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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Direct Anticoagulants and Risk of Myocardial Infarction, a Multiple Treatment Network Meta-Analysis
Péter Kupó1, Zsolt Szakács2,3, Margit Solymár2
1Heart Institute, Medical School, University of Pécs, Pécs, Hungary.
Abstract:
We assessed the cardiovascular safety of long-term direct-acting oral anticoagulant (DOAC) treatment. A search of the medical literature was performed from inception until May 31, 2019. Inclusion criteria were (1) randomized trial that assessed the clinical efficacy and/or safety of 1 or more DOAC, (2) control group including oral anticoagulation and/or antiplatelet and/or placebo treatment, and (3) the incidence of acute coronary syndrome during follow-up was reported. Fixed-effect and random-effects models were applied. The analyzed outcomes were myocardial infarction (MI), major bleeding, and mortality. Twenty-eight randomized clinical trials (196 761 patients) were included. Rivaroxaban was associated with a 21% reduction in the relative risk of MI when compared to placebo (relative risk [RR]: 0.79 [95% credible interval, CrI: 0.65-0.94]) and a 31% reduction (RR: 0.70 [95% CrI: 0.53-0.89]) when compared to dabigatran. Apixaban resulted in 24% (RR: 0.76 [95% CrI: 0.58-0.99]) and vitamin K antagonists anticoagulation resulted in 19% (RR: 0.81 [95% CrI: 0.65-0.98]) risk reduction compared to dabigatran. The computed probability of being the first best choice of treatment was 61.8% for rivaroxaban. Cardiovascular safety shows considerable heterogeneity among oral anticoagulants. Treatment with rivaroxaban is associated with reduced rate of MI.
Insights
Long-term direct-acting oral anticoagulant (DOAC) treatment shows varied cardiovascular safety. Rivaroxaban demonstrated a reduced risk of myocardial infarction (MI) compared to placebo and dabigatran.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Direct-acting oral anticoagulants (DOACs) are widely used for thromboprophylaxis.
- Assessing the long-term cardiovascular safety of DOACs is crucial for clinical decision-making.
- Heterogeneity in cardiovascular safety profiles among different oral anticoagulants necessitates comparative analysis.
Purpose of the Study:
- To evaluate the cardiovascular safety of long-term direct-acting oral anticoagulant (DOAC) treatment.
- To compare the incidence of myocardial infarction (MI) among various DOACs, vitamin K antagonists (VKAs), and placebo.
Main Methods:
- Systematic literature search of randomized clinical trials (RCTs) up to May 31, 2019.
- Inclusion of 28 RCTs involving 196,761 patients assessing DOAC efficacy and/or safety.
- Application of fixed-effect and random-effects models to analyze outcomes including MI, major bleeding, and mortality.
Main Results:
- Rivaroxaban showed a 21% relative risk reduction in MI versus placebo (RR: 0.79) and 31% versus dabigatran (RR: 0.70).
- Apixaban demonstrated a 24% risk reduction in MI compared to dabigatran (RR: 0.76).
- Vitamin K antagonists offered a 19% risk reduction in MI compared to dabigatran (RR: 0.81).
Conclusions:
- Cardiovascular safety profiles exhibit significant heterogeneity across different oral anticoagulants.
- Rivaroxaban is associated with a reduced rate of myocardial infarction, suggesting it as a potentially favorable option.
- Further comparative studies are warranted to fully elucidate the long-term cardiovascular safety of DOACs.
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