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治疗持续时间与新发心力衰竭患者心室功能的改善:心力衰竭优化研究。

Therapy duration and improvement of ventricular function in de novo heart failure: the Heart Failure Optimization study.

机构信息

Department of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.

Heart Center Bremen, Electrophysiology Bremen, Senator-Wessling-Str. 1, 28277 Bremen, Germany.

出版信息

Eur Heart J. 2024 Aug 9;45(30):2771-2781. doi: 10.1093/eurheartj/ehae334.

Abstract

BACKGROUND AND AIMS

In patients with de novo heart failure with reduced ejection fraction (HFrEF), improvement of left ventricular ejection fraction (LVEF) is expected to occur when started on guideline-recommended medical therapy. However, improvement may not be completed within 90 days.

METHODS

Patients with HFrEF and LVEF ≤ 35% prescribed a wearable cardioverter-defibrillator between 2017 and 2022 from 68 sites were enrolled, starting with a registry phase for 3 months and followed by a study phase up to 1 year. The primary endpoints were LVEF improvement > 35% between Days 90 and 180 following guideline-recommended medical therapy initiation and the percentage of target dose reached at Days 90 and 180.

RESULTS

A total of 598 patients with de novo HFrEF [59 years (interquartile range 51-68), 27% female] entered the study phase. During the first 180 days, a significant increase in dosage of beta-blockers, renin-angiotensin system inhibitors, and mineralocorticoid receptor antagonists was observed (P < .001). At Day 90, 46% [95% confidence interval (CI) 41%-50%] of study phase patients had LVEF improvement > 35%; 46% (95% CI 40%-52%) of those with persistently low LVEF at Day 90 had LVEF improvement > 35% by Day 180, increasing the total rate of improvement > 35% to 68% (95% CI 63%-72%). In 392 patients followed for 360 days, improvement > 35% was observed in 77% (95% CI 72%-81%) of the patients. Until Day 90, sustained ventricular tachyarrhythmias were observed in 24 wearable cardioverter-defibrillator carriers (1.8%). After 90 days, no sustained ventricular tachyarrhythmia occurred in wearable cardioverter-defibrillator carriers.

CONCLUSIONS

Continuous optimization of guideline-recommended medical therapy for at least 180 days in HFrEF is associated with additional LVEF improvement > 35%, allowing for better decision-making regarding preventive implantable cardioverter-defibrillator therapy.

摘要

背景与目的

在射血分数降低的新发心力衰竭(HFrEF)患者中,开始接受指南推荐的医学治疗后,左心室射血分数(LVEF)有望得到改善。然而,改善可能无法在 90 天内完成。

方法

2017 年至 2022 年期间,68 个地点的 HFrEF 且 LVEF≤35%的患者被纳入研究,首先进行为期 3 个月的登记阶段,然后进行长达 1 年的研究阶段。主要终点为指南推荐的医学治疗开始后 90 至 180 天之间 LVEF 改善>35%,以及 90 至 180 天达到目标剂量的百分比。

结果

共有 598 名新发 HFrEF 患者[59 岁(四分位距 51-68),27%为女性]进入研究阶段。在最初的 180 天内,β受体阻滞剂、肾素-血管紧张素系统抑制剂和盐皮质激素受体拮抗剂的剂量显著增加(P<0.001)。在第 90 天,46%[95%置信区间(CI)41%-50%]的研究阶段患者 LVEF 改善>35%;第 90 天 LVEF 持续较低的 46%(95%CI 40%-52%)患者在第 180 天 LVEF 改善>35%,使改善>35%的总比率增加到 68%(95%CI 63%-72%)。在 392 名随访 360 天的患者中,77%(95%CI 72%-81%)的患者观察到 LVEF 改善>35%。直到第 90 天,24 名穿戴式除颤器携带者中观察到持续性室性心律失常(1.8%)。90 天后,穿戴式除颤器携带者中未发生持续性室性心律失常。

结论

HFrEF 患者接受至少 180 天的指南推荐的医学治疗持续优化与额外的 LVEF 改善>35%相关,这有助于更好地决策预防性植入式心脏复律除颤器治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c29/11313580/0493eb0bbc9c/ehae334_sga.jpg

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