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Published on: August 16, 2021
Anticoagulation alone as an effective and safe antithrombotic therapy in LVAD: When less is more
Vincenzo Tarzia1, Chiara Tessari1, Lorenzo Bagozzi1
1Cardiac-Surgery-Unit, Department of Cardio-Thoracic-Vascular Sciences and Public Health, University of Padova, Padova, Italy.
Insights
Aspirin avoidance in HeartMate3 patients significantly reduced bleeding events without increasing clotting risks, demonstrating a safe and effective anticoagulation strategy for improved hemocompatibility.
Area of Science:
- Cardiovascular Medicine
- Biomedical Engineering
- Hematology
Background:
- HeartMate3 left ventricular assist device (LVAD) recipients require careful antithrombotic management to balance thrombosis and bleeding risks.
- Optimizing anticoagulation regimens is crucial for long-term LVAD performance and patient safety.
Purpose of the Study:
- To assess the safety and efficacy of anticoagulation strategies in HeartMate3 patients.
- To compare hemocompatibility-related adverse events (HRAEs) and hemocoagulative markers between patients on warfarin plus aspirin versus warfarin alone.
Main Methods:
- A prospective study divided 50 HeartMate3 patients into two groups: Group-1 (warfarin + aspirin) and Group-2 (warfarin alone).
- Evaluated HRAEs, hemocompatibility score (HCS), and laboratory markers over a median follow-up of 590 days.
Main Results:
- Significantly fewer HRAEs occurred in Group-2 (2%) compared to Group-1 (34%) (P < 0.001).
- Group-1 had a higher net HCS (24 points) than Group-2 (1 point) (P = 0.023).
- Hemocoagulative markers remained stable, with no intergroup differences except for the ASPI-test (P = 0.003).
Conclusions:
- HeartMate3 demonstrates high hemocompatibility irrespective of the antithrombotic regimen.
- Omitting aspirin from the antithrombotic therapy in HeartMate3 patients is a safe and effective strategy, reducing hemorrhagic events without elevating thrombotic risk.
Abstract:
To evaluate the safety and effectiveness of anticoagulation alone in HeartMate3 patients. According to antithrombotic regimen, patients were divided into 2 groups: Group-1(warfarin+aspirin) and Group-2(warfarin). A comparison of hemocompatibility-related adverse events (HRAEs), hemocompatibility score (HCS), and hemocoagulative laboratory markers, both qualitative and quantitative, between the 2 groups were performed. Fifty patients were enrolled, 28 (56%) in Group-1 and 22 in Group-2 (44%), without statistical differences at baseline. Median time of follow-up was 590 days (IQR: 410.25-1007.50). Eighteen HRAEs (36.0%) occurred: 17 in Group-1 (34%) and 1 in Group-2 (2%) (P < 0.001). The net HCS for Group-1 versus Group-2 was 24 points and 1 point (OR 12.116[2.034-233.226], P = 0.023), respectively. Hemocoagulative values turned into the normality and remained stable during follow-up, without differences between groups, except for ASPI-test (P = 0.003). HeartMate3 showed a high hemocompatibility independently from antithrombotic therapy. Aspirin avoidance resulted a safe and effective strategy since it reduced hemorrhagic events, without increasing thrombotic risk.
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