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Published on: February 28, 2012
Direct Oral Anticoagulants Compared with Vitamin K Antagonists for Left Ventricular Thrombus: A Systematic Review and
Shu Fang1, Bao-Zhen Zhu1, Fan Yang1
1Department of Cardiology, Peking University First Hospital, Beijing 100034, China.
Insights
Direct oral anticoagulants (DOACs) and vitamin K antagonists (VKAs) show similar safety and efficacy for left ventricular thrombus (LVT) treatment. However, DOACs may offer improved outcomes for patients post-acute myocardial infarction (AMI).
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Direct oral anticoagulants (DOACs) are guideline-recommended for hypercoagulable diseases.
- Their use for left ventricular thrombus (LVT) is off-label due to limited evidence.
- This meta-analysis compares DOACs with vitamin K antagonists (VKAs) for LVT treatment.
Purpose of the Study:
- To assess the safety and efficacy of DOACs versus VKAs in treating left ventricular thrombus (LVT).
- To evaluate outcomes including stroke, systemic embolism, thrombus resolution, bleeding, and mortality.
Main Methods:
- A meta-analysis of 12 observational studies involving 2262 patients.
- Searched PubMed, EMBASE, Cochrane Library, and Web of Science databases.
- Analyzed data using Review Manager 5.3; registered at PROSPERO.
Main Results:
- No significant differences were found between DOACs and VKAs for stroke or systemic embolism (SSE), thrombus resolution, bleeding risk, or mortality.
- Subgroup analysis indicated DOACs may reduce SSE and bleeding risk in post-acute myocardial infarction (AMI) patients.
- Overall efficacy and safety profiles were comparable across treatments.
Conclusions:
- DOACs and VKAs demonstrate similar safety and efficacy for LVT treatment.
- DOACs may present a superior option for LVT management in post-AMI patients.
- Further research could solidify DOACs' role in specific LVT patient populations.
Background:
Direct oral anticoagulants (DOACs) are the guideline-recommended therapy for some hypercoagulable diseases but are used off-label for left ventricular thrombus (LVT) owing to a paucity of evidence. We performed a meta-analysis to assess the safety and efficacy of DOACs compared with vitamin K antagonists (VKAs) for LVT treatment.
Methods:
We comprehensively searched PubMed, EMBASE, Cochrane Library, and Web of Science databases for studies that compared DOACs with VKAs for LVT treatment. Outcome indicators included stroke or systemic embolism (SSE), thrombus resolution, bleeding, and death. The Newcastle-Ottawa scale was used to evaluate the quality of included studies. Data were analyzed using Review Manager 5.3, and the meta-analysis is registered at PROSPERO (CRD 42020211376).
Results:
We included 12 observational studies (n = 2262 patients). SSE was similar for DOACs and VKAs groups (odds ratio (OR) = 1.01, 95% confidence interval (CI) 0.66-1.54, P = 0.95). For thrombus resolution, DOACs were not significantly different to VKAs (OR = 1.15, 95% CI 0.54-2.45, P = 0.71). DOACs and VKAs had a similar bleeding risk (OR = 0.78, 95% CI 0.45-1.35, P = 0.37). DOACs and VKAs groups had a comparable mortality (OR = 0.91, 95% CI 0.50-1.65, P = 0.76). Subgroup analysis showed that post-acute myocardial infarction (AMI) patients using DOACs had a lower risk of SSE (OR = 0.24, 95% CI 0.07-0.87, P = 0.03) and bleeding (OR = 0.38, 95% CI 0.18-0.81, P = 0.01).
Conclusion:
DOACs and VKAs showed no difference in the safety and efficacy of patients with LVT. DOACs might be superior to VKAs for LVT treatment in post-AMI patients.
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