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射血分数差异作为心力衰竭伴射血分数降低患者随机对照试验的纳入标准:系统评价。

Differences in ejection fraction as inclusion criterion in randomized controlled trials among patients with heart failure with reduced ejection fraction: a systematic review.

机构信息

Department of Internal Medicine, Einstein Medical Center, Philadelphia, PA, USA.

Department of Medicine, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

出版信息

Expert Rev Cardiovasc Ther. 2022 Jun;20(6):481-484. doi: 10.1080/14779072.2022.2085687. Epub 2022 Jun 6.

DOI:10.1080/14779072.2022.2085687
PMID:35654018
Abstract

INTRODUCTION

Heart failure (HF) with reduced ejection fraction (HFrEF) has been defined by varying ejection fraction (EF) criteria in clinical trials, leading to differences in quantifying treatment effects.

AREAS COVERED

The definitions of HFrEF in randomized controlled trials from 2010 until 2020 were collected. The EF ranges were clustered into very low (<30%), low (30-39%) and mildly reduced (40-49%) stratified by intervention. A time series regression analysis was performed. A total of 3052 articles were screened and 706 were included. Interventions included were pharmacologic (37%), device therapy (10%), and a combination of programs, procedural, and laboratory testing (53%). Regarding EF cutoffs, 41% of the studies utilized <40% while 26% used <35%. About 31% did not have a clearly defined EF. Between 2010 and 2020, studies with HFrEF ranges 30-39% have significantly decreased (p value < 0.001 for trend), but those which included very low EF (<30%) and mildly reduced EF (40-49%) have remained the same.

EXPERT OPINION

EF definitions across clinical trials in HFrEF varied widely. Defining the specific target HF population phenotype when designing trials or in patient treatment is important as various beneficial effects of different heart failure treatment modalities can be modified or even attenuated across the spectrum of EF.

摘要

简介

心力衰竭(HF)伴射血分数降低(HFrEF)在临床试验中通过不同的射血分数(EF)标准进行定义,导致治疗效果的量化存在差异。

涵盖领域

收集了 2010 年至 2020 年随机对照试验中 HFrEF 的定义。根据干预措施,EF 范围分为极低(<30%)、低(30-39%)和轻度降低(40-49%)。进行了时间序列回归分析。共筛选了 3052 篇文章,纳入了 706 篇。干预措施包括药物治疗(37%)、器械治疗(10%)以及程序、实验室检测和综合项目治疗(53%)。关于 EF 截止值,41%的研究使用<40%,26%使用<35%。约 31%的研究没有明确定义 EF。2010 年至 2020 年间,EF 范围为 30-39%的研究显著减少(趋势 p 值<0.001),但包括 EF 极低(<30%)和轻度降低(40-49%)的研究则保持不变。

专家意见

HFREF 临床试验中的 EF 定义差异很大。在设计试验或患者治疗时,明确特定的心力衰竭患者表型目标非常重要,因为不同心力衰竭治疗方式的各种有益效果可能会在 EF 谱的各个方面发生改变甚至减弱。

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