Traceability in Laboratory Medicine

被引:128
作者
Vesper, Hubert W. [1 ]
Thienpont, Linda M. [1 ]
机构
[1] Univ Ghent, Analyt Chem Lab, Fac Pharmaceut Sci, B-9000 Ghent, Belgium
关键词
CLINICAL-CHEMISTRY; SERUM TESTOSTERONE; WORKING GROUP; STANDARDIZATION; QUALITY; IMMUNOASSAYS; TRUENESS; ASSAYS; WOMEN; HARMONIZATION;
D O I
10.1373/clinchem.2008.107052
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: In patient and population samples, generation of analytical results that are comparable and independent of the measurement system, time, and location is essential for the utility of laboratory information supplied in healthcare. Obtaining analytical measurement results with such characteristics is the aim of traceability in laboratory medicine. As awareness of the benefits of having traceable measurement results has increased, associated efforts have been directed toward making traceability a regulatory requirement and developing approaches to enable and facilitate the implementation of traceability. Although traceability has been a main focus of many laboratory Standardization activities in the past, discussions are still ongoing with regard to traceability and its implementation. CONTENT: This review provides information about the traceability concept and what needs can be fulfilled and benefits achieved by the availability of traceable measurement results. Special emphasis is given to the new metrological terminology introduced with this concept. The review addresses and describes approaches for technical implementation of traceable methods as well as the associated challenges. Traceability is also discussed in the context of other activities to improve the overall measurement process. SUMMARY: Establishing metrological traceability of measurement results satisfies basic clinical and public health needs, thus improving patient care and disease control and prevention. Large advances have been made to facilitate the implementation of traceability. However, details in the implementation process, such as lack of available commutable reference materials and insufficient resources to develop new reference measurement systems continue to challenge the laboratory medicine community. (C) 2009 American Association for Clinical Chemistry
引用
收藏
页码:1067 / 1075
页数:9
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