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Updated: Feb 7, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Feasibility of left atrial appendage device closure following chronically failed surgical ligation
Christopher R Ellis1, Mohamed Metawee1, Robert N Piana1
1Department of Medicine, Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Insights
Watchman device closure is feasible for patients with incomplete surgical left atrial appendage occlusion (S-LAAO), even with narrow necks. This approach offers a viable option for patients previously excluded from trials.
Area of Science:
- Cardiology
- Interventional Cardiology
- Medical Devices
Background:
- Incomplete surgical left atrial appendage occlusion (S-LAAO) with narrow necks is linked to higher embolic stroke rates.
- Patients with prior S-LAAO attempts were excluded from LAA closure device trials.
Purpose of the Study:
- To assess the feasibility of using the Watchman device for left atrial appendage (LAA) closure in patients with prior incomplete S-LAAO.
Main Methods:
- A prospective, single-arm feasibility study was conducted.
- Patients underwent Watchman LAA closure following incomplete S-LAAO.
- Pre- and post-implant imaging (CTA, TEE) and registry follow-up were utilized.
Main Results:
- All six attempted Watchman LAA closures were successful.
- Complete device seal and no thrombus were observed at 45-day follow-up.
- The procedure was feasible even in patients with narrow ostial necks (≤9 mm).
Conclusions:
- Watchman LAA closure appears feasible for patients with chronically incomplete S-LAAO.
- This includes individuals with narrow ostial necks, addressing a previously unmet clinical need.
Background:
Incomplete surgical left atrial appendage occlusion (S-LAAO) with a narrow neck has been shown to predict an increased rate of embolic stroke. Patients with a previously attempted S-LAAO were systematically excluded from all clinical trials of LAA closure devices.
Objective:
The purpose of this study was to evaluate the feasibility of Watchman LAA device closure for patients referred with chronically incomplete S-LAAO.
Methods:
A prospective single-arm feasibility cohort evaluated only subjects undergoing Watchman LAA closure following incomplete S-LAAO. Patients referred and implanted were followed in the Vanderbilt LAA Registry. Preprocedure computed tomographic angiography and transesophageal echocardiography (TEE) were performed to evaluate suitability for closure, with 45-day follow-up TEE postimplant.
Results:
All attempted LAA closures after incomplete S-LAAO were successful (n = 6). Mean age was 76.3 ± 7 years. Mean CHADS2Vasc score was 3.8 ± 0.8, and HAS-BLED score was 3.5 ± 0.5. At 45-day follow up, all subjects had complete device seal with no thrombus on device and had transitioned to clopidogrel plus aspirin. Three subjects had narrow ostial necks with a maximum diameter ≤9 mm. In all cases, the 4.7-mm Watchman access sheath was able to cross the ostial stricture. Mean occluder size implanted was 28 ± 4 mm. Mean LAA dimension by TEE in the 45° and 135° views for depth was 31 mm and ostial diameter was 11 × 16 mm, below the minimum Watchman indication for use of 17 mm. No major intraoperative complications occurred.
Conclusion:
Watchman LAA closure seems to be feasible in patients with chronically incomplete S-LAAO, including subjects with a narrow neck ≤9 mm in width.
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