Key result
Clopidogrel monotherapy is linked to ~24% lower MACE risk and less major bleeding vs aspirin.
Why the study?
Long-term antiplatelet monotherapy is advised after DAPT following PCI, but the optimal agent in real-world practice remains uncertain.
Does clopidogrel monotherapy reduce major adverse cardiovascular events and major bleeding compared to aspirin monotherapy in stable post-PCI patients?
Cohort (n=133,454)
Yes
Does clopidogrel monotherapy reduce major adverse cardiovascular events and major bleeding compared to aspirin monotherapy in stable post-PCI patients?
In stable post-PCI patients, long-term clopidogrel monotherapy significantly reduces both ischemic events and major bleeding compared to aspirin monotherapy.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“Long-term clopidogrel monotherapy may be a preferable alternative to aspirin monotherapy for secondary prevention in real-world clinical practice.”
Clopidogrel monotherapy lowers MACE versus aspirin; confirms benefit in large Asian RCT.
BACKGROUND: After guideline-recommended dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI), long-term antiplatelet monotherapy is advised, but the optimal agent in real-world practice remains uncertain. OBJECTIVES: The authors aimed to compare efficacy and safety of clopidogrel versus aspirin monotherapy in stable post-PCI patients. METHODS: Using the Korean nationwide claims and health examination database, we identified PCI-treated patients maintained on clopidogrel or aspirin monotherapy between 2009 and 2019. The co-primary outcomes were major adverse cardiovascular events (a composite of cardiovascular death, myocardial infarction or ischemic stroke) and major bleeding. RESULTS: Among 133,454 patients receiving DAPT, 67,652 (50.7%) continued with clopidogrel monotherapy and 65,802 (49.3%) continued with aspirin monotherapy. The median durations of DAPT and monotherapy duration were 1.0 year (IQR: 0.8-1.2) and 3.3 years (IQR: 1.3-6.2), respectively. After stabilized inverse probability of treatment weighting, clopidogrel monotherapy was associated with lower risks of major adverse cardiovascular events (HR: 0.759; 95% CI: 0.733-0.785; P < 0.0001) and major bleeding (HR: 0.895; 95% CI: 0.848-0.945; P < 0.0001) compared with aspirin monotherapy. Clopidogrel monotherapy was associated with lower risks of cardiovascular death (HR: 0.605; 95% CI: 0.573-0.638; P < 0.0001), myocardial infarction (HR: 0.921; 95% CI: 0.877-0.968; P = 0.0011), and ischemic stroke (HR: 0.674; 95% CI: 0.624-0.729; P < 0.0001) than aspirin monotherapy. The treatment effects were consistent across prespecified subgroups and DAPT durations. CONCLUSIONS: In the stable post-PCI period, clopidogrel monotherapy may be preferred over aspirin monotherapy for long-term prevention due to its efficacy and safety.
No takes yet. Share an insight, caveat, or question.
Cho et al. (2026) conducted a cohort in Stable post-PCI (n=133,454). Clopidogrel monotherapy vs. Aspirin monotherapy was evaluated on Major adverse cardiovascular events (a composite of cardiovascular death, myocardial infarction or ischemic stroke) (HR 0.759, 95% CI 0.733-0.785, p=< 0.0001). Clopidogrel monotherapy was associated with lower risks of major adverse cardiovascular events (HR 0.759; 95% CI 0.733-0.785; P<0.0001) and major bleeding compared with aspirin monotherapy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: