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Review
. 2014 Dec;15(12):873-9.
doi: 10.2459/JCM.0000000000000206.

Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis

Affiliations
Review

Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis

Wenbin Fu et al. J Cardiovasc Med (Hagerstown). 2014 Dec.

Erratum in

  • J Cardiovasc Med (Hagerstown). 2015 Feb;16(2):148

Abstract

Background: Much direct evidence has proved that the novel oral anticoagulants (NOACs) are noninferior or superior to warfarin for stroke prevention in patients with nonvalvular atrial fibrillation, and lead to a relevant decrease in bleeding profiles. However, no study has compared NOACs with each other head-to-head. The current study is a network meta-analysis aiming to assess the efficacy and safety of NOACs.

Methods: Cochrane library, Pubmed NCBI, EMBASE and MEDLINE were systematically searched for randomized controlled trials that assessed the efficacy and safety profiles of NOACs compared with warfarin. The primary outcome was the rate of stroke or systemic embolism, and the secondary outcome was the rate of bleeding events. Network meta-analysis was performed using Markov chain Monte Carlo methods.

Results: A total of four phase III randomized controlled trials (n = 71683) met the inclusion criteria. All NOACs except low dose of edoxaban showed noninferior efficacies to warfarin in stroke prevention. In the field of hemorrhage, apixaban was safer than edoxaban 60 mg in any bleeding events and had fewer major bleeding events compared with dabigatran 150 mg and rivaroxaban.

Conclusion: NOACs are promising candidates for stroke prevention in patients with nonvalvular atrial fibrillation due to a favorable risk-benefit profile. All NOACs other than edoxaban 30 mg had parallel efficacies with respect to stroke prevention. Apixaban had an advantage over the other NOACs in safety.

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Figures

Fig. 1
Fig. 1
Flow diagram of selection process of randomized controlled trials included in meta-analysis.

References

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