How to evaluate fixed clinical QC limits vs. risk-based SQC strategies
Author:
Affiliation:
1. University of Wisconsin School of Public Health , Madison WI , USA
2. Westgard QC, Inc. , Madison WI , USA
3. Sina Medical Laboratory , Qaem Shahr , Iran
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://www.degruyter.com/document/doi/10.1515/cclm-2022-0539/pdf
Reference10 articles.
1. CLSI C24-Ed4. Statistical quality control for quantitative measurement procedures: principles and definitions, 4th ed. Wayne PA: Clinical and Laboratory Standards Institute; 2016.
2. Braga, F, Pasqualetti, S, Aloisio, E, Panteghini, M. The internal quality control in the traceability era. Clin Chem Lab Med 2021;59:291–300. https://doi.org/10.1515/cclm-2020-0371.
3. Westgard, JO, Quam, EF, Barry, PL. Establishing and evaluating QC acceptability criteria. Med Lab Observ 1994;26:22–6.
4. Braga, F, Panteghini, M. Performance specifications for measurement uncertainty of common biochemical measurands according to Milan models. Clin Chem Lab Med 2021;59:1362–8. https://doi.org/10.1515/cclm-2021-0170.
5. Bayat, H, Westgard, SA, Westgard, JO. Planning risk-based SQC strategies: practical tools to support the new CLSI C24Ed4 guidance. J Appl Lab Med 2017;2:211–21. https://doi.org/10.1373/jalm.2017.023192.
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