Anand, A;
Lee, KK;
Chapman, AR;
Ferry, AV;
Adamson, PD;
Strachan, FE;
Berry, C;
Findlay, I;
Cruikshank, A;
Reid, A;
et al.
Anand, A; Lee, KK; Chapman, AR; Ferry, AV; Adamson, PD; Strachan, FE; Berry, C; Findlay, I; Cruikshank, A; Reid, A; Collinson, PO; Apple, FS; McAllister, DA; Maguire, D; Fox, KAA; Newby, DE; Tuck, C; Harkess, R; Keerie, C; Weir, CJ; Parker, RA; Gray, A; Shah, ASV; Mills, NL; HiSTORIC Investigators†
(2021)
High-Sensitivity Cardiac Troponin on Presentation to Rule Out Myocardial Infarction: A Stepped-Wedge Cluster Randomized Controlled Trial.
Circulation, 143 (23).
pp. 2214-2224.
ISSN 1524-4539
https://doi.org/10.1161/CIRCULATIONAHA.120.052380
SGUL Authors: Collinson, Paul
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Abstract
Background: High-sensitivity cardiac troponin assays enable myocardial infarction to be ruled out earlier, but the safety and efficacy of this approach is uncertain. We investigated whether an early rule-out pathway is safe and effective for patients with suspected acute coronary syndrome. Methods: We performed a stepped-wedge cluster randomized controlled trial in the emergency departments of 7 acute care hospitals in Scotland. Consecutive patients presenting with suspected acute coronary syndrome between December 2014 and December 2016 were included. Sites were randomized to implement an early rule-out pathway where myocardial infarction was excluded if high-sensitivity cardiac troponin I concentrations were <5 ng/L at presentation. During a previous validation phase, myocardial infarction was ruled out when troponin concentrations were <99th percentile at 6 to 12 hours after symptom onset. The coprimary outcome was length of stay (efficacy) and myocardial infarction or cardiac death after discharge at 30 days (safety). Patients were followed for 1 year to evaluate safety and other secondary outcomes. Results: We enrolled 31 492 patients (59±17 years of age [mean±SD]; 45% women) with troponin concentrations <99th percentile at presentation. Length of stay was reduced from 10.1±4.1 to 6.8±3.9 hours (adjusted geometric mean ratio, 0.78 [95% CI, 0.73–0.83]; P<0.001) after implementation and the proportion of patients discharged increased from 50% to 71% (adjusted odds ratio, 1.59 [95% CI, 1.45–1.75]). Noninferiority was not demonstrated for the 30-day safety outcome (upper limit of 1-sided 95% CI for adjusted risk difference, 0.70% [noninferiority margin 0.50%]; P=0.068), but the observed differences favored the early rule-out pathway (0.4% [57/14 700] versus 0.3% [56/16 792]). At 1 year, the safety outcome occurred in 2.7% (396/14 700) and 1.8% (307/16 792) of patients before and after implementation (adjusted odds ratio, 1.02 [95% CI, 0.74–1.40]; P=0.894), and there were no differences in hospital reattendance or all-cause mortality. Conclusions: Implementation of an early rule-out pathway for myocardial infarction reduced length of stay and hospital admission. Although noninferiority for the safety outcome was not demonstrated at 30 days, there was no increase in cardiac events at 1 year. Adoption of this pathway would have major benefits for patients and health care providers.
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Additional Information: | © 2021 The Authors. Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made. | ||||||||||||||||||||||||||||||||||||
Keywords: | biomarkers, chest pain, myocardial infarction, randomized controlled trial, troponin, HiSTORIC Investigators†, : high-sensitivity cardiac troponin, early rule-out pathway, randomized controlled tria, stepped-wedge cluster, Cardiovascular System & Hematology, 1103 Clinical Sciences, 1102 Cardiorespiratory Medicine and Haematology, 1117 Public Health and Health Services | ||||||||||||||||||||||||||||||||||||
SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) | ||||||||||||||||||||||||||||||||||||
Journal or Publication Title: | Circulation | ||||||||||||||||||||||||||||||||||||
ISSN: | 1524-4539 | ||||||||||||||||||||||||||||||||||||
Language: | eng | ||||||||||||||||||||||||||||||||||||
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Publisher License: | Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0 | ||||||||||||||||||||||||||||||||||||
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PubMed ID: | 33752439 | ||||||||||||||||||||||||||||||||||||
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URI: | https://openaccess.sgul.ac.uk/id/eprint/113124 | ||||||||||||||||||||||||||||||||||||
Publisher's version: | https://doi.org/10.1161/CIRCULATIONAHA.120.052380 |
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