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Published on: August 26, 2025
Postprocedural Management: Anticoagulation and Beyond
Moniek Maarse1, Martin J Swaans1, Lucas V A Boersma2
1Department of Cardiology, St. Antonius Hospital, Koekoekslaan 1, 3435CM Nieuwegein, The Netherlands.
Insights
Excluding the left atrial appendage reduces stroke risk in nonvalvular atrial fibrillation. However, closure devices may cause thrombus, necessitating tailored antithrombotic therapy based on individual patient risks.
Area of Science:
- Cardiology
- Vascular Surgery
Background:
- Left atrial appendage exclusion is a strategy to mitigate stroke risk in nonvalvular atrial fibrillation.
- Closure devices are exposed to blood flow during endothelialization, potentially activating coagulation and leading to device-related thrombus.
Purpose of the Study:
- To evaluate the risks and benefits of antithrombotic treatment following left atrial appendage closure.
- To explore alternative antithrombotic strategies for patients with contraindications to standard anticoagulation.
Main Methods:
- Review of existing literature on left atrial appendage closure devices and antithrombotic therapies.
- Analysis of patient/procedural characteristics influencing thromboembolic and bleeding risks.
Main Results:
- Device-related thrombus is a potential complication requiring antithrombotic treatment.
- Standard antithrombotic protocols may not be suitable for all patients, particularly those with anticoagulation contraindications.
- Less intensive antithrombotic regimens show promise but require further investigation.
Conclusions:
- A personalized antithrombotic treatment approach, balancing bleeding and thromboembolic risks, is likely optimal for patients undergoing left atrial appendage closure.
- Further research is needed to define the best antithrombotic strategies for diverse patient populations.
Abstract:
Excluding the left atrial appendage in patients with nonvalvular atrial fibrillation is a mechanical way to decrease stroke risk. During endothelialization, the closure device is exposed to circulating blood, which might activate the coagulation cascade. In excessive proportions, possibly resulting in the development of device-related thrombus, requiring a bridging period with optimal antithrombotic treatment. Initial protocol treatment is less suitable for patients with contraindications to anticoagulation. Less intensive antithrombotic regimens investigated suggest safety and efficacy, however further research is required. A tailored treatment, considering bleeding and thromboembolic risk based on patient/procedural characteristics in every patient, is probably the best approach.
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