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High-sensitivity cardiac troponin I at presentation in patients with suspected acute coronary syndrome: a cohort study.

Shah, ASV; Anand, A; Sandoval, Y; Lee, KK; Smith, SW; Adamson, PD; Chapman, AR; Langdon, T; Sandeman, D; Vaswani, A; et al. Shah, ASV; Anand, A; Sandoval, Y; Lee, KK; Smith, SW; Adamson, PD; Chapman, AR; Langdon, T; Sandeman, D; Vaswani, A; Strachan, FE; Ferry, A; Stirzaker, AG; Reid, A; Gray, AJ; Collinson, PO; McAllister, DA; Apple, FS; Newby, DE; Mills, NL; High-STEACS investigators (2015) High-sensitivity cardiac troponin I at presentation in patients with suspected acute coronary syndrome: a cohort study. Lancet, 386 (10012). pp. 2481-2488. ISSN 1474-547X https://doi.org/10.1016/S0140-6736(15)00391-8
SGUL Authors: Collinson, Paul

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Abstract

BACKGROUND: Suspected acute coronary syndrome is the commonest reason for emergency admission to hospital and is a large burden on health-care resources. Strategies to identify low-risk patients suitable for immediate discharge would have major benefits. METHODS: We did a prospective cohort study of 6304 consecutively enrolled patients with suspected acute coronary syndrome presenting to four secondary and tertiary care hospitals in Scotland. We measured plasma troponin concentrations at presentation using a high-sensitivity cardiac troponin I assay. In derivation and validation cohorts, we evaluated the negative predictive value of a range of troponin concentrations for the primary outcome of index myocardial infarction, or subsequent myocardial infarction or cardiac death at 30 days. This trial is registered with ClinicalTrials.gov (number NCT01852123). FINDINGS: 782 (16%) of 4870 patients in the derivation cohort had index myocardial infarction, with a further 32 (1%) re-presenting with myocardial infarction and 75 (2%) cardiac deaths at 30 days. In patients without myocardial infarction at presentation, troponin concentrations were less than 5 ng/L in 2311 (61%) of 3799 patients, with a negative predictive value of 99·6% (95% CI 99·3-99·8) for the primary outcome. The negative predictive value was consistent across groups stratified by age, sex, risk factors, and previous cardiovascular disease. In two independent validation cohorts, troponin concentrations were less than 5 ng/L in 594 (56%) of 1061 patients, with an overall negative predictive value of 99·4% (98·8-99·9). At 1 year, these patients had a lower risk of myocardial infarction and cardiac death than did those with a troponin concentration of 5 ng/L or more (0·6% vs 3·3%; adjusted hazard ratio 0·41, 95% CI 0·21-0·80; p<0·0001). INTERPRETATION: Low plasma troponin concentrations identify two-thirds of patients at very low risk of cardiac events who could be discharged from hospital. Implementation of this approach could substantially reduce hospital admissions and have major benefits for both patients and health-care providers. FUNDING: British Heart Foundation and Chief Scientist Office (Scotland).

Item Type: Article
Additional Information: © Shah et al. Open Access article distributed under the terms of CC BY-NC-ND.
Keywords: Acute Coronary Syndrome, Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Myocardial Infarction, Prognosis, Prospective Studies, Risk Factors, Scotland, Sensitivity and Specificity, Troponin I, High-STEACS investigators, Humans, Myocardial Infarction, Troponin I, Prognosis, Risk Factors, Sensitivity and Specificity, Prospective Studies, Adult, Aged, Aged, 80 and over, Middle Aged, Scotland, Female, Male, Acute Coronary Syndrome, General & Internal Medicine, 11 Medical And Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cardiac (INCCCA)
Journal or Publication Title: Lancet
ISSN: 1474-547X
Language: eng
Dates:
DateEvent
19 December 2015Published
8 October 2015Published Online
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
PG/15/51/31596British Heart FoundationUNSPECIFIED
WT103782AIAWellcome TrustUNSPECIFIED
FS/10/024/28266British Heart FoundationUNSPECIFIED
SP/12/10/29922British Heart FoundationUNSPECIFIED
HICG/1/40Chief Scientist OfficeUNSPECIFIED
103782Wellcome TrustUNSPECIFIED
CH/09/002British Heart FoundationUNSPECIFIED
PubMed ID: 26454362
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/108955
Publisher's version: https://doi.org/10.1016/S0140-6736(15)00391-8

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