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Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Discontinuation of antithrombotic therapy for a year or more in patients with continuous-flow left ventricular assist
Naveen L Pereira1, Dong Chen, Sudhir S Kushwaha
1Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic, 200 First Street S.W., Rochester, MN 55905, USA. pereira.naveen@mayo.edu
Insights
Patients with left ventricular assist devices (LVADs) experiencing gastrointestinal bleeding may safely discontinue anticoagulation if they have an acquired von Willebrand factor (VWF) abnormality, avoiding thrombotic events.
Area of Science:
- Cardiology
- Hematology
- Medical Devices
Background:
- Continuous-flow axial left ventricular assist devices (LVADs) require anticoagulation with aspirin and warfarin (target INR 2.0-3.0).
- Recurrent gastrointestinal bleeding is a known complication in LVAD patients on anticoagulation.
Observation:
- Two LVAD patients with recurrent gastrointestinal bleeding required discontinuation of anticoagulation for over a year.
- Neither patient experienced thrombotic complications during 29 months of follow-up after stopping anticoagulation.
Findings:
- Both patients demonstrated an acquired von Willebrand factor (VWF) abnormality, characterized by reduced high-molecular-weight multimers.
- Platelet function tests were normal, suggesting an acquired VWF syndrome as the primary hemostatic defect.
Implications:
- Discontinuation of standard anticoagulation may be feasible in select LVAD patients with acquired VWF abnormalities.
- Further clinical trials are necessary to validate the safety of reduced or absent anticoagulation in this patient population.
Abstract:
The recommended anticoagulation regimen during continuous-flow axial left ventricular assist device (LVAD) support is aspirin and warfarin with a targeted international normalized ratio of 2.0-3.0. We report two patients in whom recurrent gastrointestinal bleeding during LVAD support necessitated discontinuation of this anti-thrombotic regimen for a year or more. Despite this, neither patients developed thrombotic complications during 29 patient-months of follow-up. An acquired von Willebrand factor (VWF) abnormality reflected by the absence or decreased abundance of the highest molecular weight multimers was demonstrated in both patients. The gold standard test for platelet function, light transmission platelet aggregometry was measured in one patient and was normal, indicative that the predominant abnormality in the coagulation profile of these patients is an acquired VWF syndrome. Clinical trials are required to address the question whether it is safe to discontinue anticoagulation in LVAD patients with acquired VWF abnormalities.
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