Prognostic impact of inducible ischaemia in ischaemic left ventricular dysfunction: the REVIVED-BCIS2 trial

Retrospective observational data suggest that the presence and extent of inducible myocardial ischaemia predict future adverse cardiac events in patients with ischaemic heart disease. However, several randomized trials have failed to identify an association between the burden of inducible ischaemia and outcomes in patients with stable coronary artery disease (CAD) assigned to medical therapy alone or revascularization.1,2 Despite this, the presence and extent of ischaemia are commonly used to guide revascularization of stable patients. Notably, many of these analyses excluded patients with impaired left ventricular (LV) function. REVIVED-BCIS2 was a prospective, multi-centre, randomized controlled trial, investigating whether percutaneous coronary intervention (PCI) improved clinical outcomes in patients with severe ischaemic LV dysfunction (ILVD), compared with optimal medical therapy (OMT) alone.3,4 Whilst ischaemia testing was not mandated by protocol, it was performed as part of routine clinical practice in selected patients. Based on these data, we sought to determine whether the presence and extent of ischaemia detected on stress perfusion cardiac magnetic resonance (CMR) imaging predict clinical outcomes and response to PCI, in patients with ILVD.

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Publication Details

Journal
European Heart Journal
Published
2024-12-11
DOI
https://doi.org/10.1093/eurheartj/ehae844
Citations
7
Primary Topic
Cardiac Imaging and Diagnostics
Type
article
Field-Weighted Citation Impact
2.83

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article

Prognostic impact of inducible ischaemia in ischaemic left ventricular dysfunction: the REVIVED-BCIS2 trial

Adam K McDiarmid, John Pierre Greenwood, Gerry P McCann, Holly Morgan et al.
7 citations
European Heart Journal
Cardiac Imaging and Diagnostics
2.83
article

Prognostic impact of inducible ischaemia in ischaemic left ventricular dysfunction: the REVIVED-BCIS2 trial

Adam K McDiarmid, John Pierre Greenwood, Gerry P McCann, Holly Morgan, Muhummad Sohaib Nazir, Amedeo Chiribiri, Divaka Perera, M. J. Ryan, Matthew Dodd, Matthew Li Kam Wa
article en
7 citations

Abstract

Retrospective observational data suggest that the presence and extent of inducible myocardial ischaemia predict future adverse cardiac events in patients with ischaemic heart disease. However, several randomized trials have failed to identify an association between the burden of inducible ischaemia and outcomes in patients with stable coronary artery disease (CAD) assigned to medical therapy alone or revascularization.1,2 Despite this, the presence and extent of ischaemia are commonly used to guide revascularization of stable patients. Notably, many of these analyses excluded patients with impaired left ventricular (LV) function. REVIVED-BCIS2 was a prospective, multi-centre, randomized controlled trial, investigating whether percutaneous coronary intervention (PCI) improved clinical outcomes in patients with severe ischaemic LV dysfunction (ILVD), compared with optimal medical therapy (OMT) alone.3,4 Whilst ischaemia testing was not mandated by protocol, it was performed as part of routine clinical practice in selected patients. Based on these data, we sought to determine whether the presence and extent of ischaemia detected on stress perfusion cardiac magnetic resonance (CMR) imaging predict clinical outcomes and response to PCI, in patients with ILVD.

European Heart JournalVol. 46(5)
University of London (GB), Baker Heart and Diabetes Institute (AU), University of Leicester (GB), King's College London (GB), Guy's and St Thomas' NHS Foundation Trust (GB), Leeds Teaching Hospitals NHS Trust (GB), Newcastle upon Tyne Hospitals NHS Foundation Trust (GB), British Heart Foundation (GB), London School of Hygiene & Tropical Medicine (GB), Royal Brompton Hospital (GB), NIHR Leicester Biomedical Research Centre (GB)
National Institute for Health and Care Research, British Heart Foundation
Good health and well-being
Openalex Percentile: Top 9%
Cardiac Imaging and Diagnostics
2.83
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