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J Am Coll Cardiol, 2006; 48:1755-1762, doi:10.1016/j.jacc.2006.05.075
(Published online 16 October 2006). © 2006 by the American College of Cardiology Foundation |
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* Division of Cardiology
Department of Emergency Medicine
Department of Pathology, Beth Israel Medical Center, New York, New York
|| St. Luke's-Roosevelt Hospital, New York, New York
Manuscript received February 15, 2006; revised manuscript received April 21, 2006, accepted May 15, 2006.
* Reprint requests and correspondence: Dr. Daniel A. Waxman, Beth Israel Medical Center, Department of Emergency Medicine, First Avenue at 16th Street, New York, New York 10003 (Email: dwaxman{at}chpnet.org).
OBJECTIVES: We evaluated log-transformed troponin I as a predictor of mortality in 2 independent populations.
BACKGROUND: The troponin I result is typically dichotomized by a single diagnostic cutoff. Its performance as a continuous prognostic variable has not previously been well-characterized.
METHODS: We studied the first troponin I sent from the emergency department (ED) as a predictor of all-cause inpatient mortality, with retrospectively gathered data. We performed our study in 2 stages, deriving our model with data from a single medical center and validating it with data from another. Subjects included every patient who had a troponin I sent from the ED during the period from November 2002 to January 2005. We assessed prognostic independence by including other potential confounders in nested logistic regression models. The troponin assay was identical at both sites (Ortho-Clinical Diagnostics, Rochester, New York).
RESULTS: There were a total of 34,227 patients (12,135 derivation and 22,092 validation). Odds ratio for mortality as a function of log10-troponin was 2.08 (95% confidence interval [CI] 1.85 to 2.32) in the derivation set and 2.07 (95% CI 1.92 to 2.24) for the validation set. Troponin I remained a strong predictor after inclusion of age, electrocardiogram normality, renal insufficiency, arrival mode, chief complaint, admission diagnosis, and abnormal vital signs into bivariate and nested multivariate models.
CONCLUSIONS: The presence of any detectible troponin I at ED presentation is associated with increased inpatient mortality. In 2 distinct clinical populations, the odds of death approximately doubled with any 10-fold increase in troponin result. This held true at levels below current diagnostic cutoffs. The placement and utility of dichotomous cutoffs might merit reconsideration.
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