Long-term stability of laboratory tests and practical implications for quality management

Author:

Van Houcke Sofie K.1,Stepman Hedwig C.M.1,Thienpont Linda M.1,Fiers Tom2,Stove Veronique3,Couck Pedro4,Anckaert Ellen4,Gorus Frans4

Affiliation:

1. Laboratory for Analytical Chemistry, Faculty of Pharmaceutical Sciences, Ghent University , Ghent , Belgium

2. Laboratory for Hormonology and Department of Endocrinology, Ghent University Hospital , Ghent , Belgium

3. Department of Clinical Chemistry, Ghent University Hospital , Ghent , Belgium

4. Laboratory of Clinical Chemistry and Radioimmunology, University Hospital of the Free University Brussels , Brussels , Belgium

Abstract

Abstract Background: Long-term stability of analytical performance is required for adequate patient management. We investigated the use of patient data to document test stability, and the relevance of observed instabilities on a surrogate medical outcome. We used multiyear patient and internal quality control (IQC) data from two laboratories for tests to monitor chronic kidney and thyroid disease. Methods: We plotted moving means of the 50th percentiles of stratified patient data and of the daily IQC means. We evaluated observed instabilities based on goals inferred from the analytes’ biological variation and investigated their effect on classification of results against reference intervals. Results: Patient and IQC data generally matched well, except for analytes, for which other than analytical variation sources prevailed. Analytical instabilities were predominantly due to reagent/calibrator lot changes, however, for immunoassays also to within-lot instabilities, urging frequent recalibrations. The relevance of biased results on medical decisions ranged from negligible to very pronounced, indicating the need for assessment of analytical performance in relation to quality goals inferred from biological variation. Conclusions: Patient percentiles offer great potential to assess/monitor the medium- to long-term analytical stability of a test within certain constraints. Differences in analytical quality between assays can significantly affect medical outcome.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

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3. Lot-to-lot variation and verification;Clinical Chemistry and Laboratory Medicine (CCLM);2022-11-24

4. Analyte stability in whole blood using experimental and datamining approaches;Scandinavian Journal of Clinical and Laboratory Investigation;2022-02-03

5. Integrating quality control and external quality assurance;Clinical Biochemistry;2021-09

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