Trueness verification of actual creatinine assays in the European market demonstrates a disappointing variability that needs substantial improvement An international study in the framework of the EC4 creatinine standardization working group

被引:45
作者
Delanghe, Joris R. [1 ]
Cobbaert, Christa [2 ]
Galteau, Marie-Madeleine [3 ]
Harmoinen, Aimo [4 ]
Jansen, Rob [5 ]
Kruse, Rolf [6 ]
Laitinen, Paeivi [7 ,8 ]
Thienpont, Linda M.
Wuyts, Birgitte [1 ]
Weykamp, Cas [9 ]
Panteghini, Mauro [10 ,11 ]
机构
[1] Ghent Univ Hosp, B-9000 Ghent, Belgium
[2] Amphia Hosp, Breda & Dutch Fdn Qual Assessment Clin Labs, Nijmegen, Netherlands
[3] Ctr Med Prevent, Nancy, France
[4] Savonlinnan Keskussairaala, Savonlinna, Finland
[5] St Anna Hosp, Dept Clin Chem, Geldrop, Netherlands
[6] Referenzinst Bioanalyt, DGKL, Bonn, Germany
[7] Univ Hosp Oulu, Oulu, Finland
[8] Univ Ghent, Dept Analyt Chem, B-9000 Ghent, Belgium
[9] Queen Beatrix Hosp, Winterswijk, Netherlands
[10] Univ Milan, Ctr Metrol Traceabil Lab Med CIRME, Milan, Italy
[11] Univ Milan, Dept Clin Sci Luigi Sacco, Milan, Italy
关键词
analytical error; bias; calibration; creatinine; external quality assessment; glomerular filtration; rate; reference methods;
D O I
10.1515/CCLM.2008.256
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: The European In Vitro Diagnostics (IVD) directive requires traceability to reference methods and materials of analytes. It is a task of the profession to verify the trueness of results and IVD compatibility. Methods: The results of a trueness verification study by the European Communities Confederation of Clinical Chemistry (EC4) working group on creatinine standardization are described, in which 189 European laboratories analyzed serum creatinine in a commutable serum-based material, using analytical systems from seven companies. Values were targeted using isotope dilution gas chromatography/mass spectrometry. Results were tested on their compliance to a set of three criteria: trueness, i.e., no significant bias relative to the target value, between-laboratory variation and within-laboratory variation relative to the maximum allowable error. Results: For the lower and intermediate level, values differed significantly from the target value in the Jaffe and the dry chemistry methods. At the high level, dry chemistry yielded higher results. Between-laboratory coefficients of variation ranged from 4.37% to 8.74%. Total error budget was mainly consumed by the bias. Non-compensated Jaffe methods largely exceeded the total error budget. Best results were obtained for the enzymatic method. The dry chemistry method consumed a large part of its error budget due to calibration bias. Conclusions: Despite the European IVD directive and the growing needs for creatinine standardization, an unacceptable inter-laboratory variation was observed, which was mainly due to calibration differences. The calibration variation has major clinical consequences, in particular in pediatrics, where reference ranges for serum and plasma creatinine are low, and in the estimation of glomerular filtration rate. Clin Chem Lab Med 2008; 46: 1319-25.
引用
收藏
页码:1319 / 1325
页数:7
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