Key result
DAPT >12 months after bifurcation PCI is linked to ~79% lower MACE risk versus <6 months.
Why the study?
The optimal duration of DAPT after PCI remains debated, particularly for bifurcation lesions associated with increased thrombotic risk.
Does shorter duration of dual antiplatelet therapy increase the risk of major adverse cardiac events in patients undergoing percutaneous coronary intervention for bifurcation lesions?
Cohort (n=6,729)
Does shorter duration of dual antiplatelet therapy increase the risk of major adverse cardiac events in patients undergoing percutaneous coronary intervention for bifurcation lesions?
Hazard Ratio: 4.8 (95% CI 1.8–12.8)
Absolute Event Rate: 19.5% vs 5.9%
p-value: p=<0.001
In patients undergoing PCI for bifurcation lesions, particularly those with acute coronary syndrome, DAPT duration >12 months is associated with a significantly lower risk of MACE compared to shorter durations.
Longer DAPT was associated with lower MACE after bifurcation PCI; leaves open optimal duration pending randomized trials.
Background The optimal duration of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) remains debated, particularly for bifurcation lesions, which are associated with increased thrombotic risk. Purpose To evaluate the impact of different DAPT duration regimens on clinical outcomes in a large cohort of patients treated with PCI on bifurcation lesions. Methods This study analyzed data from the BIFURCAT-ULTRA registry, including patients treated with PCI for bifurcation lesions. DAPT duration was categorized as <6, 6–11, 12, and >12 months. The primary endpoint was major adverse cardiac events (MACE), a composite of all-cause death, myocardial infarction, target lesion revascularization, and stent thrombosis. Results Among 6,729 patients, 425 received DAPT <6 months, 568 for 6–11 months, 2,878 for 12 months, and 2,858 for >12 months. At 800-day follow-up, MACE rates were higher with shorter DAPT (19.5% vs. 10.2% vs. 9.9% vs. 5.9%, p<0.001). Adjusted hazard ratios for MACE were significantly higher for DAPT <6 months (HR 4.8, 95% CI 1.8–12.8), 6–11 months (HR 2.8, 95% CI 1.5–5.0), and 12 months (HR 2.7, 95% CI 1.4–5.0) compared to >12 months (Figure 1, Table 1). This trend was consistent in acute coronary syndrome (ACS) patients but not in stable patients. Conclusion In PCI-treated bifurcation lesions, particularly in ACS patients, shorter DAPT duration is associated with a higher risk of adverse events. These findings highlight the need to consider bifurcation lesions as a key factor in tailoring DAPT duration.Figure 1 Table 1
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Nebiolo et al. (2025) conducted a cohort in Bifurcation lesions treated with PCI (n=6,729). Shorter DAPT duration (<6 months) vs. DAPT >12 months was evaluated on Major adverse cardiac events (MACE), a composite of all-cause death, myocardial infarction, target lesion revascularization, and stent thrombosis (HR 4.8, 95% CI 1.8-12.8, p=<0.001). Shorter DAPT duration (<6 months) after PCI for bifurcation lesions was associated with a higher risk of MACE compared to >12 months (19.5% vs 5.9%; HR 4.8, 95% CI 1.8-12.8, p<0.001).
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