• J. Am. Coll. Cardiol. · Oct 2013

    Randomized Controlled Trial Multicenter Study

    Validation of high-sensitivity troponin I in a 2-hour diagnostic strategy to assess 30-day outcomes in emergency department patients with possible acute coronary syndrome.

    • Louise Cullen, Christian Mueller, William A Parsonage, Karin Wildi, Jaimi H Greenslade, Raphael Twerenbold, Sally Aldous, Bernadette Meller, Jillian R Tate, Tobias Reichlin, Christopher J Hammett, Christa Zellweger, Jacobus P J Ungerer, Maria Rubini Gimenez, Richard Troughton, Karsten Murray, Anthony F T Brown, Mira Mueller, Peter George, Tamina Mosimann, Dylan F Flaws, Miriam Reiter, Arvin Lamanna, Philip Haaf, Christopher J Pemberton, A Mark Richards, Kevin Chu, Christopher M Reid, William Frank Peacock, Allan S Jaffe, Christopher Florkowski, Joanne M Deely, and Martin Than.
    • Royal Brisbane and Women's Hospital, Herston, Australia; Queensland University of Technology, Brisbane, Australia. Electronic address: louise_cullen@health.qld.gov.au.
    • J. Am. Coll. Cardiol. 2013 Oct 1;62(14):1242-9.

    ObjectivesThe study objective was to validate a new high-sensitivity troponin I (hs-TnI) assay in a clinical protocol for assessing patients who present to the emergency department with chest pain.BackgroundProtocols using sensitive troponin assays can accelerate the rule out of acute myocardial infarction in patients with low-risk (suspected) acute coronary syndrome (ACS).MethodsThis study evaluated 2 prospective cohorts of patients in the emergency department with ACS in an accelerated diagnostic pathway integrating 0- and 2-h hs-TnI results, Thrombolysis In Myocardial Infarction (TIMI) risk scores, and electrocardiography. Strategies to identify low-risk patients incorporated TIMI risk scores= 0 or ≤ 1. The primary endpoint was a major adverse cardiac event (MACE) within 30 days.ResultsIn the primary cohort, 1,635 patients were recruited and had 30-day follow-up. A total of 247 patients (15.1%) had a MACE. The finding of no ischemic electrocardiogram and hs-TnI ≤ 26.2 ng/l with the TIMI = 0 and TIMI ≤ 1 pathways, respectively, classified 19.6% (n = 320) and 41.5% (n = 678) of these patients as low risk; 0% (n = 0) and 0.8% (n = 2) had a MACE, respectively. In the secondary cohort, 909 patients were recruited. A total of 156 patients (17.2%) had a MACE. The TIMI = 0 and TIMI ≤ 1 pathways classified 25.3% (n = 230) and 38.6% (n = 351), respectively, of these patients as low risk; 0% (n = 0) and 0.8% (n = 1) had a MACE, respectively. Sensitivity, specificity, and negative predictive value for TIMI = 0 in the primary cohort were 100% (95% confidence interval [CI]: 98.5% to 100%), 23.1% (95% CI: 20.9% to 25.3%), and 100% (95% CI: 98.8% to 100%), respectively. Sensitivity, specificity, and negative predictive value for TIMI ≤ 1 in the primary cohort were 99.2 (95% CI: 97.1 to 99.8), 48.7 (95% CI: 46.1 to 51.3), and 99.7 (95% CI: 98.9 to 99.9), respectively. Sensitivity, specificity, and negative value for TIMI ≤ 1 in the secondary cohort were 99.4% (95% CI: 96.5 to 100), 46.5% (95% CI: 42.9 to 50.1), and 99.7% (95% CI: 98.4 to 100), respectively.ConclusionsAn early-discharge strategy using an hs-TnI assay and TIMI score ≤ 1 had similar safety as previously reported, with the potential to decrease the observation periods and admissions for approximately 40% of patients with suspected ACS. (Advantageous Predictors of Acute Coronary Syndromes Evaluation [APACE] Study, NCT00470587; A 2 hr Accelerated Diagnostic Protocol to Assess patients with chest Pain symptoms using contemporary Troponins as the only biomarker [ADAPT]: a prospective observational validation study, ACTRN12611001069943).Copyright © 2013 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

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