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NEQAS SCHEME 3

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No B62 or B70 Ab detected therefore unlikely (Bead anomaly) Sample 306 ... beads, given DR1,10,103 and DR51 specificities, multi antigen beads would not discriminate ... – PowerPoint PPT presentation

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Title: NEQAS SCHEME 3


1
NEQAS SCHEME 3
  • Cycle 1 2008 samples 301-06

2
NEQAS SCHEME 3
  • Cycle 2 2008 samples 307-12

3
Class I
  • Sample 301
  • No real problems
  • Sample 302
  • No real problems

4
  • Sample 303
  • Most penalty points awarded for not reporting
    what might be considered weaker reactions against
    HLA-A antigens. Stronger reactions suggest Bw4
    specific antibody (which incidentally cannot be
    reported)

5
  • Sample 304
  • No problems with class I, all labs reported as
    negative

6
  • Sample 305
  • As with sample 303, lots of PPs for not
    reporting weaker reactivity (HLA-B antigens this
    time)
  • Many labs had difficulty detecting B12 and B17
    Abs
  • Many reported B76 as ve. No B62 or B70 Ab
    detected therefore unlikely (Bead anomaly)

7
  • Sample 306
  • Same story Lots of PPs for not listing weak
    specificities as positive
  • Majority behaviour at the moment seems to be if
    its positive put it down

8
  • Class II antibody analysis
  • No real difficulties with any samples other
    than reporting of weak positive reactions

9
Cycle Performance
  • All labs averaged 99
  • Mostly for not reporting weak positives
    (?experienced vs novice luminex users)
  • Large Nos PPs only apparent for CI ??
  • CII all labs 11
  • Most for not reporting weak positive

10
  • Class I
  • Sample 307
  • A26 specific Ab caused problems for non-UK labs
  • Cluster of UK labs had difficulty detecting B57

11
  • Sample 308
  • A25 specific Ab caused difficulty across the
    board
  • Same cluster of UK labs had difficulty detecting
    B57 and B44 specific Abs

12
  • Sample 309
  • Same cluster of UK labs had difficulty detecting
    A9 and B17 specific Abs

13
  • Sample 310
  • A group of UK labs penalised for not detecting
    A29,32,43,66,74,80 B17,21,52,62 and 63 specific
    Abs. All weaker reactions

14
  • Sample 311
  • Split decision over /- B7
  • 1 lab had real problems with this sample
  • Failed to detect B13,38,44,49,63 and B77 specific
    Abs (all 5pps)

15
  • Sample 312
  • Same lab had problems with this sample
  • Failed to detect A28,33,34 and B57specific Abs
    (all 5pps)
  • Failed to detect B54 and B55 specific Abs (all 3
    PPs)
  • This lab had problems with all samples and may
    need assistance/guidance
  • 3 or 4 non-UK labs in similar position

16
  • Class II
  • Sample 311
  • DQ9 specific Ab caused difficulty with some
    non-UK labs failing to detect (3PPs)

17
  • Sample 312
  • Problem with detection of DQ6 specific Ab. Same
    labs also penalised for not detecting DQ5
    specific Ab
  • ? Problem with detecting DQ1?
  • - Unlikely - labs not reporting DQ1 specific Ab
    probably using single antigen beads, given
    DR1,10,103 and DR51 specificities, multi antigen
    beads would not discriminate

18
  • Overall Performance
  • Big increase in PPs for Class I - ? Reflection
    of changes to scoring system
  • Patterns of cycle performance perpetuated in
    2008 If you scored high number of PPs in 07
    then the same in 08 etc
  • Patterns of scoring per cycle perpetuated also
    low score cycle 1 then high cycle 2 etc
  • Overall not much has changed!
  • Class II, general improvement from 07 despite
    change to scoring

19
  • Questions
  • Is it time to ignore 1pp scores and concentrate
    on the more disparate results?
  • Why is class II so much less problematic?
  • Does this reflect less antigens to report on Kit
    performance
  • Is there a need for a forum to discuss what is
    considered a positive reaction?
  • Is there a schism between experienced and novice
    users?
  • Should we add clinical relevance to the scheme?
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