苏比里尔/缬沙坦和伊伐布雷定:两种治疗低射血分数心力衰竭(EFrEF)的化合物,通过创新机制起作用

F. Cacciapuoti
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引用次数: 0

摘要

评价了两种新化合物——沙比利/缬沙坦和伊伐布雷定在治疗收缩期心力衰竭(HFrEF)中的作用。Sacubitril/缬沙坦(也称为enterresto),与其他最佳药物治疗一起拮抗HFrEF,增强利钠肽(NP)的有益作用,并通过血管紧张素受体阻滞剂(ARB)缬沙坦对抗血管紧张素II。PARADIGM-HF研究表明,Sacubitril/缬沙坦在降低HFrEF的死亡和住院风险方面优于单独使用血管紧张素转换酶(ACE)。相反,伊伐布雷定是一种选择性的窦房结“滑稽”通道电流抑制剂,对窦性心律患者的HFrEF起抑制作用,导致心率降低。由于左室舒张充盈增加,这种减少产生了卒中容量的改善,改善了HFrEF症状。SHIFT试验报告的结果支持伊伐布雷定降低心率对改善HFrEF临床结果的重要性,并证实心率在该疾病的病理生理学中的重要作用。两种药物以两种不同和创新的机制起作用,并与剩余的最佳药物治疗一起,代表了HFrEF治疗的有效改进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sacubitril/Valsartan and Ivabradine: Two Compounds for Heart Failure with Low Ejection Fraction (EFrEF), Acting by Innovative Mechanisms
The role of two new compounds - Sacubitril/valsartan and Ivabradine in treatment of systolic heart failure (HFrEF) was evaluated. Sacubitril/valsartan (also called as Entresto), together the remaining optimal medical therapy, antagonize HFrEF both strengthening the beneficial effects of natriuretic peptides (NP) and acting against angiotensin II by angiotensin receptor blocker (ARB), valsartan. PARADIGM-HF study has demonstrated that Sacubitril/valsartan is superior to angiotensin-converting-enzyme (ACE) alone in reducing the risks of death and hospitalization for HFrEF. On the contrary Ivabradine, a selective inhibitor of the “funny” channel current present in the sino-atrial node, acts against HFrEF inducing a reduction of heart rate in sinus rhythm patients. This reduction yields an improvement in stroke volume due to the increased of LV diastolic filling, improving the HFrEF symptoms. The results reported in the SHIFT Trial support the importance of heart rate reduction obtained with Ivabradine for improvement of clinical outcomes in HFrEF and confirm the important role of heart rate in the pathophysiology of this disorder. Two drugs act with two diverse and innovative mechanisms and, together the remaining optimal medical therapy, represent an effective improvement in HFrEF therapy.
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