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UK National Renal Transplant EQA Scheme
Ian Roberts
Department of Cellular Pathology,
Oxford Radcliffe Hospitals
The National Renal Transplant EQA Scheme is sponsored by Fujisawa Ltd
EQA in Histopathology
• maintenance & improvement of diagnostic standards
• education vs performance assessment
• required for CPD and CPA
• RCPath EQA steering committee -
sets performance standards
investigates substandard performance
EQA in Histopathology
• substandard performance:
anonymous letter of enquiry
NQA Advisory panel informed and determine whether low EQA scores reflect standards of routine practice
site visit
review panel
Medical Director informed
EQA in Histopathology
“ these procedures should be activated only in exceptional circumstances, and should cause no more concern to EQA participants than the possibility of being reported for incompetence by a colleague”
slides circulated to participants
responses submitted to scheme organiser
feedback of group diagnoses to participants
cases discussed at participants meeting
diagnoses scored
persistent substandard performers identified
remedial action
EQA in Histopathology
slides circulated to participants
responses submitted to scheme organiser
feedback of group diagnoses to participants
cases discussed at participants meeting
Renal Transplant EQA Scheme
slides circulated to participants
responses submitted to scheme organiser
feedback of group diagnoses to participants
cases discussed at participants meeting
diagnoses scored
persistent substandard performers identified
remedial action
Renal Transplant EQA Scheme
• 44 participants from 31 centres
• Case submission:
7 sets of slides (H&E and PAS/silver)
diagnostic lesion is present in all slides
biopsy is adequate by Banff criteria
NATIONAL RENAL TRANSPLANT EQA SCHEMECASE SUBMISSION FORM
Provided by: Original lab No.
Donor age Transplant date
Recipient age Biopsy date
Best creatinine Creatinine at biopsy
Donor type cadaveric Cause of recipientÕs renal failure(tick) living
non-heart beating
Delayed graft function Y / N HLA mismatches
Immunosuppressive regimen:
Prednisolone Mycophenolate
Azathioprine ATG, etc
Cyclosporine Other (please specify below)
FK/Prograf
Number of previous acute rejections
Is this acute rejection? (retrospective diagnosis when follow-up makes it clearwhat the ÒtrueÓ diagnosis is)
Major diagnosis
Supplementary diagnosis
Banff codes
Clinical information available at the time the original report was produced:
Clinical follow-up:
Renal Transplant EQA Scheme
• participants divided into 6 cells
• Circulations organised using Genpath software:
sets circulation dates
automatic reminder letters
RESPONSE SHEET Please return to the EQA secretary: Mrs Lynn Bradbury
NB: Please write something in every box, either a precise number (not more or less than),+/- or Banff score, as indicated.
Participant code number Circulation letter Case number
Information provided Slides
Tubules Interstitium
Tubulitis (Banff t0-3) oedema (+/-)
Tubules with tubilitis/10 hpf mononuclear cell infiltration (%) (number)Tubular atrophy (%) nucleolated lymphocytes (+/-)
Glomeruli eosinophils (+/-)
Glomerulitis (Banff g0-3) neutrophils (+/-)
Other interstitial haemorrhage (%)
Vessels interstitial fibrosis (%)
Intimal/transmural arteritis(Banff v0-3)Arteriolitis (+/-)
Arteriolar hyalinosis (Banff 0-3)
Major diagnosis
Supplementary diagnosis
Banff codes
Comments
Educational value
• enables pathologists to compare their diagnoses and their Banff grading with the whole group
• identifies differences in use of terminology
• identifies misunderstanding of the Banff classification and its application
• ongoing measure of the reproducibility of Banff criteria
• highlights areas of diagnostic difficulty
TerminologyCase 4 Number of responses 26
Diagnoses Numberacute rejection* 22Banff IB 11Banff IA 5Banff I 3severe acute rejection 4III 1chronic nephropathy 1interstitial nephritis 1
*acute cellular rejection 9*acute rejection, grade 1 6*acute tubulointerstitial rejection 3*acute rejection NOS 1*acute parenchymal rejection 1*acute tubular rejection 1*active rejection 1*severe acute rejection, 4I 1
ApplicationCase 5 Number of responses 26
Diagnoses Numberacute rejection* 13Banff IA 9Banff IB 1Banff II 1borderline changes* 6no rejection (infection 6, ATN4) 7
*On the basis of the Banff t and i scores provided:acute rejection 6borderline changes 13
Supplementary diagnosesinfection 20acute tubular necrosis 8donor vascular disease 6?CyA toxicity 2
Reproducibility
0%
20%
40%
60%
80%
100%
I t g vBanff criteria
Case 6
3
2
1
0
Reproducibility
mononuclear cell interstitial inflammation i1 (i2,t0,v0)
acute cellular rejection, type IA (i1,t1,v1)
acute rejection mild grade 1 (i1,t2,v0)
acute rejection, typeIA
acute rejection, typeIIA
acute rejection, typeIIB
acute vascular rejection, NOS
1
1
1
1
15
8
1
acute tubular necrosis
donor vascular disease
2
1
Case 21
Reproducibility
Case 22 borderline changes/suspicious of rejection
acute rejection, typeIA (i2/3,t1,v0)
acute rejection, typeIA
acute rejection, typeIB
severe acute parenchymal rejection, type IIA (i3,t2,v0)
acute rejection, moderate grade 2 (i3,t3,v0)
acute cellular rejection
chronic allograft nephropathy
?polyoma virus infection
3
5
9
3
1
1
1
4
1
CAN
?CsA/tacrolimus toxicity
acute tubular injury
arteriolitis
7
2
1
1
Difficult diagnoses
acute pyelonephritis, no rejection
borderline changes/suspicious of rejection
acute rejection (i?,t1)
acute rejection, typeIA
acute rejection, typeIB
chronic allograft nephropathy
inadequate specimen
Case 23 11
4
1
9
1
1
1
12
8
4
2
1
1
acute pyelonephritis
donor vascular disease
chronic allograft nephropathy
CsA toxicity
exclude obstruction
?interstitial nephritis
Difficult diagnoses
Case 25 hyperacute rejection 6
antibody-mediated rejection (Banff 2B) 2
acute rejection, typeIIB ?antibody mediated 1
acute rejection, typeIII 6
infarction ?large vessel thrombosis ?antibody-mediated rejection 7
arterial/venous thrombosis +/- infarction 2
macroscopic polyangiitis/vasculitis with infarction 3
Renal Transplant EQA Scheme
• identifies practical difficulties in the application of the Banff schema in routine practice
• identifies areas of diagnostic difficulty that should be specifically addressed in the future
Renal Transplant EQA Scheme
• identifies practical difficulties in the application of the Banff schema in routine practice
• identifies areas of diagnostic difficulty that should be specifically addressed in the future
• for the patients:
improves the diagnostic accuracy of the pathologist looking at their biopsy