Selepressin in Septic Shock.

Elio Antonucci, Manuela Giovini, Sara Agosta, Yasser Sakr, Marc Leone
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Abstract

Abstract: Sepsis and septic shock usually show a high mortality rate and frequently need of intensive care unit admissions. After fluid resuscitation, norepinephrine (NE) is the first-choice vasopressor in septic shock patients. However, high-NE doses are associated with increased rates of adverse effects and mortality. In this perspective, many authors have proposed the administration of non-adrenergic vasopressors (NAV). Selepressin is a selective vasopressin type 1A (V1A) receptor agonist and may be a valid option in this field, because it can decrease NE requirements and also limit the deleterious effects induced by high doses of catecholamines. Only few clinical data actually support selepressin administration in this setting. Here, we review the current literature on this topic analyzing some pathophysiological aspects, the rationale about the use of NAV, the possible use of selepressin differentiating animal, and human studies. Various issues remain unresolved and future trials should be focused on early interventions based on a multimodal activation of the vasopressive pathways using both alpha and V1A receptors pathways.

selepresin在感染性休克中的作用。
摘要:脓毒症和感染性休克死亡率高,经常需要重症监护病房。脓毒性休克患者液体复苏后,去甲肾上腺素(NE)是首选血管加压剂。然而,高ne剂量与不良反应和死亡率增加有关。从这个角度来看,许多作者建议使用非肾上腺素能性血管加压药(NAV)。Selepressin是一种选择性抗利尿激素1A型(V1A)受体激动剂,可能是该领域的有效选择,因为它可以减少NE的需求,也限制了高剂量儿茶酚胺引起的有害影响。只有很少的临床数据支持在这种情况下使用自我加压素。在此,我们回顾了目前关于这一主题的文献,分析了一些病理生理方面,使用NAV的基本原理,以及在动物和人类研究中可能使用的自我表达素。各种问题仍未解决,未来的试验应侧重于基于使用α和V1A受体途径的血管抑制途径的多模态激活的早期干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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