Percutaneous left atrial appendage closure followed by single antiplatelet therapy: Short- and mid-term outcomes

Zakaria Jalal1, Marie-Lou Dinet1, Nicolas Combes2

  • 1Department of paediatric and adult congenital cardiology, university hospital of Bordeaux, avenue Magellan, 33600 Pessac, France.

Insights

Left atrial appendage closure (LAAC) with the AMPLATZER™ Cardiac Plug (ACP) device, followed by single antiplatelet therapy, offers a safe and effective stroke prevention strategy. This approach shows promising results for patients with atrial fibrillation who cannot take oral anticoagulants.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Medical Devices

Background:

  • Optimal antithrombotic strategies post-left atrial appendage closure (LAAC) remain debated.
  • Various antithrombotic protocols exist, necessitating further research into effective post-procedural management.

Purpose of the Study:

  • To evaluate the efficacy and safety of LAAC using the AMPLATZER™ Cardiac Plug (ACP) device.
  • To assess the outcomes of a single antiplatelet therapy regimen following LAAC.

Main Methods:

  • A cohort of 76 patients with non-valvular atrial fibrillation and contraindications for oral anticoagulants underwent LAAC with an ACP device.
  • Follow-up included clinical assessments and cardiac CT scans at 3 months to evaluate device performance and complications.
  • Patients received single antiplatelet therapy for at least 12 months post-procedure.

Main Results:

  • Successful LAAC was achieved in all patients, with low rates of major periprocedural complications.
  • Device thrombosis occurred in 6.8% of patients, all asymptomatic.
  • After a mean follow-up of 13 months, observed rates of death (2.6%), stroke (4.0%), and major bleeding (1.3%) were lower than predicted by risk scores.

Conclusions:

  • Left atrial appendage closure (LAAC) with the ACP device, combined with single antiplatelet therapy, presents a viable alternative for stroke prevention.
  • This strategy demonstrates favorable safety and efficacy profiles in high-risk patients.
Abstract