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DR NILESH KATE MBBS,MD ASSOCIATE PROF DEPT. OF PHYSIOLOGY BLOOD GROUPS

BLOOD GROUP SYSTEM

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Page 1: BLOOD GROUP SYSTEM

DR NILESH KATE

MBBS,MDASSOCIATE PROF

DEPT. OF PHYSIOLOGY

BLOOD GROUPS

Page 2: BLOOD GROUP SYSTEM

OBJECTIVES. BLOOD GROUPS

Introduction Classical ABO blood

grouping system Rh blood grouping

system Clinical applications of

blood groups.

BLOOD TRANSFUSION. Indications Donors & recipient. Precautions during

blood transfusion. Hazards Autologous BT. Storage of blood for

transfusion.

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INTRODUCTION Agglutinogens –

Antigens present on cell membrane of RBC

Agglutinins – antibodies against Agglutinogens present in plasma.

Agglutination – of RBC is reaction between these 2

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BLOOD GROUPING SYSTEM. Major blood group system – based on Agglutinogens on cell

membrane, present widely & causes severe transfusion reaction ABO Rh system

Minor blood group system – based on Agglutinogens but present in few populations & causes mild transfusion reaction. MNS P

Familial blood group system – found in few families KELL. DUFFY, LUTHERAN, BOMBAY LEWIS, DEIGO, KIDD

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LANDSTEINER’S LAWKARL LANDSTEINER 1900

If an Agglutinogens is present on surface of RBC corresponding agglutinins must be absent in plasma.

& if an Agglutinogens is absent on surface of RBC corresponding Agglutinins must be present in plasma.

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CLASSICAL ABO BLOOD GROUPING SYSTEM

A & B Agglutinogens- these are complex oligosaccharides differing in terminal sugar

In Antigen A – N-acetylgalactosamine & in Antigen B – galactose.

Other than RBC also present in salivary glands, pancreas, kidney, liver, lung, testes also in body fluids like saliva, semen & amniotic fluid

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CLASSICAL ABO BLOOD GROUPING SYSTEM

Anti-A (α)and anti-B (β) Agglutinins – IgM type & cannot cross placenta.

Absence of these are determined by Landsteiner’s law

Act best at low temperature so called Cold Antibodies.

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TYPES OF ABO BLOOD GROUPS.

BLOOD GROUP ANTIGEN ANTIBODIES

A A ANTI B OR β

B B ANTI A OR α

AB AB ---------------------

O -----------ANTI A (α) & ANTI B

(β)

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POPULATION DISTRIBUTION OF ABO BLOOD GROUPS

BLOOD GROUPS PERCENTAGE (%)

A 20

B 40

AB 08

O 32

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INHERITANCE OF ABO BLOOD GROUPS

PHENOTYPE(BLOOD GROUP)

GENOTYPE

A AA,AO

B BB,BO

AB AB

O OO

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APPERANCE OF ANTIGENS & ANTIBODIES

Antigens A & B appears in 6th week of fetal life, at birth 1/5th of adult level & rises during puberty & adolescence.

Antibodies are absent at birth, appear 10-15 days after birth, reach maximum at 10 yrs.

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MECHANISM Antigens similar to A & B are present in

intestinal bacteria & foods, when newborn exposed to these absorbed in blood, stimulate formation of antibodies against antigens recognized as non-self by immune system.

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DETERMINATION OF ABO BLOOD GROUPS

Covered in

Practicals “ Determination of Blood Groups”

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Rh BLOOD GROUPING SYSTEM Rh Antigens – called Rh as these were first

discovered in RBC of rhesus monkey. Discovered by Landsteiner & weiner in 1940. 3 types of Rh antigen, C,D & E, D IS COMMONEST & causes severe transfusion

reaction. Rh antigens are integral membrane proteins & not

found in other tissues.

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Rh Antibodies. No natural antibodies like

ABO blood groups system Rh antibodies are produced

when Rh -ve individual is transfused with Rh +ve blood.

These are IgG type & crosses placenta.

Warm Antibodies.

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INHERITANCE OF Rh BLOOD GROUPS

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HEMOLYTIC DISEASE OF NEWBORN.

Incompatibility of Rh blood groups between fetus & mother.

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MECHANISM OF HEMOLYTIC DISEASE OF NEWBORN IN RH INCOMPATIBILITY.

Entrance of Rh +ve fetal RBC into Rh –ve mother’s circulation during first pregnancy.

Production of Rh antibodies.

Rh incompatibility reaction during second pregnancy.

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MANIFESTATIONS OF HEMOLYTIC DISEASE OF NEWBORN.

Erythroblastosis fetalis. Erythroblastosis Anaemia.

Icterus gravis Neonatorum. Jaundice Enlarged liver & spleen.

Kernicterus – excess (<18mg%) bilirubin deposition in brain mainly basal ganglia

Hydrops fetalis – Grossly edematous fetus.

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PREVENTION OF HEMOLYTIC DISEASE OF NEWBORN.

Injecting single dose of Rh antibodies (anti-D) to mother soon after child birth.

So active antibodies will not be formed by mother.

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TREATMENT OF HEMOLYTIC DISEASE OF NEWBORN.

Replacement of baby’s Rh+ve blood by Rh –ve blood.

This is called Exchange Transfusion.

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CLINICAL APPLICATIONS OF BLOOD GROUPS.

In blood transfusion. In Preventing Hemolytic Disease. In Paternity Disputes. In Medicolegal Cases. In knowing Susceptibility to Diseases.

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BLOOD TRANSFUSION. Life saving measure Should be carried out

when absolutely necessary.

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INDICATIONS Blood loss – Accidents, major operations, rupture

peptic ulcer, rupture aortic aneurysm & rupture ectopic pregnancy.

For Quick restoration of haemoglobin. Exchange transfusion. Blood diseases- Aplastic anaemia, agranulocytosis,

leukemias, purpurae & clotting defects Acute poisoning – carbon Monoxide poisoning.

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DONORS & RECIPIENT. Donor – person who

donate the blood Recipient – person who

receives the blood. Universal donor – O

Rh Negative. Universal recipient –

AB Rh positive

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PRECAUTIONS TO BE TAKEN WHILE SELECTING DONOR.

Should be Healthy Age – 18- 60 yrs Contraindicated in

pregnant & lactating mothers

Screening for – AIDS, viral hepatitis, malaria, syphilis.

Hb & PCV should be normal

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PRECAUTIONS DURING BLOOD TRANSFUSION.

Absolute indication. Cross matching

Major – Donor’s RBC + Recipient plasma

Minor -Donor’s plasma+ Recipient RBC

Rh +ve blood should never be transfused to Rh –ve person.

Donor’s blood should always be screened for diseases.

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PRECAUTIONS DURING BLOOD TRANSFUSION.

Blood bag/bottle should be checked. Blood transfusion should be given at slow rate. Proper Aseptic measures. Careful watch on recipient condition – for first 10-

15min. Should stop if any reaction

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HAZARDS OF BLOOD TRANSFUSION.

Mismatched transfusion reaction. Agglutination of donor’s RBC Tissue ischemia – chest pain or back pain Haemolysis of agglutinated RBC- Haemoglobinemia Haemolytic Jaundice Renal vasoconstriction Circulatory shock Haemoglobinuria. Renal tubular damage, acute renal shutdown & Uraemia.

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HAZARDS OF BLOOD TRANSFUSION.

Circulatory overload - Hypervolemia Transmission of blood borne infections – AIDS, viral

hepatitis Pyrogenic reactions – fever with chills Allergic reactions – skin rashes , asthma Hyperkalemia – after excessive transfusion Hypocalcaemia – Tetany due to chelation of Ca by citrate Reduced tissue oxygenation – stored RBC has low 2,3-DPG Haemosiderosis – Iron overload & deposition in liver, heart Thrombophlebitis – at Venepuncture site Air embolism – entry of air into blood.

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AUTOLOGOUS BT. Transfusion of

individual own blood withdrawl & stored

For elective surgery During surgery Sports persons

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STORAGE OF BLOOD FOR TRANSFUSION.

One unit 420 ml mixed with 120 ml ACD ( Acid citrate dextrose)

Contents – Acid citrate 0.48 gm Trisodium citrate – 1.32 gm Dextrose – 1.47gm Distilled water -100ml

Dextrose – provide energy for Na-K pump

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IMPORTANT FACTS ABOUT BLOOD TRANFUSION.

One can safely donate 1 unit of blood every 6 month.

Blood can be stored for 21 days with above conditions

WBC & platelet virtually absent after 24 hrs of storage.

After transfusion 80% RBC survive for 24 hrs & destroyed at a rate of 1% per day.

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Thank You