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Omission of Antiplatelet Therapy in Patients With HeartMate 3 Left Ventricular Assist Devices: A Systematic Review
Maximilian Tscharre1,2, David Mutschlechner3, Thomas Schlöglhofer4
1From the Department of Internal Medicine, Cardiology and Nephrology, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Vitamin K antagonist monotherapy significantly reduces bleeding events in HeartMate 3 patients. This approach lowers hemocompatibility-related adverse events without increasing thromboembolic risks.
Area of Science:
- Cardiovascular Surgery
- Medical Devices
- Pharmacology
Background:
- The HeartMate 3 (HM3) left ventricular assist device (LVAD) reduces thromboembolic events but high bleeding complications persist with combined antithrombotic therapy (VKA and aspirin).
- Limited data exists on the safety of vitamin K antagonist (VKA) monotherapy in HM3 patients.
Approach:
- A systematic literature search identified observational studies and randomized trials evaluating VKA monotherapy versus VKA and aspirin in HM3 patients.
- Hemocompatibility-related adverse events (HRAE) were analyzed as the primary endpoint, with secondary analysis of individual event components.
- A random-effects model was used to calculate the odds ratio (OR) for outcome measures.
Key Points:
- Five studies including 785 patients (381 on VKA monotherapy, 404 on VKA and aspirin) were analyzed.
- VKA monotherapy significantly reduced HRAE (OR: 0.11) and bleeding complications (OR: 0.12).
- No significant increase in thromboembolic events was observed with VKA monotherapy (OR: 0.69).
Conclusions:
- Vitamin K antagonist monotherapy is associated with a significant reduction in bleeding events in HM3 patients.
- This approach does not increase the risk of thromboembolic complications.
- VKA monotherapy represents a safer antithrombotic strategy for HM3 patients compared to combined therapy.
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