Affiliation:
1. Department of Cardiology, Peking University First Hospital, Beijing 100034, China
2. Department of Pharmacy, Peking University
First Hospital, Beijing 100034, China
3. Department of Pharmacy, Peking University First Hospital, Beijing, China
Abstract
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.
Registration No:
A review protocol (number: CRD 42020211376) was registered in the PROSPERO International
prospective register of systematic reviews.
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology
Cited by
3 articles.
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