Effect of Digoxin vs Bisoprolol for Heart Rate Control in Atrial Fibrillation on Patient-Reported Quality of Life

医学 比索洛尔 地高辛 心房颤动 内科学 心脏病学 心力衰竭 心率 血压
作者
Dipak Kotecha,Karina V Bunting,Simrat Gill,Samir Mehta,Mary Stanbury,J. C. H. Jones,Sandra Haynes,Melanie Calvert,Jonathan J Deeks,Richard P. Steeds,Victoria Y. Strauss,Kazem Rahimi,A. John Camm,Michael Griffith,Gregory Y.H. Lip,John Townend,Paulus Kirchhof,Rate Control Therapy Evaluation in Permanent Atrial Fibrillation (RATE-AF) Team
出处
期刊:JAMA [American Medical Association]
卷期号:324 (24): 2497-2497 被引量:229
标识
DOI:10.1001/jama.2020.23138
摘要

Importance: There is little evidence to support selection of heart rate control therapy in patients with permanent atrial fibrillation, in particular those with coexisting heart failure. Objective: To compare low-dose digoxin with bisoprolol (a β-blocker). Design, Setting, and Participants: Randomized, open-label, blinded end-point clinical trial including 160 patients aged 60 years or older with permanent atrial fibrillation (defined as no plan to restore sinus rhythm) and dyspnea classified as New York Heart Association class II or higher. Patients were recruited from 3 hospitals and primary care practices in England from 2016 through 2018; last follow-up occurred in October 2019. Interventions: Digoxin (n = 80; dose range, 62.5-250 μg/d; mean dose, 161 μg/d) or bisoprolol (n = 80; dose range, 1.25-15 mg/d; mean dose, 3.2 mg/d). Main Outcomes and Measures: The primary end point was patient-reported quality of life using the 36-Item Short Form Health Survey physical component summary score (SF-36 PCS) at 6 months (higher scores are better; range, 0-100), with a minimal clinically important difference of 0.5 SD. There were 17 secondary end points (including resting heart rate, modified European Heart Rhythm Association [EHRA] symptom classification, and N-terminal pro-brain natriuretic peptide [NT-proBNP] level) at 6 months, 20 end points at 12 months, and adverse event (AE) reporting. Results: Among 160 patients (mean age, 76 [SD, 8] years; 74 [46%] women; mean baseline heart rate, 100/min [SD, 18/min]), 145 (91%) completed the trial and 150 (94%) were included in the analysis for the primary outcome. There was no significant difference in the primary outcome of normalized SF-36 PCS at 6 months (mean, 31.9 [SD, 11.7] for digoxin vs 29.7 [11.4] for bisoprolol; adjusted mean difference, 1.4 [95% CI, -1.1 to 3.8]; P = .28). Of the 17 secondary outcomes at 6 months, there were no significant between-group differences for 16 outcomes, including resting heart rate (a mean of 76.9/min [SD, 12.1/min] with digoxin vs a mean of 74.8/min [SD, 11.6/min] with bisoprolol; difference, 1.5/min [95% CI, -2.0 to 5.1/min]; P = .40). The modified EHRA class was significantly different between groups at 6 months; 53% of patients in the digoxin group reported a 2-class improvement vs 9% of patients in the bisoprolol group (adjusted odds ratio, 10.3 [95% CI, 4.0 to 26.6]; P < .001). At 12 months, 8 of 20 outcomes were significantly different (all favoring digoxin), with a median NT-proBNP level of 960 pg/mL (interquartile range, 626 to 1531 pg/mL) in the digoxin group vs 1250 pg/mL (interquartile range, 847 to 1890 pg/mL) in the bisoprolol group (ratio of geometric means, 0.77 [95% CI, 0.64 to 0.92]; P = .005). Adverse events were less common with digoxin; 20 patients (25%) in the digoxin group had at least 1 AE vs 51 patients (64%) in the bisoprolol group (P < .001). There were 29 treatment-related AEs and 16 serious AEs in the digoxin group vs 142 and 37, respectively, in the bisoprolol group. Conclusions and Relevance: Among patients with permanent atrial fibrillation and symptoms of heart failure treated with low-dose digoxin or bisoprolol, there was no statistically significant difference in quality of life at 6 months. These findings support potentially basing decisions about treatment on other end points. Trial Registration: ClinicalTrials.gov Identifier: NCT02391337 and clinicaltrialsregister.eu Identifier: 2015-005043-13.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
长孙烙完成签到 ,获得积分10
6秒前
7秒前
LY完成签到,获得积分10
16秒前
18秒前
19秒前
su完成签到 ,获得积分0
21秒前
英吉利25发布了新的文献求助10
23秒前
wj发布了新的文献求助10
25秒前
Eric完成签到,获得积分10
25秒前
knight7m完成签到 ,获得积分10
26秒前
dawn完成签到 ,获得积分10
31秒前
九万里发布了新的文献求助10
32秒前
34秒前
包子完成签到 ,获得积分10
41秒前
44秒前
夕阳下仰望完成签到 ,获得积分10
44秒前
英吉利25发布了新的文献求助10
48秒前
彦成发布了新的文献求助10
49秒前
50秒前
56秒前
宋笨笨完成签到 ,获得积分10
1分钟前
pengpengpeng完成签到,获得积分10
1分钟前
1分钟前
charih完成签到 ,获得积分10
1分钟前
泥嚎完成签到,获得积分10
1分钟前
香蕉新儿完成签到,获得积分10
1分钟前
leilei完成签到,获得积分10
1分钟前
高CA完成签到 ,获得积分10
1分钟前
稻草人完成签到,获得积分10
1分钟前
112完成签到,获得积分10
1分钟前
FFFFFFG完成签到,获得积分10
1分钟前
chen完成签到,获得积分10
1分钟前
林韵悠扬完成签到 ,获得积分10
2分钟前
关畅澎完成签到 ,获得积分10
2分钟前
鱼鱼完成签到 ,获得积分10
2分钟前
2分钟前
369ninja发布了新的文献求助10
2分钟前
Kelly完成签到,获得积分10
2分钟前
无用的老董西完成签到 ,获得积分10
2分钟前
CipherSage应助369ninja采纳,获得10
2分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Cronologia da história de Macau 5000
Petrology and Plate Tectonics 800
Electrode Potentials 550
Matrix Methods in Data Mining and Pattern Recognition 510
Trees of tropical Asia : an illustrated guide to diversity 500
Materials Informatics Molecules, Crystals and Beyond A volume in Acta Materialia Book Series 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7042808
求助须知:如何正确求助?哪些是违规求助? 8709633
关于积分的说明 18444574
捐赠科研通 6554192
什么是DOI,文献DOI怎么找? 3117297
关于科研通互助平台的介绍 2201439
邀请新用户注册赠送积分活动 2092713