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Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Direct current cardioversion of atrial fibrillation in patients with left atrial appendage occlusion devices
Xin Xie1, Zijun Chen1, Xiaorong Li1
1Department of Cardiology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Insights
Direct current cardioversion (DCCV) is safe and effective in patients with left atrial appendage occlusion (LAAO) devices. This study found no increased risk of adverse events or thromboembolism in patients undergoing DCCV after LAAO device implantation.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Devices
Background:
- Limited data exists on the safety and efficacy of direct current cardioversion (DCCV) in patients with left atrial appendage occlusion (LAAO) devices.
- Understanding the impact of DCCV on thromboembolic prevention in this population is crucial for clinical decision-making.
Purpose of the Study:
- To investigate the safety and efficacy of DCCV in patients who have undergone LAAO procedures.
- To assess DCCV-related risks and its impact on thromboembolic events in patients with LAAO devices.
Main Methods:
- An ambispective cohort study included 196 patients undergoing LAAO, with 95 receiving DCCV post-procedure.
- Safety endpoints included DCCV-related death, device dislodgement/embolization, and major bleeding.
- Efficacy endpoints comprised all-cause death, cardiovascular death, stroke/transient ischemic attack, and systemic embolism.
Main Results:
- No DCCV-related deaths, device dislodgements, or embolizations occurred.
- Safety endpoints (3.2% vs. 6.9%) and efficacy endpoints (1.1% vs. 4.0%) showed no significant difference between DCCV and no-DCCV groups at 12 months.
- Transesophageal echocardiography revealed minor, non-adverse changes in device diameter post-DCCV.
Conclusions:
- Direct current cardioversion (DCCV) can be safely performed in patients with left atrial appendage occlusion (LAAO) devices.
- No increased risk of adverse events or thromboembolic complications was observed.
- Minor device diameter changes noted on TEE were not associated with adverse outcomes.
Background And Aims:
Data on the safety of direct current cardioversion (DCCV) in patients with left atrial appendage occlusion (LAAO) devices and its impact on thromboembolic prevention are limited. This study aimed to investigate the safety and efficacy of DCCV in patients with LAAO devices.
Methods:
This single-center, ambispective cohort included patients undergoing one-stop procedures [LAAO combined with radiofrequency catheter ablation (RFCA)], where LAAO was performed first. DCCV was performed to restore sinus rhythm after LAAO. Patients were divided into the DCCV group and the no-DCCV group. Safety endpoints included DCCV-related death, device dislodgment, device embolization, and major bleeding events. Efficacy endpoints contained all-cause death, cardiovascular death, stroke/transient ischemic attack, and systemic embolism.
Results:
A total of 196 patients (age 72.5 ± 7.4 years, 51.0% male) were enrolled, with 95 patients undergoing DCCV after LAAO. No DCCV-related death, device dislodgement, or device embolism was observed. At 12 months, the safety endpoints occurred in 3.2% of the DCCV group vs. 6.9% of the no-DCCV group (p = 0.238). Similarly, the efficacy endpoints were observed in 1.1% of the DCCV group vs. 4.0% of the no-DCCV group (p = 0.339). By performing pre- and post-DCCV transesophageal echocardiography (TEE) in the prospective cohort, a significant increase in device diameter at 45° and 90° (p = 0.044; 0.027), and an insignificant decline trend of peri-device leak and shoulder at 135° were noted (p = 0.051; 0.103).
Conclusions:
No signal of excess risk was observed when performing DCCV in patients with LAAO devices. Tiny changes in device diameter after DCCV were noted on TEE at 45° and 90°, but these were not associated with adverse effects.
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