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Published on: February 26, 2013
Optimal Antithrombotic Regimen in Left Atrial Appendage Occlusion: The Gordian Knot?
Shazia Afzal1, Lisa Dannenberg1, Dominika Kanschik1
1Division of Cardiology, Pulmonology, and Vascular Medicine, Heinrich Heine University Medical Center Düsseldorf, Cardiovascular Research Institute Düsseldorf (CARID), Düsseldorf, Germany.
Insights
Device-related thrombosis (DRT) after left atrial appendage occlusion (LAAO) varies significantly. Different antithrombotic strategies and devices appear to influence DRT rates, necessitating further controlled studies.
Area of Science:
- Cardiology
- Medical Devices
- Thrombosis
Background:
- Percutaneous left atrial appendage occlusion (LAAO) offers stroke risk reduction for patients with atrial fibrillation and high bleeding risk.
- Device-related thrombosis (DRT) is a significant complication following LAAO procedures.
- Variations in DRT incidence across studies suggest potential influences from antithrombotic regimens and occluder devices.
Discussion:
- A comparative analysis of DRT incidence revealed significant differences: 25.3% in the DRT study, 3.8% in the Amplatzer IDE trial, and 3.3% in the Düsseldorf LAAO registry.
- Antithrombotic strategies differed, with oral anticoagulation more common in the DRT study and dual antiplatelet therapy more prevalent in the Düsseldorf registry.
- The Amplatzer Amulet device was used more frequently in the Düsseldorf registry compared to the DRT study, suggesting a potential device-related factor.
Key Insights:
- DRT incidence is substantially lower with the Amplatzer Amulet device compared to other devices in the analyzed studies.
- The choice of antithrombotic treatment (oral anticoagulation vs. dual antiplatelet therapy) appears to correlate with DRT rates.
- These findings highlight the complex interplay between LAAO devices, antithrombotic therapy, and the risk of device-related thrombosis.
Outlook:
- Further clinical trials are essential to definitively establish the impact of specific LAAO devices and antithrombotic regimens on DRT.
- Optimizing antithrombotic protocols and device selection could mitigate the risk of DRT, improving patient outcomes after LAAO.
- Understanding these factors is crucial for refining LAAO procedures and reducing stroke risk in vulnerable patient populations.
Abstract:
Percutaneous left atrial appendage occlusion (LAAO) is an option to reduce the risk of stroke in patients with atrial fibrillation and high bleeding risk. However, device-related thrombosis (DRT) post LAAO is feared as complication. Simard et al. found a very high incidence of DRT compared to other trials. However, antithrombotic regimen and used devices have not been compared between studies. We compared DRT formation, antithrombotic regimen and used device in the recent DRT study, the Amplatzer IDE trial, and the Düsseldorf (DUS) LAAO registry. Occluder thrombosis occurred in 25.3% in the DRT study, 3.8% in the Amulet IDE trial, and 3.3% in the DUS LAAO registry (p < 0.0001). Oral anticoagulation-based regimen was more frequent in the DRT study compared to the DUS LAAO registry, whereas dual antiplatelet regimen was more frequent in the DUS LAAO registry (p < 0.0001). Amplatzer amulet was more frequently used in the DUS LAAO registry as compared to the DRT study (p < 0.0001). DRT is a feared complication after LAAO and seems to be dependent on antiplatelet treatment and underlying device. A clinical study controlling for device and antithrombotic regimen is needed to smash this Gordian knot.
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