Huang Wilbert, Nurhafizah Apridya, Frederich Alvin, Khairunnisa Alya Roosrahima, Kezia Capella, Fathoni Muhammad Irfan, Samban Sean, Flindy Samuel
Faculty of Medicine, University of Padjadjaran, Bandung, Indonesia.
Curr Cardiol Rep. 2025 Jan 6;27(1):4. doi: 10.1007/s11886-024-02180-w.
Heart failure with improved ejection fraction (HFimpEF) patients could still develop adverse outcomes despite EF improvement. This study evaluates the risk and protective factors of poor clinical outcomes in HFimpEF patients.
Systematic searching was done to include studies that evaluate the risks of developing poor outcomes in HFimpEF patients. HFimpEF is defined as improvement of 5-10% EF within 6-12 months or normalization of EF > 40%. Poor clinical outcome is defined as a composite of all-cause mortality, cardiovascular events, HF rehospitalization, and requirement of LVAD/ transplant. Odds ratios of outcome are pooled with random effects model. A subgroup analysis of multivariate analysis-only studies was also conducted.
32 studies comprising 10,740 HFimpEF patients are included. Poor clinical outcomes followed up for approximately 3 years, are seen in 18.9% of HFimpEF patients. Twelve statistically significant factors that increase the risk of outcome are found. Among them, anemia (OR 7.69, CI 3.48-16.99, I 0%) and baseline NT pro-BNP (OR 3.25) are the two most important predictors. Other significant risk factors are increasing age, ischemic heart disease, NYHA III/IV, diabetes mellitus, atrial fibrillation, dyslipidemia, cerebrovascular disease, hypertension, use of diuretics, and baseline LVEDD. Alternately, protective factors of poor clinical outcome are regression of left atrial diameter (LAD) (OR 0.33, CI: 0.18-0.61, p 0.0003, I 0%), use beta-blockers, SGLT- 2 inhibitors, and baseline LVEF level (OR 0.60, 0.78, 0.90, respectively).
HFimpEF patients are not fully recovered and patient stratification based on risk and protective factors is recommended.
射血分数改善的心力衰竭(HFimpEF)患者尽管射血分数有所改善,但仍可能出现不良结局。本研究评估HFimpEF患者临床结局不佳的风险和保护因素。
进行系统检索,纳入评估HFimpEF患者出现不良结局风险的研究。HFimpEF定义为在6 - 12个月内射血分数提高5 - 10%或射血分数>40%恢复正常。不良临床结局定义为全因死亡率、心血管事件、心力衰竭再住院以及左心室辅助装置/移植需求的综合指标。结局的比值比采用随机效应模型进行汇总。还对仅进行多变量分析的研究进行了亚组分析。
纳入了32项研究,共10740例HFimpEF患者。对HFimpEF患者进行约3年的随访,发现18.9%的患者出现不良临床结局。发现了12个增加结局风险的具有统计学意义的因素。其中,贫血(比值比7.69,95%置信区间3.48 - 16.99,I² 0%)和基线N末端B型利钠肽原(比值比3.25)是两个最重要的预测因素。其他显著的风险因素包括年龄增长、缺血性心脏病、纽约心脏协会心功能分级III/IV级、糖尿病、心房颤动、血脂异常、脑血管疾病、高血压、使用利尿剂以及基线左心室舒张末期内径。相反,不良临床结局的保护因素是左心房直径(LAD)缩小(比值比0.33,95%置信区间:0.18 - 0.61,p 0.0003,I² 0%)、使用β受体阻滞剂、钠 - 葡萄糖协同转运蛋白2(SGLT - 2)抑制剂以及基线左心室射血分数水平(分别为比值比0.60、0.78、0.90)。
HFimpEF患者并未完全康复,建议基于风险和保护因素对患者进行分层。