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Clinical Chemistry 50: 327-332, 2004. First published December 4, 2003; 10.1373/clinchem.2003.026815
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(Clinical Chemistry. 2004;50:327-332.)
© 2004 American Association for Clinical Chemistry, Inc.


Proteomics and Protein Markers

Evaluation of Imprecision for Cardiac Troponin Assays at Low-Range Concentrations

Mauro Panteghini1,a, Franca Pagani1, Kiang-Teck J. Yeo2, Fred S. Apple3, Robert H. Christenson4, Francesco Dati5, Johannes Mair6, Jan Ravkilde7 and Alan H.B. Wu8 on behalf of the Committee on Standardization of Markers of Cardiac Damage of the IFCC

1 Laboratorio Analisi Chimico Cliniche 1, Azienda Ospedaliera ‘Spedali Civili’, 25125 Brescia, Italy.
2 Department of Pathology, Dartmouth-Hitchcock Medical Center and Dartmouth Medical School, Lebanon, NH 03756.
3 Department of Laboratory Medicine and Pathology, Clinical Laboratories, Hennepin County Medical Center and the University of Minnesota School of Medicine, Minneapolis, MN 55415.
4 Department of Pathology, University of Maryland Medical School of Medicine, Baltimore, MD 21201.
5 IVD Consulting, D-35041 Marburg, Germany.
6 Department of Internal Medicine, Division of Cardiology, University of Innsbruck School of Medicine, 6020 Innsbruck, Austria.
7 Department of Cardiology, Aalborg University Hospital, DK-9100 Aalborg, Denmark.
8 Clinical Chemistry Laboratory, Hartford Hospital, Hartford, CT 06102.

aAuthor for correspondence. Fax 39-030-3995369; e-mail panteghi{at}bshosp.osp.unibs.it.

Background: The European Society of Cardiology/American College of Cardiology Committee for the Redefinition of Myocardial Infarction (MI) has recommended that an increased cardiac troponin should be defined as a measurement above the 99th percentile value of the reference group. A total imprecision (CV) at the decision limit of <=10% is recommended. However, peer-reviewed data on assay imprecision are lacking. The purpose of this study was to construct the clinically relevant imprecision profiles for each of the commercially available cardiac troponin assays. Pools of human sera containing cardiac troponin concentrations around the MI decision limit were assessed to identify the lowest concentration associated with a 10% CV.

Methods: Eight serum pools targeting different concentrations of cardiac troponin (I and T) were prepared and stored at -70 °C until usage. The cardiac troponin measurement protocol consisted of two replicates per specimen per run, and one run per day for 20 days, using two reagent lots and three calibrations. Manufacturers of each cardiac troponin assay directly performed the measurements. Data analysis for each assay was centralized and performed according to the NCCLS EP5-A guideline.

Results: The lowest concentrations (µg/L) providing a 10% CV were as follows: AxSYM, 1.22; ACS:180, 0.37; Centaur, 0.33; Immuno 1, 0.34; Access, 0.06; Vidas, 0.36; Liaison, 0.065; Dimension, 0.26; Opus, 0.90; Stratus CS, 0.10; Immulite, 0.32; Vitros ECi, 0.44; Elecsys, 0.04; AIA 21, 0.09.

Conclusion: No cardiac troponin assay was able to achieve the 10% CV recommendation at the 99th percentile reference limit defined by the manufacturer.




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