Presentation cardiac troponin and early computed tomography coronary angiography in patients with suspected acute coronary syndrome: a pre-specified secondary analysis of the RAPID-CTCA trial.

Acute coronary syndrome Cardiac troponin Computed tomography coronary angiography Non-invasive testing

Journal

European heart journal. Acute cardiovascular care
ISSN: 2048-8734
Titre abrégé: Eur Heart J Acute Cardiovasc Care
Pays: England
ID NLM: 101591369

Informations de publication

Date de publication:
21 Jul 2022
Historique:
received: 25 02 2022
revised: 06 05 2022
accepted: 09 05 2022
pubmed: 2 6 2022
medline: 26 7 2022
entrez: 1 6 2022
Statut: ppublish

Résumé

To evaluate the potential associations between presentation cardiac troponin and the clinical impact of early computed tomography coronary angiography (CTCA) in intermediate-risk patients with suspected acute coronary syndrome. In a large multicentre randomized controlled trial of patients with intermediate-risk chest pain due to suspected acute coronary syndrome, early CTCA had no effect on the primary outcome-death or subsequent Type 1 or 4b myocardial infarction-but reduced the rate of invasive coronary angiography. In this pre-specified secondary analysis, cardiovascular testing and clinical outcomes were compared between those with or without cardiac troponin elevation at presentation. Of 1748 patients, 1004 (57%) had an elevated cardiac troponin concentration and 744 (43%) had a normal concentration. Patients with cardiac troponin elevation had a higher Global Registry of Acute Coronary Events score (132 vs. 91; P < 0.001) and were more likely to have obstructive coronary artery disease (59 vs. 33%; P < 0.001), non-invasive (72 vs. 52%; P < 0.001) and invasive (72 vs. 38%; P < 0.001) testing, coronary revascularization (47 vs. 15%; P < 0.001), and the primary outcome (8 vs. 3%; P = 0.007) at 1 year. However, there was no evidence that presentation cardiac troponin was associated with the relative effects of early CTCA on rates of non-invasive (Pinteraction = 0.33) and invasive (Pinteraction = 0.99) testing, coronary revascularization (Pinteraction = 0.57), or the primary outcome (Pinteraction = 0.41). Presentation cardiac troponin had no demonstrable associations between the effects of early CTCA on reductions in non-invasive and invasive testing, or the lack of effect on coronary revascularization or the primary outcome in intermediate-risk patients with suspected acute coronary syndrome.

Identifiants

pubmed: 35642464
pii: 6596491
doi: 10.1093/ehjacc/zuac057
pmc: PMC9302931
doi:

Substances chimiques

Troponin 0

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

570-579

Subventions

Organisme : National Institute for Health
Organisme : British Heart Foundation
ID : CH/F/21/90010
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/20/10/34966
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/5/34216
Pays : United Kingdom
Organisme : UK National Institute for Health Research Health Technology Assessment Programme
Organisme : Wellcome Trust
Pays : United Kingdom

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

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Auteurs

Kang Ling Wang (KL)

Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.
School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
General Clinical Research Center, Taipei Veterans General Hospital, Taipei, Taiwan.

Carl Roobottom (C)

Department of Radiology, University Hospitals Plymouth NHS Trust, Plymouth, UK.

Jason E Smith (JE)

Emergency Department, University Hospitals Plymouth NHS Trust, Plymouth, UK.

Steve Goodacre (S)

School of Health and Related Research, University of Sheffield, Sheffield, UK.

Katherine Oatey (K)

Edinburgh Clinical Trials Unit, University of Edinburgh, Edinburgh, UK.

Rachel O'Brien (R)

Department of Emergency Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.

Robert F Storey (RF)

Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Nick Curzen (N)

Faculty of Medicine, University of Southampton, Southampton, UK.
Department of Cardiology, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Liza Keating (L)

Department of Emergency Medicine, Royal Berkshire NHS Foundation Trust, Reading, UK.

Attila Kardos (A)

Translational Cardiovascular Research Group, Milton Keynes University Hospital NHS Foundation Trust, Milton Keynes, UK.
Faculty of Medicine and Health Science, University of Buckingham, Buckingham, UK.

Dirk Felmeden (D)

Department of Cardiology, Torbay and South Devon NHS Foundation Trust, Torquay, UK.

Praveen Thokala (P)

School of Health and Related Research, University of Sheffield, Sheffield, UK.

Nicholas L Mills (NL)

Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.
Usher Institute, University of Edinburgh, Edinburgh, UK.

David E Newby (DE)

Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.

Alasdair J Gray (AJ)

Department of Emergency Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK.
Usher Institute, University of Edinburgh, Edinburgh, UK.

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