Key result
Early measurements of cTn-I (RR 3.87), cTn-T (RR 3.03), and CK-MB (RR 6.45) significantly predicted 14-day adverse events, with CK-MB being a stronger predictor than either troponin.
Why the study?
Do early measurements of cTn-I, cTn-T, and CK-MB predict adverse events in ED patients with possible myocardial ischemia?
Cohort (n=401)
Yes
Do early measurements of cTn-I, cTn-T, and CK-MB predict adverse events in ED patients with possible myocardial ischemia?
Relative Risk: 3.87 (95% CI 2.39–6.26)
Early, single-sample measurements of cTn-I, cTn-T, and CK-MB are all predictive of 14-day adverse events in ED patients with possible myocardial ischemia, with CK-MB being the strongest predictor.
Early marker positivity flags high-risk ED patients for intensified care; leaves open optimal single- vs. multi-marker strategies in modern cohorts.
OBJECTIVES: To determine and compare the prognostic abilities of early, single-sample measurements of cardiac troponin I (cTn-I), cardiac troponin T (cTn-T), and creatine kinase-MB (CK-MB) among ED patients with possible myocardial ischemia. METHODS: Prospective collection of clinical and serologic data using an identity-unlinked technique from patients with possible myocardial ischemia at 2 urban EDs. Outcome data concerning the occurrence of adverse events (AEs) during the 14 days after enrollment were used to calculate and compare the relative risks (RRs) and predictive values (with 95% confidence intervals) of the 3 markers for predicting AEs. RESULTS: Among the 401 study patients, 105 AEs occurred in 67 patients. cTn-I, cTn-T, and CK-MB were all significantly predictive of AEs, with RRs of 3.87 (2.39, 6.26), 3.03 (1.92, 4.79), and 6.45 (4.74, 8.77), respectively. For prediction of AEs, sensitivity for each of the 3 markers was low (cTn-I = 15.38, cTn-T = 24.62, CK-MB = 15.38), while specificity was high (cTn-I = 97.62, cTn-T = 93.15, CK-MB = 99.70). No significant difference in predictive ability was found between cTn-I and cTn-T. However, a positive CK-MB result was a stronger predictor of AEs than either cTn-I (p = 0.01) or cTn-T (p = 0.001). CONCLUSIONS: No significant difference in predictive abilities was found between cTn-I and cTn-T. However, routine testing for both CK-MB and either of the troponins may optimize early identification of high-risk patients so they may be targeted for a higher level of care and consideration of more aggressive therapies.
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Green et al. (1998) conducted a cohort in Possible myocardial ischemia (n=401). Early, single-sample measurements of cTn-I, cTn-T, and CK-MB was evaluated on Occurrence of adverse events during the 14 days after enrollment (RR 3.87, 95% CI 2.39-6.26). Early measurements of cTn-I (RR 3.87), cTn-T (RR 3.03), and CK-MB (RR 6.45) significantly predicted 14-day adverse events, with CK-MB being a stronger predictor than either troponin.
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