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Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis

BACKGROUND: Several studies have investigated the effect of non–vitamin K antagonist oral anticoagulants (NOACs) in atrial fibrillation (AF) patients with cancer, but the results remain controversial. Therefore, we conducted a meta‐analysis to compare the efficacy and safety of NOACs versus warfarin...

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Autores principales: Deng, Yuqing, Tong, Yifan, Deng, Yuanyuan, Zou, Le, Li, Shunhui, Chen, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662149/
https://www.ncbi.nlm.nih.gov/pubmed/31310583
http://dx.doi.org/10.1161/JAHA.119.012540
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author Deng, Yuqing
Tong, Yifan
Deng, Yuanyuan
Zou, Le
Li, Shunhui
Chen, Hui
author_facet Deng, Yuqing
Tong, Yifan
Deng, Yuanyuan
Zou, Le
Li, Shunhui
Chen, Hui
author_sort Deng, Yuqing
collection PubMed
description BACKGROUND: Several studies have investigated the effect of non–vitamin K antagonist oral anticoagulants (NOACs) in atrial fibrillation (AF) patients with cancer, but the results remain controversial. Therefore, we conducted a meta‐analysis to compare the efficacy and safety of NOACs versus warfarin in this population. METHODS AND RESULTS: We systematically searched the PubMed and Embase databases until February 16, 2019 for studies comparing the effect of NOACs with warfarin in AF patients with cancer. Risk ratios (RRs) with 95% CIs were extracted and pooled by a random‐effects model. Five studies involving 8908 NOACs and 12 440 warfarin users were included. There were no significant associations between cancer status and risks of stroke or systemic embolism, major bleeding, or death in AF patients. Compared with warfarin, NOACs were associated with decreased risks of stroke or systemic embolism (RR, 0.52; 95% CI, 0.28–0.99), venous thromboembolism (RR, 0.37, 95% CI, 0.22–0.63), and intracranial or gastrointestinal bleeding (RR, 0.65; 95% CI, 0.42–0.98) and with borderline significant reductions in ischemic stroke (RR, 0.63; 95% CI, 0.40–1.00) and major bleeding (RR, 0.73; 95% CI, 0.53–1.00). In addition, risks of efficacy and safety outcomes of NOACs versus warfarin were similar between AF patients with and without cancer. CONCLUSIONS: In patients with AF and cancer, compared with warfarin, NOACs had lower or similar rates of thromboembolic and bleeding events and posed a reduced risk of venous thromboembolism.
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spelling pubmed-66621492019-08-02 Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis Deng, Yuqing Tong, Yifan Deng, Yuanyuan Zou, Le Li, Shunhui Chen, Hui J Am Heart Assoc Systematic Review and Meta‐analysis BACKGROUND: Several studies have investigated the effect of non–vitamin K antagonist oral anticoagulants (NOACs) in atrial fibrillation (AF) patients with cancer, but the results remain controversial. Therefore, we conducted a meta‐analysis to compare the efficacy and safety of NOACs versus warfarin in this population. METHODS AND RESULTS: We systematically searched the PubMed and Embase databases until February 16, 2019 for studies comparing the effect of NOACs with warfarin in AF patients with cancer. Risk ratios (RRs) with 95% CIs were extracted and pooled by a random‐effects model. Five studies involving 8908 NOACs and 12 440 warfarin users were included. There were no significant associations between cancer status and risks of stroke or systemic embolism, major bleeding, or death in AF patients. Compared with warfarin, NOACs were associated with decreased risks of stroke or systemic embolism (RR, 0.52; 95% CI, 0.28–0.99), venous thromboembolism (RR, 0.37, 95% CI, 0.22–0.63), and intracranial or gastrointestinal bleeding (RR, 0.65; 95% CI, 0.42–0.98) and with borderline significant reductions in ischemic stroke (RR, 0.63; 95% CI, 0.40–1.00) and major bleeding (RR, 0.73; 95% CI, 0.53–1.00). In addition, risks of efficacy and safety outcomes of NOACs versus warfarin were similar between AF patients with and without cancer. CONCLUSIONS: In patients with AF and cancer, compared with warfarin, NOACs had lower or similar rates of thromboembolic and bleeding events and posed a reduced risk of venous thromboembolism. John Wiley and Sons Inc. 2019-07-16 /pmc/articles/PMC6662149/ /pubmed/31310583 http://dx.doi.org/10.1161/JAHA.119.012540 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Systematic Review and Meta‐analysis
Deng, Yuqing
Tong, Yifan
Deng, Yuanyuan
Zou, Le
Li, Shunhui
Chen, Hui
Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title_full Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title_fullStr Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title_full_unstemmed Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title_short Non–Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Cancer and Atrial Fibrillation: A Systematic Review and Meta‐Analysis
title_sort non–vitamin k antagonist oral anticoagulants versus warfarin in patients with cancer and atrial fibrillation: a systematic review and meta‐analysis
topic Systematic Review and Meta‐analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662149/
https://www.ncbi.nlm.nih.gov/pubmed/31310583
http://dx.doi.org/10.1161/JAHA.119.012540
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