# Feasibility and Impact of Left Atrial Appendage Closure in Patients with Cardiac Implantable Electronic Devices: Insights from a Prospective Registry

**Authors:** Tommaso Bini, Sven Ledwoch, Roberto Galea, Antanas Gasys, Marco Gamardella, George C. M. Siontis, Lorenz Räber, Laurent Roten

PMC · DOI: 10.3390/jcm14113857 · Journal of Clinical Medicine · 2025-05-30

## TL;DR

This study examines the safety and feasibility of left atrial appendage closure in patients with heart devices, finding it generally safe but with mixed effects on atrial fibrillation burden.

## Contribution

The study provides new insights into the safety and feasibility of LAAC in patients with cardiac implantable electronic devices.

## Key findings

- LAAC was feasible and safe in 6% of patients with cardiac implantable electronic devices.
- No CIED lead dislodgement occurred, but AF burden increased slightly after LAAC.
- Larger studies are needed to confirm the impact on AF burden.

## Abstract

Background—Percutaneous left atrial appendage (LAA) closure (LAAC) offers a valid alternative to oral anticoagulation in patients with atrial fibrillation (AF) at high risk of bleeding. However, its impact on AF burden and device function in patients with cardiac implantable electronic devices (CIEDs) remains largely unexplored. Methods—From our prospective LAAC registry (clinicaltrial.gov—NCT04628078), which includes all consecutive LAAC procedures performed at our institution, we identified patients with a CIED and retrospectively analyzed procedural and follow-up data. The primary endpoint was defined as a composite of death, TIA/stroke, systemic or pulmonary embolism and major bleeding (BARC 3-5) within 7 days of the procedure. The secondary endpoint was CIED lead dislodgement. Additionally, AF burden was compared before and after LAAC. Results—Of the 586 LAAC procedures performed between August 2015 and January 2023, 36 patients (6%) had a CIED. The median CHA2DS2-VASC and HAS-BLED scores were 4.0 and 3.0, respectively. The primary endpoint occurred in one (3%) patient, and no patient experienced CIED lead dislodgement. AF burden data before and after LAAC were available in 20 patients. The mean AF burden increased from 6% to 31% following LAAC (p = 0.064). Conclusions—A CIED was present in 6% of LAAC procedures, and LAAC appears feasible and safe in this patient population. Larger, prospective studies are warranted to further evaluate the impact of LAAC on AF burden.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981), stroke (MONDO:0005098)

## Full-text entities

- **Diseases:** stroke (MESH:D020521), AF (MESH:D001281), TIA (MESH:D002546), bleeding (MESH:D006470), Left Atrial Appendage (MESH:D059446), death (MESH:D003643), systemic or pulmonary embolism (MESH:D011655)
- **Chemicals:** LAAC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12156788/full.md

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Source: https://tomesphere.com/paper/PMC12156788