Outcome of left atrial appendage closure using cerebral protection system for thrombosis: no patient left behind

Luca Rosario Limite1, Andrea Radinovic1, Lorenzo Cianfanelli2

  • 1Department of Arrhythmology, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Insights

Percutaneous left atrial appendage closure (LAAC) using a cerebral protection device (CPD) is safe and effective for managing left atrial appendage thrombosis or sludge (LAAT). This approach offers a viable therapeutic option for patients at risk of stroke.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Thrombosis Management

Background:

  • Left atrial appendage (LAA) thrombosis poses a significant stroke risk, necessitating effective management strategies.
  • Left atrial appendage thrombosis or sludge (LAAT) can occur despite anticoagulant therapy or after its withdrawal due to bleeding complications.

Purpose of the Study:

  • To evaluate the safety and efficacy of a standardized percutaneous left atrial appendage closure (LAAC) approach.
  • To assess the routine use of a cerebral protection device (CPD) during LAAC in patients with LAAT.

Main Methods:

  • Prospective enrollment of 14 consecutive patients with atrial fibrillation and LAAT.
  • Standardized LAAC procedure using a CPD, guided by transesophageal echocardiography.
  • Transradial access was utilized in the majority of patients (92.8%).

Main Results:

  • Procedural success was achieved in all patients, with no reported neurological consequences despite one instance of thrombus embolization.
  • The study included patients with high stroke risk (CHA2DS2-VASc score 3.3 ± 1.6) and bleeding risk (HAS-BLED score 2.3 ± 1.1).
  • During a mean follow-up of 426 days, no embolic events or major bleeding were reported; one patient died from a non-cardiac cause.

Conclusions:

  • Percutaneous LAAC with routine CPD use is a feasible, safe, and effective therapeutic option for LAAT.
  • The approach demonstrated both acute and long-term safety and efficacy in an unselected patient cohort.
Abstract

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