Propafenone- vs. amiodarone-associated adverse cardiac outcomes in patients with atrial fibrillation and heart failure.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Yi-Cheng Lin, Bi-Li Chen, Chien-Yi Hsu, Li-Ying Chen, Shing-Jong Lin, Gregory Y H Lip, Li-Nien Chien, Chun-Yao Huang
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引用次数: 0

Abstract

Aims: Clinical trials have shown an increased risk of death in patients with recent myocardial infarction who received antiarrhythmic drugs such as flecainide, encainide or moricizine, especially in the presence of associated structural heart disease such as cardiac dysfunction. This study aimed to evaluate the safety outcomes of propafenone use in atrial fibrillation patients with heart failure when compared to those of amiodarone use.

Methods: This population-based cohort study used the National Health Insurance Research Database in Taiwan. Eligible patients were those who had atrial fibrillation or atrial flutter diagnosis, had heart failure diagnosis, and first received propafenone or amiodarone between 2002 and 2018. The primary endpoints were death due to arrhythmia and the composite proarrhythmic outcome, which consisted of sudden cardiac arrest, arrhythmic death, ventricular arrhythmia and implantation of defibrillator.

Results: After propensity score matching, the study cohort consisted of 7235 propafenone and 14 470 amiodarone users. Compared to amiodarone, propafenone was associated with significantly lower risk of the composite proarrhythmic outcome (adjusted hazard ratio: 0.52; 95% confidence interval: 0.42-0.64; P < .001). Propafenone users also had lower risk of death owing to arrhythmia compared to amiodarone users (adjusted hazard ratio: 0.22; 95% confidence interval: 0.08-0.65; P = .006). Subgroup analysis and sensitivity analysis showed similar trends, favouring propafenone.

Conclusion: Propafenone was not significantly associated with increased risk of proarrhythmia and mortality when compared to amiodarone in atrial fibrillation patients with heart failure in contemporary real-world settings. Prospective studies are needed to determine whether propafenone should definitely be avoided in these patients.

心房颤动和心力衰竭患者与普罗帕酮和胺碘酮相关的不良心脏结局。
目的:临床试验表明,近期心肌梗死患者接受抗心律失常药物(如flecainide、encainide或moricizine)的死亡风险增加,特别是在存在相关结构性心脏病(如心功能障碍)的情况下。本研究旨在评价心房颤动合并心力衰竭患者使用普罗帕酮与使用胺碘酮的安全性结果。​符合条件的患者是2002年至2018年间首次接受普罗帕酮或胺碘酮治疗的房颤或心房扑动诊断、心力衰竭诊断的患者。主要终点为心律失常所致死亡和复合致心律失常结局,包括心脏骤停、心律失常死亡、室性心律失常和除颤器植入。结果:倾向评分匹配后,研究队列包括7235名普罗帕酮使用者和14470名胺碘酮使用者。与胺碘酮相比,普罗帕酮与复合心律失常结局的风险显著降低相关(校正风险比:0.52;95%置信区间:0.42-0.64;结论:与胺碘酮相比,普罗帕酮与心衰房颤患者心律失常和死亡率的风险增加没有显著相关。需要前瞻性研究来确定这些患者是否应该绝对避免使用普罗帕酮。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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