Beta-Blocker Interruption or Continuation after Myocardial Infarction

心肌梗塞 继续 心脏病学 β受体阻滞剂 内科学 医学 BETA(编程语言) 计算机科学 心力衰竭 程序设计语言
作者
Johanne Silvain,Guillaume Cayla,Émile Ferrari,Grégoire Rangé,Étienne Puymirat,Nicolas Delarche,Paul Guedeney,Thomas Cuisset,Fabrice Ivanes,Thibault Lhermusier,Thibault Petroni,Gilles Lemesle,François Bresoles,Jean-Noël Labèque,Thibaut Pommier,Jean-Guillaume Dillinger,Florence Leclercq,Franck Boccara,Pascal Lim,Timothée Besseyre des Horts
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:391 (14): 1277-1286 被引量:134
标识
DOI:10.1056/nejmoa2404204
摘要

BACKGROUND: The appropriate duration of treatment with beta-blocker drugs after a myocardial infarction is unknown. Data are needed on the safety and efficacy of the interruption of long-term beta-blocker treatment to reduce side effects and improve quality of life in patients with a history of uncomplicated myocardial infarction. METHODS: In a multicenter, open label, randomized, noninferiority trial conducted at 49 sites in France, we randomly assigned patients with a history of myocardial infarction, in a 1:1 ratio, to interruption or continuation of beta-blocker treatment. All the patients had a left ventricular ejection fraction of at least 40% while receiving long-term beta-blocker treatment and had no history of a cardiovascular event in the previous 6 months. The primary end point was a composite of death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for cardiovascular reasons at the longest follow-up (minimum, 1 year), according to an analysis of noninferiority (defined as a between-group difference of <3 percentage points for the upper boundary of the two-sided 95% confidence interval). The main secondary end point was the change in quality of life as measured by the European Quality of Life-5 Dimensions questionnaire. RESULTS: A total of 3698 patients underwent randomization: 1846 to the interruption group and 1852 to the continuation group. The median time between the last myocardial infarction and randomization was 2.9 years (interquartile range, 1.2 to 6.4), and the median follow-up was 3.0 years (interquartile range, 2.0 to 4.0). A primary-outcome event occurred in 432 of 1812 patients (23.8%) in the interruption group and in 384 of 1821 patients (21.1%) in the continuation group (risk difference, 2.8 percentage points; 95% confidence interval [CI], <0.1 to 5.5), for a hazard ratio of 1.16 (95% CI, 1.01 to 1.33; P = 0.44 for noninferiority). Beta-blocker interruption did not seem to improve the patients' quality of life. CONCLUSIONS: In patients with a history of myocardial infarction, interruption of long-term beta-blocker treatment was not found to be noninferior to a strategy of beta-blocker continuation. (Funded by the French Ministry of Health and ACTION Study Group; ABYSS ClinicalTrials.gov number, NCT03498066; EudraCT number, 2017-003903-23.).
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