Allergen Specific IgE EQA

Accreditation Status: UKAS Schedule of Accreditation
Date Scheme started: 1988
Clinical Applicability:

Diagnosis and management of allergic disease

Analytes:

(SER/032) The programme includes the assessment of common or clinically important, individual IgE specificities, for example:

     D1       Dermatophagoides pteronyssinus
     E1       Cat epithelium
     E5       Dog dander
     F1       Egg white
     F2       Cow’s milk
     F13     Peanut
     F17     Hazel nut
     G6      Timothy grass
     I1        Bee venom
     I3        Wasp venom
     K82     Latex
     M3      Aspergillus fumigatus
     M6      Alternaria alternata
     T3        Birch
     W6      Mugwort

Other allergen specificities may be included, subject to the availability of clinically validated donor serum units

Units for Reporting:

Grade and kU/L (arbitrary)

Samples Distributed: Liquid format. Normal and pathological human serum
Number of Distributions per year: 6
Number of Samples per Distribution:

2

Frequency of Distributions: Every two months as outlined in the Distribution Schedule. Four allergen specific IgE tests will be analysed on each specimen.
Schedule of Analysis: Data entry is via the web for the submission of results. Data analysis commences 21 days after sample dispatch. Late returns are accepted and will contribute to the laboratory's cumulative performance statistics.
Data Analysis:

Analysis by grade shows the overall response and the method specific responses.

Reports show method specific statistics. Individual laboratory performance is expressed in terms of MRBIS, SDBIS and MRVIS, the DV for calculation of VI being taken from the MLTM, GLTM or ALTM as appropriate.

Chosen Coefficient of Variation for Allergen Specific IgE is 12%

Performance Scoring: Cumulative performance scores are based on the quantitative response with MRVIS scoring over a running window of twelve samples or twelve months
Criteria of Performance:

Performance assessment is allergen specific. Quantitative performance is assessed for each allergen, and is over a running period of 6 distributions containing that allergen (12 months)

  MRVIS
Ideal < 50
Good 50 - 100
Adequate 101 - 200
Poor >200 or SDBIS > 200


Overall MIS (OMIS) greater than 4 will also be considered as poor performance

Persistent Poor Performance:

Defined as being in the Poor Performance category for two or more successive Distributions