Evaluation of a point-of-care system for quantitative determination of troponin T and myoglobin

被引:35
作者
Müller-Bardorff, M
Sylvén, C
Rasmanis, G
Jorgensen, B
Collinson, PO
Waldenhofer, U
Hirschl, MM
Laggner, AN
Gerhardt, W
Hafner, G
Labaere, I
Leinberger, R
Zerback, R
Katus, HA
机构
[1] Med Univ Lubeck, Med Klin 2, D-23562 Lubeck, Germany
[2] Huddinge Hosp, Dept Cardiol, S-14186 Huddinge, Sweden
[3] Aalborg Hosp, Dept Clin Biochem, Aalborg, Denmark
[4] Mayday Univ Hosp, Dept Pathol, London, England
[5] Univ Klin Vienna, Notfallaufnahme,Allgemeines Krankenhaus, Vienna, Austria
[6] Helsingborg Hosp, Dept Clin Chem, Helsingborg, Sweden
[7] Univ Mainz, Inst Klin Chem, D-6500 Mainz, Germany
[8] Roche Diagnost GmbH, Evaluat Dept Patient Care, Mannheim, Germany
关键词
troponin T; myoglobin; cardiac enzymes; point-of-care testing; myocardial infarction; unstable angina pectoris;
D O I
10.1515/CCLM.2000.083
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
We present the results of a multicenter evaluation of a new point-of-care system (Cardiac Reader) for the quantitative determination of cardiac troponin T (CARDIAC T Quantitative test) and myoglobin (CARDIAC M test) in whole blood samples. The Cardiac Reader is a CCD camera that optically reads the immunochemical test strips. The measuring range is 0.1 to 3 mu g/l for CARDIAC T Quantitative and 30 to 700 mu g/l for CARDIAC M. Both tests are calibrated by the manufacturer. The reaction times of the tests are 12 or 8 minutes, respectively. Method comparisons were performed with 281 heparinized blood samples from patients with suspected acute coronary syndromes. The results obtained with CARDIAC T Quantitative showed a good agreement compared with cardiac troponin T ELISA (r = 0.89; y = 0.93x + 0.02). The method comparison between CARDIAC M and Tina-quant Myoglobin also showed a good agreement between both assays (r = 0.98; y = 0.92x + 1.6). Test lot-to-lot comparisons yielded differences of 2% and 6% for CARDIAC T Quantitative and of 0 to 11% for CARDIAC M. The within-run imprecision with blood samples and control materials was acceptable for CARDIAC T Quantitative (CV 10 to 15%) and good for CARDIAC M (CV 5 to 10%). The between-instrument CV was below 7% for CARDIAC T Quantitative and below 5% for CARDIAC M. The cross-reactivity of CARDIAC T Quantitative with skeletal troponin T was approximately 0.003%. No significant analytical interference was detected for any of the assays in investigations with biotin (up to 100 mu g/l), hemoglobin (up to 0.125 mmol/l), hematocrit (26 to 52%), bilirubin (up to 340 mu mol/l), triglycerides (up to 5.0 mmol/l), and 18 standard drugs. With the Cardiac Reader reliable quantitative results can be easily obtained for both cardiac markers. The system is, therefore, particularly suitable for use in emergency rooms, coronary care units and small hospitals.
引用
收藏
页码:567 / 574
页数:8
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