Verification of examination procedures in clinical laboratory for imprecision, trueness and diagnostic accuracy according to ISO 15189:2012: a pragmatic approach

Author:

Antonelli Giorgia1ORCID,Padoan Andrea2,Aita Ada2,Sciacovelli Laura3,Plebani Mario23ORCID

Affiliation:

1. Department of Medicine-DIMED , University of Padova , Padova , Italy , Phone: +390498217978

2. Department of Medicine-DIMED , University of Padova , Padova , Italy

3. Department of Laboratory Medicine , University-Hospital of Padova , Padova , Italy

Abstract

Abstract Background The International Standard ISO 15189 is recognized as a valuable guide in ensuring high quality clinical laboratory services and promoting the harmonization of accreditation programmes in laboratory medicine. Examination procedures must be verified in order to guarantee that their performance characteristics are congruent with the intended scope of the test. The aim of the present study was to propose a practice model for implementing procedures employed for the verification of validated examination procedures already used for at least 2 years in our laboratory, in agreement with the ISO 15189 requirement at the Section 5.5.1.2. Methods In order to identify the operative procedure to be used, approved documents were identified, together with the definition of performance characteristics to be evaluated for the different methods; the examination procedures used in laboratory were analyzed and checked for performance specifications reported by manufacturers. Then, operative flow charts were identified to compare the laboratory performance characteristics with those declared by manufacturers. Results The choice of performance characteristics for verification was based on approved documents used as guidance, and the specific purpose tests undertaken, a consideration being made of: imprecision and trueness for quantitative methods; diagnostic accuracy for qualitative methods; imprecision together with diagnostic accuracy for semi-quantitative methods. Conclusions The described approach, balancing technological possibilities, risks and costs and assuring the compliance of the fundamental component of result accuracy, appears promising as an easily applicable and flexible procedure helping laboratories to comply with the ISO 15189 requirements.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Reference39 articles.

1. International Organization for Standardization (ISO). Medical laboratories-particular requirements for quality and competence. ISO 15189, Geneva, Switzerland, 2012.

2. Farmer T. Toward a culture shift in laboratory quality: application of the full ISO 15189 standard. MLO Med Lab Obs 2015;47:38–9.

3. Plebani M, Sciacovelli L, Chiozza ML, Panteghini M. Once upon a time: a tale of ISO 15189 accreditation. Clin Chem Lab Med 2015;53:1127–9.

4. EU Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices (1998). Available at: www.europa.eu/legislation_summaries/internal_market/single_market_for_goods/technical_harmonisation/l21010c_en.htm

5. Clinical Pathology Accreditation (UK). Standards for Medical Laboratory. Version 2.01, CPA, UK, March 2009.

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