血管紧张素受体奈普利素抑制剂用于HFrEF:这是第一个导致利尿需求大幅减少的疾病修饰治疗药物类别吗?

International Journal of Heart Failure Pub Date : 2021-02-25 eCollection Date: 2021-04-01 DOI:10.36628/ijhf.2020.0043
Brian Kerr, Rebabonye B Pharithi, Matthew Barrett, Carmel Halley, Joe Gallagher, Mark Ledwidge, Kenneth McDonald
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引用次数: 2

摘要

尽管心力衰竭(HF)的疾病修饰治疗取得了重大进展,利尿剂仍然是所有HF表型容量管理的基石。利尿剂,除了他们明确的急性血流动力学和症状的好处,也有许多可能有害的副作用。此外,关于长期使用利尿剂对预后影响的问题仍然存在。迄今为止,很少有数据表明,在心力衰竭伴射血分数降低(HFrEF)的个体化传统指导药物治疗中,利尿剂减少。然而,从PARADIGM研究以及我们自己的小组和其他小组的上市后报告来看,苏比里尔/缬沙坦(血管紧张素受体-奈普利素抑制剂[ARNi])已被证明具有利尿作用。ARNi化合物是否代表了一个新时代的曙光,在这个新时代,有效的治疗方法将更显著地减少利尿剂的需求,还有待观察。葡萄糖转运2钠抑制剂和鸟苷酸环化酶刺激剂的出现可能进一步证明了这一问题,并可能将这种益处扩展到HFrEF表型以外的HF患者。总之,HFrEF的新疗法可以减少对利尿剂的依赖。这些发展进一步强调了通过仔细的容量评估来持续评估个人利尿剂需求的临床重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Angiotensin Receptor Neprilysin Inhibitors in HFrEF: Is This the First Disease Modifying Therapy Drug Class Leading to a Substantial Reduction in Diuretic Need?

Angiotensin Receptor Neprilysin Inhibitors in HFrEF: Is This the First Disease Modifying Therapy Drug Class Leading to a Substantial Reduction in Diuretic Need?

Angiotensin Receptor Neprilysin Inhibitors in HFrEF: Is This the First Disease Modifying Therapy Drug Class Leading to a Substantial Reduction in Diuretic Need?

Despite significant advances in disease modifying therapy in heart failure (HF), diuretics have remained the cornerstone of volume management in all HF phenotypes. Diuretics, alongside their definite acute haemodynamic and symptomatic benefits, also possess many possible deleterious side effects. Moreover, questions remain regarding the prognostic impact of chronic diuretic use. To date, few data exist pertaining to diuretic reduction as a result of individual traditional guideline directed medical therapy in HF with reduced ejection fraction (HFrEF). However, diuretic reduction has been demonstrated with sacubitril/valsartan (angiotensin receptor-neprilysin inhibitor [ARNi]) from the PARADIGM study, as well as, post-marketing reports from our own group and others. Whether the ARNi compound represents the dawn of a new era, where effective therapies will have a more noticeable reduction on diuretic need, remains to be seen. The emergence of sodium glucose transport 2 inhibitors and guanylate cyclase stimulators may further exemplify this issue and potentially extend this benefit to HF patients outside of the HFrEF phenotype. In conclusion, emerging new therapies in HFrEF could reduce the reliance on diuretics in the management of this phenotype of HF. These developments further highlight the clinical importance to continually assess an individual's diuretic requirements through careful volume assessment.

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