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埃及射血分数保留的心力衰竭:专家意见

Heart Failure with Preserved Ejection Fraction in Egypt: An Expert Opinion.

作者信息

Abdelhamid Magdy, Salem Amr Zaki, Kabil Hamza, Ragy Hany, Hasan-Ali Hosam, Elnoamany Mohamed, Elsetiha Mohamed, Shaheen Sameh

机构信息

Faculty of Medicine, Cairo University, Cairo, Egypt.

Faculty of Medicine, Alexandria University, Alexandria, Egypt.

出版信息

Glob Heart. 2025 Mar 20;20(1):31. doi: 10.5334/gh.1411. eCollection 2025.

Abstract

Heart failure with preserved ejection fraction (HFpEF) is an ongoing challenge for healthcare systems. Major limitations that hinder adequate control of the disease, including an incomplete understanding of its pathophysiology, limited therapy options, and the absence of sufficient information on the management of comorbidities. Diagnosis and management of HFpEF in Egypt lack standardization as they are complicated with multiple comorbidities and limited by the lack of resources and data on epidemiology and patient characteristics. Diagnostic procedures for HFpEF should be implemented through guideline-specified scoring systems, due to the heterogeneity of clinical presentations and the absence of a golden standard for confirming HFpEF. In Egypt, the HFPEF scoring system is more commonly used for establishing HFpEF diagnosis. All HFpEF patients should be treated through multidrug regimens tailored for their state, symptoms, and comorbidities, with sodium-glucose cotransporter-2 (SGLT2) inhibitors as the mainstay of treatment together with either one or a combination of loop diuretic and aldosterone antagonists. This paper provides an integrated review of epidemiology, means of diagnosis, current and novel pharmacological therapy options for HFpEF patients in the light of the recent advances in treatment of HFpEF, discussing means of healthcare delivery and unmet needs, and proposing recommendations for clinical practice and pathways for future research.

摘要

射血分数保留的心力衰竭(HFpEF)对医疗系统来说仍是一项持续的挑战。阻碍对该疾病进行充分控制的主要限制因素包括对其病理生理学的理解不完整、治疗选择有限以及缺乏关于合并症管理的充分信息。在埃及,HFpEF的诊断和管理缺乏标准化,因为它与多种合并症相关,并且受到资源以及流行病学和患者特征数据缺乏的限制。由于临床表现的异质性以及缺乏确诊HFpEF的金标准,HFpEF的诊断程序应通过指南规定的评分系统来实施。在埃及,HFPEF评分系统更常用于确立HFpEF诊断。所有HFpEF患者都应通过针对其病情、症状和合并症量身定制的多药治疗方案进行治疗,以钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂作为主要治疗药物,并联合使用袢利尿剂和醛固酮拮抗剂中的一种或两者的组合。本文根据HFpEF治疗的最新进展,对HFpEF患者的流行病学、诊断方法、当前和新型药物治疗选择进行了综合综述,讨论了医疗服务提供方式和未满足的需求,并提出了临床实践建议和未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8a7/11927671/8c3316cd1729/gh-20-1-1411-g1.jpg

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