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Updated: Oct 11, 2025

A Thrombotic Stroke Model Based On Transient Cerebral Hypoxia-ischemia
Published on: August 18, 2015
Large Device-Related Thrombus Detected following Symptoms of Transient Ischemic Attack
Osayi Lawani1, Edward Baptista2
1University of Houston College of Medicine/HCA Houston Healthcare, USA.
Insights
Atrial fibrillation increases stroke risk. Left atrial appendage occlusion devices, while effective, can cause device-related thrombus. Prolonging anticoagulation may benefit high-risk patients to prevent this complication.
Area of Science:
- Cardiology
- Medical Devices
- Stroke Prevention
Background:
- Atrial fibrillation is a major risk factor for embolic stroke, primarily due to thrombus formation in the left atrial appendage.
- Left atrial appendage occlusion (LAAO) devices offer an alternative to anticoagulation for stroke prevention in patients with contraindications.
- Implantation of LAAO devices, such as WATCHMAN, is associated with a 3-6% incidence of device-related thrombus (DRT).
Abstract:
As an independent risk factor for stroke, atrial fibrillation has been shown to be associated with a fivefold increase in the cause of embolic stroke in comparison to healthy individuals without atrial fibrillation. This risk may be compounded by other factors; however, the main probable cause of stroke leading from atrial fibrillation is thrombus formation in the left atrial appendage. In patients for whom anticoagulation is contraindicated, left atrial appendage occlusion has become a leading alternative option for therapeutic prevention of thromboembolism and stroke in patients with this condition. Unfortunately, these devices (particularly the WATCHMAN) have been associated with a 3-6% incidence of intracardiac thrombus development postimplantation. Some risk factors for the development of device-related thrombus are high platelet count, permanent atrial fibrillation, resistance to clopidogrel, and prior transient ischemic attack or stroke. Despite following an anticoagulant regimen, thrombus formation was reported in 5.6% of participants of a randomized clinical trial, and further analysis showed that some of these patients continued to develop either ischemic stroke or thromboembolism five years later as compared to patients without initial thrombus development. We present a case of an elderly male with prior history of stroke and transient ischemic attack who developed a large device-related thrombus five months following WATCHMAN FLX™ implantation. Currently, there are no specific recommendations on the management of this rare complication; however, we discuss possible consideration of initially prolonging anticoagulation therapy following implantation for high-risk individuals, as there is an increased possibility for thrombus formation in this population. Management options should continue to be studied for therapeutic benefit in streamlining postprocedural therapy and improve future outcomes in the use of left atrial appendage occlusion devices, as well as continual thrombus prevention.
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