The changing landscape of heart failure: translating management into the modern era

医学 重症监护医学 范围(计算机科学) 疾病 心力衰竭 药物治疗 医疗保健系统 射血分数 病因学 心脏再同步化治疗 心脏病 疾病管理 精密医学 基因检测 临床实习 医疗保健 诊断试验 个性化医疗 临床表型 药物治疗 风险分析(工程) 临床试验 梅德林 情感(语言学) 射血分数保留的心力衰竭
作者
Cristina Madaudo,Wasyla Ibrahim,Daniela Noakes,Daniel I. Bromage,Gianfranco Sinagra,Theresa McDonagh,Antonio Cannatà
出处
期刊:European Journal of Internal Medicine [Elsevier BV]
卷期号:145: 106633-106633
标识
DOI:10.1016/j.ejim.2025.106633
摘要

Heart failure (HF) is a complex clinical syndrome associated with high morbidity and mortality, accounting for approximately 2 % of total healthcare expenditures. Despite advances in pharmacological and device-based therapies, HF continues to affect over 70 million people globally, with an increasing prevalence driven by an aging population. The classification remains imperfect due to the pathophysiological complexity of the syndrome. Recent attention has focused on aetiological characterisation, particularly in non-ischaemic cardiomyopathies, where genetic testing may provide diagnostic, prognostic, and therapeutic insights. Left ventricular reverse remodeling (LVRR) and the recognition of HF with improved ejection fraction (HFimpEF) have highlighted the dynamic nature of HF and the importance of continued therapy despite apparent recovery. Guideline-directed medical therapy (GDMT), based on four foundational drug classes for HFrEF, has demonstrated significant benefit, yet its implementation remains suboptimal. For HFpEF, all effective drugs have however failed to reduce mortality. Device therapy, including implantable cardioverter-defibrillators (ICDs), cardiac resynchronisation therapy (CRT) and valve replacement offers additional benefit in select patients and may facilitate optimisation of medical therapy. New avenues such as multiomic profiling, gene therapy, and artificial intelligence (AI) are expanding our ability to phenotype HF, predict disease progression, and personalize treatment strategies. This viewpoint summarises the current understanding of HF, with an emphasis on the classification, aetiology, phenotypes and evidence-based management including newer therapies and their scope of use across the spectrum of LVEF.
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