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Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis

BACKGROUND AND AIM: Current observational studies have compared the effectiveness and safety of edoxaban with other oral anticoagulants in patients with AF, but the results are still disputed. This meta-analysis was conducted to compare the effect of edoxaban in patients with AF. METHODS: We perform...

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Autores principales: Zhang, Bailin, Cheng, Winglam, Kaisaier, Wulamiding, Gu, Zhenbang, Zhu, Wengen, Jiang, Qiuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665752/
https://www.ncbi.nlm.nih.gov/pubmed/38027839
http://dx.doi.org/10.1016/j.heliyon.2023.e21740
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author Zhang, Bailin
Cheng, Winglam
Kaisaier, Wulamiding
Gu, Zhenbang
Zhu, Wengen
Jiang, Qiuhua
author_facet Zhang, Bailin
Cheng, Winglam
Kaisaier, Wulamiding
Gu, Zhenbang
Zhu, Wengen
Jiang, Qiuhua
author_sort Zhang, Bailin
collection PubMed
description BACKGROUND AND AIM: Current observational studies have compared the effectiveness and safety of edoxaban with other oral anticoagulants in patients with AF, but the results are still disputed. This meta-analysis was conducted to compare the effect of edoxaban in patients with AF. METHODS: We performed systematic research from the PubMed, EMBASE, and Cochrane Library databases until November 2022 to obtain relevant observational studies. Adjusted risk ratios (RRs) and 95 % confidence intervals (CIs) of the outcomes were collected and pooled by a random-effects model. This study was prospectively registered in PROSPERO (CRD42022314222). RESULTS: A total of 17 observational studies were included in this meta-analysis. Compared with vitamin K antagonists, edoxaban was associated with lower risks of stroke or systemic embolism (RR = 0.67, 95 % CI:0.61–0.74), major bleeding (RR = 0.54, 95 % CI:0.44–0.67), and intracranial hemorrhage (RR = 0.51, 95 % CI:0.29–0.90). Compared with dabigatran or rivaroxaban, edoxaban was associated with reduced risks of stroke or systemic embolism (dabigatran [RR = 0.76, 95 % CI:0.66–0.87]; rivaroxaban [RR = 0.81, 95 % CI:0.70–0.94]) and major bleeding (dabigatran [RR = 0.82, 95 % CI:0.69–0.98]; rivaroxaban [RR = 0.81, 95 % CI:0.70–0.94]). Compared with apixaban, edoxaban was associated with a reduced risk of stroke or systemic embolism (RR = 0.87, 95 % CI:0.79–0.97), but had similar risks of bleeding events. CONCLUSIONS: Our current evidence suggested that edoxaban might have superior effectiveness and/or safety outcomes than vitamin K antagonists, dabigatran, rivaroxaban, and apixaban for stroke prevention in patients with AF.
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spelling pubmed-106657522023-11-03 Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis Zhang, Bailin Cheng, Winglam Kaisaier, Wulamiding Gu, Zhenbang Zhu, Wengen Jiang, Qiuhua Heliyon Review Article BACKGROUND AND AIM: Current observational studies have compared the effectiveness and safety of edoxaban with other oral anticoagulants in patients with AF, but the results are still disputed. This meta-analysis was conducted to compare the effect of edoxaban in patients with AF. METHODS: We performed systematic research from the PubMed, EMBASE, and Cochrane Library databases until November 2022 to obtain relevant observational studies. Adjusted risk ratios (RRs) and 95 % confidence intervals (CIs) of the outcomes were collected and pooled by a random-effects model. This study was prospectively registered in PROSPERO (CRD42022314222). RESULTS: A total of 17 observational studies were included in this meta-analysis. Compared with vitamin K antagonists, edoxaban was associated with lower risks of stroke or systemic embolism (RR = 0.67, 95 % CI:0.61–0.74), major bleeding (RR = 0.54, 95 % CI:0.44–0.67), and intracranial hemorrhage (RR = 0.51, 95 % CI:0.29–0.90). Compared with dabigatran or rivaroxaban, edoxaban was associated with reduced risks of stroke or systemic embolism (dabigatran [RR = 0.76, 95 % CI:0.66–0.87]; rivaroxaban [RR = 0.81, 95 % CI:0.70–0.94]) and major bleeding (dabigatran [RR = 0.82, 95 % CI:0.69–0.98]; rivaroxaban [RR = 0.81, 95 % CI:0.70–0.94]). Compared with apixaban, edoxaban was associated with a reduced risk of stroke or systemic embolism (RR = 0.87, 95 % CI:0.79–0.97), but had similar risks of bleeding events. CONCLUSIONS: Our current evidence suggested that edoxaban might have superior effectiveness and/or safety outcomes than vitamin K antagonists, dabigatran, rivaroxaban, and apixaban for stroke prevention in patients with AF. Elsevier 2023-11-03 /pmc/articles/PMC10665752/ /pubmed/38027839 http://dx.doi.org/10.1016/j.heliyon.2023.e21740 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Zhang, Bailin
Cheng, Winglam
Kaisaier, Wulamiding
Gu, Zhenbang
Zhu, Wengen
Jiang, Qiuhua
Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title_full Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title_fullStr Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title_full_unstemmed Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title_short Effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: A meta-analysis
title_sort effect of edoxaban compared with other oral anticoagulants for stroke prevention in patients with atrial fibrillation: a meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665752/
https://www.ncbi.nlm.nih.gov/pubmed/38027839
http://dx.doi.org/10.1016/j.heliyon.2023.e21740
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