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The impact of cardiac magnetic resonance viability assessment on the management of patients with ischaemic heart disease and left ventricular dysfunction
Journal of Cardiovascular Magnetic Resonance volume 17, Article number: P140 (2015)
Background
Identifying patients with ischaemic left ventricular dysfunction that would benefit from revascularisation as opposed to medical therapy alone is challenging. Viability assessment has in many centres become a gatekeeper to revascularisation, however its use remains controversial with several prospective randomised trials showing no mortality benefit with this strategy. The aim of this study was to investigate the role of cardiovascular magnetic resonance (CMR) imaging in the decision making process in patients being considered for revascularisation at our institution.
Methods
All patients referred for CMR viability assessment at a single regional centre were identified retrospectively between January 2011 and March 2013 inclusive. CMR scans were reviewed and segmental viability was determined using the AHA segmental model with viability defined as less than 50% delayed contrast enhancement. Patient records were reviewed to determine the ultimate revascularisation strategy as well as patient outcomes.
Results
324 consecutive patients were identified, of which 256 were being considered for revascularisation. The remainder were undergoing viability assessment for other reasons, for example valvular heart disease. Of the patients being considered for revascularisation, 38 (14.4%) had preserved left ventricular (LV) systolic function, 33 (17.3%) mild LV dysfunction, 77 (28.4%) moderate LV dysfunction and 108 (39.9%) severe LV dysfunction. Of the patients with severe LV dysfunction 22 subsequently underwent coronary artery bypass grafting (CABG), 30 had percutaneous coronary intervention (PCI) and the remaining 56 patients were managed medically. The patient characteristics are detailed in table 1. All patients undergoing CABG had at least partial viability in the left anterior descending artery territory. In those who underwent PCI, the results of viability testing changed the proposed management strategy in 30%. By the end of the follow period (median, 28 months), death from any cause occurred in 3 patients (14%) in the CABG group, 4 (13%) in the PCI group and 14 (25%) in the medical-therapy group (p=0.32). Hospitalisation for cardiac causes occurred in 1 patient (5%) in the CABG group, 1 (3%) in the PCI group and 28 (50%) in the medical-therapy group (p <0.001). Hospitalisation in the medical therapy group was primarily related to admissions with heart failure (73%).
Conclusions
Patients undergoing surgical revascularisation had significantly less adverse remodelling than those managed with PCI or medical therapy. Patients undergoing CABG with viability prior to revascularisation demonstrated good outcomes, similar to those undergoing PCI. The medical therapy group had a significantly higher number of non-viable segments and outcome was poor. Further randomised controlled trials using CMR assessment of viability may provide evidence that viability assessment is still beneficial prior to revascularisation in patients with ischaemic cardiomyopathy.
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No external funding.
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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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Cole, B., Douglas, H., Soong, C.M. et al. The impact of cardiac magnetic resonance viability assessment on the management of patients with ischaemic heart disease and left ventricular dysfunction. J Cardiovasc Magn Reson 17 (Suppl 1), P140 (2015). https://doi.org/10.1186/1532-429X-17-S1-P140
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DOI: https://doi.org/10.1186/1532-429X-17-S1-P140