Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/45325
Title: | Multicenter evaluation of Cystatin C measurement after assay standardization | Authors: | Bargnoux, Anne Sophie Piéroni, Laurence Cristol, Jean Paul Kuster, Nils Delanaye, Pierre Carlier, Marie Christine Fellahi, Soraya Boutten, Anne Lombard, Christine González-Antuña, Ana Delatour, Vincent Cavalier, Etienne |
UNESCO Clasification: | 32 Ciencias médicas 2403 Bioquímica |
Keywords: | Cystatin C Assay Standardization |
Issue Date: | 2017 | Journal: | Clinical chemistry (Baltimore, Md.) | Abstract: | Background: Since 2010, a certified reference material ERM-DA471/IFCC has been available for cystatin C (CysC). This study aimed to assess the sources of uncertainty in results for clinical samples measured using standardized assays. Methods: This evaluation was performed in 2015 and involved 7 clinical laboratories located in France and Belgium. CysC was measured in a panel of 4 serum pools using 8 automated assays and a candidate isotope dilution mass spectrometry reference measurement procedure. Sources of uncertainty (imprecision and bias) were evaluated to calculate the relative expanded combined uncertainty for each CysC assay. Uncertainty was judged against the performance specifications derived from the biological variation model. Results: Only Siemens reagents on the Siemens systems and, to a lesser extent, DiaSys reagents on the Cobas system, provided results that met the minimum performance criterion calculated according to the intraindividual and interindividual biological variations. Although the imprecision was acceptable for almost all assays, an increase in the bias with concentration was observed for Gentian reagents, and unacceptably high biases were observed for Abbott and Roche reagents on their own systems. Conclusions: This comprehensive picture of the market situation since the release of ERM-DA471/IFCC shows that bias remains the major component of the combined uncertainty because of possible problems associated with the implementation of traceability. Although some manufacturers have clearly improved their calibration protocols relative to ERM-DA471, most of them failed to meet the criteria for acceptable CysC measurements. | URI: | http://hdl.handle.net/10553/45325 | ISSN: | 0009-9147 | DOI: | 10.1373/clinchem.2016.264325 | Source: | Clinical Chemistry [ISSN 0009-9147], v. 63, p. 833-841 |
Appears in Collections: | Artículos |
Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.