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Extended Dual Antiplatelet Therapy for Multivessel Coronary Artery Disease
Jinwei Tian1,2,3,4, Zhuozhong Wang1,4, Yan Wang1
1Department of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Extending dual antiplatelet therapy (DAPT) for 12 months in patients with multivessel coronary artery disease significantly reduced ischemic events without increasing bleeding risk. This extended DAPT regimen offers a safer and more effective treatment option for these patients.
Area of Science:
- Cardiology
- Interventional Cardiology
- Clinical Trials
Background:
- Multivessel coronary artery disease (CAD) management often involves 12 months of dual antiplatelet therapy (DAPT) post-stenting to prevent ischemic events.
- The optimal duration of DAPT in event-free patients with multivessel CAD remains uncertain.
Purpose of the Study:
- To evaluate the efficacy and safety of extending DAPT beyond 12 months in patients with multivessel CAD.
Main Methods:
- An open-label, randomized trial involving 8250 patients across 97 centers in China.
- Patients received either an additional 12 months of DAPT (clopidogrel plus aspirin) or aspirin monotherapy.
- Primary endpoints included major adverse cardiovascular events and clinically relevant or major bleeding (BARC type ≥2).
Main Results:
- Extended DAPT showed a significantly lower incidence of primary efficacy endpoint events (5.8% vs. 6.8%; HR, 0.82; P=0.03).
- No significant increase in clinically relevant or major bleeding was observed between the extended DAPT group and the aspirin monotherapy group (1.4% vs. 1.5%; HR, 0.89; P=0.54).
Conclusions:
- Extending DAPT for an additional 12 months in stable patients with multivessel CAD after drug-eluting stent implantation reduces ischemic events.
- This extended DAPT strategy is safe, showing no increased risk of bleeding compared to aspirin monotherapy.
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