Real-world evidence comparing oral anticoagulants in non-valvular atrial fibrillation: a systematic review and network meta-analysis

Author:

Deitelzweig Steven1ORCID,Bergrath Evelien2ORCID,di Fusco Manuela3ORCID,Kang Amiee4,Savone Mirko3,Cappelleri Joseph C3ORCID,Russ Cristina3ORCID,Betts Marissa5ORCID,Cichewicz Allie5ORCID,Schaible Kassandra5,Tarpey Jialu5,Fahrbach Kyle5ORCID

Affiliation:

1. Ochsner Health System, Department of Hospital Medicine, New Orleans, LA 70121, USA

2. Regeneron Pharmaceuticals, Inc., Health Economics and Outcomes Research, Tarrytown, NY 10591, USA

3. Pfizer, Inc., Health Economics and Outcomes Research, New York, NY 10017, USA

4. Bristol Myers Squibb Company, Health Economics and Outcomes Research, Lawrenceville, NJ 08648, USA

5. Evidera, Evidence Synthesis, Modeling & Communication, Waltham, MA 02451, USA

Abstract

Aim: To compare real-world effectiveness/safety of non-vitamin K antagonist oral anticoagulants and vitamin K antagonists among patients with non-valvular atrial fibrillation. Materials & methods: A systematic review of electronic databases yielded 7661 citations published from January 2013 to January 2020. Fifty-five studies were included in Bayesian network meta-analyses of hazard ratios. Results & conclusion: In comparison with vitamin K antagonists, apixaban, dabigatran and rivaroxaban were associated with a reduced risk of stroke or systemic embolism, ischemic stroke, intracranial hemorrhage and all-cause mortality. Apixaban, dabigatran and edoxaban, but not rivaroxaban, were associated with a reduced risk of major bleeding. This study confirmed the effectiveness and safety of non-vitamin K antagonist oral anticoagulants for the treatment of non-valvular atrial fibrillation in real-world settings, consistent with clinical trial evidence.

Funder

Bristol-Myers Squibb

Pfizer

Publisher

Future Medicine Ltd

Subject

Cardiology and Cardiovascular Medicine,Molecular Medicine

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