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

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...

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Autores principales: Fu, Wenbin, Guo, Hongyang, Guo, Jianping, Lin, Kun, Wang, Haijun, Zhang, Yu, Wang, Yutang, Shan, Zhaoliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244213/
https://www.ncbi.nlm.nih.gov/pubmed/25304034
http://dx.doi.org/10.2459/JCM.0000000000000206
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author Fu, Wenbin
Guo, Hongyang
Guo, Jianping
Lin, Kun
Wang, Haijun
Zhang, Yu
Wang, Yutang
Shan, Zhaoliang
author_facet Fu, Wenbin
Guo, Hongyang
Guo, Jianping
Lin, Kun
Wang, Haijun
Zhang, Yu
Wang, Yutang
Shan, Zhaoliang
author_sort Fu, Wenbin
collection PubMed
description 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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spelling pubmed-42442132014-11-26 Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis Fu, Wenbin Guo, Hongyang Guo, Jianping Lin, Kun Wang, Haijun Zhang, Yu Wang, Yutang Shan, Zhaoliang J Cardiovasc Med (Hagerstown) Systematic Reviews 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. Lippincott Williams & Wilkins 2014-12 2014-11-07 /pmc/articles/PMC4244213/ /pubmed/25304034 http://dx.doi.org/10.2459/JCM.0000000000000206 Text en © 2014 Italian Federation of Cardiology http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Systematic Reviews
Fu, Wenbin
Guo, Hongyang
Guo, Jianping
Lin, Kun
Wang, Haijun
Zhang, Yu
Wang, Yutang
Shan, Zhaoliang
Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title_full Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title_fullStr Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title_full_unstemmed Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title_short Relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
title_sort relative efficacy and safety of direct oral anticoagulants in patients with atrial fibrillation by network meta-analysis
topic Systematic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244213/
https://www.ncbi.nlm.nih.gov/pubmed/25304034
http://dx.doi.org/10.2459/JCM.0000000000000206
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