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Updated: Aug 26, 2025

Use of a Percutaneous Ventricular Assist Device/Left Atrium to Femoral Artery Bypass System for Cardiogenic Shock
Published on: August 16, 2021
Impact of time off anticoagulation in patients with continuous-flow left ventricular assist devices
Christian A Inchaustegui1,2, Ashley Patel3, Harveen K Lamba4
1Department of Medicine, Baylor College of Medicine, McNair Campus (MCHA) A10.193 MS: BCM903, 7200 Cambridge Street, Houston, TX, 77040, USA. cc22@bcm.edu.
Insights
Discontinuing anticoagulation for 30 days or more in patients with left ventricular assist devices (LVADs) significantly increases the risk of ischemic stroke and death. Shorter interruptions do not show the same increased risk.
Area of Science:
- Cardiology
- Medical Devices
- Thrombosis Research
Background:
- Patients with left ventricular assist devices (LVADs) require anticoagulation to prevent thrombosis.
- Discontinuation of anticoagulation is sometimes necessary but carries undefined risks.
Purpose of the Study:
- To investigate the impact of temporary anticoagulation cessation on thrombosis and mortality rates in LVAD patients.
- To define the risks associated with different durations of anticoagulation interruption post-LVAD implantation.
Main Methods:
- Retrospective review of 245 LVAD implantation procedures.
- Patients were categorized by days off anticoagulation: none, <30 days (short-term), and ≥30 days (long-term).
- International Normalized Ratio (INR) ≤1.5 used as a threshold for anticoagulation discontinuation.
Main Results:
- 70 patients (28.6%) experienced anticoagulation interruption.
- Long-term discontinuation (≥30 days) was associated with significantly higher rates of ischemic stroke (aHR 8.5) and death (aHR 3.9).
- No significant difference in pump thrombosis rates was observed among the groups.
Conclusions:
- Anticoagulation interruption for 30 days or more after LVAD implantation is an independent risk factor for ischemic stroke and mortality.
- Careful consideration of anticoagulation management is crucial in LVAD patients requiring temporary cessation.
Abstract:
Patients with left ventricular assist devices (LVADs) receive anticoagulation to decrease the risk of thrombosis. Various circumstances require discontinuing anticoagulation in LVAD patients, but the risks entailed are not well defined. In a retrospective review of LVAD implantation procedures, we examined the effect of time off anticoagulation on thrombosis and mortality rates after implantation. An international normalized ratio ≤ 1.5 was used to screen for patients taken off anticoagulation. Patients were divided into three groups by the cumulative number of days off anticoagulation: no discontinuation, short-term discontinuation (< 30 days), and long-term discontinuation (≥ 30 days). Rates of ischemic stroke, pump thrombosis, and mortality were compared among groups. Of 245 patients who underwent LVAD implantation during the study, 70 (28.6%) were off anticoagulation during follow-up: 37 (15.1%) had short-term discontinuation (median, 11 days), and 33 (13.5%) had long-term discontinuation (median, 124 days). Patients with long-term discontinuation had a higher rate of ischemic stroke (adjusted hazard ratio 8.5, p = 0.001) and death (adjusted hazard ratio 3.9, p = 0.001). The three groups did not differ in pump thrombosis rate. We conclude that after LVAD implantation, discontinuing anticoagulation for ≥ 30 days is independently associated with an increased risk of ischemic stroke and death.
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