Back to Search Start Over

Clinical outcomes for chest pain patients discharged home from emergency departments using high-sensitivity versus conventional cardiac troponin assays.

Authors :
Lau G
Koh M
Kavsak PA
Schull MJ
Armstrong DWJ
Udell JA
Austin PC
Wang X
Ko DT
Source :
American heart journal [Am Heart J] 2020 Mar; Vol. 221, pp. 84-94. Date of Electronic Publication: 2019 Dec 11.
Publication Year :
2020

Abstract

Background: High-sensitivity cardiac troponin (hs-cTn) assays enhance detection of lower circulating troponin concentrations, but the impact on outcomes in clinical practice is unclear. Our objective was to compare outcomes of chest pain patients discharged from emergency departments (EDs) using hs-cTn and conventional troponin (cTn) assays.<br />Methods: We conducted an observational study of chest pain patients aged 40-105 years who presented to an ED from April 1, 2013, to March 31, 2017, and were discharged home. We compared 30-day and 1-year outcomes of EDs that used hs-cTn versus cTn assays. The primary outcome was a composite of all-cause death, myocardial infarction or unstable angina. Comparisons were conducted with (1) no adjustment; (2) adjustment for demographic, socioeconomic, and hospital characteristics; and (3) full clinical adjustment.<br />Results: Among the 394,910 patients, 62,138 (15.7%) were evaluated at hs-cTn EDs and 332,772 (84.3%) were evaluated at cTn EDs. Patients discharged from hs-cTn EDs were less likely to have diabetes, hypertension, or prior heart disease. At 30 days, the unadjusted primary outcome rate was lower in hs-cTn EDs (0.9% vs 1.0%, P < .001). The 30-day hazard ratios for the primary outcome were 0.84 (95% CI 0.77-0.92) for no adjustment and 0.98 (95% CI 0.88-1.08) for full adjustment. Over 1 year, patients discharged from hs-cTn EDs had significantly fewer primary outcomes (3.7% vs 4.1%, P < .001) and lower hazard ratio (0.93; 95% CI 0.89-0.98) even after full adjustment.<br />Conclusions: Hs-cTn testing was associated with a significantly lower adjusted hazard of myocardial infarction, angina, and all-cause hospitalization at 1 year but not 30 days.<br />Competing Interests: Disclosures Dr Kavsak has received grants/reagents/consultant/advisor /honoraria from Abbott Laboratories, Abbott Point of Care, Abbott Diagnostics Division Canada, Beckman Coulter, Ortho Clinical Diagnostics, Randox Laboratories, Roche Diagnostics, and Siemens Healthcare Diagnostics. McMaster University has filed patents with Dr Kavsak listed as an inventor in the acute cardiovascular biomarker field. Dr Udell is supported in part by a Heart and Stroke Foundation of Canada National New Investigator/Ontario Clinician Scientist Award, Women's College Research Institute, and the Department of Medicine, Women's College Hospital; Peter Munk Cardiac Center, University Health Network; and Department of Medicine and Heart and Stroke Richard Lewar Center of Excellence in Cardiovascular Research, University of Toronto. Dr Ko and Dr Austin are supported by Mid-Career Investigator Awards from the Heart and Stroke Foundation, Ontario Provincial Office.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-6744
Volume :
221
Database :
MEDLINE
Journal :
American heart journal
Publication Type :
Academic Journal
Accession number :
31954328
Full Text :
https://doi.org/10.1016/j.ahj.2019.12.007