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Updated: May 23, 2026

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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
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Contrast-free left atrial appendage occlusion in patients using the LAMBRE™ device
Vivian Vij1, Tobias Friedrich Ruf2, Jean-Benoit Thambo3
1Herzzentrum Bonn, University Hospital Bonn, Germany.
International Journal of Cardiology
|March 8, 2024
Summary
Contrast-free left atrial appendage closure (LAAC) using the LAMBRE device is safe and feasible, demonstrating high device success rates. This echocardiography-guided approach offers a viable alternative for patients with high risks.
Area of Science:
- Cardiology
- Medical Imaging
- Interventional Procedures
Background:
- Left atrial appendage closure (LAAC) procedures are increasingly optimized with advanced imaging techniques.
- Contrast-free approaches guided by echocardiography are emerging but lack extensive data.
- This study evaluates the LAMBRE LAAC device in a contrast-free setting.
Purpose of the Study:
- To assess the safety and feasibility of contrast-free LAAC using the LAMBRE device.
- To analyze procedural outcomes and complications in a real-world patient cohort.
- To contribute data on echocardiography-guided LAAC without contrast dye.
Main Methods:
- A multicenter retrospective analysis (BoBoMa-Registry) of 118 patients undergoing LAAC with LAMBRE devices.
- Procedures were performed without contrast dye, guided solely by echocardiography.
- Baseline characteristics, procedural details, and complications were evaluated.
Main Results:
- High device success rate of 97.5% was achieved in elderly patients with high thromboembolic and bleeding risks.
- Mean procedural time was 47.2 minutes with a mean radiation dose of 4.75 Gy*cm².
- Periprocedural complications occurred in 6.8% of cases, with no relevant peri-device leakage observed.
Conclusions:
- Echocardiography-guided, contrast-free LAAC with the LAMBRE device is a safe and feasible procedure.
- The study supports the use of this technique in selected patient populations.
- Further prospective studies comparing devices and imaging modalities are recommended.
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