Why the study?
Does revascularisation improve ischaemia burden compared with medical therapy in patients with CAD and EF ≤40%?
Does revascularisation improve ischaemia burden compared with medical therapy in patients with CAD and EF ≤40%?
In patients with CAD and reduced EF, revascularisation improves ischaemia burden compared to medical therapy, though ischaemia worsening on nuclear imaging may paradoxically indicate viable myocardium and is associated with reduced death/MI risk.
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May support revascularisation for ischaemia reduction in low-EF CAD; hypothesis-generating for worsening ischaemia as viability marker, needing RCTs.
OBJECTIVE: Nuclear imaging data demonstrate that revascularisation leads to favourable effects on ischaemia burden and improved outcomes compared with medical therapy (MT). In patients with heart failure (HF), the effects of MT versus revascularisation on ischaemia change and its independent prognostic significance requires investigation. METHODS: From the Duke Databank, we performed a retrospective analysis of 278 consecutive patients with coronary artery disease (CAD) and ejection fraction (EF) ≤40%, who underwent 2 serial myocardial perfusion scans between 1993 and 2009. Ischaemia change was calculated for patients undergoing MT alone, or revascularisation. Cox proportional hazards regression modelling was used to identify factors associated with death/myocardial infarction (MI). RESULTS: The magnitude of ischeamia reduction was greater with revascularisation than with MT alone (median change of -6% vs 0%, p<0.001). With revascularisation, more patients experienced ≥5% ischaemia reduction compared with MT (52% vs 25%, p<0.01) and a similar percentage experienced ≥5% ischaemia worsening (13% vs 18%, p=0.37). After risk adjustment, ≥5% ischaemia worsening was associated with decreased death/MI (HR=0.58; 95% CI 0.36 to 0.96). CONCLUSIONS: In patients with HF with CAD, revascularisation improves long-term ischaemia burden compared with MT. Ischaemia worsening on nuclear imaging was associated with reduced risk of death/MI, potentially related to development of ischaemic viable myocardium as opposed to scar tissue.
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Mentz et al. (2015) studied this question.
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