IFCC Working Group Recommendations for Correction of Bias Caused by Noncommutability of a Certified Reference Material Used in the Calibration Hierarchy of an End-User Measurement Procedure

Author:

Miller W Greg1,Budd Jeffrey2,Greenberg Neil3,Weykamp Cas4,Althaus Harald5,Schimmel Heinz6,Panteghini Mauro7,Delatour Vincent8,Ceriotti Ferruccio9,Keller Thomas10,Hawkins Douglas11,Burns Chris12,Rej Robert13,Camara Johanna E14,MacKenzie Finlay15,van der Hagen Eline4,Vesper Hubert16

Affiliation:

1. Virginia Commonwealth University, Richmond, VA

2. Jeff Budd Consulting, St. Paul, MN

3. Neil Greenberg Consulting, LLC, Rochester, NY

4. Queen Beatrix Hospital, Winterswijk, the Netherlands

5. Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany

6. European Commission, Joint Research Centre, Directorate F, Geel, Belgium

7. Research Centre for Metrological Traceability in Laboratory Medicine (CIRME), University of Milan, Milan, Italy

8. Laboratoire national de métrologie et d’essais (LNE), Paris, France

9. Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy

10. ACOMED Statistic, Leipzig, Germany

11. School of Statistics, University of Minnesota, Minneapolis, MN

12. National Institute for Biological Standards and Control, A Centre of the MHRA, Hertfordshire, UK

13. Wadsworth Center for Laboratories and Research, New York State Department of Health, and School of Public Health State University of New York at Albany, Albany, NY

14. National Institute of Standards and Technology, Gaithersburg, MD

15. Birmingham Quality/UK NEQAS, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK

16. Centers for Disease Control and Prevention, Atlanta, GA

Abstract

AbstractEstablishing metrological traceability to an assigned value of a matrix-based certified reference material (CRM) that has been validated to be commutable among available end-user measurement procedures (MPs) is central to producing equivalent results for the measurand in clinical samples (CSs) irrespective of the clinical laboratory MPs used. When a CRM is not commutable with CSs, the bias due to noncommutability will be propagated to the CS results causing incorrect metrological traceability to the CRM and nonequivalent CS results among different MPs. In a commutability assessment, a conclusion that a CRM is commutable or noncommutable for use with a specific MP is made when the difference in bias between the CRM and CSs meets or does not meet a criterion for that specific MP when compared to other MPs. A conclusion regarding commutability or noncommutability requires that the magnitude of the difference in bias observed in the commutability assessment remains unchanged over time. This conclusion requires the CRM to be stable and no substantive changes in the MPs. These conditions should be periodically reverified. If an available CRM is determined to be noncommutable for a specific MP, that CRM can be used in the calibration hierarchy for that MP when an appropriately validated MP-specific correction for the noncommutability bias is included. We describe with examples how a MP-specific correction and its uncertainty can be developed and applied in a calibration hierarchy to achieve metrological traceability of results for CSs to the CRM’s assigned value.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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