1- or 3-Month DAPT in Patients With HBR With or Without Oral Anticoagulant Therapy After PCI
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Updated: Jul 14, 2025

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Marco Valgimigli1, Alessandro Spirito2, Samantha Sartori2
1Cardiocentro Ticino Institue, Ente Ospedaliero Cantonale, Lugano and Bern University Hospital, Bern, Switzerland.
Insights
Shorter dual antiplatelet therapy (DAPT) of 1 month, compared to 3 months, showed similar risks for death or myocardial infarction (MI) in patients on oral anticoagulation (OAC). One-month DAPT also significantly reduced bleeding events, regardless of OAC use.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Pharmacology
Background:
- Optimal duration of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) in patients on long-term oral anticoagulation (OAC) is not well-established.
- Patients on OAC often have high bleeding risk, complicating antiplatelet therapy decisions post-PCI.
Purpose of the Study:
- To evaluate the comparative effectiveness and safety of 1-month versus 3-month DAPT in patients undergoing PCI with a cobalt-chromium everolimus-eluting stent.
- To specifically assess outcomes in patients with and without concomitant OAC therapy within the XIENCE Short DAPT program.
Main Methods:
- Analysis of the XIENCE Short DAPT program, enrolling high bleeding risk patients post-PCI.
- Comparison of 1-month vs. 3-month DAPT discontinuation in patients free from ischemic events.
- Propensity score stratification used to compare outcomes (all-cause death, MI, BARC 2-5 bleeding) between 1- and 3-month DAPT groups, with and without OAC.
Main Results:
- Among patients on OAC, 1-month DAPT showed similar rates of death or MI compared to 3-month DAPT (7.4% vs. 8.8%; P=0.139).
- One-month DAPT significantly reduced Bleeding Academic Research Consortium (BARC) types 2-5 bleeding in OAC patients (adjusted HR: 0.71; P=0.046).
- These findings were consistent across patients with and without OAC, indicating no significant interaction.
Conclusions:
- A 1-month DAPT duration is associated with similar ischemic event rates but lower bleeding rates compared to 3-month DAPT after PCI in high bleeding risk patients.
- These benefits of shorter DAPT duration are maintained irrespective of concomitant oral anticoagulation therapy.
Background:
The optimal duration of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) in patients on long-term oral anticoagulation (OAC) therapy is still uncertain.
Objectives:
The aim of this analysis was to assess the effects of 1- vs 3-month DAPT in patients with and those without concomitant OAC included in the XIENCE Short DAPT program.
Methods:
The XIENCE Short DAPT program enrolled patients with high bleeding risk who underwent successful PCI with a cobalt-chromium everolimus-eluting stent. DAPT was discontinued at 1 or 3 months in patients free from ischemic events and adherent to treatment. The effect of 1- vs 3-month DAPT was compared in patients with and those without OAC using propensity score stratification. The primary endpoint was all-cause death or any myocardial infarction (MI). The key secondary endpoint was Bleeding Academic Research Consortium (BARC) types 2 to 5 bleeding. Outcomes were assessed from 1 to 12 months after index PCI.
Results:
Among 3,364 event-free patients, 1,462 (43%) were on OAC. Among OAC patients, the risk for death or MI was similar between 1- and 3-month DAPT (7.4% vs 8.8%; adjusted HR: 0.74; 95% CI: 0.49-1.11; P = 0.139), whereas BARC types 2 to 5 bleeding was lower with 1-month DAPT (adjusted HR: 0.71; 95% CI: 0.51-0.99; P = 0.046). These effects were consistent in patients with and those without OAC (P for interaction = NS).
Conclusions:
Between 1 and 12 months after PCI, 1-month compared with 3-month DAPT was associated with similar rates of all-cause death or MI and a reduced rate of BARC types 2 to 5 bleeding, irrespective of OAC treatment.
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