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Updated: Feb 12, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Device-Related Thrombosis After Percutaneous Left Atrial Appendage Occlusion for Atrial Fibrillation
Laurent Fauchier1, Alexandre Cinaud1, François Brigadeau2
1Trousseau University Hospital, Faculty of Medicine, François Rabelais University, Tours, France.
Device-related thrombus is common after left atrial appendage (LAA) closure for atrial fibrillation (AF) stroke prevention. This thrombus increases the risk of ischemic stroke, highlighting the need for careful patient monitoring.
Area of Science:
- Cardiology
- Interventional Cardiology
- Medical Devices
Background:
- Transcatheter left atrial appendage (LAA) occlusion offers an alternative stroke prevention strategy for patients with atrial fibrillation (AF).
- Understanding the risks associated with LAA closure devices is crucial for patient management.
Purpose of the Study:
- To determine the incidence of thrombus formation on LAA closure devices in patients with AF.
- To identify predictors of device-related thrombus.
- To assess the prognostic impact of thrombus on stroke risk.
Main Methods:
- Retrospective analysis of 469 patients undergoing LAA closure with Watchman or Amplatzer devices across 8 French centers (2012-2017).
- Evaluation of LAA imaging, adverse events, and clinical outcomes during a mean follow-up of 13 months.
Main Results:
- The incidence of device-related thrombus was 7.2% per year among patients with LAA imaging.
- Older age and history of stroke were predictors of thrombus formation.
- Dual antiplatelet therapy and oral anticoagulation at discharge were protective.
- Device-related thrombus and vascular disease independently predicted ischemic strokes and transient ischemic attacks.
Conclusions:
- Thrombus formation on LAA closure devices is a significant concern in AF patients.
- Device-related thrombus is associated with an increased risk of ischemic stroke during follow-up.
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