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Updated: Sep 23, 2025

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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
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Left Atrial Appendage Closure with the LAmbre Device - Initial Multicentre Experience in Brazil
Francisco Chamié1,2, Enio Guerios3, Daniel Peralta E Silva1,2
1Hospital Federal dos Servidores do Estado - Cardiologia Intervencionista, Rio de Janeiro, RJ - Brasil.
Arquivos Brasileiros De Cardiologia
|May 11, 2022
Summary
Left atrial appendage (LAA) closure using the LAmbre device is a safe and effective alternative for stroke prevention in non-valvular atrial fibrillation patients. This initial multicenter study in Brazil shows promising results for LAA occlusion.
Area of Science:
- Cardiology
- Medical Devices
- Interventional Procedures
Background:
- Left atrial appendage (LAA) closure offers an alternative to oral anticoagulation (OAC) for stroke prevention in patients with non-valvular atrial fibrillation (NVAF).
- This study focuses on LAA closure as a therapeutic option for NVAF patients who cannot tolerate long-term OAC.
Purpose of the Study:
- To report the initial multicenter experience in Brazil with LAA closure using the LAmbre device.
- To evaluate the feasibility, safety, and efficacy of the LAmbre device for LAA occlusion in NVAF patients.
Main Methods:
- A total of 51 consecutive NVAF patients underwent LAA closure with the LAmbre device across 18 centers in Brazil.
- Patients had restrictions for long-term OAC due to bleeding, stroke, or other contraindications.
- Procedural and follow-up data were collected, including device success and complication rates.
Main Results:
- The study included 51 patients (49% male, 51% female) with a mean age of 76 years and high CHA2DS2-VASc and HAS-BLED scores.
- Procedural success rate was 100%, with minor immediate complications in 3 patients (pericardial effusion, device embolization).
- After a mean follow-up of 18 months, no deaths or strokes were reported, with small residual shunts in 4 patients.
Conclusions:
- LAA occlusion with the LAmbre device demonstrated safety and effectiveness in this initial series of NVAF patients.
- The findings suggest LAmbre is a viable option for stroke prevention in patients unsuitable for OAC.
- Further research with larger cohorts and longer follow-up is recommended to confirm these encouraging results.

