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Published on: February 26, 2013
Antithrombotic Strategy in Atrial Fibrillation Patients Undergoing Percutaneous Coronary Intervention
1Department of Internal Medicine, Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.
Insights
Dual therapy with non-vitamin K antagonist oral anticoagulants (NOACs) offers a safer alternative to traditional triple therapy for patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI), significantly reducing bleeding risks.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Managing antithrombotic therapy for patients with atrial fibrillation (AF) after percutaneous coronary intervention (PCI) is complex.
- Traditional warfarin-based triple therapy is associated with high rates of major bleeding (up to 12% annually).
Purpose of the Study:
- To review the evidence supporting dual antithrombotic therapy with non-vitamin K antagonist oral anticoagulants (NOACs) in AF patients post-PCI.
- To emphasize the potential for reduced bleeding complications.
Main Methods:
- Review of clinical trial data, focusing on the WOEST trial and subsequent studies.
- Analysis of efficacy and safety outcomes for dual versus triple antithrombotic regimens.
Main Results:
- Dual therapy without aspirin demonstrated significantly lower bleeding risks compared to triple therapy.
- Thromboembolic event rates were similar between dual and triple therapy groups.
- NOAC-based dual therapy is emerging as an optimal regimen.
Conclusions:
- Dual therapy, particularly with NOACs, represents a favorable strategy for AF patients undergoing PCI.
- This approach balances the need for thromboembolic event prevention with a substantial reduction in bleeding risk.
Abstract:
Choosing antithrombotic regimens for patients with atrial fibrillation (AF) who underwent percutaneous coronary intervention (PCI) with stent placement is challenging. Until recently, the guidelines recommended warfarin-based triple therapy, which causes frequent major bleeding events in up to 12% of patients during the first year of treatment. The WOEST trial, however, revealed that dual therapy, by without aspirin, resulted in significantly lower bleeding risks with similar thromboembolic events to triple therapy. Subsequently, efforts to seek the optimal dual therapy regimens, especially with the combination of a non-vitamin K antagonist oral anticoagulant (NOAC), were initiated. This review highlights the evidence for dual therapy using an NOAC for patients with AF who underwent PCI, with an emphasis on reduced bleeding risk.
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