Effectiveness and safety of oral anticoagulants in older adults with non-valvular atrial fibrillation and heart failure

拜瑞妥 阿哌沙班 危险系数 达比加群 华法林 医学 狼牙棒 心房颤动 内科学 心力衰竭 心脏病学 冲程(发动机) 维生素K拮抗剂 置信区间 瓣膜性心脏病 依杜沙班 人口 抗凝剂 心肌梗塞 经皮冠状动脉介入治疗 工程类 机械工程
作者
Alpesh Amin,Alessandra Garcia Reeves,Xiaoyan Li,Amol Dhamane,Xuemei Luo,Manuela Di Fusco,Anagha Nadkarni,Keith Friend,Lisa Rosenblatt,Jack Mardekian,Xiangbin Pan,Hüseyin Yüce,Allison Keshishian
出处
期刊:PLOS ONE [Public Library of Science]
卷期号:14 (3): e0213614-e0213614 被引量:26
标识
DOI:10.1371/journal.pone.0213614
摘要

Direct oral anticoagulants (DOACs) are at least as efficacious and safe as warfarin among non-valvular atrial fibrillation (NVAF) patients; limited evidence is available regarding NVAF patients with heart failure (HF). US Medicare enrollees with NVAF and HF initiating DOACs (apixaban, rivaroxaban, dabigatran) or warfarin were selected. Propensity score matching and Cox models were used to estimate the risk of stroke/systemic embolism (SE), major bleeding (MB), and major adverse cardiac events (MACE) comparing DOACs versus warfarin and DOACs versus DOACs. We identified 10,570 apixaban-warfarin, 4,297 dabigatran-warfarin, 15,712 rivaroxaban-warfarin, 4,263 apixaban-dabigatran, 10,477 apixaban-rivaroxaban, and 4,297 dabigatran-rivaroxaban matched pairs. Compared to warfarin, apixaban had lower rates of stroke/SE (hazard ratio = 0.64, 95% confidence interval = 0.48–0.85), MB (hazard ratio = 0.66, 0.58–0.76), and MACE (hazard ratio = 0.73,0.67–0.79); dabigatran and rivaroxaban had lower rates of MACE (hazard ratio = 0.87,0.77–0.99; hazard ratio = 0.84, 0.79–0.89, respectively). Rivaroxaban had a lower stroke/SE rate (hazard ratio = 0.65, 0.52–0.81) and higher MB rate (hazard ratio = 1.18, 1.08–1.30) versus warfarin. Compared to dabigatran and rivaroxaban, apixaban had lower MB (hazard ratio = 0.71, 0.57–0.89; hazard ratio = 0.55, 0.49–0.63) and MACE rates (hazard ratio = 0.80, 0.69–0.93; hazard ratio = 0.86, 0.79–0.94), respectively. All DOACs had lower MACE rates versus warfarin; differences were observed in stroke/SE and MB. Our findings provide insights about OAC therapy among NVAF patients with HF.

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