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Comparison of Direct Oral Anticoagulants and Vitamin K Antagonists for Left Ventricular Thrombus: A Global
Zhihong Yao1, Ying Gue2, Gregory Y H Lip3
1Liverpool Heart and Chest Hospital, United Kingdom.
Insights
Direct oral anticoagulants (DOACs) show improved safety and efficacy for left ventricular thrombus treatment compared to vitamin K antagonists (VKAs). These findings apply to patients with and without recent acute coronary syndrome, indicating DOACs as a preferred option.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Limited guidelines exist for managing left ventricular thrombus (LVT), especially with oral anticoagulants and dual antiplatelet therapy in acute myocardial infarction.
- This study addresses the need for comparative data on direct oral anticoagulants (DOACs) versus vitamin K antagonists (VKAs) for LVT management.
Purpose of the Study:
- To assess the safety and efficacy of DOACs compared to VKAs in patients with left ventricular thrombus.
- To evaluate outcomes in patients with and without recent acute coronary syndrome.
Main Methods:
- Retrospective observational study utilizing the TriNetX research network.
- Inclusion of patients with LVT treated with DOACs or VKAs from December 2013 to December 2023.
- Subgroup analyses for patients with/without recent acute coronary syndrome, with 90-day risk and survival analysis.
Main Results:
- DOACs showed significantly lower rates of stroke, major bleeding, and systemic embolism compared to VKAs in the overall cohort.
- In the acute coronary syndrome subgroup, DOACs demonstrated reduced risks of stroke and systemic embolism.
- The non-acute coronary syndrome subgroup also showed lower stroke and major bleeding risks with DOACs.
Conclusions:
- Direct oral anticoagulants (DOACs) offer superior safety and efficacy compared to vitamin K antagonists (VKAs) for treating left ventricular thrombus.
- These benefits were consistent across patient groups, including those with and without recent acute coronary syndrome.
Introduction:
Guidelines for managing left ventricular thrombus remain limited, particularly when incorporating oral anticoagulants into dual antiplatelet therapy for acute myocardial infarction. This study aims to assess the safety and efficacy of direct oral anticoagulants (DOACs) vs vitamin K antagonists (VKAs) in managing left ventricular thrombus among patients with and without recent myocardial infarction.
Methods:
This retrospective observational study used data from the TriNetX research network. Patients with left ventricular thrombus treated with either DOACs or VKAs between December 1, 2013 and December 1, 2023, were included. Subgroup analyses were conducted for patients with or without recent acute coronary syndrome (<1 month). Risk and Kaplan-Meier survival analysis were conducted at 90 days after the indexed event.
Results:
A total of 39,770 patients were included. DOACs treatment had lower rates of stroke (11.8% vs 13.7%; relative risk [RR] 0.859; 95% confidence interval [CI], 0.816-0.905; P < .001), major bleeding (4.8% vs 5.3%; RR 0.902; 95% CI, 0.829-0.982; P = .018), and systemic embolism (3.5% vs 4.2%; RR 0.841; 95% CI, 0.762-0.928; P = .001) compared with VKAs in overall cohort. Within the acute coronary syndrome group (n = 14,302), DOACs had lower stroke (12.3% vs 14.4%, RR 0.860; 95% CI, 0.791-0.935; P < .0001) and systemic embolism (3.1% vs 4%; RR 0.774; 95% CI, 0.651-0.919; P = .003) risks. For non-acute coronary syndrome group (n = 24,162), DOACs had lower stroke (11.4% vs 13.1%; RR 0.868; 95% CI, 0.811-0.929; P < .001) and major bleeding (4.8% vs 5.5%; RR 0.877; 95% CI, 0.787-0.977; P = .017) risks. No significant differences in all-cause mortality were observed across groups.
Conclusion:
DOACs demonstrated better safety and efficacy outcomes when compared with VKAs in left ventricular thrombus treatment, with or without recent acute coronary syndrome.
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