Key result
Complete revascularization linked to ~26% lower MACCE risk vs culprit-only PCI in multivessel NSTE-ACS.
Why the study?
Evidence on long-term outcomes after different index PCI strategies in high-risk NSTE-ACS with multivessel disease remained limited.
Does complete revascularisation PCI reduce major adverse cardiac and cerebrovascular events (MACCE) compared to culprit-only revascularisation PCI in patients with high-risk non-ST-elevation acute coronary syndrome and multivessel coronary artery disease?
Cohort (n=754)
Yes
Does complete revascularisation PCI reduce major adverse cardiac and cerebrovascular events (MACCE) compared to culprit-only revascularisation PCI in patients with high-risk non-ST-elevation acute coronary syndrome and multivessel coronary artery disease?
In patients with high-risk NSTE-ACS and multivessel disease, complete revascularisation during index PCI was associated with a modestly lower 5.5-year risk of major adverse cardiac and cerebrovascular events compared to culprit-only PCI without temporal heterogeneity, though the association was sensitive to unmeasured confounding and exclusion of chronic total occlusions.
May support complete revascularization in high-risk NSTE-ACS; hypothesis-generating pending RCTs and sensitivity to unmeasured confounding.
Evidence on long-term outcomes after different index percutaneous coronary intervention (PCI) strategies remains limited in high-risk non-ST-elevation acute coronary syndrome (NSTE-ACS) with multivessel disease. We examined the associations between recorded PCI strategies and outcomes, including whether the primary association varied over time. This multicentre retrospective cohort included 754 patients treated at four tertiary centres from 2016 to 2019: 375 were classified as culprit-only revascularisation (COR-PCI) and 379 as complete revascularisation (CR-PCI). The primary outcome was major adverse cardiac and cerebrovascular events (MACCE), comprising all-cause death, myocardial infarction, stroke, or unplanned revascularisation. The primary analysis used a 25-variable pretreatment propensity score, winsorised stabilised average-treatment-effect inverse probability weights, and a robust Cox model. We also assessed temporal variation, conducted landmark and sensitivity analyses, and calculated E-values. Median follow-up was 66 months. Group-specific effective sample sizes after weighting were 300.0 in the COR-PCI group and 303.9 in the CR-PCI group. CR-PCI was associated with a lower estimated hazard of MACCE than COR-PCI (hazard ratio [HR], 0.74; 95% confidence interval [CI], 0.55–0.999; P = 0.049). HRs were 0.70 (95% CI, 0.35–1.42) during 0–12 months and 0.75 (95% CI, 0.54–1.04) thereafter; temporal heterogeneity was not detected ( P = 0.865). HRs for myocardial infarction, unplanned revascularisation, and major bleeding were 0.61 (95% CI, 0.36–1.05), 0.65 (95% CI, 0.41–1.03), and 1.02 (95% CI, 0.43–2.43), respectively. Excluding patients with recorded total occlusion yielded a MACCE HR of 0.84 (95% CI, 0.60–1.19). E-values were 1.77 for the point estimate and 1.03 for the confidence limit. CR-PCI was associated with a lower estimated hazard of MACCE after weighting, with no evidence of temporal variation.
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Ding et al. (2026) conducted a cohort in High-risk non-ST-elevation acute coronary syndrome (NSTE-ACS) with multivessel coronary artery disease (n=754). Complete revascularization percutaneous coronary intervention (CR-PCI) vs. Culprit-only revascularization percutaneous coronary intervention (COR-PCI) was evaluated on Major adverse cardiac and cerebrovascular events (MACCE: composite of all-cause death, myocardial infarction, stroke, or unplanned revascularisation) (HR 0.74, 95% CI 0.55-0.999, p=0.049). Complete revascularization PCI was associated with a lower long-term hazard of MACCE compared to culprit-only PCI (HR 0.74, 95% CI 0.55-0.999; P=0.049) in high-risk NSTE-ACS with multivessel disease.
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