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Articles |
1
Department of Laboratory Medicine and Pathology, Hennepin County Medical Center, Minneapolis, MN 55415.
2
Departments of Pathology and Medical Research
Technology, University of Maryland School of Medicine, Baltimore, MD
21201.
3
Department of Pathology and Laboratory Medicine,
University of Louisville, School of Medicine, Louisville, KY 40292.
4
Department of Pathology, Hartford Hospital, Hartford, CT
06102.
a Address correspondence to this author at: Hennepin County Medical Center, Clinical Laboratories No. 812, 701 Park Ave., Minneapolis, MN 55415. Fax 612-904-4229; e-mail fred.apple{at}co.hennepin.mn.us.
This multicenter study evaluated the Biosite Triage® Cardiac Panel as a quantitative, multimarker, whole blood system for the detection of acute myocardial infarction (MI). Optimum cutoffs for the discrimination of acute MI (n = 192 patients, 59 with MI) as determined by ROC curve analyses were as follows: 0.4 µg/L for cardiac troponin I (cTnI); 4.3 µg/L for the creatine kinase MB isoenzyme (CK-MB); and 107 µg/L for myoglobin. The Triage Panel showed the following concordances for detection or rule-out of MI compared with established devices: cTnI >89%; CK-MB >81%; myoglobin >69%. No significant differences were present between methods for the same marker. Diagnostic efficiencies demonstrated comparable sensitivities and specificities for the diagnosis of MI in patients presenting with symptoms compared with the Dade, Beckman, and Behring CK-MB, cTnI, and myoglobin assays; the ratio of sensitivity to specificity for each marker was as follows: cTnI, 98%:100%; CK-MB, 95%:91%; myoglobin, 81%:92%. The areas under the ROC curves for the Biosite myoglobin, CK-MB, and cTnI were 0.818, 0.905, and 0.970, respectively; the areas were significantly different, P <0.05. In patients with skeletal muscle injury and renal disease, the Triage cTnI showed 94% and 100% specificity, respectively. The Triage panel offers clinicians a whole blood, point-of-care analysis of multiple cardiac markers that provides excellent clinical sensitivity and specificity for the detection of acute MI.
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