The multicentre, randomised-controlled PREVENT trial (NCT02316886) compared OMT alone with OMT plus preventive PCI of vulnerable non-flow-limiting coronary plaques [1]. The 1,606 participants from research hospitals in South Korea, Japan, Taiwan, and New Zealand) were randomised 1:1 to PCI and OMT or OMT alone. Among the inclusion criteria were stenosis >50% and a negative fractional flow reserve (FFR) of ≥0.80. The primary endpoint was a composite of death from cardiac causes, target vessel myocardial infarction, ischaemic-driven target vessel revascularisation, or hospitalisation for unstable/progressive angina summarised as target vessel failure at 2 years. Prof. Seung-Jung Park (University of Ulsan College of Medicine; Asan Medical Center, South Korea) presented the results.
At 2 years, the results showed a cumulative incidence of target vessel failure in 0.4% of the OMT plus PCI arm, compared with 3.4% on OMT alone. This resulted in a significant hazard ratio of 0.11 (95% CI 0.03–0.36; P=0.0003). After a longer follow-up at 7 years, a consistent advantage of preventive PCI was seen with target vessel failure rates of 6.5% versus 9.4%, respectively (HR 0.54; 95% CI 0.33–0.87; P=0.0097).
Furthermore, the patient-oriented composite of any-cause death, any MI, or any repeat revascularisation at 7 years was significantly reduced in the intervention group: HR 0.69 (95% CI 0.50–0.95; P=0.022). Among the individual primary outcome components, only ischaemia-driven revascularisation and hospitalisation for angina were significantly in favour of the PCI group, other components showed no between-group difference. Also, no statistical differences were determined for secondary endpoints like bleeding events and stroke.
“Our key findings might provide a novel insight into the role of a preventive PCI on non-flow-limiting high-risk vulnerable plaques in the future,” concluded Prof. Park.
- Park SJ. Preventive PCI or medical therapy alone for atherosclerotic coronary vulnerable plaques. LB5, Session 412, ACC 2024 Scientific Session, 6–8 April, Atlanta, USA.
- Park SJ, et al. Lancet; April 8. DOI: 10.1016/S0140-6736(24)00413-6.
Medical writing support was provided by Karin Drooff, MPH
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