Use of High-Sensitivity Troponin T to Identify Patients With Acute Heart Failure at Lower Risk for Adverse Outcomes
dc.contributor.author | Pang, Peter S. | |
dc.contributor.author | Teerlink, John R. | |
dc.contributor.author | Voors, Adriaan A. | |
dc.contributor.author | Ponikowski, Piotr | |
dc.contributor.author | Greenberg, Barry H. | |
dc.contributor.author | Filippatos, Gerasimos | |
dc.contributor.author | Felker, G. Michael | |
dc.contributor.author | Davison, Beth A. | |
dc.contributor.author | Cotter, Gad | |
dc.contributor.author | Kriger, Joshua | |
dc.contributor.author | Prescott, Margaret F. | |
dc.contributor.author | Hua, Tsushung A. | |
dc.contributor.author | Severin, Thomas | |
dc.contributor.author | Metra, Marco | |
dc.contributor.department | Department of Emergency Medicine, IU School of Medicine | en_US |
dc.date.accessioned | 2016-11-03T15:01:06Z | |
dc.date.available | 2016-11-03T15:01:06Z | |
dc.date.issued | 2016-07 | |
dc.description.abstract | Objectives The aim of this study was to determine if a baseline high-sensitivity troponin T (hsTnT) value ≤99th percentile upper reference limit (0.014 μg/l [“low hsTnT”]) identifies patients at low risk for adverse outcomes. Background Approximately 85% of patients who present to emergency departments with acute heart failure are admitted. Identification of patients at low risk might decrease unnecessary admissions. Methods A post-hoc analysis was conducted from the RELAX-AHF (Serelaxin, Recombinant Human Relaxin-2, for Treatment of Acute Heart Failure) trial, which randomized patients within 16 h of presentation who had systolic blood pressure >125 mm Hg, mild to moderate renal impairment, and N-terminal pro–brain natriuretic peptide ≥1,600 ng/l to serelaxin versus placebo. Linear regression models for continuous endpoints and Cox models for time-to-event endpoints were used. Results Of the 1,076 patients with available baseline hsTnT values, 107 (9.9%) had low hsTnT. No cardiovascular (CV) deaths through day 180 were observed in the low-hsTnT group compared with 79 CV deaths (7.3%) in patients with higher hsTnT. By univariate analyses, low hsTnT was associated with lower risk for all 5 primary outcomes: 1) days alive and out of the hospital by day 60; 2) CV death or rehospitalization for heart failure or renal failure by day 60; 3) length of stay; 4) worsening heart failure through day 5; and 5) CV death through day 180. After multivariate adjustment, only 180-day CV mortality remained significant (hazard ratio: 0.0; 95% confidence interval: 0.0 to 0.736; p = 0.0234; C-index = 0.838 [95% confidence interval: 0.798 to 0.878]). Conclusions No CV deaths through day 180 were observed in patients with hsTnT levels ≤0.014 μg/l despite high N-terminal pro–brain natriuretic peptide levels. Low baseline hsTnT may identify patients with acute heart failure at very low risk for CV mortality. | en_US |
dc.eprint.version | Final published version | en_US |
dc.identifier.citation | Pang, P. S., Teerlink, J. R., Voors, A. A., Ponikowski, P., Greenberg, B. H., Filippatos, G., ... & Prescott, M. F. (2016). Use of High-Sensitivity Troponin T to Identify Patients With Acute Heart Failure at Lower Risk for Adverse Outcomes: An Exploratory Analysis From the RELAX-AHF Trial. JACC: Heart Failure. http://dx.doi.org/10.1016/j.jchf.2016.02.009 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/11348 | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | 10.1016/j.jchf.2016.02.009 | en_US |
dc.relation.journal | JACC: Heart Failure | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | Publisher | en_US |
dc.subject | acute heart failure | en_US |
dc.subject | emergency department | en_US |
dc.subject | risk stratification | en_US |
dc.title | Use of High-Sensitivity Troponin T to Identify Patients With Acute Heart Failure at Lower Risk for Adverse Outcomes | en_US |
dc.type | Article | en_US |