The Imaging Spectrum of Device-Related Thrombus After Percutaneous Left Atrial Appendage Occlusion

Joshua Rezkalla1, Hasan Alarouri1, Ratnasari Padang1

  • 1Department of Cardiovascular Diseases, Mayo College of Medicine, Rochester, Minnesota, USA.

JACC. Case Reports
|December 2, 2024
PubMed

Insights

Surveillance imaging after left atrial appendage closure can detect device-related thrombus (DRT), increasing stroke risk. Standardized imaging definitions are needed due to variability in DRT detection.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Interventional Cardiology

Background:

  • Transcatheter left atrial appendage occlusion (LAAO) is an alternative to anticoagulation for stroke risk reduction in atrial fibrillation.
  • Post-procedural surveillance imaging, typically with transesophageal echocardiography (TEE) or cardiac computed tomography (CT), is crucial for assessing device position and detecting complications.
  • Device-related thrombus (DRT) is a significant complication, associated with a higher risk of stroke and systemic embolization.

Observation:

  • Current surveillance protocols for DRT detection after LAAO show considerable variability in timing, frequency, and imaging modality.
  • The distinction between early device endothelization and pathological DRT formation remains unclear.
  • Imaging findings on TEE and CT can be diverse, making consistent interpretation challenging.

Findings:

  • DRT detection during surveillance is linked to a substantially increased risk of thromboembolic events within six months.
  • Variability in surveillance practices contributes to inconsistent DRT detection rates.
  • The spectrum of imaging findings for DRT and benign device healing requires further elucidation.

Implications:

  • Standardized definitions and reporting criteria for surveillance imaging are essential for consistent DRT detection and risk stratification.
  • Unified imaging protocols may improve the accuracy of identifying patients at high risk for stroke after LAAO.
  • Further research is needed to understand the pathophysiology of DRT formation versus device endothelization.