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Who Watches the "Watchman" and How Often?
Kyaw M Hlaing1, Thein T Aung2, Kevin Kravitz2
1Internal Medicine, LewisGale Medical Center, Salem, USA.
Cureus
|October 1, 2020
Summary
Patients with atrial fibrillation (AF) who cannot take anticoagulants may receive a Watchman device. This case highlights the risk of device-related thrombosis (DRT) and the need for prolonged monitoring and anticoagulation.
Area of Science:
- Cardiology
- Medical Devices
- Thrombosis
Background:
- Atrial fibrillation (AF) is a common arrhythmia requiring anticoagulation to prevent stroke.
- Bleeding risks often preclude anticoagulation in some AF patients.
- Left atrial appendage (LAA) closure devices, like the Watchman, offer an alternative stroke prevention strategy.
Observation:
- A patient with AF and epistaxis necessitating anticoagulation cessation underwent Watchman device implantation.
- The patient developed device-related thrombosis (DRT) post-implantation.
- This complication required extended anticoagulation and echocardiographic surveillance.
Findings:
- Device-related thrombosis (DRT) is a potential complication following LAA closure.
- There is a lack of established guidelines for monitoring DRT and determining the duration of anticoagulation after LAA device placement.
- Prolonged anticoagulation and regular echocardiographic follow-up may be necessary to manage DRT.
Implications:
- This case underscores the importance of vigilant monitoring for DRT after LAA device implantation.
- Further research is needed to establish optimal anticoagulation strategies and follow-up protocols for patients with LAA closure devices.
- Individualized patient management is crucial when balancing bleeding risks and thrombotic events in AF patients.
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