CLINICAL STUDY: ACUTE CORONARY SYNDROMES
Cardiac troponin I for stratification of early outcomes and the efficacy of enoxaparin in unstable angina: a TIMI-11B substudy
David A. Morrow, MDa,
Elliott M. Antman, MD, FACCa,
Milenko Tanasijevic, MDb,
Nader Rifai, PhDc,
James A. de Lemos, MDa,
Carolyn H. McCabe, BSa,
Christopher P. Cannon, MD, FACCa and
Eugene Braunwald, MD, FACCa
a Department of Medicine, Brigham and Womens Hospital, Boston, Massachusetts, USA
b Department of Pathology, Brigham and Womens Hospital, Boston, Massachusetts, USA
c Department of Laboratory Medicine, Childrens Hospital, Boston, Massachusetts, USA
Manuscript received December 30, 1999;
revised manuscript received May 8, 2000,
accepted June 28, 2000.
Reprint requests and correspondence: Dr. David A. Morrow, Cardiovascular Division, Brigham and Womens Hospital, 75 Francis Street, Boston, Massachusetts 02115 damorrow{at}bics.bwh.harvard.edu
Objectives
We sought to evaluate cardiac troponin I (cTnI) for predicting early clinical outcomes and the efficacy of enoxaparin among patients with nonST segment elevation acute coronary syndrome (ACS) and negative creatine kinase, MB fraction (CK-MB) levels.
Background
Cardiac TnI identifies patients with unstable angina who are at higher risk of death or myocardial infarction (MI) by 30 days. The utility of cTnI for predicting very early clinical events, including recurrent ischemia, and the efficacy of enoxaparin are not yet established.
Methods
At baseline and 12 h to 24 h after enrollment in the Thrombolysis in Myocardial Infarction (TIMI)-11B trial, samples were collected for cTnI determination.
Results
Among 359 patients with negative serial CK-MB values, 50.1% had a cTnI result 0.1 ng/ml within the first 24 h. Patients with elevated cTnI were at higher risk of death or MI at 48 h (3.9 vs. 0%, p = 0.01) and 14 days (13.9 vs. 2.2%, p < 0.0001). Elevated cTnI also correlated with higher risk of recurrent ischemia requiring urgent revascularization by 48 h (10.0 vs. 1.7%, p = 0.001) and 14 days (20.6 vs. 5.6%, p 0.0001). Enoxaparin had a greater benefit among patients with elevated vs. normal cTnI (p = 0.03), achieving a 47% reduction in the risk of death, MI or urgent revascularization by 14 days in cTnI-positive patients (p = 0.007).
Conclusions
Elevation of cTnI among patients with nonST segment elevation ACS and negative levels of CK-MB identifies those at higher risk for very early adverse outcomes, including severe recurrent ischemia. Treatment with enoxaparin reduces the risk associated with elevated cTnI.
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Abbreviations and Acronyms
| | ACS | = acute coronary syndrome | | CABG | = coronary artery bypass graft surgery | | CI | = confidence interval | | CK-MB | = creatine kinase, MB fraction | | cTnI | = cardiac troponin I | | MI | = myocardial infarction | | PTCA | = percutaneous transluminal coronary angioplasty | | TIMI | = Thrombolysis in Myocardial Infarction | | UFH | = unfractionated heparin | | ULN | = upper limit of normal |
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