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Updated: Mar 15, 2026

In Vitro Thrombosis Test for Ventricular Assist Devices
Published on: March 21, 2025
Thrombosis in Continuous Flow Left Ventricular Assist Devices: Our Clinical Experience With Medical and Surgical
U Köksel1, O Erbasan1, Ö Bayezid1
1Department of Cardiovascular Surgery, Akdeniz University Hospital, Antalya, Turkey.
Insights
Pump thrombosis in continuous-flow left ventricular assist devices (CF-LVADs) is linked to high blood pressure and poor anticoagulation. Thrombolytic therapy is an option but carries bleeding risks.
Area of Science:
- Cardiology
- Biomedical Engineering
- Medical Device Technology
Background:
- Continuous-flow left ventricular assist devices (CF-LVADs) are crucial alternatives to heart transplantation.
- Pump thrombosis is a significant complication affecting CF-LVADs, including HeartMate II and HeartWare devices.
- Understanding predisposition factors and treatment strategies for CF-LVAD thrombosis is vital.
Purpose of the Study:
- To analyze predisposition factors for pump thrombosis in CF-LVAD patients.
- To evaluate the center's approach to treating pump thrombosis.
- To assess patient outcomes following treatment for pump thrombosis.
Main Methods:
- Retrospective review of a CF-LVAD database (January 2011 - January 2015).
- Comparison of patients with pump thrombosis (n=13) versus without (n=85).
- Analysis of device type, predisposition factors, treatment, and outcomes.
Main Results:
- Pump thrombosis occurred in 13 of 98 patients; no difference between HeartMate II and HeartWare devices.
- High mean arterial blood pressure and noncompliance with anticoagulation were significant risk factors.
- Thrombolytic therapy was used for most patients, with some requiring pump exchange; bleeding complications occurred.
Conclusions:
- Optimizing blood pressure and anticoagulation adherence may reduce CF-LVAD pump thrombosis.
- Thrombolytic therapy is a less invasive treatment option for pump thrombosis but has risks.
- Careful patient selection and monitoring are essential when using thrombolytic therapy for CF-LVAD thrombosis.
Background:
Continuous-flow left ventricular assist devices (CF-LVADs) such as the HeartMate II and HeartWare left ventricular assist device are important alternatives to heart transplantation. Thrombosis is a serious complication in both devices and we present our approach to treating thrombosis and analysis of predisposition factors.
Methods:
Our center's CF-LVADs database was retrospectively reviewed for pump thrombosis between January 2011 and January 2015. The patients were grouped for pump thrombosis (n = 13) and nonpump thrombosis (n = 85). Patients with pump thrombosis were further divided by device type (n = 5 HeartMate II and n = 8 HeartWare left ventricular assist device). Predisposition factors for pump thrombosis, our treatment approach, and patient outcomes were evaluated.
Results:
Pump thrombosis was diagnosed in 13 of 98 patients. The rate of pump thrombosis did not differ between the 37 HeartMate II and 61 HeartWare left ventricular assist device patients. High mean arterial blood pressure (P < .01) and noncompliance with the anticoagulation regimen (P = .04) were associated significantly with thrombosis. Twelve patients with stable hemodynamics were treated initially with intravenous tissue plasminogen activator and 1 patient who had end-organ damage underwent pump exchange. Two patients failed to respond to medical treatment and underwent pump exchange. Two patients with recurrent thrombosis were administered intracardiac tissue plasminogen activator. Five patients died after medical treatment and 4 deaths were due to cerebral hemorrhage.
Conclusions:
Avoiding increased mean arterial blood pressures and ensuring optimal anticoagulation may help to decrease pump thrombosis. In patients with pump thrombosis, thrombolytic therapy is an alternative that is less invasive than pump exchange, but carries the risk of hemorrhage and thromboembolism.
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