jurisprudence talks of the patient giving an “informed
consent” (see the case of Canterbury v Spence [1972] 464 F (2d) 772). The difference is
this. “Broad terms” essentially means the health carer telling the patient about the broad
risks and benefits associated with the treatment as determined by the health carer not the
patient (so following what other health carers would do in similar circumstances would
suffice for the rule : shades of Bolam here). On the other hand “informed consent”
requires the health carer to tell the patient what the patient would want to know, not what
the health carer thinks should be told. Consequently it could be maintained that an
American patient would have volunteered to him/her more information than his English
equivalent.
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together’. In particular paragraph 9 lists areas of information to be given to
patients. In relation to answering questions, paragraph 12 states:- ‘You must
answer patient’s questions honestly and as far as practical, answer as fully as
they wish.’
Paragraphs 13-17 list reasons when information might not be shared with a patient.
Paragraphs 28-36 consider discussion of side effects and complications. In particular
paragraph 32 states:- ‘you must tell patients if an investigation or treatment might result in
a serious adverse outcome, even if the likelihood is very small.’
11.10.1 Understanding the Information
Does it have to be shown that the patient actually understood the information or is it
sufficient that the health carer has taken reasonable and appropriate steps to satisfy
himself that the patient understood the information? Under s.3 of the MCA the test is not
whether the patient understood the information but whether he has the capacity to
understand. This means that the health carer must reasonably believe that the patient
has the ability to understand the information (see for example Hamwi v Johnson and NW
London Hospitals NHS Trust [2005] EWHC 206 ). In assisting the patient understand the
information The Code details the steps the heathcarer must take.
The GMC Guidance emphasises that a doctor should check whether his patient hasunderstood the information and whether he requires additional information before making
a decision.
11.11 VOLUNTARILY
The patient’s consent must be given voluntarily; that means it must be devoid of any
physical or moral pressure or undue influence or fraud or mistake or misrepresentation on
the part of the health carer or the patient’s relatives or spouse; consent given in such
circumstances is not, in general, true consent. In Re T (An Adult) (Consent for Medical
Treatment) [1992] 2 FLR 458, the patient who was pregnant and injured in a car accident
refused a blood transfusion while her mother was with her; the mother was a Jehovah’s
Witness. There was evidence that the daughter was not as deeply attached to the
Jehovah’s Witness faith as her mother. When an application was made to the courts for
a blood transfusion to be administered the court granted it, holding that the patient’s
refusal was not genuine, vitiated as it was by the mother’s pressure; in other wor ds the
mother’s undue influence raised the spectre that the daughter’s refusal was not true.
Lord Donaldson said at p 473:
“If …. [his] will was overborne, the refusal will not have represented a true
decision. In this context the relationship of the persuader to the patient – for
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example, spouse, parents or religious adviser – will be important, because
some relationships more readily lend themselves to overbearing the patient’s
independent will than do others”. (See also the GMC Guidance Consent:
patients and doctors making decisions together” ).
11.11.1 Fraud and Consent
In R v Tabassum [2000] Lloyds Rep Med. 404 a man who impersonated a health carer
and subsequently deceived women into agreeing to participate in a breast cancer survey
and to undergo breast examinations was held to be rightly convicted of indecent assault;
his fraud “as to the nature and quality of the conduct” vitiated the women’s consent.
11.12 SIGNIFICANCE OF CAUSATION
It can be argued that if no consent at all has been obtained or if the consent has been
obtained fraudulently etc, then the claim should be pursued in trespass; in other
circumstances the claim should be pursued in negligence. So is causation a problem
where the claim is properly brought in trespass? Not really, as Mister Justice Bristow said
in 1980.
“Once it is shown that the consent is unreal then what the plaintiff wouldhave decided if she had been given the information which would have
prevented vitiation of the reality of her consent is irrelevant ” (per Bristow J.
in Chatterton v Gerson [1980] 3 WLR 1003 at p 1013).
And Brazier agrees. At page 117 (Medicine, Patients and the Law”) this is what she says:
“The essence of the wrong of battery is the un -permitted contact. There is
no requirement that the patient prove that if he had been asked to consent to
the relevant treatment he would have refused.”
On the other hand if the claim is to be pursued in negligence then
“… the plaintiff must prove not only the breach of duty to inform but that had
the duty not been broken [she] would not have chosen to have the
operation.” (per Bristow J in Chatterton v Gerson at p 1012). But how is this
tested?
11.12.1 Subjective or Objective Test?
Causation means that the claimant has to show that, had the appropriate advice and
information been given by the health carer, then he (the claimant) would not have agreed
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SUMMARY
At the end of this chapter you should be able to appreciate:
* the distinction between informed consent and true consent;
* the position of the adult, 16/17 year old and the ‘mature’ minor;
* the impact of and position under the MCA 2005;
* the ingredients necessary to sue in trespass where it is argued that no true
consent has been given
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SELF-TEST QUESTIONS – CHAPTER 11
1. List three ingredients which make up true consent.
2. What is the ratio of the Gillick case?
3. When can you treat an unconscious patient?
4. Distinguish between “informed consent” and “broad terms” insofar as it relates
to the volume of information which should be imparted to a patient.
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NOTES
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CHAPTER 12
MEDICAL CONFIDENTIALITY
12.1 INTRODUCTION
Most people will be aware of the medical profession’s duty of confidentiality to patients,
however, the basis of this duty may not be so well known. It is clear that there will be
both a legal and ethical obligation to maintain confidences (although neither would
impose an ‘absolute’ obligation). It is also important to appreciate that the Human Rights
Act 1998 will impact on the law in this area.
12.2 BASIS OF THE OBLIGATION OF CONFIDENCE
12.2.1 Ethical/ professional basis
The Hippocratic Oath provides:
“ All that may come to my knowledge in the exercise of my profession or
outside of my profession or in daily commerce with men, which ought not to
spread abroad, I will keep secret and never reveal .”
And the Declaration of Geneva states:
“I will respect the secrets which are confided in me, even after the patient
has died .”
It is clear that the obligation of confidence is not an absolute obligation and that
there will be circumstances which justify disclosure of confidential information. It is
also clear that a medical professional cannot simply choose what to disclose
without reference to the appropriate professional guidance.
The General Medical Council (GMC) sets out detailed guidance regarding the
nature and extent of the ethical/ professional obligation of confidence in its
guidance document Confidentiality (2009).
In Good Medical Practice it is stated at paragraph 37 that:
“Patients have a right to expect that information about them will be
held in confidence by their doctors. You must treat information about
patients as confidential, including after a patient has died. If you are
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considering disclosing confidential information without a patient’s
consent, you must follow the guidance in with Confidentiality.”
Where a doctor breaches the ‘duty of confidentiality’ a patient may wish to file a
complaint against the doctor with the General Medical Council. However, even if adisciplinary sanction does follow, this would not in itself give the aggrieved patient
a remedy. The patient would simply have to satisfy himself that a disciplinary
sanction was imposed. To gain a ‘legal remedy’ the aggrieved patient would have
to pursue a legal claim. At the outset it is worthy of note that the extent of the legal
and ethical/professional obligations may differ. You will note above that ‘Good
Medical Practice’ makes reference to the obligation of confidence surviving after
the patient’s death (see paragraph 37). The legal position here is not quite so clear
cut.
12.2.2 Legal basis
Iis there a common law rule which governs medical and other confidences? And
does this legal duty of confidentiality arise via contract or tort (of negligence) or
equity? In A.G. v Guardian Newspapers (No 2) 1988 the House of Lords had
established -- in a non-medical case -- that a duty of confidence did come into
existence where confidential information was imparted to someone in
circumstances where that recipient must have been aware that the information wasboth confidential and not disclosable. Applying this to the private patient he is
able to argue that the duty of confidentiality was/is an implied (or perhaps an
express) term of the contract to provide private health care – hence a claim in
contract for breach of that term if there is an unauthorised disclosure. But what
about the NHS patient who has no contract? In Furniss v Fitchett (a New Zealand
case in 1958 [1958] NZLR 396) it was argued that a claim could be made in tort
arguing that the health carer owed a duty to respect the patient’s confidence and
that, by wrongfully revealing the confidence, a breach of that duty had occurred.
But this approach is somewhat questionable since negligence suggests
inadvertence whereas the disclosure envisaged here is deliberate. The better legal
approach seems to be to argue that the claim could be made in equity.
The case of W v Egdell concerned proceedings brought following disclosure of a
psychiatric repor t without the patient’s consent. It was stated by Bingham LJ (at
p.848) that:
“It has never been doubted that the circumstances here were such to
impose on Dr. Egdell a duty of confidence owed to W….It is not in issue
here that a duty of confidence existed. The breadth of such a duty in any
case is, however, dependent on circumstances.”
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Note, this case is considered later in relation to the public interest exception to the
obligation of confidence. Reference was made in the case to GMC advice regarding
the existence of a confidentiality obligation and Bingham LJ commented at p.849:
“I do not doubt that this accurately states the general rule as the law
now stands…”
The Law Commission recommended that a statutory offence of breach of confidence be
created, however this recommendation was not taken forward. See Law Commission
Report No.110 Breach of Confidence (Cmnd 8388, 1981) paragraph 6.1.
There are, however, specific situations where an obligation of confidence has been
established by statute/ statutory instrument. Examples are noted below:
Abortion Regulations 1991 (SI 1991 No 499)
Health Service Commissioners Act 1993, section 15
The relevant provisions both provide for an obligation of confidence and also
specify circumstances where disclosure is possible
12.3 WHAT IS CONFIDENTIAL INFORMATION? WHAT TRIGGERS THE ‘DUTY
OF CONFIDENCE’?
In Attorney-General v Guardian Newspapers (No 2), it was stated that the information
should have
It was also stated (at p.658) that the “duty of confidence arises when
confidential information comes to the knowledge of a person (the confident) in
circumstances where he has notice, or is held to have agreed, that the
information is confidential, with the effect that it would be just and reasonable
in all the circumstances that he should be precluded from disclosing the
information to others.”
Thus we have the requirements that:
The information is confidential
That information must be communicated in circumstances where the confident has
notice/ agrees the information is confidential.
It is clear that information passing between the patient and healthcare professional would
satisfy these requirements
12.4 THE IMPACT OF THE HUMAN RIGHTS ACT 1998
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12.4.1 Article 8
Consideration of issues of confidentiality must also include a consideration of the
impact of HRA, and in particular Article 8. Article 8 provides:
1. Everyone has the right to respect for his private and family life, his home and
his correspondence.
2. There shall be no interference by a public authority with the exercise of this
right except such as is in accordance with the law and is necessary in a
democratic society in the interests of national security, public safety or the
economic well being of the country, for the protection of health or morals, or
for the protection of the rights and freedoms of others.
It is clear that confidentiality could be protected under Article 8(1). It is also clear
that this obligation is not absolute and this ‘right’ could be interfered with in
appropriate circumstances.
Examples of the application of Article 8 are set out below.
In Campbell v Mirror Group Newspapers [2004] 2 All ER 995 it becomes apparent
that the focus is on ‘whether there is a reasonable expectation of privacy’ when
determining whether there has been a breach of Article 8.
It must be made clear that Article 8(2) does set out justifications for disclosure even
when a ‘right to privacy’ can be established under Article 8(1) see Z v Finland(1998) 25 EHRR 371 .
In A HA v X [2001] 61 BMLR 22 it was held that disclosure of patient records could
be justified in accordance with Article 8 if conditions were in place to prevent any
abuse. Thus the issue of ensuring that stringent safeguards are in place is
necessary if disclosure is to be justified under Article 8(2).
It is suggested in Confidentiality: NHS Code of Practice (at paragraph 34) that:
“Current understanding is that compliance with the Data Protection Act 1998
and the common law of confidentiality should satisfy Human Rights
requirements.”
12.4.2 Article 10
Article 10 provides:
“Everyone has the right to freedom of expression. This right shall
include freedom to hold opinions and to receive and impart information
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and ideas without interference by public authority and regardless of
frontiers…”
Again this right is qualified. See Article 10(2), the Article 10(1) right can be
interfered with provided that three conditions are satisfied, namely:
The interference must be in accordance with the law;
It must pursue one of the aims set out in Article 10(2), namely ‘the protection
of the reputation or rights of others’ and ‘preventing the disclosure of
information received in confidence.’
The interference must be ‘necessary in a democratic society’, meeting a
‘pressing social need’ and be proportionate to the legitimate aim pursued.
Article 10 issues can arise where material is published. Where the material
published is confidential in nature Article 8 and Article 10 both need to be
considered as there will be a potential conflict.Consider the following cases as a
starting point:
Campbell v Mirror Group Newspapers Ltd [2004] 2 All ER 995.
There is a need to ‘strike a balance’. It was stated at p.1026 that:
“Any restriction of the right to freedom of expression must be subjected
to very close scrutiny. But so too must any restriction of the right to
respect for private life. Neither art 8 nor art 10 has any pre-eminence
over the other in the conduct of this ex ercise….they are neither absolute
nor in any hierarchical order, since they are of equal value in ademocratic society.”
See also H (A Healthcare Worker) v Associated Newspapers Limited and H
(A Healthcare Worker) v N Health Authority [2002] E.W.C.A. Civ 195 and R
(on the application of Stone) v South East Coast Strategic Health Authority
and others [2006] EWHC 1668 (Admin). Venables & Thompson v News
Group Newspapers and others [2001] 1 ALL ER 908
12.5 RELEVANT GUIDANCE
12.5.1 General Medical Council ‘Confidentiality’ 2009
The GMC has provided updated guidance for doctors regarding confidentiality
issues. The guidance sets out the extent of the professional obligations and
attempts to identify the circumstances when disclosure can be justified.
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Note, the GMC website also contains ‘learning materials’ to support the
confidentiality guidance. Various case studies are set out which deal with different
problem scenarios.
12.5.2 The NHS Confidentiality Code of Practice (November 2003)
The document is described (at p.3) as a:
“guide to required practice for those who work within or under contract to
NHS organisations concerning confidentiality and patients’ consent to
the use of t heir health records….For the purposes of this document, the
term ‘staff’ is used as a convenience to refer to all those to whom this
code of practice should apply. Whilst directed at NHS staff, the Code is
also relevant to anyone working in and around health. This includes
private and voluntary sector staff.”
Its application is therefore quite far reaching. Practical guidance regarding the
scope of the confidentiality obligation, disclosure issues and practical steps to be
taken to ensure compliance is set out in the Code.
Recent supplemental guidance has been issues which focuses on public interest
disclosure (Confidentiality: NHS Code of Practice supplemental guidance: public
interest disclosures, November 2010).
12.5.3 Guidance document supplied by defence organisations etc
Consider, for example, available information/ guidance supplied by:
British Medical Association (BMA) www.bma.org.uk
Medical Defence Union (MDU) www.the-mdu.com
Medical Protection Society (MPS) www.medicalprotection.org/uk
12.6 THE DUTY OF CONFIDENTIALITY: EXCEPTIONS TO THE
OBLIGATION
In the context of medical law the duty of confidentiality was considered in Hunter v Mann
([1974] QB 767) and more recently in the cases of W v Egdell [1990] 1 ALL ER 835
and R (on the application of S) v Plymouth City Council EWCA Civ 388, para 33 .
However it is clear that the duty of confidence is not absolute. There will be
circumstances where disclosure of confidential information can be justified.
.”
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In brief confidential information may be disclosed in certain limited circumstances:
where the person to whom the duty is owed consents to information being shared;
where the public interest in disclosure outweighs the public interest in the
maintenance of confidentiality;
where disclosure is required by a court order or other legal obligation.
[Note:- in considering whether information can be lawfully disclosed, regard must also
be had to HRA implications, in particular Article 8 (see below), and the DPA (see
below). In practical terms, however, it seems sensible to address the common law and
professional guidance first, since if disclosure can be justified in accordance with those
provisions, then it is likely to be justifiable in HRA and DPA terms too.]
12.7 CONSENT
12.7.1 Issues regarding express consent
Whether it is an ‘exception’ or something which defeats the existence of the
duty/obligation, the importance of the role of consent needs to be considered.
For consent to be valid the patient must:
(i) have capacity;
(ii) be given sufficient information for a decision to be reached;
(iii) the patient must act voluntarily.
You will note that in relation to the level of information that must be supplied to
satisfy (ii) this is not a particularly onerous requirement. For the consent to be
valid, information in broad terms should suffice.
There is GMC guidance on the issue of when ‘express consent’ should be sought.
In ‘Confidentiality’ (2009) paragraphs 33 to 35 deal with ‘disclosures for which
express consent should be sought.’ Paragraph 33 provides that:
“As a general rule, you should seek a patient’s express consent before
disclosing identifiable information for purposes other than the provision
of their care or local clinical audit, such as financial audit and insurance
or benefits claims.”
Thus, unless you are disclosing information in relation to a patient’s care or for
local clinical audit, express consent should be obtained. If express consent is
refused, you may still be able to disclose if you can establish a public interest
reason.
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Paragraph 34 deals with situations where doctors are asked to provide information
to third parties (for example, an insurer or employer) either following examination
or from existing medical records. It includes the requirement that the patient
should have “sufficient information” regarding the purpose and consequences of
the disclosure and that “relevant information cannot be concealed or withheld.” Ifthey wish the patient should be shown or given a copy of any report prepared
unless “disclosure would be likely to cause serious harm to the patient or anyone
else” or “disclosure would be likely to reveal information about another person who
does not consent.”
.
12.7.2 Implied consent
Can consent to disclosure of information ever be implied? Certainly the
professional guidance suggests this is the case.
The GMC guidance ‘Confidentiality’ (2009) has a section dealing with
‘circumstances in which patients may give implied consent to disclosure’. Read
paragraphs 25-32 of the guidance document.
Paragraphs 25-29 deal with the issues of sharing information in the healthcare
team or with others providing care. Paragraph 25 makes clear:
“Most patients understand and accept that information must be sharedwithin the healthcare team in order to provide their care. You should
make sure information is readily available to patients explaining that,
unless they object, personal information about them will be shared within
the healthcare team, including administrative and other staff who
support the provision of their care.”
Thus on the basis of this guidance, information can be shared on the basis of
implied consent.
The courts have continually stressed that care must be taken to limit the amount of
information disclosed to those “who need to know” and to ensure that the recipient of
that information understands the requirement of confidentiality, see W v Egdell [1990]
1 ALL ER 835 at page 850. See also paragraph 28 of the ‘Confidentiality’
guidance: “You must ensure that anyone you disclose personal information to
understands that you are giving it to them in confidence, which they must respect.”
12.8 PUBLIC INTEREST
Consider the following two situations. Firstly, A is diagnosed as HIV positive. He is
counselled by his health carer and this includes the advice that he should inform
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his wife of his condition, especially if they intend to continue to have unprotected
sexual intercourse. He refuses to do so. He dies. After his death A’s spouse
discovers that she is now HIV positive. Can she sue the health carer? Could she
argue that, in the public interest, the health carer should have ignored the
confidentiality between himself and her husband and disclose the information toher in order to protect her from such a harmful illness? Secondly, a health carer
diagnoses B, a long-distance lorry driver, to be going blind. He urges B to inform
the DVLA; B refuses to do so. Should the health carer inform the DVLA?
Possibly in both cases an argument could be made out for saying that the public
interest demands that there should be a breach of the confidentiality rule. The
difficulty is in defining “public interest”; it is suggested that the phrase should be
given a wide interpretation and on this basis if only one member of the public is
likely to be harmed then the public interest is affected. But it will always be a
balancing exercise that the health carer will have to perform: balancing the public
interest confidentiality of the patient against the public interest desire to protect the
public from harm. It is more than likely that, if the health carer performs this
exercise and places his thoughts on the records, an English court will not find him
or her liable for unauthorised disclosure.
There are public interest considerations which may justify disclosure of confidential
information. There are potentially competing public interest considerations:
(i) the public interest in maintaining confidences
(ii) the public interest in disclosing confidential material if the circumstances can justify
it.
In essence to justify disclosure, the public interest in disclosure must be stronger than
the public interest in maintaining the confidentiality.
12.8.1 Case law
Consider relevant case law regarding the public interest exception.
See Attorney-General v Guardian Newspapers (No 2) [1988] 3 All ER 545. This
case highlights the need for a balancing exercise to take place, see the following
comment per Lord Griffiths:
“This involves the judge in bal ancing the public interest in upholding the
right to confidence….against some other public interest that will be
served by the publication of the confidential material.”
See also Lord Goff:
“…although the basis of the law’s protection of confidence is that there is
a public interest that confidences should be preserved and protected by
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the law, nevertheless that public interest may be outweighed by some
other countervailing public interest which favours disclosure.”
A key factor in deciding whether or not to disclose confidential information is
proportionality.
In X v Y [1988] 2 All ER 648 employees of a health authority had supplied
information from hospital records to a newspaper reporter which identified that two
doctors with AIDS were working in general practice. A general article was
published in the newspaper regarding doctors with AIDS practising in Britain. The
newspaper wished to publish a further article which identified the doctors. An
injunction was sought to restrain the defendants from publishing the identity of the
two doctors. The issue to be addressed was whether the publication of the
information could be justified in the public interest. The following issues were
identified:
“On the one hand there are the public interests in having a free press
and an informed public debate; on the other, it is in the public interest
that actual or potential AIDS sufferers should be able to resort to
hospitals without fear of this being revealed….I accept that there is
some public interest in knowing that which the defendants seek to
publish….in my judgment those public int erests are substantially
outweighed when measured against the public interests in relation to
loyalty and confidentiality both generally and with particular reference to
AIDS patients’ hospital records.”
So what ‘public interest’ will justify disclosure? In W v Egdell [1990] 1 ALL ER 835
proceedings were brought against a doctor following disclosure of a psychiatric
report without the patient’s consent. The patient was detained in a secure hospital
due to the threat he posed (having killed five people and wounded two people).
The defendant, a consultant psychiatrist, was asked to prepare a report by the
patient’s solicitors to support an application for discharge/ transfer. The report
opposed the discharge/ transfer on the basis of the conclusions drawn about the
patient (for instance his interest in firearms). The patient’s solicitors therefore
withdrew the application. The defendant contacted the medical director of the
hospital and a copy of the report was provided on the basis it was considered
beneficial regarding further treatment. There was also concern regarding future
discharge/ transfer. A copy was also sent to the Secretary of State and then to the
mental health review tribunal. When the patient discovered the report had been
disclosed without permission he sought an injunction and damages.
It was held (at p.846) that:
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“The balance of public interest clearly lay in the restricted disclosure of
vital information to the director of the hospital and to the Secretary of
State who had the onerous duty of safeguarding public safety.”
Also, per Bingham LJ at p.851:
“the crucial question in the present case was how, on the special facts ofthe case, the balance should be struck between the public interest in
maintaining professional confidences and the public interest in
protecting the public against possible violence.”
At pp.852-853 it was held:
“There is one consideration which in my judgment, as in that of the
judge, weighs the balance of public interest decisively in favour of
disclosure. It may be shortly put. Where a man has committed multiple
killings under the disability of serious mental illness, decisions which
may lead directly or indirectly to his release from hospital should not be
made unless a responsible authority is properly able to make an
informed judgment that the risk of repetition is so small as to be
acceptable. A consultant psychiatrist who becomes aware, even in the
course of a confidential relationship, of information which leads him, in
the exercise of what the court considers a sound professional judgment,
to fear that such decisions may be made on the basis of inadequate
information and with a real risk of consequent danger to the public is
entitled to take such steps as are reasonable in all the circumstances to
communicate the grounds of his concern to the responsible authorities.”
Thus confidential information can be disclosed where there is a ‘real risk’ of
‘danger to the public’. It should be stressed however that (as was the case in W v
Egdell ) disclosure should be made ‘to the responsible authorities’. For instance,
disclosure to a newspaper may not be permitted.
This was quite an ‘extreme’ example, where it was relatively easy to see the public
interest element should weigh heavily in favour of disclosure. But how far reaching
can this public interest exception be? To what extent will other third party interests
outweigh the public interest in confidence?
Also, in such a situation the ‘public interest’ justification would provide the clinician
with a power to disclose rather than impose an obligation. If Dr. Egdell had not
disclosed the information and W then injured a member of the public, a legal action
by the injured person would not have been successful. See later for further
discussion of whether there are any circumstances where an injured third party
could bring an action against a clinician where, for example, risks posed by the
patient were not disclosed and the third party suffers harm as a result.
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Other cases to note:
R v Crozier [1991] Criminal. LR.138
Hay v University of Alberta Hospital [1991]; X v Y [1988].
H v N (a Health Authority) [2001];
C v Dr A.J. Cairns [2003]
Ackroyd v Mersey Care NHS Trust [2003].
12.8.2 GMC guidance: ‘Public inter est’ justification
The GMC guidance ‘Confidentiality’ (2009) acknowledges the balancing act that
would have to be undertaken when deciding whether disclosure was appropriate.
See paragraphs 36-39 for the general position regarding disclosure in the public
interest. Paragraph 36 provides:
“Confidential medical care is recognised in law as being in the public
interest. However, there can also be a public interest in disclosing
information…”
Thus, under paragraph 37:
“Personal information may, therefore, be disclosed in the public interest,
without patients’ consent, and in exceptional cases where patients havewithheld consent, if the benefits to an individual or to society of the
disclosure outweigh both the public and the patient’s interest in keeping
the information confidential.”
You should still try to seek consent (unless this is not practicable) and should
consider whether the information could be anonymised (see paragraph 38).
12.8.3 GMC guidance: Disclosures to protect the patient/ to protect others
Read paragraphs 51-56 of the GMC ‘Confidentiality’ guidance.
What is the position where a patient with capacity refuses to consent to disclosure
even where this puts the patient at risk of harm? See paragraph 51:
“…you should usually abide by a competent adult patient’s refusal to
consent to disclosure, even if their decision leaves them, but nobody
else [my emphasis], at risk of serious harm.”
If somebody else could be put at risk (for example, a domestic violence case where
children are also potentially at risk) paragraph 53 would come into play:
“Disclosure of personal information about a patient without consent may
be justified in the public interest if failure to disclose may expose others
to a risk of death or serious harm.” [my emphasis]
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Paragraph 55 goes on to explain how disclosure can be justified where a failure to
disclose “leaves others exposed to a risk so serious that it outweighs the patient’s
and the public interest in maintaining conf identiality.”
Note, even where a ‘public interest’ justification exists consent should still be
sought or the patient should be informed of the intent to disclose where possible.
12.8.4 GMC guidance: Supplementary guidance on specific issues
Note the GMC has also issued specific supplementary guidance on the following
issues:
Reporting concerns about patients to the DVLA
Disclosing records for financial and administrative purposes
Reporting gunshot and knife wounds
Disclosing information about serious communicable diseases
Disclosing information for insurance, employment or similar purposes
Disclosing information for education and training
Responding to criticism in the press.
12.8.5 NHS Code of Practice: Public interest
The NHS guidance regarding confidentiality also includes reference to public
interest issues (see Confidentiality: NHS Code of Practice (November 2003.
Examples of where disclosure may be necessary to protect the public are set out at
p.35 of the Code (see figure 7). These include disclosure on the grounds of serious
crime and national security or risk of harm.
Identifying which circumstances will justify public interest disclosure is a difficult
task. The Department of Health has recently issued supplemental guidance
(Confidentiality: NHS Code of Practice- supplemental guidance: public interest
disclosures, November 2010) to assist with the decision making process. The
guidance is said to expand upon the principles set out in the 2004 Code of
Practice.
At paragraph 2 of the 2010 supplemental guidance, it is stated that there are
certain considerations which should be taken into account:
“Extent of the information which is to be disclosed- it will be easier to justify
disclosure of demographic data or the fact that someone attended a clinic
rather than detailed health information.
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12.9.6 Terrorism Act 2000
See section 19 which imposes a duty to disclose if it is believed that an offence has
been committed, otherwise a criminal offence is committed by the person failing to
disclose.
12.9.7 Public Health (Control of Disease) Act 1984
Section 10 authorises the disclosure of notifiable diseases such as cholera etc.
12.10 DISCLOSURE IN THE COURSE OF LITIGATION
Disclosure of information about the patient may be sought by the patient/claimant’s
lawyer from the defendant Trust in anticipation of or during litigation. It is vital thatany communication requesting the records from the Trust etc. be accompanied by
the patient’s express consent to such a disclosure. At the same time the lawyer
should make sure all communications are directed to him and not to his medical
adviser. Usually requests for disclosure of medical records in litigation will be made
under the DPA (see the following chapter).
If the defendants refuse to give voluntary disclosure then an application may be
made to the court under sections 33(2) and 34(2) of the Supreme Court Act 1981
for an order for disclosure. The order may be obtained not only against the
defendants but also against a third party, for example, if the defendant is a
pharmaceutical company, the order may be sought against the Prescription Pricing
Authority. (The legal practitioner should be aware that valuable information may
also be obtained from other sources, such as inquests (where applicable) (see R v
HM Coroner for N Humberside ex parte Jamieson [1994), and the NHS complaints
system.
The defendant may refuse disclosure on the grounds that the records are subject
to lawyer / client privilege and should therefore remain confidential, i.e.
communications between a solicitor and his client or communications between a
lawyer and a third party for the purposes of the litigation. Where a document has
two purposes, one of which is to assist in the litigation and the other is for the
client’s own use then, for the document to remain privileged, the dominant purpose
for which it was prepared must be to assist in the litigation. To illustrate this point
see Waugh v British Railways Board (1980), Lask v Gloucester H A The Times 13
Dec 1985, and Lee v South West Thames HA [1985].
Disclosure may also be refused on the ground that revelation would be
embarrassing to the defendant or damaging to the public interest (see S35 of the
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Supreme Court Act 1981). In Re HIV Haemophiliac Litigation (1990) 140 NLJ 1349
the claimants sued the Department of Health for becoming infected with the HIV
virus. The defendant argued that document disclosure should be refused on the
grounds that it would be damaging to the public interest in that it would reveal
communications between government ministers. This argument was rejected; itwas held to be more important that the claimants were given the opportunity of a
fair trial of the matter.
If either of the above situations arises then a determination of this issue will have to
be arrived at before the trial of the main issue(s).
12.11 ANONYMISED DATA
The case of R v Department of Health, ex p. Source Informatics Ltd [2000] 1 All ER 786
considered the issue of whether disclosure of anonymised patient information could
constitute a breach of confidence. The case concerned use of anonymised information
supplied to a data protection company by pharmacists. The information related to GPs
prescriptions. At first instance, the court held that disclosure of anonymised information
without consent could constitute breach of confidence. The judge considered public
interest issues and considered that patients may not want information from their
prescription forms to be used.
The Court of Appeal took a different view.Simon Brown LJ held (at p.797):
“What interest, one must ask, is the law here concerned to protect? In my
judgment the answer is plain. The concern of the law here is to protect the
confider’s personal privacy. That and that alone is the right at issue in this
case. The patient has no proprietorial claim to the prescription form or to the
information it contains….This appeal concerns, as all agree, the application of
the broad principle of equity. I propose its resolution on a similarly broad
basis….pharmacists’ consciences ought not reasonably to be troubled by co-
operation with Source’s proposed scheme. The patient’s privacy will have
been safeguarded not invaded. The pharmacist’s duty of confidence will not
have been breached.”
See also H (a health care worker) v Associated Newspapers Limited and H (a health care
worker) v NHA [2002] EWCA Civ 195
12.12 DATA PROTECTION ACT 1998
In addition to considering the common law position (above) and the impact of HRA
(below), in order to fully understand the obligations in relation to confidentiality, we also
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need to consider the application of the Data Protection Act 1998 (DPA).The provisions of
the act are complex and cover all manner of data and its processing. We will only
consider its provisions and their application to medical information briefly here. For further
information on the DPA, see the Information Commissioner’s (ICO) web site, and in
particular, the ICO ‘Data Protection Act 1998 Legal Guidance’.
Essentially the DPA provides certain protections in relation to personal data. This
includes the obligation on those ‘controlling’ such data to do so in accordance with 8 key
principles. In addition it also provides individuals a right of access to certain data held
about them.
Considering (very briefly) the implications of the DPA the following points should be
noted.
12.12.1 Terminology
The act contains a number of key terms. The act applies to all ‘personal data’-
which is data referable to a living individual, the ‘data subject’. Further medical
information will usually be ‘sensitive personal data’, which means additional
safeguards apply. The safeguards are contained in the 8 ‘principles’ and apply any
time data is ‘processed’. This is a very wide definition and will include almost
anything from filing, amending, updating records, manually or on computer, as well
as to allowing access to the records. The principles apply to the ‘data controller’,usually the relevant NHS Trust in this context, when processing information.
12.12.2 Principles
As considered above, the DPA imposes certain safeguards through requirement to
process data in accordance with the 8 principles. In addition schedules 2 and 3
(where the data is sensitive personal data) of the DPA include additional criteria
which must be satisfied for data to be lawfully processed. Essentially for lawful
processing at least one of a list of conditions in schedule 2, and where data is
‘sensitive’, schedule 3, must be satisfied. Consent is not necessarily required,
although consent (‘express consent’ for schedule 3) is one of the categories for
both schedules.
Arguably the most important of those principles, practically speaking, is the first
principle, that of ‘fair and lawful processing’. As may be self evident this includes a
number of obligations, including the requirement that any processing be compliant
with common law and HRA provisions.
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Establishing capacity, therefore, is important. In relation to ‘older’ children the
confidentiality issues seem most likely to arise in relation to contraceptive advice/
treatment and abortion. For children under 16, the position in relation to consent to
treatment was considered in the case of ‘Gillick’ Gillick v West Norfolk and Wisbech Area Health Authority [1985] 3 All ER 402, (see chapter on consent). For the
purposes of the Data Protection Act and rights of access, there is a general
presumption that a child of 12 is ‘mature’ enough to exercise their right of access.
The Gillick decision was re-visited in the case of R (on the application of Axon) v
Secretary of State for Health [2006] All ER (D) 148 (Jan) . Part of the claimant’s
claim was that “a doctor was under no obligation to keep confidential advice and
treatment which he proposed to provide to a young person under the age of 16 in
respect of contraception, sexually transmitted infections and abortion and therefore
should not provide such advice and treatment without the parents’ knowledge
unless to do so would or might prejudice the child’s physical or mental health so
that it was in the child’s best interests not to do so.” The claimant challenged the
Secretary of State’s guidance document ‘Best Practice Guidance for Doctors and
other Health Professionals on the Provision of Advice and Treatment to Young
People under Sixteen on Contraception, Sexual and Reproductive Health’ (the
2004 Guidance). The claimant sought a declaration that doctors and other health
professionals have “a duty to consult the parents” before advising/treating
regarding contraception, sexually transmitted infections or abortions and that the
parents “have a right to be informed about” proposed provision of such
advice/treatment.
Mr. Justice Silber acknowledged (see paragraph 7) that this raised a tension
between two principles:
(i) a competent child is an autonomous person and is entitled to confidentiality;
and
(ii) the parent has responsibility for the young person’s health and moral
welfare.
He also acknowledged:
“There is also a significant public policy dimension because there is
evidence that without the guarantee of confidentiality, some of these
young people might not seek advice or treatment from medical
professionals on sexual matters with potentially disturbing
consequences.”
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For various reasons Mr. Justice Silber did not agree that there should be an
exception to the duty of confidence, at paragraph 62:
“the very basis and nature of the information which a doctor or a
medical professional receives relating to the sexual and reproductive
health of any patient of whatever age deserves the highest degree ofconfidentiality and this factor undermines the existence of a limitation
on the duty of disclosure…”
and at paragraph 80 Mr. Justice Silber concluded:
“In the light of this change in the landscape of family matters, in
which the rights of children are becoming increasingly important, it
would be ironic and indeed not acceptable now to retreat from the
approach adopted in Gillick and to impose additional new duties
on medical professionals to disclose information to parents of their
younger patients.”
The claimant also had argued that she had a right to be notified on the basis of
article 8 of the European Convention of Human Rights (article 8(1) ‘Everyone has
the right to respect for his private and family life, his home and his
correspondence’) and that the relevant 2004 guidance was unlawful.
At paragraph 132 Mr. Justice Silber concludes:
“…parents do not have article 8 rights to be notified of any advice of a
medical professional after the young person is able to look after
himself or herself and make his or her own d ecisions.”
Suggested reading
Hall, “Children’s Rights, Parents’ Wishes and the State: the Medical Treatment of
Children” Fam Law 36(317) 1 April 2006
Samiloff, “Knowing all- a parent’s prerogative?” 156 NLJ 570 (7 April 2006)
12.13.2 Children who lack capacity to consent to treatment
There appears to be some academic dispute regarding the nature and extent of the
confidentiality obligations in relation to the child who lacks capacity to give consent
to treatment, but who seeks confidentiality and requests that their parents should
not be informed.
See Montgomery, Health Care Law, 2nd
Ed, Oxford University Press, 2003, at
pp.308-311.
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Montgomery suggests (at p.309) that the reasoning in Gillick implies that if a child
can understand the obligation of confidence, this can impose an obligation of
confidence, even if the child does not understand the relevant treatment. He
suggests this view can be supported “based on the fact that the preconditions of
the legal obligation of confidence are made out in relation to children who claim theright to secrecy on exactly the same basis as in relation to adults.” He also notes
that it is apparent from Gillick that:
“children can take decisions which they are competent to make as
they reach that stage of competence and not at a single radical rite
of passage whereby they become adults for all purposes. There is
no reason of principle why the obligation of confidence cannot be
created independently of any later treatment decision.”
This argument runs counter to other academics who argue only a capable child is
owed a duty of confidentiality..
What is the position in relation to young children who neither have capacity to
consent to treatment or capacity to appreciate the notion of confidence. Here the
role a person with parental responsibility is significant. Parental rights do not exist
for the benefit of the parent, they exist for the benefit of the child. For instance, a
parent could consent to information being disclosed and exercise DPA rights on
behalf of the child. Note, however that this does not mean a child has no
protection. The exercise of parental responsibility is expected to be done
responsibly and in accordance with the child’s interests. If a person with parental
responsibility acts against the interests of the child an application to court for a
prohibited steps order (under section 8, Children Act 1989) can be made to prevent
this.
12.13.3 Professional guidance
o GMC ‘Confidentiality Guidance’
The GMC document ‘Confidentiality’ (2009) offers some limited guidance in relation
to confidentiality and children.
Paragraph 58 of the ‘Confidentiality’ guidance directs you to the GMC’s
guidance in relation to children generally ‘0-18 years: guidance for all
doctors’.
Paragraph 61 of the ‘Confidentiality’ guidance provides:
“If a patient who lacks capacity asks you not to disclose
personal information about their condition or treatment, you
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should try to persuade them to allow an appropriate person
to be involved in their consultation. If they refuse, and you
are convinced that it is in their best interests, you may
disclose relevant information to an appropriate person or
authority.”
Paragraph 63 deals with ‘disclosures when a patient may be a victim of
neglect or abuse.’ It provides:
“If you believe that a patient may be a victim of neglect or
physical, sexual or emotional abuse, and that they lack
capacity to consent to disclosure, you must give information
promptly to an appropriate responsible person or authority, if
you believe that the disclosure is in the patient’s best
interests or necessary to protect others from a risk of seriousharm.”
GMC ‘0-18 years: guidance for all doctors’
Paragraphs 45-52 of the ‘0-18 years’ guidance are of particular relevance. For
instance, paragraphs 47-50 consider the public interest justifications for disclosure
that apply in relation to children.
GMC ‘Protecting children and young people: the responsibilities of all
doctors’
The GMC has recently published additional guidance which focuses on how to
protect children and young people from abuse and neglect. This guidance was
published in July 2012 and came into effect on 3.9.12. Paragraphs 28-60 of this
guidance focus on issues regarding confidentiality and sharing information.
Paragraph 31 states that public interest can be used to justify sharing information
“if the benefits to a child or young person that will arise from sharing theinformation outweigh both the public and the individual’s interest in keeping the
information confidential.
The obligation to share information where there is a concern that a child is at risk of
abuse/neglect is framed quite strongly. A decision not to share information would
have to be justified (see paragraphs 39-41). The guidance does state that
consent should be sought first “unless there is a compelling reason for not doing
so” such as if “asking for consent may increase the risk of harm to the child, young
person, you or anyone else” (see paragraph 34).
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12.14 ADULTS WHO LACK CAPACITY
12.14.1 The Impact of the Mental Capacity Act 2005
Where a person lacks capacity to consent to any disclosure, then difficult issues
can arise. In the case of a child, someone with parental responsibility (PR) will
(may) be able to consent. With adults the position is more complex. Until
implementation (in October 07) of the Mental Capacity Act 2005 (MCA) no one
could take healthcare/ welfare decisions on behalf on another adult. As the MCA
has now been fully implemented it is important to consider what impact it will have
for confidentiality. Although the MCA does not specifically refer to confidentiality as
such it does set out a statutory legal framework for decision making for those who
lack capacity and you should refer back to this and in particular sections 2, 3 and 4
MCA. Once it has been established however that a person lacks capacity, then
certain acts can be carried out under section 5 of the MCA. To what extent the
disclosure of information would fall within section 5 is not clear though the
application of section 5 has been widely interpreted (see Code chapter 6). The
MCA Code of Practice then continues at chapter 16 to assess the impact of the Act
for confidentiality.
The Code reiterates the basic legal framework, including reference to the common
law duty of confidentiality, HRA and DPA. It then considers the position in relationto ‘proxy decision makers’, LPAs and Deputies (see s 9-11 MCA). The Code
suggests that a proxy decision maker will be entitled to access information relevant
to the decision they are empowered to make, subject to certain limitations (see the
DPA position discussed later). In relation to others, paragraph 16.19 refers to
disclosure of information by healthcare and social care staff ‘only when it is in the
best interests of the person concerned to do so, or when there is some other,
lawful reason for them to do so.’
Information disclosed should always be limited to that which it is necessary for the
person to know, and their will be obligations of confidentiality on the recipient of the
information. In cases of dispute an application can be made to the Court of
Protection.
See the case of Stevens v Plymouth City Council [2002] EWCA Civ 388 , para
33 for consideration of the position in relation to disclosure in the context of the
Mental Health Act 1983, and the ‘competing’ rights of mother and son.
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12.14.2 Professional guidance
Reference is again made to the new GMC ‘Confidentiality’ guidance. Paragraphs
57-63 are of particular relevance. The new guidance has clearly been drafted to
take into account the MCA provisions. See for example paragraph 60 which
stresses the need to consider whether the lack of capacity is permanent or
temporary (and whether the disclosure decision could wait if temporary), evidence
of previously expressed preferences and the views of anyone the patient asks you
to consult...
Paragraph 61 provides:
“If a patient who lacks capacity asks you not to disclose personal
information about their condition or treatment, you should try to persuade
them to allow an appropriate person to be involved in their consultation.
If they refuse, and you are convinced that is essential in their best
interests, you may disclose relevant information to an appropriate person
or authority.”
Disclosure must therefore be justified based on best interests. Note also that only
relevant information can be disclosed and this must be to an appropriate person or
authority.
Even where a patient lacks capacity, relatives and carers are not automaticallyentitled to full access to the patient’s medical records. See paragraph 62 on this
point:
“You may need to share personal information with a patient’s relatives,
friends or carers to enable you to assess the patient’s best interests. But
that does not mean they have a general right of access to the patient’s
records or to have irrelevant informati on about, for example, the patient’s
past healthcare.”
As highlighted in 3.1.4, there is an obligation under paragraph 63 to disclose
information to “an appropriate responsible person or authority” where “the patient
may be a victim of neglect or physical, sexual or emotional abuse, and that they
lack capacity to consent to disclosure.” If a decision is made not to disclose, this
must be carefully justified.
Read paragraphs 11-15 of annex B of the Department of Health document
‘Confidentiality: NHS Code of Practice’ November 2003 which sets out guidance
where ‘patients are unable to give consent.’ The need to justify disclosure is again
stressed.
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12.15 CONFIDENTIALITY AND DECEASED PATIENTS.
12.15.1 Professional guidance
Professional guidance on this issue seems clear. In the GMC document
‘Confidentiality’ (2009) guidance is set out regarding disclosure of personal information
after a patient’s death. At paragraph 70 it is stated:
“Your duty of confidentiality continues after a patient had died. Whet her and
what personal information may be disclosed after a patient’s death will depend
on the circumstances. If the patient has asked for information to remain
confidential, you should usually respect their wishes.”
If the patient had made no such request, paragraph 70 provides guidance regarding the
factors to be taken into account should a request for information be made. Paragraph
71 sets out circumstances where disclosure should take place.
12.15.2 Legal position
The nature and extent of the legal obligations is less straightforward.
At paragraphs 4.105-4.106 of the Law Commission Report referred to above the
position under section 1(1) of the Law Reform (Miscellaneous Provisions) Act 1934 is
set out. Consider the following example given in paragraph 4.105:
“where X is in breach of an obligation of confidence which he owes to Y and Y
dies before he has started or concluded proceedings for breach of confidence,
the personal representatives of Y may bring, or as the case may be, continue an
action for breach of confidence against X in respect of his breach of confidence
vis-à-vis Y.”
Two recent decisions have pointed towards a legal obligation of confidence after death:
Bluck v Information Commissioner & Epsom & St Helier University NHS Trust
EA/2006/0090
Lewis v Secretary of State for Health [2008] EWHC 2196
12.16 REMEDIES FOR A WRONGFUL DISCLOSURE?
An injunction and/or damages. For these two remedies, the normal rules as laid down
in the American Cyanamid case [1975] are applicable.
As above, a breach of the DPA will also give rise to a claim.
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12.17 CAN A THIRD PARTY SUE FOR NON-DISCLOSURE?
If a health carer decides not to disclose information he will (generally) not be liable
to a third party who is subsequently harmed by the patient. (See Smith v
Littlewoods Organisation [1987]). With the development of human rights and the
concept of duties to disclose, it will be interesting to see how this area develops.
However this is not necessarily the position in the United States of America – see the
earlier reference to:
* Tarasoff v Regents of the University of California (1976) 551 P. (2d) 334;
* Bradshaw v Daniel (1994) Med.L.Rev. 237
* Webb v Jarvis (1991) 575 NE (2d_ 992)
READING:
Stauch & Wheat: Text, Cases and Materials on Medical Law &
Ethics (5th ed) (Routledge) Chapter 5
Pattinson Chapter 6Jackson Chapter 7
Brazier Chapter 4
Khan/Robson/Swift Chapter 1
Montgomery Chapter 11
Mason/McCall Smith (2013) Chapter 8
Guidance:
NHS Confidentiality Code of Practice GMC
Guidance referred to in chapter
Code of Practice to MCA
Nov 2003( on D o H website)
As referred to in chapter
Chapter 16
SUMMARY
At the end of this chapter you should understand:
* what is meant by confidentiality;
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* when a health carer may legally disclose information about his patients;
* the remedy the patient may have for an unauthorised disclosure.
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SELF-TEST QUESTIONS – CHAPTER 12
1. Mention the circumstances in which a health carer may legally disclose a
patient’s confidential information.
2. What is meant by a claim in equity for breach of confidential information?
3. What is meant by a disclosure in the public interest?
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NOTES
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CHAPTER 13
ACCESS TO MEDICAL RECORDS
13.1 INTRODUCTION
A patient’s medical records are not the property of the patient; rather they are owned
(generally) by the NHS Trust (see R v Mid Glamorgan FHSA ex p Martin [1995] and the
reader should note that some authors make a distinction between the paper on which the
records are written and the information within the records—the latter “belonging”, it is
said, to the patient). As a result the patient had no right in English law to see his own
records; his health carer could, in a benevolent mood, allow him to have sight of such or
he could see the records in the course of any litigation he was pursuing. This has
however changed with the introduction of the DPA 1998.
The topic of medical records has already been touched upon, because when one talks of
medical confidentiality, essentially one is talking of keeping the patient’s medical records
confidential. But while Chapter 14 focuses on disclosure of those records to a third party,
this chapter will reflect on the patient himself /herself getting hold of his/her own medical
records (what he/she chooses to do with them subsequently is a matter for the patient), inother words rights of access.
13.2 DISCLOSURE TO THE PATIENT/CLIENT
This may be done voluntarily on the part of the health carer in possession of the records.
Statutory provisions now exist to enable (generally) a patient to see (have access to) his
own records subject to whatever limitations the statute itself may impose.
13.2.1
The legislation dealing with such access includes/ included the Data Protection Act
1984 (dealing with computerised medical records- now replaced by the DPA 1998),
the Access to Personal Files Act 1987, the Access to Medical Reports Act 1988 (re
employment and insurance), the Access to Health Records Act 1990 (for non-
computerised records made since 1/11/91, now repealed by DPA 1998, except in
so far as it relates to the deceased). But the most important provision is the Data
Protection Act 1998.
13.2.2 Data Protection Act 1984
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This Act allowed a patient to see all of his computerised records although access
could be refused on the grounds that it would damage the physical or mental
health of the patient or that it identified a third party whose consent had not been
obtained.
13.2.3 Access to Personal Files Act 1987 / Access to Medical
Reports Act 1988 (S1)
The patient is permitted to see his records in certain circumstances, for example
where a report is prepared for his employer.
13.2.4 Access to Health Records Act [1991]
This Act allowed patients access to all their health records post November 1991.
But again there are exceptions e.g. there is no access where there is a genuine
risk to the physical or mental health of the applicant or a third party or if access
would reveal information about any individual other than the patient. This Act has
been repealed in part by the 1998 Data Protection Act except in relation to
deceased patients. Consequently it only has application to the seeking of
disclosure of records relating to a deceased patient.
13.2.5 The Data Protection Act 1998
We have already considered the DPA in chapter 14 above. In terms of access to
records, the most significant change introduced by this Act was that the application
of the 1984 act would effectively be extended to all medical records.
Section 7 of the DPA establishes the right of every individual (subject to stated
exceptions), to require the relevant data controller to confirm the nature and extent
of the data being held and the recipients to whom they are or may be disclosed.
Any person may also be entitled to a copy of the information in an intelligible form.
The data controller is required to supply the information within 40 days of a written
request (and payment of the appropriate fee).
Although s. 7 confers a right of access, the right is modified in certain
circumstances by the DATA PROTECTION (SUBJECT ACCESS MODIFICATION)
(HEALTH) ORDER 2000 (‘The Order’). This effectively restricts access/ disclosure,
where such disclosure ‘would be likely to cause serious harm to the physical or
mental health of the data subject or any other person’.
In relation to children, no age limits as such are provided within the act. What about
a child wishing to access their own records? A capable child should be able tomake their own access request. Further, general guidance is ‘that by the age of 12
a child can be expected to have sufficient maturity to understand the nature of the
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request’, and make a request. However ‘a child may, of course, reach sufficient
maturity earlier and it will be a question of fact in each case’ (ICO Guidance, para.
4.1.6).
It is important to note at the outset that the right of access under the DPA is onlyconferred on the data subject (eg the patient) themselves. It does not provide any
authority to access ‘third party’ information (eg about a person other than the
person making the request). Special rules apply to third party information
introduced by the above Order . Consequently NHS Trusts need to take care when
disclosing records that information about other patients, for example, is not
included.
Although the DPA does not provide any authority for someone to access
information about someone else, in certain circumstances, namely in relation to
children and incapable adults, it may be that authority to access information can be
derived from other legal provisions. Examples may be the Children Act 1989, in
relation to someone with parental responsibility for a child, or in relation to an
incapable adult, via the court of protection provisions or post October 07, the MCA
2005. In such circumstances the DPA introduces further restrictions on access.
This essentially restricts disclosure where the child/ incapable adult has provided
information expressly/ impliedly on the basis it would not be shared with the person
seeking such disclosure.
For example where a parent may have the right legally to access their child’s
health records since they have parental responsibility for them, then this right may
be restricted in accordance with the Order, if the child has provided the information
on the basis that any such information would not be disclosed to that parent.
We have already noted above that these provisions do not apply to the deceased
and access to a deceased patient’s records will have to be sought under the
Access to Heath Records Act, noted above.
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READING:
See reading for Confidentiality chapter
Stauch & Wheat: Text, Cases and Materials on Medical Law &
Ethics (5th ed) (Routledge) Chapters 3,4 & 9
Brazier Pp 93-94
Khan/Robson/Swift Chapter 1
Mason/ McCall Smith Chapter 8
Montgomery Chapter 11
SUMMARY
At the end of this chapter you should be able to:
* The significance of legislation such as the Data Protection Act 1998;
* When, as the patient’s legal advisor, you may not see your client’s medical
records;
* When, as the patient, you may not see your medical records.
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SELF-TEST QUESTIONS – CHAPTER 15
1. As a lawyer how would you go about getting your client/patient’s records from
the defendant Trust?
2. What arguments might a Trust use to avoid sending the lawyer the records?
3. When can a patient see his/her own records?
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NOTES
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CHAPTER 14
THE BEGINNING OF LIFE
14.1 CONTRACEPTION
(a) This can be achieved by surgical methods such as (voluntary) sterilisation and
vasectomy, both of which should be regarded as forms of medical treatment and
therefore the health carer may be liable in contract or negligence or trespass.
(Refer back to your trespass and clinical negligence notes and in particular to such
matters as consent, duty of care, causation, damages and note the importance of
contract law in these areas, since more and more people are likely to have
sterilisations etc. done privately). What may be of greater significance here is the
fact that the health carer is under a legal duty to warn the patient of the risks
associated with a particular form of contraception; failure to do so may well result in
a claim in negligence.
See Walkin v South Manchester H.A. [1995], Allen v Bloomsbury H.A. [1993] and
McFarlane v Tayside Health Board [2002], Rees v Darlington Memorial Hospital
[2003] UKHL 52.
◦ Compulsory sterilisation will raise issues of consent or lack of consent as well
as human rights issues. There is a strong argument for saying that the lack of
consent in sterilisation cases is a denial of the patient’s human rights, but there
is growing evidence that treatment in a patient’s best interests will not infringe
their human rights: and in some cases compulsory sterilisation will be effected
because it is deemed to be in a patient’s best interests. See cases such as Re
B (A Minor) [1987] 2 All ER 206 A Local Authority v Mrs A and Mr A [2010]EWHC 1549 and the MCA s.4 and new case
(b) Non-surgical methods of contraception:
(i) condoms;
(ii) IUD (intra uterine device - coil);
(iii) long acting injectable contraceptive (Depo-Provera);
(iv) female contraceptive pill (male contraceptive pill?);
(v) post-coital birth control (morning after pill);
(vi) Abortion pill (RU486).
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Apart from (i) above, all the other methods could involve the services of a health
carer, in which case issues of consent, care, counselling etc are again all relevant.
14.2 CONTRACEPTION OR ABORTION?
Are methods which are described as contraceptive truly contraceptive? Or might they be
abortive? Take the IUD, as an example. This acts to prevent implantation of the fertilised
ovum and can be taken up to 72 hours after unprotected sex. Is this contraceptive? Yes,
if one were to argue that at day 3 there is no ‘life’ which is likely to be affected. But if ‘life’
was to begin at day 1, then the IUD may be seen as aborting that life, in which case the
law on abortion would become relevant.
So, the issue now is: when does life begin? Some argue for day 1, others day 10
(implantation), some for day 15/16 (appearance of the ‘primitive streak’), others when the
baby is born, still others when certain features appear, for example lungs. Although at
present there is no definitive answer, an appreciation of what the argument entails is vital
as newer or more sophisticated forms of contraception come on the market. (Read
(1984) Criminal Law Review p 608). If the ‘contraception’ is abortive, then leg al protection
will have to be sought under the Abortion Act 1967 as amended by the Human
Fertilisation and Embryology Act 1990 (HFE act), since offences under the Offences
Against the Person Act 1861 ( sections 58 and 59) will (otherwise) have been committed.
In R v Secretary of State for Health ex p Smeaton [2002] EWHC 610 , the Society for the
Protection of the Unborn Child sought judicial review of a statutory instrument which
permitted the sale of the morning after pill to under 16 year olds under the supervision of
a pharmacist. The Court held that miscarriage in sections 58 and 59 of the 1861 Act
presupposed that implantation of a fertilised egg had already taken place , and since the
morning after pill acted on an egg which was not yet fertilised then no offence was being
committed; therefore no judicial review. “There is no miscarriage if a fertilised egg is lost
prior to implantation. Current medical understanding ……..excludes result brought about
by the pill, the mini-pill or the morning after pill.”(Munby J)
READING:
Stauch & Wheat: Text, Cases and Materials on Medical Law &
Ethics (5th ed) (Routledge) Chapter 7
Pattinson Chapters 7-9
Jackson Chapter 14
Montgomery Chapter 16
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Brazier Chapters 11 & 12 & pp 354-356
SUMMARY
After this part of the chapter you should be able to:
* apply the principles of negligence to claims associated with failed
contraceptive devices;
* possibly decide when life begins;
* decide what are contraceptive devices and what are abortive measures.
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14.3 SELECTIVE FETICIDE OR SELECTIVE REDUCTION
This occurs where, after being treated with a fertility drug, the woman produces a number
of foetuses but some are destroyed (or stored) and she continues to term where she
delivers the surviving child or children. What is the legality of this selective reduction?
See s 37(5) of HFE Act 1990 which introduced new wording into s. 5(2) of the Abortion
Act, and states that such a procedure must now be related to one of the grounds for a
lawful abortion; otherwise it is illegal.
14.4 CHILDLESSNESS
It has to be accepted that childlessness is a feature of many relationships. Today the
technology does exist to assist childless couples to achieve the family unit they long for.
But the techniques available raise significant ethical issues, the major one being that the
scientists are playing God. In addition to this and other ethical issues, there are important
legal problems which need to be considered.
14.4.1
Does anyone have a legal right to have a family? Should a couple be allowed
access to all available techniques without reference to such conditions as age?
Are such conditions legal? According to cases like R v Sheffield Health Authority
ex.p. Seale (1994) and R v Ethical Advisory Committee of St Mary’s Hospital ex pHarriott [1988] the answer is, no. Essentially the decision will be one for individual
fertility clinics to make in accordance with the code of practice issued by the HFEA
(Human Fertilisation and Embryology Authority see below). Although judicial review
is available in respect of decisions not to admit someone to an IVF programme, the
conditions in Harriott’s and Seale’s case, namely, looking at her background and
lifestyle and age, were considered to be reasonable conditions. See also s 14 of
the new Human and Fertilisation and Embryology Act 2008 (and guidance in the
HFA Code), which requires an assessment to be made of ‘the welfare of any child
who may be born as a result of the treatment (including the need of that child for
supportive parenting (replacing the wording under the 1990 Act “the need of that
child for a father”) and of any other child who may be affected by the birth’. It could
be that to succeed an applicant would have to show that there was “Wednesbury
unreasonableness” in dealing with the request for IVF treatment. However might
an applicant now use the Human Rights Act (Articles 12 and/or 8) to argue a right
to a family? Might conditions such as age and background be seen as an
infringement of these Articles?
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14.4.2 Techniques resorted to when childlessness is present include:
AID – Artificial Insemination by Donor. Note until recently the anonymity of the
donor was respected—see section 31(3) of the 1990 Act – but following the Human
Fertilisation and Embryology Authority (Disclosure of Donor Information)
Regulations 2004, information can now be provided to someone aged 18 and
over who was born as a result of assisted conception services, although the donor
will still not be legally and financially liable.(Note, anyone donating sperm before
April 2005 will remain anonymous unless they elect to waive their right to
anonymity). See also the case of Rose & Anor v Secretary of State for Health
[2002] EWHC Admin 1593 and the successful challenge under Article 8 by two AID
children to access to certain Donor information. This did not, however consist of
information which would have disclosed the identity of the donors. Such an Article
8 challenge is likely to fail (see Odievre v France [2003] 1FCR 621), but will be
rendered unnecessary in any event for post April 05 donors.
* AIH – Artificial Insemination by Husband;
* Surrogacy;
* IVF – In Vitro Fertilisation;
* GIFT – Gamete intra-fallopian transfer.
These techniques throw up a number of very important legal and ethical issues
(see Quintavalle v HFEA [2003] UKHL 13), not least as the law attempts to keepup with scientific developments. So much so that the Warnock Committee was set
up with the following terms of reference,
“to consider recent and potential developments in medicine and
science related to human fertilization and embryology; to consider
what policies and safeguards should be applied, including
consideration of the social, ethical and legal implications of these
developments; and to make recommendations.”
The Report (Report of the Committee of Inquiry into Human Fertilisation and
Embryology Cmd 9314) was published in 1984 and could be said to be responsible
for both the Surrogacy Arrangements Act 1985 and the Human Fertilisation and
Embryology Act 1990 (the 1990 Act). The following set of notes take into
consideration the Human and Fertilisation and Embryology Act 2008 (the 2008 Act)
which amends the 1990 Act.
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14.4.3 Stemming from the various forms of assisted conception, what are
the legal issues that need to be addressed?
(The following is not an exhaustive list)
* Definition of (legal) mother (see s 27(1) of 1990 Act; now s.33(1) 2008 Act);
* Definition of (legal) father (see s 28(2) of 1990 Act; now s.35 2008 Act);
* Legal position as regards unmarried couples ( s 28(3) of 1990 Act; now see
ss 35, 36 2008 Act)
* Legal position of same sex couples (see s.42 2008 Act);
* Legal status of child ( now see ss 40,41,46 of 2008 Act);
* Status of the “agreement” in surrogacy arrangements;
* Issue of payments.
14.4.3 What are the Ethical Issues?
(Again not an exhaustive list)
* The various techniques go against God’s will;
* They disturb the natural order of things;
* They treat children as commodities not as human beings;
* There is a potential for abuse of the techniques e.g. by people who can have
children but do not want their careers disturbed.
14.5 SURROGACY.
This is defined as “the practice whereby one woman carries a child for another with the
intention that the child should be handed over after birth”.
The ethical arguments for and against surrogacy may well depend on what form the
surrogacy takes. There is partial and full surrogacy.
Partial surrogacy: where SM (surrogate mother) provides the ova and carries the child
and CF (commissioning father) provides the sperm. Here there is a genetic link with SM.
Full surrogacy (womb leasing): where CF provides the sperm, CM (commissioning
mother) provides the ova and SM carries the child. Here there is no genetic link with SM.
Ethical Arguments for surrogacy* SM using her body as she wishes – autonomy.
* CM and CF using technology that exists.
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* CM and CF only chance to have a child that is genetically related
* Surrogacy is voluntary and consequently not exploitative
* Surrogacy is just another cure for infertility
Ethical Arguments against surrogacy* Commercial aspects reprehensible e.g. if SM is paid anything other than expenses
for her part in carrying the child;
* Can be used by people without infertility problems;
* Can be used by two people of the same sex;
* Children seen as “commodities”;
* Weakening of the family ties;
* A form of prostitution.
* Psychological harm to some of the parties e.g. SM who may well bond with the
child she is carrying and refuse to hand it over.
* Psychological harm to the child.
* SM may not “take care” of herself during pregnancy.
* The resulting child may not be perfect
* The risks of pregnancy are too great (see in this regard
http://news.bbc.co.uk/1/hi/england/gloucestershire/4224349.stm 31 Jan 2005 -
Natasha Caltabiano died shortly after giving birth to a surrogate baby. Although the
cause of death was an aneurism and was said not to be pregnancy related the
stress of the pregnancy could have perhaps caused the aneurism to occur earlier.)
The view of English law is that it is better to regulate surrogacy than leave it unregulated.
No statutory provisions were in force prior to the 1985 Surrogacy Arrangements Act; until
then the common law applied (along with certain other non-surrogacy-statutes). Under
this pre-1985 law it could be said that:
* the surrogacy contract was unenforceable as being contrary to public policy;
* even if not void under the above, some of the contractual terms would clearly be
unenforceable e.g. a requirement that SM should not smoke or drink or take drugs;
* Criminal offences may have been committed by parties to the agreement. (See the
Adoption Act 1976).
The Warnock Committee was charged with looking at surrogacy and other related areas.
However it was the public outrage over the “Baby Cotton” affair in January 1985 (see
[1985] 1 FLR 846) which ultimately led to the Surrogacy Arrangements Act 1985. That
Act effectively banned some of the more heinous forms of commercialisation associated
with surrogacy such as advertising; put another way it effectively sought to stop third
parties from profiting from other peoples’ “misery”. See the provisions on:
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* Advertising (s 3 and the case of A v C [1985] );
* Agencies (s 2).
It was not until the Human Fertilisation and Embryology Act 1990 (HFE act) that the
surrogacy contract was made legally unenforceable (s.36), that the legal status and rightsof the mother, father and child were determined and that the issue of confidentiality was
tackled. “Most of the new rules allocate parental status without the need to litigate the
issue”. (Montgomery p.410) The key provisions of the 1990 Act are set out below
alongside the new provisions introduced by the 2008 HFEA:
* S.27 (now s.33 2008 Act) (legal definition of mother) – the legislation gives the
status to the gestational mother. Contrast this with the American cases of
Johnson v Calvert [1993] 851 P 2nd
776 where the intent of the parties was
regarded as the dominant feature and as such the status of legal mother was given
to the commissioning woman. See also In the Matter of Baby M (1998) 537 A 2d
1227.
* S.28(2) (now s.35 2008 Act) (legal definition of father) – here, if the surrogate is
married then the surrogate’s husband becomes the legal father, because of the
presumption of legitimacy under common law. S38(2) 2008 Act preserves the
common law rule that says a child born during the subsistence of a marriage shall
be deemed to the child of the parties to the marriage. But this is only a
presumption – it can be rebutted by DNA evidence. Further, the surrogate’s
husband becomes the legal father unless he has objected, before the insemination,
to the insemination. In the case of Leeds Teaching Hospitals NHS Trust v A and
Others [2003] EWHC 259, the court had to consider the legal situation following the
accidental mix-up of sperm. The court ruled that a man does not consent where
another man’s sperm is mistakenly used in the provision of treatment services. See
also Re R (a child) [2003] EWCA Civ 182 and Re D [2005] UKHL 33.
* s.28(3) (now replaced by s.36 2008 Act) – where there is no consenting husband
or civil partner (see s.42 2008 Act) another man may be the father of a child
created from donor sperm where the implantation takes place in the UK and the
agreed fatherhood conditions in s.37 are met. Briefly these conditions include:
licensed treatment was provided to a woman;
a man consents to being treated as the father and the woman also consents
to this;
neither party subsequently withdraws their consent;
the woman has not subsequently consented to another person being the
other parent;
the consents (or withdrawals) are in writing.
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* Implantation after death - In relation to posthumous use of sperm the 2008
Act replaces the provisions of the Human and Fertilisation and Embryology
(Deceased Fathers) Act 2003.) Now the deceased man providing the sperm
may have his name registered on the birth certificate only, if he consented
(in writing) to the use of his sperm or embryo after his death, to being thechild’s father, and the mother elects for him to be so treated within 42 days
of the child’s birth (s.39). Where donor sperm is used, the mother may elect
another person to be treated as the legal parent where that person was her
husband or civil partner and consented in writing, ss40(1) and 46(1). If that
other person was not the mother’s husband or civil partner, the agreed
fatherhood and conditions must be met prior to that person’s death and the
embryo must be created in the course of license treatment services (ss40(2)
and 46(2).
* A mother’s female partner – now s 42 of the 2008 Act treats a woman in a
civil partnership in exactly the same way as s.35 applies to husbands. In
other words the mother’s civil partner will be treated as the other parent
unless she can show that she did not consent. S.43 also allows another
woman to be the legal parent where neither s.35 nor s,.2 apply and the
agreed female parenthood conditions apply which effectively are identical to
those applying in the case of a man.
* S.30 (parental orders).- (now s.54 2008 Act) – this is probably the one
section which could be regarded as encouraging rather than discouraging
surrogacy (see Briody v St Helens and Knowsley AHA [2001] EWCA Civ
1010). It is the section which allows the commissioning parents (the
childless couple) to apply for a Parental Order to make them the legal
mother and father with parental responsibility. But note the strict conditions
which must be satisfied, (for example the child must have been created
using a variant of IVF, GIFT or by AI using the gametes of at least one of the
commissioning couple, the commissioning couple must be married, civil
partners, or living as partners in an enduring family relationship, the child
must already be living with the commissioning couple and no payments
(excluding reasonable expenses) may have been made) before a Parental
Order can be granted by the courts. See Re Q (Parental Order) [1996] 1
FLR 369. In Re P ( A Child) [2007] EWCA Civ 1053, the judge, Mr Justice
Lloyd, found that P (the SM) had deliberately embarked on a path of
deception, driven by Mrs P’s compulsive desire to bear a child or further
children; she never had any other objective than to obtain insemination by
surrogacy with the single purpose of acquiring for herself and her family
another child. He therefore granted custody to the commissioning couple.
P’s arguments that the court had not given due weight to the attachment the
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child had formed with P and her capacity as a parent failed. N.B. Mr Justice
Lloyd observed however the limitation of the then 1990 Act and the fact that
under the Act the biological father is not the father and cannot apply for s.30
parental order because of the passage of time and the absence of consent.
* Note from October 2013 the child will be able to obtain details of his/her birth
on attaining 18 which will include the name of the surrogate mother, seethe
HFEA Code of Practice update.
* The welfare of the child - section 14(2)(b) of the 2008 Act amends the
need for a father to the child’s need for “supportive parenting”. This is
defined under s.14(2) as Supportive parenting is a commitment to the health,
well being and development of the child. It is presumed that all prospective
parents will be supportive parents, in the absence of any reasonable cause
for concern that any child who may be born, or any other child, may be at
risk of significant harm or neglect. Where centres have concern as to
whether this commitment exists, they may wish to take account of wider
family and social networks within which the child will be raised. See Re N
(Child) [2008] 1 FLR 198.
* Payments - section 59 of the 2008 Act allows bodies that operate on a
not-for-profit basis to receive payment for providing surrogacy services e.g.
negotiations, compiling information, advertising.
Surrogacy – Reform or Not
Most of the 1985 and 1990 Acts can be said to be anti-surrogacy. However according to
Lee and Morgan (Human Fertilisation and Embryology, p.201-2), “Since [1985],
surrogacy has undergone a metamorphosis, or more accurately, a series of
metamorphoses, from: (i) the sexual to the medical; (ii) the private and invisible to the
public and intermittently invisible; (iii) the altruistic to the commercial and back again; and
(iv) the contested and controversial to the accepted and clinically mediated, and back
again. The ‘medicalisation of surrogacy’ has occurred in parallel with the remarkable
turnaround in the legal approach to surrogacy in the [1990] Act and in the decisions in
cases …. Which have been almost universally pragmatic and usually sympathetic”.
In Oct 1997 the Government announced that a committee, chaired by Margaret Brazier,
was going to look into certain aspects of the law on surrogacy. The committee’s terms of
reference were:
* ‘to consider whether payments, including expenses, to surrogate mothers should
continue to be allowed…..’
* ‘to examine whether there is a case for the regulation of surrogacy arrangements
through a recognised body…..’
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* ‘…..to advise whether changes are needed to the Surrogacy Arrangements Act
1985 and/ or s 30…..’
The following is a summary of the Brazier Report:
Payments
1. Payments to surrogate mothers should cover only genuine expenses associated
with the pregnancy;
2. Additional payments should be prohibited in order to prevent surrogacy
arrangements being entered into for financial benefit;
3. The basis on which expenses will be met should be established before any attempt
is made to create a surrogacy pregnancy, with a requirement for documentary
evidence of expenses incurred in association with the surrogacy arrangement to be
produced by the surrogate mother;
4. Legislation should define expenses in broad terms of principle and empower
Ministers to issue directions on what constitutes reasonable expenses and the
methods by which expenses shall be proven;
Regulation
5. Agencies involved in surrogacy arrangements should be required to be registered
by the UK Health Departments and to operate in accordance with the Code of
Practice required under the terms of the proposed new Surrogacy Act;
6. The Department of Health, in consultation with the other UK Health Departments,
should draw up a Code of Practice after discussion with relevant bodies and
individuals. The Code should be binding on registered agencies. The Code
should also operate as an advisory Code to provide guidance in relation to all
surrogacy arrangements whether made through a registered agency or privately;
7. As an interim measure (prior to the necessary legislation) the UK Health
Departments should draw up and promulgate a voluntary code and invite relevant
bodies to seek voluntary registration. The Code should also be drawn to the
attention of professional bodies and of the Human Fertilisation and Embryology
Authority, so that they could consider incorporating advice on relevant aspects of it
into the guidance they issue to practitioners and clinics;
8. In addition to the Code, the Health Departments should also consider establishing
requirements for full record keeping and reporting of specified statistics; and clear
guidelines on how research will be facilitated into the outcomes of the
arrangements;
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Legislation
9. Consideration should be given to the repeal of both the Surrogacy Arrangements
Act 1985 and section 30 of the Human Fertilisation and Embryology Act 1990, andtheir replacement by a new Surrogacy Act. The Surrogacy Act would seek to
address in the one statute the main legal principles governing surrogacy
arrangements in the United Kingdom, to offer a surrogacy ‘code’ and include;
(i) the continuation of the current provisions of Section 1A of the 1985 Act
relating to the non-enforceability of surrogacy contracts;
(ii) the continuation of current provisions prohibiting commercial agencies from
assisting in the creation of surrogacy arrangements and related provisions
prohibiting advertisements in relation to surrogacy arrangements;
(iii) new statutory provisions defining and limiting lawful payments to surrogate
mothers;
(iv) provision for the promulgation by the UK Departments of Health of a Code
of Practice governing surrogacy arrangements generally;
(v) provision for the registration of non profit-making surrogacy agencies by
the Departments of Health and that such agencies should be required to
comply with the Departments’ Code of Practice on surrogacy
arrangements;
(vi) provision to prohibit the operation of unregistered agencies;
(vii) new provisions for the grant of a parental order to commissioning couples
(a revised section 30 order). The revised order should provide that
applicants for a parental order should establish compliance with the
Surrogacy Act and the Code of Practice; and that they have complied with
the statutory limitations on payments. The revised order should not
authorise the judge to approve otherwise impermissible payments.
10. Parental orders should only be obtained in the High Court; Judges should be able
to order DNA tests; and Guardians ad litem should be able to check criminal
records;
11. In order for a parental order to be granted, the commissioning couple should be
habitually resident in the United Kingdom, the Channel Islands or the Isle of Man
for a period of 12 months immediately preceding the application for a parental
order;
The Brazier Report has been criticised by COTS (Childlessness Overcome Through
Surrogacy) who vigorously oppose a prohibition on payments. This criticism in echoed in
the article by Michael Freeman listed below. To date no legislation has been forthcoming,
save for the minor amendments introduced by the 2008 Act highlighted above.
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Further Reading
Stauch & Wheat: Text, Cases and Materials on Medical Law &
Ethics (5
th
ed) (Routledge) Chapter 7
Medicine, Patients and the law, Brazier & Cave (4th ed) Penguin Chapter 13 pp 32-
349
Medical Law and Ethics, Pattinson (3rd ed) Sweet & Maxwell Chapter 8
paragraphs 8.6-8.8
Medical Law, Text, Cases and Materials, Jackson, (3rd
ed) OUP Chapter 16
Health Care Law, Montgomery J, Oxford University Press (2nd ed) chapter 16
pp402-404; 409-414
Sourcebook on Medical Law, Stauch, Wheat and Tingle, Cavendish Press Limited
(2nd ed) chapter 7 pp413-429
Human Fertilisation & Embryology Regulating the Reproductive Revolution, Lee &
Morgan Oxford University Press (2nd ed) chapter 8 pp 191-217
“Does Surrogacy Have A Future After Brazier” Michael Freeman, Medical Law
Review 7 Spring 1999 pages 1-20
Briody v St Helen’s & Knowsley Health Authority [2000] 3 Lloyd’s Rep Med 127 –
no-one has the right to be supplied with a child as per Article 12 ECHR. The costs
of a commercial surrogacy agreement were not recoverable.
14.6 EMBRYOLOGY
16.6.1 Protection of the embryo
One of the consequences of some of the afore-mentioned techniques is the
creation of an embryo. We need to examine closely what protection an embryo
has in English law. But first, note the distinction between a foetus and an embryo.
An embryo generally covers the period from fertilisation to the end of the 8th week
of pregnancy. The word 'foetus' covers the developing embryo from week 8 to
birth. Also note the distinction between in vitro and in vivo; the former means in a
test tube, the latter means occurring within the body.
As a general rule it can be stated that the foetus, while it is in vitro, has no
enforceable rights in civil law; while in vivo it has some protection but no rights.
The Congenital Disabilities (Civil Liability) Act 1976 does give rights in tort to a
child (but not – generally- against its mother) in certain circumstances but those
rights can only be enforced once the child is born and born alive. This, it could beargued, means that the foetus/embryo is being recognised to some extent in law by
giving it a contingent right. Put another way, the interests of the foetus are
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protected by the law. Health carers may be liable to the child but only after it is
born. Again it could be argued that since, under the HFE Act 1990, licences have
to be obtained before, for example, research can be carried out on an embryo and
only up to a certain “age”, namely 14 days, then some protection is being afforded
to the foetus. On the other hand, the abortion laws would seem to suggest thatthere is no real true protection for the foetus/embryo.
The following are two significant quotes from an article by Michael Jones in
Professional Negligence (Jan/Feb 1985 at p 20).
“The foetus while still in utero has no rights in civil law…This [the 1976
Act]. recognises that the foetus and even the embryo has ‘interests’
worthy of protection, but since the cause of action depends upon live
birth, it could be argued that the object of the legislation is to provide
compensation to damaged children, not to confer a right upon a foetus
to be born at all.”
“…the foetus is not accorded the full status of a person by the criminal
law, although it is given some degree of protection.”
NB The Human Rights Act 1998 and the ECHR do not extend to the
embryo/foetus.
14.6.2 Embryos
Is there such a thing as a property right in an embryo? The Warnock Report
suggested that the concept of ownership of an embryo was undesirable; the 1990
Act does not expressly deal with this point. For example: H and W agree in 1998
to store an embryo, reasoning that in the year 2004 they will be financially able to
start a family. In 2003 H and W divorce in acrimonious circumstances. In the year
2004 W wants to have the embryo implanted in her since she has recently been
told that for other reasons she will be unable to have a baby in the future. Should
the frozen embryo be part of the divorce settlement? In Evans v Amicus
Healthcare Ltd [2004] EWCA Civ 727 two women had undergone IVF treatment
with their consenting male partners, and embryos had been created. Subsequently
the parties separated and the males withdrew their consents. The women wanted
to use the embryos and among the arguments advanced on their behalf was that to
deny them would be a breach of their human rights. Could they use the embryos?
The courts said, no; consent of the males was vital and since that had been
withdrawn that was an end of the matter.
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Nathalie Evans’s claim also failed in the European Court (see Evans v UK,
application no 6339/05). The Court held that there had been no breach of Evans’s
Article 8 rights, and that, there being no right to life under Article 2 recognised in
respect of a foetus under English law, consequently no breach of Article 2 either.
Now under the new 2008 Act para 7 of Sched 3 inserts a new para 4A to Sched 3into the 1990 Act and introduces a cooling off period where one person withdraws
consent to the storage of the embryo or donated gametes. This amendment
however would still not have helped Natalie Evans however what the Evans case
did was to highlight the deficiencies with the consent provisions in the 1990 Act
which have now been amended by the 2008 Act.
Consent was also shown to be of the utmost significance in the case of R v HFEA
ex.p. Blood (1997) 2 WLR 806, where it was held that Mrs Blood could not use her
dead husband’s sperm because the husband had not consented in writing to its
use, even though before his coma and subsequent death the couple had been
receiving IVF treatment. (Using European law Mrs Blood was able to take the
sperm to Belgium where the insemination took place and she has had two healthy
children. Now see the new provisions on deceased fathers introduced by the
Human Fertilisation and Embryology Act 2008 and considered above.
14.6.3 “DESIGNER BABIES”/PRE-IMPLANTATIONGENETIC
DIAGNOSIS/TISSUE TYPING.
Think of the benefits which could result if embryos, having been created, could be
tested to make sure they had no infection/disease and only those that met that
criteria would be inserted back into the woman and allow to develop as a baby (a
perfect world?). The House of Lords had to make such a decision in Josephine
Quintavalle (on behalf of Comment on Reproductive Ethics) v HFEA [2005] UKHL
28. The case involved the Hashmi family of Leeds. Mr and Mrs Hashmi had a son
who was suffering from beta thalassaemia major (a debilitating blood disorder) and
to stay alive he needed blood transfusions every month and drugs fed to him by a
drip for 12 hours per day. The clinicians were of the view that if they could use from
a sibling the same tissue type as the ill son and transplant them into that son, then
in due course that son’s body would produce its own life saving blood. But the
question was, how do you get that type of perfect match? The answer was IVF
treatment for Mrs. Hashmi, embryos created, select an embryo with matching
tissue, insert back into the woman and when that baby is born take stem cells from
the baby’s umbilical cord and transplant into the ill son. Could HFEA legally permit
such a procedure? It said it could and the House of Lords agreed.
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Now see See para 1ZA (1)(d) of the 1990 Act inserted by the HFEA 2008 Act which
permits embryo testing on the following basis:
testing is permitted to:
– (a) Test for chromosome, gene or mitochondrial abnormality
–
(b) Where there is a risk that the embryo has chromosome, gene ormitochondrial abnormality to establish whether it has or any other
©To establish the sex of the embryo if there is a gender related physical or mental
disability; serious illness, serious medical condition
thus testing may now be licensed where the sibling suffers from a serious medical
condition that could be treated with matched tissue from the child to be born. This
includes stem cells, bone marrow or other tissue but excludes a whole organ. Note
however HFEA Sex Selection: Option for Regulation (HFEA 2003)
“ A license…cannot authorise any practice designed to secure that any resulting child
will be of one sex rather than the other” HFEA 1990 Sch 2, para 1ZB. Thus sex
selection for social and not medical reasons is not permitted.
14.7 “WRONGFUL” LIFE / BIRTH / CONCEPTION
A wrongful life claim is brought by a handicapped child who has been born as a result of
the defendant's negligence, e.g. a failed abortion attempt. The claimant’s claim is thathad the defendant not been negligent then he would not have been born, i.e. that non-
existence is preferable to the existence he now has. In McKay v Essex AHA [1982] QB
1166 the court held that damages could not be awarded against a doctor for failing to
advise a mother to have an abortion. The court gave a variety of reasons for disallowing
the claim but one of the more significant was that to award damages would mean that the
court would have to compare non-existence with existence and that would mean
assessing the value of the life of a handicapped child as less worthy than that of a normal
child.
NB: Although wrongful life claims may not be possible in England at common law, what
about a claim for pre-conception negligence? It could be that this is allowed by the
Congenitial and Disabilities Act; however, the problem which the claimant will face
here is one of causation.
Example:
Father (unmarried at the time) works for an organisation which brings him into contact
with radiological substances. Unknown to him it adversely affects his sperm. He meets
and marries W who then becomes pregnant. When the child is born it is severely
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mentally and physically disfigured. Child sues for wrongful life. Is such a claim in
principle possible?
See:
X and Y v Pal [1992] (Lawtel logon) ; De Martell v Merton and Sutton HA [1993];
Burton v Islington H.A [1993].
16.7.2 Wrongful birth is the equivalent of a wrongful life claim save that the action
is brought by the parents following the birth of a handicapped child, claiming for pain,
suffering, physical injury and financial loss. In McKay this part of the claim was
successful.
16.7.3 Wrongful conception
Damages for wrongful conception have in recent years been commonly awarded. The
claim is for damages for the upkeep of a healthy child that has been born as a result of a
failed vasectomy/sterilisation operation. The mother may also claim the compensation for
the pain and suffering associated with pregnancy and childbirth. Up until fairly recently
the courts were happy to award compensation notwithstanding the child is a healthy child,
see Allen v Bloomsbury H A [1993] 1 All ER 651. However the House of Lords took the
opposite view in the Scottish case of McFarlane v Tayside Health Board [1999] 4 All ER
961. The Health Board successfully appealed against the Court of Sessions decision to
award damages for the birth of a healthy child following a negligently performed
vasectomy. The House of Lords accepted that the loss (that is the cost of bringing up the
child) was foreseeable but saw the question as a wider issue – what was the extent of the
duty of care owed to the husband and wife and what was the liability of the defendant in
what was viewed as a claim for economic loss. Lord Slynn asked was it “fair, just and
reasonable for the law to impose a duty” and that the doctors duty was only to avoid a
pregnancy and that did not extend to the costs of rearing a child if born and accepted into
the family. Lord Steyn however saw the decision as being one of corrective justiceversus distributive justice and sometimes a decision had to be made between the two
approaches. In this instance the principle of distributive justice dictated that the law of
tort did not permit parents of a healthy unwanted child to claim the costs of bringing up
the child from the health authority or doctor. The claim did not satisfy the requirements of
being fair, just and reasonable. Note however that the parents were allowed to recover
the costs of the solatium and costs attendant on the pregnancy.
In the recent case of Denise Less and Michael Carter v Sarah Hussain [2012] EWHC
3513 the court once again considered what was the scope of the duty of care owed to the
claimants in matters of conception. The claimants’ alleged that the defendant had not
given proper advice about the risks of pregnancy, namely the presence of a known
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thromboembolic condition, and had such risks been explained Ms Less would not have
fallen pregnant. The claimant’s child was stillborn. The judge accepted the argument on
breach of duty however the claimants’ case failed on causation as the court found that
even if proper advice had been given the claimants would have proceeded with
conception. Commenting obiter on the scope of the duty owed the judge concluded thatto satisfy the duty of care the doctor must give the patient sufficient information to enable
the patient to make a balanced decision. Applying Walkin the judge ruled that the starting
point for the injury was conception and given that the advice was about conception, the
judge considered that the loss of the baby during term was a kind of loss in respect of
which a duty was owed, it made no difference that the precise manner of the loss was not
foreseen. Moreover it would have been fair, just and reasonable to compensate Ms Less
for her injuries applying the same principles that a mother of a disabled child can and as
such she would have been entitled to damages for pain, suffering and loss of amenity
and some special damages. She would not be entitled however to the Rees award (see
below) as there was no loss of autonomy.
See also Parkinson v St James & Seacroft University NHS Trust [2001] 6 Lloyd’s Rep
Med 309 a case noteworthy for the Court of Appeal’s ruling on what damages are
recoverable for the birth of an unplanned disabled child.
Finally in Rees v Darlington Memorial Hospital NHS Trust MLC 1053; [2003] UKHL 52 the
Court of Appeal awarded damages to a blind woman for the costs of bringing up a
healthy child following a failed sterilisation. The Court of Appeal ruled that Miss Rees was
entitled to cover the extra costs of bringing up her son attributable to her disability. Lady
Justice Hale commented that this case raised “novel and important” issues and told the
court that “we can only imagine the difficulties facing them both.” The decision was
appealed to the House of Lords. In summary their Lordships’ majority decision was in
essence:
A disabled mother who gave birth to a healthy child after a negligently performed
sterilisation operation was not entitled to recover the extra costs of child care
occasioned by her disability. Instead a conventional award of £15,000 would be
made to mark her injury and loss of the benefit she was entitled to expect.
Note that unusually there were 7 Law Lords sitting and it was a 4-3 majority. Their
Lordships declined to reconsider their views on the McFarlane decision. There is however
little consistency in their reasoning. All their lordships agreed that applying normal tort
principles the claimant in McFarlane should have been allowed to recover but the denial of
the claimant’s remedy was not in the court’s view a question of public policy but
interestingly legal policy and yet failed to expand on this interesting concept.
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Further Reading
Emeh v Kensington & Chelsea & Westminster A.H.A [1985] QB 1012
Thake v Maurice [1986] QB 644
Goodwill v BPAS [1996] WLR 1397
Walkin v South Manchester H.A. [1996] 7 Med LR 211
Lovelace Medical v Mendez (1991) 805 P 2d 603
CES Superclinics (Australia) Pty Ltd [1996] Med L Rev 102
Provenzano v Integrated Genetics (1998) 22 F Supp 2d 406.
Roberts v Bro Taff Health Authority [2002] 4 Lloyd’s Rep Med 182
Groom v Selby [2002] Lloyd’s Rep Med 1
AD v East Kent Community NHS Trust [2002] 9 Lloyd’s Rep Med 424
“Return of the burden of blessing” Dr J Ellis Cameron-Perry, (1999) NLJ December 17
pp1887-1888
“Wrongful birth. New light from the North” Charles Foster Solicitors Journal 21 January
2000
Mason, McCall Smith & Laurie (2006) Medical Law & Ethics Chapter 6
Booth Penny “A child is a blessing heavily in disguise, right?” New Law Journal Nov 23
2001 page 1738
“Failed Sterilisations And Child Costs Revisited” Roderick Denyer, Family Law Feb
2004 Vol 34 page 123.
Hoyano: “Misconceptions about Wrongful Conception” (2002) 65 MLR 883
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SUMMARY
At the end of this part of the chapter you should be able to:
appreciate the various techniques used to alleviate infertility;
appreciate the ethics of such techniques;
understand the various rules attending surrogacy e.g. is the agreement
lawful? Can the surrogate by forced to hand over the child?
know the ingredients for the claims of wrongful life, wrongful birth, wrongful
conception.
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SELF-TEST QUESTIONS – CHAPTER 14
1. When does life legally begin?
2. At the present time does a woman have a legal right to have access to all
techniques available to relieve childlessness?
3. List two arguments in favour of surrogacy and two arguments against surrogacy.
4. How many people may be involved in surrogacy (excluding the professionals)?
5. Before 1985 was a surrogacy arrangement legal?
6. Define “legal mother” in a surrogacy arrangement.
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NOTES
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NOTES
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CHAPTER 15
THE ENDING OF LIFE
Here we will be examining the legal and ethical issues associated with the various ways in
which human life may be ended.
15.1 ABORTION
“Abortion must be one of the most controversial areas of healthcare law”.
(Montgomery p. 379).
“We should stop seeing abortion as a problem and start seeing it as a
legitimate and sensible solution to the problem of unwanted pregnancy.” Ann
Furedi chief executive of the British Pregnancy Advisory Service.
In 2012, for women resident in England and Wales:
The total number of abortions was 185,122, 2.5% less than in 2011 (189,931).
16.5 per 1,000 women aged 15-44, 5.4% lower than in 2011; the lowest rate for 16
years.The abortion rate was highest at 31 per 1,000 for women aged 21, compared to 33 per
1,000 for women aged 20 in 2011
37% of all women having an abortion had one or more previous abortions
15 1.1 Ethical arguments for and against abortion.
For
Autonomy---the woman is using her body as she wishes;
Abortion will happen anyway, therefore it is better to regulate it than leave it
unregulated;
Prevents ‘back street’ abortions and the dangers posed to women (possibly
the major reason behind the Abortion Act 1967);
If abortion was not available then it could be argued that women were being
punished for becoming pregnant;
No form of contraception is 100% effective, therefore abortion can be seen
as a sort of back-up.
Against
Could be dangerous to the woman;
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Abortion is the taking of an innocent ‘life’ (this raises yet again those
fundamental questions of when does a life come into existence and what
rights does a foetus have?);
Emotional damage can be done to the woman (and possibly her family);
Contraception more socially acceptable than abortion as a form of birth
control.
15.1.2 Key developments in the law have been:
(1) 1861 Offences against the Person Act – an unlawful abortion may well be an
offence under section 58 of this Act.
(2) 1929 Infant Life (Preservation) Act which deals with the situation where the
baby’s life is taken while it was in the process of being born (child
destruction).
(3) R v Bourne [1939] 1 KB 687 – it is a defence to a charge of procuring a
miscarriage if it could be shown that the abortion was carried out to save the
life of the mother to prevent her becoming a physical and/or emotional
wreck; (see also R v Bergmann and Ferguson [1948] 1 BMJ 1008).
(4) 1967 Abortion Act – lays down the circumstances in which an abortion can
be lawfully carried out and the procedure which has to be followed;
(5) Royal College of Nursing v DHSS [1981] AC 800;
(6) 1990 Human Fertilisation and Embryology Act. (section 37)
15.1.3 And the law is?
The important thing to note from the combined effects of the 1967 and 1990 Acts is
the list of circumstances when an abortion can be legally performed. These are:
(1) Where the pregnancy has not exceeded 24 weeks and the continuation of it
would involve a risk, greater than if the pregnancy were terminated, of injury
to the physical/mental health of the woman or any existing children of her
family (N.B. this is the only ground which has a time limit. It is also referred
to as the “social” ground for abortion and as such is the most “popular”
ground); or
(2) Where termination is necessary to avoid grave permanent injury to the
physical/mental health of pregnant woman; or
(3) Where continuation of the pregnancy would involve risk to the pregnant
woman’s life, greater than if the pregnancy were terminated; or
(4) Where there is a substantial risk that the child would be born with severe
physical/mental abnormalities (recently this ground was in the news when it
was discovered that abortions were being carried out on foetuses with cleft
palates. Was this with ground (d)? No, it was argued in the case of R (on the
application of Jepson) v Chief Constable of West Mercia [2003] EWHC
3318.
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NB: In considering (1) and (2) above “the pregnant woman’s actual or reasonably
foreseeable environment” may be taken into account; this means the general
practitioner, whose help is sought, is entitled to take on board such things as
housing factors, financial factors ,emotional support from a husband/partneretc.
15.1.4 Procedural Points
The procedure involved in carrying out a lawful abortion is governed by the 1967
Act. It involves the following rules:
A Practitioner who has conscientious objections to taking part in an abortion does
not have to (S4(i)) and Janaway v Salford HA [1989] AC 537, Greater Glasgow
Health Board v Doogan [2013], see also Barr v Matthews (1999) 52 BMLR 217;
Two registered medical practitioners must decide in good faith that one of the
afore-mentioned grounds for a legal abortion exist (NB in an emergency only one
practitioner’s decision is required); See R v Smith [1974].
The pregnancy has to be terminated by a registered medical practitioner at
approved premises. (BPAS v Sec of State for Health [2011] EWHC 235
(Admin))
The interpretation which has been put by practitioners on both the above groundsand the procedure has led to the criticism that it is too easy to obtain an abortion in
England/Wales. However it is equally clear that some people regard the law as not
sufficiently liberal, for example, is the requirement for two medical practitioners
necessary and should it be reduced to one and more recently the political parties
have been talking about a reduction in the 24 week time limit. Do you have a view
on the matter?
The Abortion Law Reform Association has put forward the following five
amendments to the current law:
(1) allow abortions on request up to and including 14 weeks of pregnancy;
(2) make abortions available with only 1 doctor’s approval from 15 to 24 weeks
using current criteria;
(3) put a duty on doctors to declare their conscientious objection to abortion
and to refer immediately to another doctor who does not share that view;
(4) place a duty on the NHS to provide sufficient abortion services to cover local
needs.
See also http://news.bbc.co.uk/1/hi/health/6242382.stm Wednesday 27th June. The
British Medical Association conference backed a motion calling for abortions
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performed in the first three months of pregnancy to be approved by just one doctor,
rather than the current two. Moreover the HFEA Bill (the precursor to the new 2007
Act) proposed:
• Removal of the need for two doctors signatures (supported by BMA)
•
Removal of the need for premises to specially licensed• Nurse practitioners to be allowed to carry out early abortions
BUT the government were criticised as only 3.5 hrs allocated to discuss
amendments…which were never discussed (3rd
Reading).
15.2 HUMAN RIGHTS ACT 1998
Is abortion a breach of Convention rights? According to Paton v UK (1981) 3 EHRR 408)
the abortion of a 10 week old foetus to protect the health of the woman did not breach
Article 2. This was probably as a result of the Court deciding that a foetus was not
included in the word ‘everyone’ in the Article. Is it a breach of the father’s Convention
rights under, say, Article 8? If yes, then what about the woman’s convention rights? The
answer is that the law will uphold patient autonomy and in so doing will support the
mother, not the father. (See also C v S [1987]).
The ECHR case of Vo v France (2004) 2 FCR 577 decided that a foetus was notprotected by Article 2 of the Human Rights Act, and that it was a matter for individual
states to decide what protection to afford the foetus. Capacity to become a person meant
it should be protected as a matter of human dignity but no right to life. Contrast this with
the approach taken by the USA (see below).
15.3 OTHER JURISDICTIONS
Northern Ireland - no statutory defence – must rely on Bourne s.58/59
Ireland - Irish Constitution – unborn and pregnant woman have an equal right to life – Art
40.3.3 (A,B,C v Ireland [2010] (App No 25579/05) but now Protection of Life During
Pregnancy Act 2013. This legislation is the direct result of the death of Savita
Halappanavar died in Galway University hospital last autumn, after being denied an
emergency abortion. The Guardian reports that 23rd
August 2013 saw the first abortion to
be performed under this legislation.
USA – see Roe v Wade (a woman’s constitutional right to request an abortion.
Often views are swayed by presidency elections. In April 2004 the Unborn Victims of
Violence Act (U.S.A.) became law. It is now a crime to harm a foetus during an attack on
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a pregnant woman. In November 2003 the USA also passed a law banning late-term
abortions i.e. abortions during the fifth or sixth month of pregnancy. This law was
declared unconstitutional by a federal judge in San Francisco in May 2004 on the ground
that it was too vague and restricted the right to choose an abortion. It would therefore
appear that in the USA there is a move to accord rights to a foetus. Contrast thatapproach with Vo above.
Conclusion
1. Why have abortion – scans only take place 18-20 weeks
2. Woman’s circumstances may have changed since becoming pregnant
3. She may not realise that she is pregnant
4. Why is the abortion pill still a criminal offence?
5. Why is there no right to an abortion?
6. The medical profession will seldom interfere with a woman’s rights
7. Why is this still a case of defence to a criminal offence?
READING:
Brazier Chapter 13
Stauch & Wheat Chapter 8
Jackson Chapter 8
Herring: Chapter 6
Hewson “Abortion Law in the Dock” SJ 12.12.03
Foster “When two freedoms collide” NLJ 28.10.05
Hewson “Foetal Rights” and obstetric malpractice” NLJ 30.9.04
Thomson JJ (1971) “A Defence of Abortion” 1 Philosophy and Public Affairs 47-66
Swift & Robson “Why doctors need not fear prosecution for gender - related abortions
JCL August 2012
15.4 NEONATICIDE
15.4.1 Introduction
This is the practice of letting new-born babies, suffering from a range of serious
ailments (physical and/or mental), die by not treating their ailments. It's usually
done with the consent of the parents and, supposedly, in the best interests of the
child (see the case of R v Arthur (1981) and contrast it with Re B (Wardship:
Medical Treatment) (1981)----is the distinction between the two cases solely that in
one case criminal proceedings were involved whereas in Re B wardship
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proceedings were involved?). Yet again the argument put forward against such a
practice is that medical technology has improved to the stage where it is possible
to treat such babies and to keep them alive. The retort to that is: what sort of life
will the baby have? Furthermore who has the right to make such a decision? The
parents? The doctors? The courts?
Note the guidance published by the Royal College of Paediatrics and Child Health,
‘Witholding or Withdrawing Life Sustaining Treatment in Children, A Framework for
Practice’, (2nd edition May 2004, Royal College of Paediatrics & Child Health -
www.rcpch.ac.uk). In the foreword to this guidance it states:-
‘Sometimes it is necessary to come to the conclusion that for an
individual child…the more humane path is one of palliation rather than
a continuation of life saving treatment. To so resolve is profoundly
difficult, challenging the doctor and all members of the Health Care
Team with issues of conscience and internal conflicts. Nevertheless
our professional responsibilities do not allow us to walk away from
such diffic ulties’.
15.4.2 What are the arguments for such an approach- that is allowing the child
to die by not providing medical treatment?
Economic – less expensive to let the child die than have the medicalfacilities utilised for what could turn out to be a failed exercise.
The wishes of the parents – it’s what they want. Is this important?
The quality of life of the child may be such that it would be immoral to keep it
alive, in other words, it is in the child’s best interests.
Avoids the family’s mental anguish.
The approach in English law is not dissimilar to the approach taken in USA
and Canada; also it is what doctors would generally do in the circumstances;
Conforms to the decision in the leading case of R v Arthur (1981);
The outcome would have been the same if the Abortion Act 1967 was
involved;
It’s not a case of action being taken – everything that is done is passive and
therefore it’s a case of nature taking its course – the distinction between acts
and omissions (see Airedale NHS Trust v Bland [1993]).
Against the above arguments are the following points:
They (the children) are “innocent” – their only ‘crime’ is to be born with
disabilities; It’s morally wrong to let children die and not try to save them;
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3. The ‘No Chance’ Situation. The child has such severe
disease that life sustaining treatment simply delays death
without significant alleviation of suffering. Treatment to sustain
life is inappropriate.
4. The ‘No Purpose’ Situation. Although the patient may be ableto survive with treatment, the degree of physical or mental
impairment will be so great that it is unreasonable to expect
them to bear it.
5. The ‘Unbearable’ Situation. The child and/or family feel that
in the face of progressive and irreversible illness further
treatment is more than can be borne. They wish to have a
particular treatment withdrawn or to refuse further treatment
irrespective of the medical opinion that it may be of some
benefit.
In situations that do not fit with these 5 categories, or where there is
uncertainty about the degree of future impairment or disagreement,
the child’s life should always be safeguarded in the best way possible
by all in the Health Care Team, until these issues are resolved.
Decisions must never be rushed and must always be made by the
team with all evidence available. In emergencies it is often doctors in
training who are called to resuscitate. Rigid rules, even for conditions
which seem hopeless, should be avoided; life sustaining treatment
should be administered and continued until a senior and more
experienced doctor arrives.
The decision to withhold or withdraw life-sustaining treatment should
always be associated wi th consideration of the child’s palliative or
terminal care needs. These include symptom alleviation and care,
which maintains human dignity and comfort.”
15.4.4
Note the potential effect of the decision of the European court in the case of David
Glass (Glass v UK [2004] 1 FLR 1019), that, other than in a true
emergency, the court should be involved where it is contemplated
treating a child contrary to a refusal of treatment by a ‘legal proxy’. See
also comments made by the Court of Appeal in GMC v Burke, in relation
to the European Court’s decision.
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On what basis then can- should- the courts conclude that medical intervention-
which is necessary to save a child’s life is not in the child’s ‘best interests’?
In the case of Re J [1991] Fam 33 AC, the court considered the ‘test’ to be applied.
In this case, J was a Ward of court. He was a premature baby, with severe braindamage and a considerably shortened life expectancy, likely to become a serious
spastic quadriplegic, without sight, hearing, and speech. It was possible he would
require further resuscitation/ ventilation in the future. The doctors treating him did
not want to provide this. An application was made to the court to determine
whether such treatment would be in J’s best interests.
The judge held that:
‘Three primary principles are not in dispute. First it is settled law that
the court’s prime and paramount consideration must be the best
interests of the child……Secondly, the court’s high respect for the
sanctity of human life imposes a strong presumption in favour of
taking all steps capable of preserving it, save in exceptional
circumstances…Thirdly… it c annot be too strongly emphasised that
the court never sanctions steps to terminate life. That would be
unlawful.’
‘The test must be whether to that child in question… life would be
intolerable’.
In the circumstances, the judge concluded that it would be lawful not to treat.
More recently the courts have been asked to reconsider the ‘test’ in the case
of Charlotte Wyatt. Charlotte Wyatt was born prematurely at 26 weeks and
had never been well enough to leave hospital. She suffered from profound
brain damage, leaving her blind, deaf and incapable of movement, with
chronic respiratory and kidney problems. There was a disagreement
between her doctors and parents as to whether, should the need arise, she
should be ventilated, to be kept alive.
Her parents believed that she should, her father’s approach being a ‘broad’
‘life at all costs’ approach, and that he was hoping for ‘a miracle’ including a
‘miracle born of divine intervention’. The doctors believed to do so [ventilate]
would only result in ‘increased suffering for no commensurate benefit’.
The issues to be addressed by the court included the question of which was
the correct best interests test applied? Hedley J held - ‘It is in my view
essential that the concept of ‘intolerable to that child’ should not be seen as
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a gloss on, much less a supplementary test to, best interests. It is a valuable
guide in the search for best interests in this kind of case’. This was approved
by the CoA, who rejected an argument that intolerability should be the
‘touchstone’, as indicated by Munby in Burke (but not approved on appeal).
Hedley J added “The term best interests encompasses medical, emotional,and all other welfare issues (Re A). The court must conduct a balancing
exercise in which all the relevant factors are weighed (Re J) and a helpful
way of undertaking this exercise is to draw up a balance sheet (Re A)’
See the CoA’s conclusions on best interests at paras 85-91 of the judgment.
The question came up for consideration again in the case of Re MB
[2006] EWHC 507. Again, the parents wanted treatment to continue, the
doctors did not. The Court held that ventilation should not be withdrawn,
although the doctors need not resort to carrying out certain other procedures
should they become necessary. The court avoided any reference to
‘intolerability’, as expressing a ‘conclusion rather than a test’.
More recently see the cases of:
Re B [2008] EWHC 1996 (Fam)
Re OT (A Baby) Unreported March 20 2009
NHS Trust v Baby X & Othrs [2012] EWHC 2188 (Fam)
KH [2012] EWHC B18 (Fam)
NHS Trust v SR [2012] EWHC 3842 (Fam)
And refer to Re A (Conjoined Twins) [2001] Fam 147 considered in the
chapter on Consent.
READING:
• Jackson, 3rd
ed Chapter 17
• Stauch & Wheat Chapter 12
• Brazier extracts
• Mason McCall Smith, chapters 15 & 18
• End of Life Treatment & Care GMC 2010
• ‘Witholding or Withdrawing Life Sustaining Treatment in Children, A Framework for
Practice’, 2nd
edition May 2004, Royal College of Paediatrics & Child Health
(www.rcpch.ac.uk)
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SUMMARY
At the end of this part of the chapter you should be able to:
* discuss the law and the ethics of the abortion rules;
* discuss what offences/protection exists for someone charged with carrying
out an illegal abortion;
* consider whether the rule in R v Arthur is sound;
* appreciate the legal rules applicable to the law on neonaticide.
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15.5 EUTHANASIA
17.5.1 INTRODUCTION
The word literally means ‘dying well’. Today the following can be used as a working
definition:
“the practice of painlessly putting to death persons suffering from
incurable and distressing diseases”
Euthanasia can be either involuntary or voluntary. We will be concentrating on voluntary
euthanasia (where the incurably ill patient begs to die), though it should be noted that
neonaticide represents a form of involuntary euthanasia.
Euthanasia can also be either active or passive. Active euthanasia is where, in response
to the patient’s wish to die, the health carer gives the patient a lethal injection or does some
other positive act. Passive euthanasia is where, in response to the patient’s wish to die,
the health carer, for example, stops treating the patient and the patient dies – in which case
it is said that nature has taken its course and the patient has died from his/her illness.
The basic rule of English Law is that almost all forms of active voluntary euthanasia are
illegal whereas passive voluntary euthanasia may be both legal and ethically acceptable.
15.5.2 Active Voluntary Euthanasia
Offences which may be committed here are murder or attempted murder (see R
v Cox (1992), manslaughter, aiding and abetting a suicide under section 2 of
the Suicide Act 1961 (see on the latter point, R v McShane (1977), Attorney
General v Able (1984)). Note that whilst a person committing suicide is not
committing a criminal offence assisted (physician assisted ) suicide is clearly
unlawful.
In Nicklinson v MoJ & Ors [2012] EWHC 304 it was argued that:
That the common law doctrine of necessity provides a defence
to assisted suicide
That the current law breaches Article 8 by criminalising assisted
suicide
That the current law breaches Article 2 by failing to adequately
regulate active euthanasia.
However these arguments ultimately failed, and the Court of Appeal refused to
create a defence of necessity to a charge of murder or assisting suicide findingthat:
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DPP policy insufficiently clear re factors to be taken into account in
deciding whether to prosecute healthcare professionals.
Ban on euthanasia and section 2 not incompatible with article 8
Matter is for parliament
See Martin, Nicklinson & Lamb [2013] EWCA CIV 961.
Finally in R (on the application of Nicklinson and another) v MOJ [2014] UKSC 38 the
Supreme Court upheld the Court of Appeal judgement and restated that any change in
the law is an issue for Parliament, not one for the courts.
NOTE TO STUDENTS: We will be considering the implications of the Nicklinson
judgment in more depth later in the programme along with the Assisted Dying Bill,
sponsored by Lord Falconer. The Bill aims to enable competent adults who are
terminally ill to be provided at their request with specified assistance to end their
own life.
15.5.3 Assisted Suicide
Pre February 2010 the law on assisted suicide was found in Suicide Act
1961, s.2 which stated that it was an Offence to aid, abet, counsel or procure
suicide. The offence itself required intent to aid, abet, counsel or procure
actual/ attempted suicide and the person to be assisted/ encouraged to
actually attempt or commit suicide. This section has now been amended by
s.59 Coroners & Justice Act 2009 which created the offence of encouraging
or assisting suicide. D commits an offence if-
• D does an act capable of encouraging or assisting the suicide or attempted
suicide of another person and
• D’s act was intended to encourage/ assist suicide or an attempt at suicide
• The person need not be a specific person or class of persons known to or
identified by D
• Offence whether or not suicide/ an attempt occurs
The DPP’s consent is still required to prosecute, see CPS – Policy for
Prosecutors in respect of Cases of Encouraging /Assisting Suicide, Feb 10.
Note however a capable refusal of medical treatment is not suicide, see B V
NHS Trust [2002] 1 FLR 1090.
15.5.4 Human Rights
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Is there a human right to die? In R (on the application of Diane Pretty) v DPP (2002), the
applicant, who was suffering from motor neurone disease, wanted to enlist the assistance
of her husband to die, but she wanted an undertaking from the DPP that her husband
would not be prosecuted (see above). The DPP refused to give such an undertaking and
both the House of Lords and the ECHR agreed with this ruling that there was no right to dieunder Art 2.
A slight variation on this point was evidenced by the case of Re Z (2004) where the patient
and her husband went abroad to a country where the law allowed the patient to receive
medical assistance to die; but was the husband committing an offence under section 2 by
helping her to get to the foreign country? Could he be prosecuted when and if he brought
his wife’s body back to this country for burial? It seems as if this matter never got to the
stage where the DPP had to make the decision.
Finally read the case of Debbie Purdy [2009] UKHL 45. Ms Purdy, a 46 year old
MS sufferer wanted to know whether husband would be prosecuted if he helped
her end her life in Switzerland. She challenged that the Code for CPS didn’t
provide sufficient guidance as to whether would be in public interest to prosecute
and so breached Art 8. Her argument was upheld by the House of Lords and this
led to the CPS interim policy being issued.
Although relatives and health carers are legally liable for acts of voluntary active
euthanasia, there maybe a marked difference in the punishment depending on whether the
accused is a health carer or a relative. In the case of a health carer a prosecution is seldom
successful and that could be for one major reason---- it could be that if the lethal injection
was administered in the last days of the patient’s life, then there may be a problem in
identifying what exactly caused the death: the illness or the injection?
Furthermore if the health carer was to give the patient medication which could both
temporarily ‘heal’ but ultimately kill, it is unlikely that mens rea could be shown by the
prosecution (this is the double effect syndrome and may be the only aspect of active
euthanasia which may be legal). In the Newcastle upon Tyne case of R v Moor (1999) the
practitioner gave his terminally ill patient a lethal dose of diamorphine, but he was acquitted
of murder on the ground that primary objective in giving the diamorphine was to ease the
patient’s pain not kill the patient.
15.5.5 LEGALISING EUTHANASIA?
Currently there is an active debate taking place in this country as to whether the English
law on euthanasia needs amending and if so what form should the amendment take. One
possibility could be to use statutes to make all forms of euthanasia illegal. This seemingly
was the objective behind two private members’ bills, the Medical Treatment (Prevention of
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Euthanasia) Bill 1999 and the Patients Protection Bill 2003, both of which failed for lack of
Government support. Also the Royal College of Nursing at its 2005 conference said it
would not change its policy of being against legalising assisted dying. A bill which would
have reversed the effect of a case like Diane Pretty’s was Lord Joffe’s bill, the Assisted
Dying for the Terminally Ill Bill 2004, which initially failed because of lack of parliamentarytime. Subsequently, after reintroduction, the Bill was rejected by the House of Lords. In
2012, the Commission on Assisted Dying, which had been chaired by Lord Falconer
published a report that concluded that the current law on assisted suicide was incoherent
and inconsistent. However because the Commission had received funding from people
who were known to be in favour of legislation, many commentators questioned the
independence of the report.
But there are other ways we could bring our law into line with a country like the
Netherlands (2002 Legislation permits VLT (voluntary lethal treatment) and PAS
(physician assisted suicide)) if the will is there; for example, we could resurrect
the Law Commission’s proposal of 1976 for the creation of a new offence of
mercy killing or we could redefine the word intent to make it clear that mercy
killing was not intent within the definition of common law murder.
So what are the arguments for making euthanasia more easily available?
* self autonomy of the patient;
* compassionate grounds;
* economic reality (ageing population, too expensive to keep people in
hospitals);
* it’s already happening, in other words it is accepted medical practice;
* avoids artificial distinction between active and passive (acts and omissions);
* would help the medical profession;
* avoid strain on relatives;
* accords with definition of euthanasia as dying with dignity.
But there are equally powerful arguments to suggest we should not make euthanasia more
easily accessible:
reduces importance of sanctity of life;
‘God giveth life, God taketh life’;
contrary to Hippocratic oath;
who will administer the lethal injections? Where will they be administered?;
what if the diagnosis is wrong?;
‘thin end of the wedge’/’slippery slope’ argument.
contrary to public policy;
hospice movement.
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For a discussion of the issues pertaining to assisted suicide refer again to R (on the
application of Purdy) V DPP (2009) EWCA Civ 92.
15.5.6 Passive Voluntary Euthanasia
N.B. Students should refer also to the chapter on Consent.
According to English case law to touch a patient against his wishes is trespass. Therefore
the competent patient who says he no longer wants to be treated should have that wish
respected. At the turn of the 20th
century that wish would have been ignored –the right to
treat would have superseded the right to autonomy. (Leigh v Goldstone 1909). Now,
however, the right of autonomy dominates (NB there are certain circumstances where the
patient’s request may be ignored e.g. if he is under age (18) or is incompetent.).
Given that the health carer can (must?) now accede to the patient’s request what can he
do? What can’t he do? He cannot give a lethal injection, but he can stop treating the
patient and he can, (must?) if requested, turn off life support equipment. This latter point
represents somewhat vividly the difference between an omission and an act. Turning off
such machines is the equivalent legally of refusing to treat even though it is being achieved
by a positive act on the part of the health carer- in other words it is treated legally as an
omission rather than a positive act – see the case of Bland and the distinction (and reason
for it) made by the court in this case. If a failure to treat is an omission rather than a
positive act, then the question of any liability (criminal or otherwise) arising for the doctor
who does not treat, will depend on whether there is a duty to treat. If there is no duty thenthe ‘failure’ can not be one for which the doctor is liable. The question of whether there is a
duty to treat will, in the case of an incapable patient, frequently depend on whether such
treatment is in the patient’s best interests and for that reference must be made to the
Mental Capacity Act 2005, s.4. For consideration of the question of best interest for the
patient in a persistent vegetative state (PVS) see Bland and commentary below.
Where the patient is capable and refuses treatment, then, in accordance with the principle
of autonomy, the doctor must (other than in certain circumstances such as under the
Mental Health Act 1983), cease the treatment. Responding to such a request is not aiding
and abetting a suicide (see Lord Goff in the Bland case at p 866 and also Home Secretary
v Robb [1995]).
Clearly, if the patient is legally and clinically dead there will be no liability if the life support
system is withdrawn (Re A [1992]).
15.5.7. What if the patient is unconscious?
The general rule is that, if withdrawing the life support is in the patient’s best interests, (and
again reference must now be made to s.4 MCA 2005) then the life support system and
nutrition /hydration can be withdrawn.
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15.5.8. What if the patient is PVS?
Persistent Vegetative State (PVS) has acquired a specific meaning. The BMA says it
refers to:
“patients who have lost the function of the cognitive part of their brain.
The clinical components of the condition [are] that such patients
resemble those in a coma as they do not react to stimuli and are
unaware, they are intermittently wakeful or in a state of chronic
wakefulness without awareness, their bodies show no behavioural or
cerebral metabolic evidence of their possessing capacity to respond to
external events or stimuli.”
The rule is that if it is in the PVS patient’s best interests, then an application must
be made to the courts for the life support etc. to be turned off. (see the cases Bland
and Frenchay NHS Trust v S (1994)).
Guidelines have been drawn up in relation to PVS patients. See the PVS
Guidelines drawn up by the Royal College Physicians. Note: has there been a relaxation of the PVS diagnostic requirement? See the following cases:
Re D 1997 (38 BMLR 1) - didn’t fit guidelines but declaration made
Re H 1997 (38 BMLR 11) - as above Re G (2001) 65 BMLR 6
Though see also W Healthcare Trust v H & anor [2004] EWCA Civ 1324
A hospital may be operating a DNR (Do Not Resuscitate) policy in respect of
certain patients. These patients may not be PVS but their lives may be
demonstrably awful and full of suffering. All NHS Trusts must have, since April
2001, agreed and published policies on when resuscitation should be
attempted. See further ‘Treatment & care towards the end of life’ GMC 2010.
For case law post the implantation of the MCA see Re C [2010] EWHC 3448 CoP
(Consideration of withdrawal of ANH from PVS patient); NHS trust v AW [2013]
EWHC 78 and Re W [2011] EWHC 2443.
15.5.8. Advance Decisions
N.B. This is also considered in the chapter on consent to treatment.
It may be that, although the patient is now unconscious, evidence exists as to whathis wishes are/were in respect of any continued medical treatment. He may, at
some earlier point in time when he had the capacity to do so, have expressed his
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wish that he did not want medical treatment to be continued should he lose the
capacity to make the decision at the appropriate time; and he might have done this
in the form of an advance decision (also known as a living will in USA).
Such directives were approved at common law (obiter) by the House of Lords inthe Bland case. However, they have now been accorded legislative authority as a
result of sections 24-26 of the Mental Capacity Act 2005.
At the outset it should be noted that the MCA refers to ‘advance refusals of
treatment’. There is no right to demand treatment of any type, though any such
requests for treatment must of course be considered in assessment of best
interests. See the Court of Appeal decision in GMC v Burke.
A further distinction to be noted is that made between ‘treatment’, which can be
refused, and ‘basic care’ which can not (see Code of Practice to MCA).
For an advance refusal of treatment to be binding under the MCA, it must be both
valid and applicable.
To be valid the following conditions must be observed:
it must be made by a person who is aged 18 and over;
the advance decision must not have been withdrawn;
that person must be mentally competent at the time of making it:
the person must be no longer capable of making the decision.
And- only where the refusal amounts to a refusal of life-sustaining treatment-
it must be in writing, signed by the patient or by someone else in the
patient’s presence and under his direction;
that signature must be witnessed;
the witness must sign/acknowledge in the patient’s presence;
To be applicable:
the refusal must relate to the particular treatment in question
If the person has, subsequent to the advance decision, created a lasting
power of attorney, giving that attorney the right to make the particular
decision, or if he has done something which can be construed as
inconsistent with the advance decision, for example a person who is a
Jehovah’s Witness who then marries a Moslem and takes that religion, thenthe advance decision may not be applicable.
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According to section 26(5) nothing in an advance decision can stop a person
providing life-sustaining treatment for the patient or doing something which the
provider reasonably believes to be necessary to prevent a serious deterioration in
the patient’s condition, whilst seeking court clarification of the validity/ applicability
of the advance decision.
During the passage of the Act there was some opposition to making advance
decisions legal; many saw it as euthanasia by the back door. It seems that this
argument was based on the view that the health carer would be able to give the
person who made the advance decision something like a lethal injection. That is
not intended. What is intended is for the health carer to “back off”, when the
advance decision “kicks in”.
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READING:
Stauch & Wheat: Chapter 12
Jackson:
Herring
MCA 2005
Code of Practice to MCA
Chapter 17
Chapter 9
Ss 4,24-26
SUMMARY
At the end of this part of the chapter you should be able to:
* discuss the pro’s and con’s of active voluntary euthanasia;
* understand the law on passive voluntary euthanasia;
* understand what is meant by persistent vegetative state;
* understand the MCA provisions on advance decisions
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SELF-TEST QUESTIONS – CHAPTER 15
1. Give two arguments for and two arguments against having an abortion.
2. There are four grounds on which a legal abortion can be obtained----one
important fact distinguishes ground one from the remaining three grounds. What
is that?
3. In what circumstance can one medical practitioner certify that the grounds existfor an abortion?
4. Can a medical practitioner refuse to participate in an abortion?
5. What is meant by neonaticide?
6. Which form of euthanasia is both legal and ethical? Which form is not legal orethical?
7. What is the relationship between section 2(1) of the Suicide Act 1961 andeuthanasia?
8. In the law on euthanasia what is meant by “double effect”?
9. If a patient is unconscious can his/her life support system be withdrawn?
10. What is an Advance Decision?
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CHAPTER 16
HUMAN RIGHTS
16.1 Introduction / The Background
The Human Rights Act 1998 came into effect on 2 October 2000. It is evident that it has
had a significant effect on health care law. The rights set out in the European Convention
of Human Rights are now incorporated into our domestic law. Now every citizen enjoys
those rights laid down in the Convention and any interference with those rights must be
justified. It is also important to realise that the Convention is a “living instrument” to be
interpreted in the light of present day conditions and so as to reflect changing social
attitudes (see Tyrer v United Kingdom [1978] 2 EHRR 1 at 10). This means that thecourts do not feel themselves bound by previous decisions if conditions have changed in
the meantime.
The Convention is incorporated into English law in three ways. Firstly Section 3 of the
Human Rights Act 1998 states that all primary and secondary legislation must be
interpreted as far as possible in a manner which is compatible with the Convention.
Second section 6 makes it unlawful for a public authority to act in such a way that is
incompatible with the Convention unless it is unable to do so by primary legislation or
inevitably incompatible secondary legislation. The Department of Health, Health
Authorities and NHS Trusts should be classified as public authorities and hence are
under a duty to act compatibly with the convention. Note that doctors will come within the
definition of a public authority only when they are treating NHS patients but not private
patients. And finally section 7 gives a right to sue for such unlawful acts provided the
claimant is the victim of the unlawful act.
Initially, the following points should be borne in mind:
(1) Convention rights are not always ‘absolute’ e.g. Articles 2 and 3 are but Article 8 is
not, being a ‘qualifiable’ right.
(2) The whole of the wording of the various Articles of the Convention must be
analysed – commentators and students frequently state the rights in their
abbreviated form.
(3) The doctrine of proportionality is key i.e. there must be a balancing of various
interests.
(4) Different States do things differently; therefore a ‘margin of appreciation’ will be
allowed and judicial precedent may not be as important.
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(5) NHS Trusts, Health Authorities, Local Authorities and other similar bodies, the
Department of Health and doctors treating NHS patients (but not private patients?)
are within the definition of Public Authority/ Public bodies.
(6) The obligation imposed by the HRA on public bodies, to ensure that what they do
is ‘Human Rights’ compliant, includes ‘positive’ as well as ‘negative’ obligations, ieobligations to take positive steps to uphold the right to respect for family life (etc),
in Article 8, as well as to refrain from unlawfully interfering with it.
16.2 DOES THE CONVENTION APPLY TO HEALTH CARE?
Although a right to healthcare is not expressly mentioned in the Convention, implicitly it
could be argued that the Convention must have been intended to apply to health care
issues. Take Article 2 as an example. Can a right to life simply mean that life should not
be taken except in well defined circumstances? Is it not more likely that the Article is also
referring to the quality of a person’s life?
This is supported to some extent by what the Home Secretary said in 1998:
“…freedoms alone are not enough; they need to be complemented by
positive rights that individuals can assert when they believe that they have
been treated unfairly by the State, or that the State and its institutions have
failed properly to protect them”.
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16.2.1 Article 2 – Right to Life
It could be argued that this Article gives some or all of the following new positive
rights to patients:
to receive medical treatment for life-threatening conditions. If this is
sustainable, then what about non life-threatening conditions?
to receive specific life saving treatment.
to receive different but better treatment e.g. better and more expensive
drugs.
to receive better medical facilities e.g. to be found a bed on a ward rather
than being left in a hospital corridor. (See also Article 3). Or perhaps it
could mean that a more senior person should have provided the treatment if
that would have avoided very serious consequences.
to be prevented from committing suicide as a result of mental health
problems
See:
Re A [2000] 4 All ER 961 – The Siamese Twins Case.
A National Health Service Trust v D [2000] 2 FLR 677 where the court, in the
best interests of the patient, upheld the approach of the Trust that in the
event of future respiratory and/or cardiac failure being suffered by a 19
month old baby the Trust should only administer full palliative care but no
resuscitation; there was, therefore, no breach of Articles 2 and 3;
R v Portsmouth Hospitals NHS Trust ex p Glass [1999]
Glass v UK 9.3.04;
R v N&E Devon HA ex p Coughlan [2000] ;
An NHS Trust A v M [2001]; An NHS Trust B v H [2001] 1 ALL ER 801
In the last two cases the courts held that discontinuing artificial nutrition and
hydration from PVS (permanent vegetative state) patients was in their best
interests and therefore there was no breach of Articles 2, 3 or 8.
16.3 LACK OF RESOURCES AS A DEFENCE
Could the NHS argue lack of resources as a defence to these new claims? Wendy
Outhwaite asserts that in the future the words of Laws J. will become very significant:
“… where the question is whether the life of a 10 year old child might be
saved by however slim a chance, the… authority… must do more than toll
the bell of tight resources.” (R v Cambridge HA ex p B [1995]).
But contrast that with the words of the court in Osman v UK (1998) 5 BHRC 293:
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“… such an obligation must be int erpreted in a way which does not impose
an impossible or disproportionate burden on the authorities… not every
claimed risk to life can entail for the authorities a Convention requirement to
take operational measures to prevent that risk from materialising .”
The European court has held that there is no convention right which guarantees
free medical care, see Penticova v Moldova, 4.1.05.
More recently the domestic courts have been reluctant to get involved with issues
involving resource allocation. Proportionality is usually the key here.
See, for example N W Lancashire Health Authority v A,D & G [2000] 1 WLR 977
(though note this predates the HRA), and more recently R (on application of F) v
Oxfordshire Mental Healthcare Trust & others [2001] EWHC Admin 535, where it
was held that refusal to fund certain treatment was an administrative resource
allocation decision and not a question for the courts to determine. In the recent
challenge relating to the availability on prescription of the cancer treatment drug
Herceptin, it is interesting to note that the challenge was not really pursued in
human rights terms (R(Rogers) v Swindon PCT [2006] EWCA Civ 392).
See also:
R(on application of H) v Mental Health Review Tribunal [2002] EWHC Admin 1522
Ex Parte Haggerty, [2003] EWHC 803 Admin
Ex parte Watts [2003] EWHC 2228 Admin
16.4 ARTICLE 3 – PROHIBITION OF INHUMAN OR DEGRADING
TREATMENT
This seems to demand a very high level of degradation. As was said in Ireland v UK
[1978]:
“Treatment will become inhuman only of it reaches a level of gravity
involving considerable mental or physical suffering, and degrading if the
person has undergone humiliation or debasement involving a minimum level
of severity.”
Consequently the majority of medical procedures carried out, for example, by general
practitioners or in hospitals will not engage this Article. This is because the defendants
would very likely argue that the treatment offered was designed to benefit the patient and
it would have to be a very brave court indeed which would conclude that such treatment
is inhuman etc. But could the same be said about life saving treatment carried out on a
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More generally, in NHS Trust A v M and NHS Trust B v H [2001] it was held (somewhat
controversially) that withdrawal of treatment where the patients were in a persistent
vegetative state did not breach Article 3.
At times there will be a tension between Articles 2 and 3. The extent to which Article 3required positive steps to be taken to end suffering and obligations under Article 2, were
considered in the case of Diane Pretty (R (Pretty) v DPP [2001] UKHL 61), where an
argument that the state was in breach of Article 3 by not allowing steps to be taken to end
Diane Pretty’s life- and thus suffering- was a breach of Article 3, was rejected.
Another key area of potential challenge under Article 3, as we have already seen in
relation to Article 2, above, relates to the obligation to provide treatment. In addition to the
considerations noted above, there have been a number of challenges over decisions to
deport those suffering from serious health problems to countries where no appropriate
health care is available.
16.5 ARTICLE 5 – RIGHT TO LIBERTY AND SECURITY OF THE PERSON
This is particularly relevant in the mental health field and to those who lack capacity.
There have been a number of challenges advanced in mental health terms under Article
5, to the detention and review process and detailed structure of the Mental Health Act.
This has resulted in a number of declarations of incompatibility. That is to say that thecourts have declared that the MHA is incompatible with Articles of the Convention.
Perhaps one of the most important cases to note here is that of HL v UK (5.10.04) known
as the ‘Bournewood’ case). Here the European Court held that where a patient, who lacks
capacity, is cared for in hospital (or other residential facility) in such circumstances that
amounts to a ‘deprivation of liberty’, and Article 5 is engaged, then where this is outside
the MHA structure and lawful authority is derived from the common law doctrine of
necessity (see Chapter 16), then, because the common law fails to sufficiently protect
against arbitrary detention, this breaches Article 5. With the implementation of the MCA,
which ‘takes over’ from the common law in this regard, it is clear that deprivation of liberty
can not be justified under the MCA (at present) without a court order.
A hugely important case, both in mental health terms, but also of wider application.
Consider for example the young adult male admitted to hospital for treatment for head
injury who lacks capacity. Such treatment can only be justified under the MCA, which
does not allow for deprivation of liberty. If he is cared for in circumstances that amount to
a deprivation of liberty, then this will be unlawful and Article 5 will be breached. Consider
also an elderly patient, lacking capacity, being cared for in a residential facility, where
doors are locked and movement restricted, to the degree which amounts to a deprivation.
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For further information relating to this problem access the Department of Health website,
where the safeguards introduced by the Mental Health Act 2007 into the MCA ( to be
implemented in 2009) are detailed.
16.6 ARTICLE 6 – RIGHT TO A FAIR AND PUBLIC HEARING
Excluding criminal cases, what in the civil litigation field, is likely to offend this Article?
Consider:
(1) Patient/claimants forced to use firms with clinical franchises;
(2) the move to use joint experts on the issue of causation (see Oxley v Penwarden
[2000] where this was strenuously criticised);
(3) conditional fee arrangements;
(4) use and appointment of assessors;
(5) summary judgment (“… in an area where the law is being developed on a case by
case basis it is not always clear to the pleader what facts may in the eyes of the
court eventually turn out to be critical. That seems to me to be an additional
reason for being reluctant to strike out a case like the present” per Shiemann LJ in
Capital and Counties plc v Hampshire CC (1997));
(6) GMC when dealing with doctors alleged to have committed an act of serious
professional misconduct – is it a fair trial? Is the GMC independent and impartial?
(See Gautrin v France (1998)).
A challenge to the detention process, e.g., Mental Health Review Tribunal hearings will
(generally) fall within Article 5, rather than 6. See however the impact of Article 6 on the
Judicial Review process in cases noted under 19.4 above (Ex parte Wilkinson etc).
Again in the mental health context, the court has held that the impact of Article 6 means
that doctors certifying treatment should be given in accordance with the statutory
requirements of the Mental Health Act (s.58), should give reasons in writing (see R
(Wooder) v Feggetter & others( [2002] EWCA Civ 554).
16.7 ARTICLE 8 – RIGHT TO RESPECT FOR PRIVATE AND FAMILY LIFE,
HOME AND CORRESPONDENCE
Arguably the Article which has/will have the greatest impact in the health care field.
Because of the very wide application of this Article it will be relevant to issues
relating to treatment, consent, admission, compulsory treatment, access to
treatment, confidentiality (as we saw in Chapter 14), and a very wide range of
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health related policies and procedures. Again, it is important to note that the Article
8 obligation is both a positive and negative one.
Indeed within Article 8 the rights conferred on different individuals may conflict.
Consider for example the mother’s right to information about her son (right to familylife), against the son’s right to confidentiality (private life).
It must be remembered from the outset that this is a qualifiable right, so that
although many policies may interfere prima facie with Article 8, they are not
unlawful because they constitute a lawful ‘qualification’. As we saw earlier
questions of proportionality are key.
Some cases so far:
October 18th – HUFEA rejected a couple’s bid to use IVF to ensure they have a
daughter.
R v Home Secretary ex p Mellor [2002]. Forbes J, faced with the argument by a
prisoner that under the Convention he had a right to artificially inseminate his wife
since he was denied conjugal visits, said the Article did not create a right to have
children. It was also said that there was no breach of Article 12.
ECHR forced Government to grant British citizenship to the surrogate twins of a
gay couple.
There is also a possible conflict between Articles 8 and 10 (see below). See:Douglas v Hello! Ltd [2001] and Theakston v MGN [2002].
David Glass case (cited above), where David’s Article 8 rights were breached by
the failure of those treating David to bring the matter before the court, when his
‘legal proxy’ (parent) had refused consent to the treatment he was given.
The provisions of the Mental Health Act relating to the role of the ‘nearest relative’
(a statutory role derived from the MHA giving certain rights to a defined individual,
regardless of whether the patient objects to that person being so involved), have
been declared to be incompatible with Article 8. (See, amongst others, Re M [2003]
EWHC 1094 admin).
Evans v UK- as already noted in chapter 17, Natalie Evans’s claim in relation to
Article 8 recently failed.
This is only a small taste of the challenges and Article 8 related issues raised so far. Yet
again, and again not surprisingly, many challenges have been advanced, both
successfully and unsuccessfully, in the mental health field.
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16.8 ARTICLE 10 – RIGHT TO FREEDOM OF EXPRESSION
What if a newspaper intends to publicise the fact that an individual (health carer or not) is
HIV positive or suffering from hepatitis? Can they be stopped under Article 8? If so, what
about Article 10? There are a number of cases where the freedom of the press in
particular has been balanced against Article 8 rights, see eg Ackroyd v MGN, Thompson
v Venables etc.
16.9 ARTICLE 12 – RIGHT TO MARRY
This right is only exercisable in accordance with national laws. Consequently it may have
only very limited applicability. .
16.10 ARTICLE 14 – NON DISCRIMINATION IN THE ENJOYMENT OF THE
CONVENTION’S RIGHTS
It could be that the current rule which says that a minor may consent to a medical
procedure if Gillick competent but cannot refuse medical treatment because he/she is not
capable of making that decision may have to be reviewed. The argument could be put on
the ground that someone (a minor) is being denied the right to say whether he/she should
be treated because of his/her age; adults have the capacity so why not competent
minors?
NB: Protocol 12 of the ECHR was opened for signature on 4 November 2000. This
creates a free standing right of freedom from discrimination.
16.11 OVERALL ASSESSMENT
Although in many aspects the HRA may be said to have had less impact than may
originally have been predicted (and indeed as portrayed by some elements of the media),
clearly in some areas there has been an important impact, for example in relation to
mental health, though some may well argue, not enough!
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SUMMARY
At the end of this chapter there should be:
* an appreciation of the way in which the HRA and the ECHR may impact on certain
areas of medical law.
READING:
See all textbooks as the Human Rights Act
is referred to in most chapters
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*