Waranugraha Yoga, Rohman Mohammad S, Setiawan Dion, Aziz Indra J
Department of Cardiology and Vascular Medicine, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
Brawijaya Cardiovascular Research Center, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.
J Taibah Univ Med Sci. 2021 Apr 13;16(4):582-590. doi: 10.1016/j.jtumed.2021.02.012. eCollection 2021 Aug.
A beta-blocker should be initiated in patients with stable acute heart failure (AHF). Beta-blocker titration should be conducted after a two-week interval. The benefits of aggressive beta-blocker titration are still unclear. This study aimed to investigate the aggressive beta-blocker titration outcomes in stabilized AHF patients with low left ventricular ejection fraction (LVEF).
In this retrospective cohort study, we analysed clinical data from the heart failure (HF) registry. AHF Patients with LVEF <40% were divided into aggressive and guideline-directed beta-blocker titration groups. The composite of worsening HF, ventricular arrhythmia, and mortality during hospitalization were defined as the primary outcomes. We considered secondary outcomes as the components of primary outcomes and also the outcomes during a 90-day follow-up after hospital discharge, including HF readmission and mortality.
The primary outcomes between both groups were not significantly different (12.3% vs 24.4%; relative risk [RR] 0.51; 95% confidence interval [CI] 0.25-1.01; = 0.055). However, the aggressive beta-blocker titration reduced ventricular arrhythmia events (5.7% vs 17.8%; RR 0.32; 95% CI 0.12-0.84; = 0.016). The 90-day HF readmission rate (2.6% vs 7.5%; RR 0.35; 95% CI 0.07-1.66; = 0.179) and mortality rate (4.3% vs 5%; RR 0.87; 95% CI 0.18-4.31; = 1.000) between both groups were not found to be significantly different.
Compared to the guideline-directed beta-blocker titration, the aggressive beta-blocker titration was safe in low LVEF AHF patients who have been previously stabilized. Additionally, aggressive beta-blocker titration effectively reduced ventricular arrhythmia events.
对于病情稳定的急性心力衰竭(AHF)患者,应开始使用β受体阻滞剂。β受体阻滞剂的滴定应在两周间隔后进行。积极的β受体阻滞剂滴定的益处仍不明确。本研究旨在调查左心室射血分数(LVEF)低的稳定型AHF患者进行积极的β受体阻滞剂滴定的结果。
在这项回顾性队列研究中,我们分析了心力衰竭(HF)登记处的临床数据。LVEF<40%的AHF患者被分为积极滴定组和遵循指南滴定组。住院期间心力衰竭恶化、室性心律失常和死亡率的复合情况被定义为主要结局。我们将次要结局视为主要结局的组成部分以及出院后90天随访期间的结局,包括心力衰竭再入院和死亡率。
两组之间的主要结局无显著差异(12.3%对24.4%;相对风险[RR]0.51;95%置信区间[CI]0.25 - 1.01;P = 0.055)。然而,积极的β受体阻滞剂滴定减少了室性心律失常事件(5.7%对17.8%;RR 0.32;95% CI 0.12 - 0.84;P = 0.016)。两组之间的90天心力衰竭再入院率(2.6%对7.5%;RR 0.35;95% CI 0.07 - 1.66;P = 0.179)和死亡率(4.3%对5%;RR 0.87;95% CI 0.18 - 4.31;P = 1.000)未发现有显著差异。
与遵循指南的β受体阻滞剂滴定相比,积极的β受体阻滞剂滴定对于先前已稳定的低LVEF AHF患者是安全的。此外,积极的β受体阻滞剂滴定有效减少了室性心律失常事件。