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根据ISO 15189:2012对临床实验室检查程序的不精密度、真实性和诊断准确性进行验证:一种实用方法。

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

作者信息

Antonelli Giorgia, Padoan Andrea, Aita Ada, Sciacovelli Laura, Plebani Mario

机构信息

.

出版信息

Clin Chem Lab Med. 2017 Aug 28;55(10):1501-1508. doi: 10.1515/cclm-2016-0894.

DOI:10.1515/cclm-2016-0894
PMID:28222014
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.

摘要

背景 国际标准ISO 15189被认为是确保高质量临床实验室服务以及促进检验医学认可程序协调统一的宝贵指南。必须对检验程序进行验证,以确保其性能特征与预期的检测范围一致。本研究的目的是根据ISO 15189第5.5.1.2节的要求,提出一种实践模式,用于实施对已在我们实验室使用至少两年的经过验证的检验程序进行验证的程序。方法 为了确定要使用的操作程序,识别了批准文件以及针对不同方法要评估的性能特征的定义;分析了实验室中使用的检验程序,并检查了制造商报告的性能规格。然后,确定操作流程图,以将实验室性能特征与制造商声明的特征进行比较。结果 验证性能特征的选择基于用作指导的批准文件以及所进行的特定目的测试,同时考虑了:定量方法的不精密度和真实性;定性方法的诊断准确性;半定量方法的不精密度和诊断准确性。结论 所描述的方法在平衡技术可能性、风险和成本以及确保结果准确性的基本要素合规方面,似乎是一种很有前景的易于应用且灵活的程序,有助于实验室符合ISO 15189的要求。

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