Klinik Für Innere Medizin III-Kardiologie, Angiologie Und Internistische Intensivmedizin, Universitätsklinikum Des Saarlandes, Kirrberger Strasse 100, 66421, Homburg, Germany.
Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Clin Res Cardiol. 2021 Aug;110(8):1150-1158. doi: 10.1007/s00392-021-01867-2. Epub 2021 May 13.
Due to remarkable improvements in heart failure (HF) management over the last 30 years, a significant reduction in mortality and hospitalization rates in HF patients with reduced ejection fraction (HFrEF) has been observed. Currently, the optimization of guideline-directed chronic HF therapy remains the mainstay to further improve outcomes for patients with HFrEF to reduce mortality and HF hospitalization. This includes established device therapies, such as implantable defibrillators and cardiac resynchronization therapies, which improved patients' symptoms and prognosis. Over the last 10 years, new HF drugs have merged targeting various pathways, such as those that simultaneously suppress the renin-angiotensin-aldosterone system and the breakdown of endogenous natriuretic peptides (e.g., sacubitril/valsartan), and those that inhibit the I channel and, thus, reduce heart rate (e.g., ivabradine). Furthermore, the treatment of patient comorbidities (e.g., iron deficiency) has shown to improve functional capacity and to reduce hospitalization rates, when added to standard therapy. More recently, other potential treatment mechanisms have been explored, such as the sodium/glucose co-transporter inhibitors, the guanylate cyclase stimulators and the cardiac myosin activators. In this review, we summarize the novel developments in HFrEF pharmacological and device therapy and discuss their implementation strategies into practice to further improve outcomes.
由于过去 30 年来心力衰竭(HF)管理的显著改善,射血分数降低的心力衰竭(HFrEF)患者的死亡率和住院率显著降低。目前,优化指南指导的慢性 HF 治疗仍然是进一步改善 HFrEF 患者预后、降低死亡率和 HF 住院率的主要方法。这包括已建立的设备治疗方法,如植入式除颤器和心脏再同步治疗,这些方法改善了患者的症状和预后。在过去的 10 年中,新的 HF 药物已经出现,针对各种途径,如同时抑制肾素-血管紧张素-醛固酮系统和内源性利钠肽分解的药物(如沙库巴曲缬沙坦),以及抑制 I 通道从而降低心率的药物(如伊伐布雷定)。此外,当添加到标准治疗中时,治疗患者合并症(如缺铁)已显示出改善功能能力和降低住院率的效果。最近,还探索了其他潜在的治疗机制,如钠/葡萄糖共转运体抑制剂、鸟苷酸环化酶刺激剂和心肌肌球蛋白激活剂。在这篇综述中,我们总结了 HFrEF 药理学和设备治疗的新进展,并讨论了将其实施策略纳入实践以进一步改善预后的问题。