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Published on: February 28, 2012
Direct oral anticoagulants versus Vitamin K antagonists for left ventricular thrombus management
Syed I Khalid1, Pranav Mirpuri2, Joanna M Roy1
1Department of Neurosurgery, University of Illinois at Chicago, Chicago, IL, USA.
Insights
Direct oral anticoagulants (DOACs) demonstrated comparable safety to vitamin K antagonists (VKAs) for managing left ventricular thrombus (LVT). This study found no significant differences in major bleeding or stroke events between DOACs and VKAs in LVT patients.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Left ventricular thrombus (LVT) management often involves anticoagulation therapy.
- Direct oral anticoagulants (DOACs) and vitamin K antagonists (VKAs) are common anticoagulant choices.
- Comparative safety data for DOACs versus VKAs in LVT management is crucial.
Purpose of the Study:
- To compare the incidence of intracranial hemorrhage (ICH), ischemic stroke, transient ischemic attack (TIA), and major bleeding events.
- To evaluate the safety profiles of DOACs versus VKAs in patients with LVT.
- To assess outcomes at 12 and 24 months post-treatment initiation.
Main Methods:
- Retrospective analysis of claims data involving 3152 patients treated for LVT.
- Exact matching of two cohorts based on age, sex, and comorbidities.
- Kaplan-Meier method used to assess differences in primary outcomes (ICH, ischemic stroke, TIA, major bleeding) at 12 and 24 months.
Main Results:
- A matched cohort of 336 patients (168 per group) was analyzed.
- No statistically significant differences were observed in the rates of ICH, ischemic stroke, TIA, or major bleeding events between DOAC and VKA groups at 12 months.
- Similar findings of no significant differences in these adverse events were noted at 24 months between the two anticoagulant groups.
Conclusions:
- Direct oral anticoagulants (DOACs) appear to be safe and effective alternatives to vitamin K antagonists (VKAs) for left ventricular thrombus (LVT) management.
- The findings support the use of DOACs in clinical practice for LVT patients.
- Further prospective studies are warranted to confirm these safety and efficacy outcomes.
Background:
This study compared the rates of intracranial hemorrhage (ICH), ischemic stroke, transient ischemic attack (TIA), and major bleeding events between patients receiving direct oral anticoagulants (DOACs) or vitamin K antagonists (VKAs) for left ventricular thrombus (LVT) management.
Methods:
In this retrospective analysis of claims data, 3152 patients receiving treatment for LVT were identified. Two cohorts were exactly matched on age, sex, and pertinent comorbidities. The primary outcomes were rates of ICH, ischemic stroke, TIA, and major bleeding events between the two groups at 12 months and 24 months. Differences were assessed using the Kaplan-Meier method. Data was analyzed using R (Version 4.1, R Foundation, Vienna, Austria).
Results:
336 patients were compared after the match. The majority were aged between 50-75 (76.2%), were male (80.1%), and had hypertension (77.38%) and hyperlipidemia (66.07%). At 12 months, there were no differences in the rates of ICH (3/168 vs. 2/168, p = 0.7), ischemic stroke (22/168 vs. 15/168, p = 0.2), TIA (9/168 vs 3/168, p = 0.08), or major bleeding events (25/168 vs 35/168, p = 0.1) between DOAC and VKA groups, respectively. Similarly, there were no differences at 24 months in ICH (4/168 vs. 4/168, p = 1), ischemic stroke (26/168 vs. 26/168, p = 0.9), TIA (10/168 vs 4/168, p = 0.1), and major bleeding events (36/168 vs 45/168, p = 0.2) between DOAC and VKA groups, respectively.
Conclusions:
DOACs appear to be safe alternatives to VKAs, substantiating their use for LVT management. Further evaluation is nevertheless warranted.
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