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Updated: Apr 1, 2026

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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
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Risk of Gastrointestinal Bleeding in Patients Who Have Undergone Left Atrial Appendage Closure
Christine Son1, Simran Koura1, Jordan Simpson2
1Department of Internal Medicine.
Journal of Clinical Gastroenterology
|March 31, 2026
Summary
Patients receiving the Watchman device for atrial fibrillation (AF) still face gastrointestinal (GI) bleeding risks. Higher CHA2DS2-VASc and HAS-BLED scores independently predict increased GI bleeding after the Watchman procedure.
Area of Science:
- Cardiology
- Gastroenterology
- Medical Devices
Background:
- Anticoagulation is standard for stroke prevention in atrial fibrillation (AF) patients at risk of gastrointestinal (GI) bleeding.
- Left atrial appendage closure (LAAC) using the Watchman device offers an alternative for patients with high thromboembolic or bleeding risks.
Purpose of the Study:
- To investigate the incidence of GI bleeding in patients with nonvalvular AF after LAAC.
- To identify predictors of GI bleeding post-Watchman device implantation.
Main Methods:
- Retrospective cohort study of 92 patients with nonvalvular AF undergoing LAAC.
- Follow-up period of 3 years to assess GI bleeding events.
- Cause-specific Cox proportional hazards models used to analyze bleeding and mortality risks.
Main Results:
- 11 bleeding events (12%) and 9 deaths (10%) were observed within 3 years.
- Increased CHA2DS2-VASc and HAS-BLED scores were independent predictors of GI bleeding.
- Prior GI bleeds increased bleeding hazard by 60% when controlling for CHA2DS2-VASc score.
Conclusions:
- Patients with Watchman devices remain at risk for GI bleeding post-implantation.
- Higher CHA2DS2-VASc and HAS-BLED scores are significant independent predictors of GI bleeding after LAAC.
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