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Non-vitamin K antagonist oral anticoagulants with amiodarone, P-glycoprotein inhibitors, or polypharmacy in patients with atrial fibrillation: Systematic review and meta-analysis

Authors
Kim, In-SooKim, Hyun-JungYu, Hee TaeKim, Tae-HoonUhm, Jae-SunKim, Jong-YounJoung, BoyoungLee, Moon-HyoungPak, Hui-Nam
Issue Date
Jun-2019
Publisher
ELSEVIER
Keywords
Atrial fibrillation; Non-vitamin K antagonist oral anticoagulants; Amiodarone; Polypharmacy; Meta-analysis
Citation
JOURNAL OF CARDIOLOGY, v.73, no.6, pp 515 - 521
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CARDIOLOGY
Volume
73
Number
6
Start Page
515
End Page
521
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/28670
DOI
10.1016/j.jjcc.2018.12.018
ISSN
0914-5087
1876-4738
Abstract
Background: Amiodarone, which inhibits CYP2C9 and P-glycoprotein, is commonly prescribed with non-vitamin K antagonist oral anticoagulants (NOACs) and polypharmacy in high-risk atrial fibrillation (AF) patients. We studied efficacy and safety of NOACs in AF patients receiving amiodarone, P-glycoprotein inhibitor, or polypharmacy. Methods: After a systematic database search (Medline, EMBASE, CENTRAL, SCOPUS, and Web of Science), four phase-III randomized trials comparing NOACs and warfarin in "with/without amiodarone," "with/without P-glycoprotein inhibitors," or "with/without multiple (>= 5, polypharmacy) concomitant drugs" subgroups were included. The outcomes were pooled using a random-effects model to determine the relative risks (RRs) for stroke/systemic thromboembolism (SSTE), major bleeding (MB), intracranial hemorrhage (ICH), and all-cause mortality. Results: Among patients taking amiodarone, superiority of NOACs over warfarin in non-amiodarone users disappeared in terms of SSTE (p = 0.11), MB (p = 0.95), ICH (p = 0.26), and mortality (p = 0.32). No safety benefit (MB) of NOACs compared to warfarin was shown in patients taking P-glycoprotein inhibitors (p = 0.47), but SSTE prevention was still superior with NOACs compared to warfarin in the same patient group [RR = 0.78 (0.61-0.99), p = 0.04, I-2 = 11%]. In AF patients with polypharmacy. NOACs showed a lower risk of SSTE [RR = 0.82 (0.71-0.96), p = 0.01, I-2 = 0%] and mortality [RR = 0.91 (0.83-0.99), p = 0.04, I-2 = 0%], but not MB (p = 0.81) compared to warfarin. Conclusions: NOACs were equivalent to warfarin among AF patients with concomitant amiodarone use in terms of efficacy, safety, and mortality. There was no safety benefit of NOACs over warfarin in patients using polypharmacy or P-glycoprotein inhibitors. Systematic review registration: The protocol of this meta-analysis was registered on PROSPERO under CRD42018104808 (htps://www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42018104808). (C) 2019 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.
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