Comparison of Thrombophilia Assay Results for the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee Plasma Standard from Different External Quality Assessment Providers—for the External Quality Assurance in Thrombosis and Haemostasis Group

Author:

Jennings Ian1,Meijer Piet2,Arunachalam Sandya3,Marlar Richard A.4,Olson John D.5,Zantek Nicole D.6,Bon Chantal7,Dean Elysse3,Hollestelle Martine J.2,Meley Roland7,Plumhoff Elizabeth A.8,Reilly-Stitt Christopher1,Salazar Eric5,Smock Kristi J.9,Spannagl Michael10,Walker Isobel D.1

Affiliation:

1. UK NEQAS (Blood Coagulation), Sheffield, United Kingdom

2. ECAT Foundation, Voorschoten, The Netherlands

3. RCPAQAP Haematology, St. Leonards, NSW, Australia

4. Department of Pathology, University of New Mexico, Albuquerque, New Mexico

5. UT Health, San Antonio, Texas

6. University of Minnesota, Minneapolis, Minnesota

7. ProBioQual Association, Lyon, France

8. North American Specialized Coagulation Laboratory Association (NASCOLA), Rochester, MN, USA

9. University of Utah and ARUP Laboratories, Salt Lake City, Utah

10. INSTAND, LMU Klinik der Universität München, Germany

Abstract

AbstractExternal quality assessment (EQA) is used to evaluate laboratory performance in tests of hemostasis; however, some esoteric tests are performed by too few centers in any one EQA program to allow valid statistical assessment. To explore the feasibility of pooling data from several EQA providers, an exercise was carried out by the External Quality Assurance in Thrombosis and Haemostasis group, using the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee (SSC) plasma standard for thrombophilia screening assays. Six EQA providers took part in this exercise, distributing the SSC plasma standard as a “blinded” sample to participants for thrombophilia tests between November 2020 and December 2021. Data were collected by each provider, anonymized, and pooled for analysis. Results were analyzed as overall results from each EQA provider, and by kit/method-specific comparisons of data from all providers pooled together. For each parameter, median results and range were determined. Over 1,250 sets of data were returned in the six EQA programs. The overall medians (all data pooled) were <4% of the assigned values for each parameter with the exception of protein C activity by clot-based assay. Method-related differences in median results were observed for free protein S antigen and protein S activity—a pattern seen across data from the different EQA providers. Antithrombin antigen results reported in mg/dL provided an example where small numbers of results for a single EQA provider may be supplemented by pooling data from multiple providers with good agreement seen among results reported by the different EQA providers. This study demonstrated that a multicenter EQA provider collaboration can be carried out and demonstrated benefit for assays with smaller number of participants. In addition, results showed good agreement with the assigned values of the SSC plasma standard. Further exercises for tests performed by only small numbers of laboratories can be planned.

Publisher

Georg Thieme Verlag KG

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