通过炎症和氧化代谢靶向败血症。

Salena Jacob, Sanjana Ann Jacob, Joby Thoppil
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引用次数: 0

摘要

感染是一个公共卫生问题,是一系列可导致败血症和感染性休克的疾病。脓毒症的特点是对感染的免疫反应失调。脓毒性休克是最严重的脓毒症,可导致分布性休克和高死亡率。脓毒症的管理已经取得了重大进展,主要集中在早期识别和治疗上。然而,使问题复杂化的是缺乏可靠的诊断工具和现有评分工具的特异性和敏感性差,即系统性炎症反应综合征标准,顺序器官衰竭评估(SOFA)或快速SOFA。这些限制强调了在降低败血症相关死亡率方面的适度进展。本文将重点介绍氧化应激靶点、细胞因子调节、内皮细胞调节等新疗法,这些新疗法正在被概念化,用于脓毒症和感染性休克的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeting sepsis through inflammation and oxidative metabolism.

Targeting sepsis through inflammation and oxidative metabolism.

Targeting sepsis through inflammation and oxidative metabolism.

Infection is a public health problem and represents a spectrum of disease that can result in sepsis and septic shock. Sepsis is characterized by a dysregulated immune response to infection. Septic shock is the most severe form of sepsis which leads to distributive shock and high mortality rates. There have been significant advances in sepsis management mainly focusing on early identification and therapy. However, complicating matters is the lack of reliable diagnostic tools and the poor specificity and sensitivity of existing scoring tools i.e., systemic inflammatory response syndrome criteria, sequential organ failure assessment (SOFA), or quick SOFA. These limitations have underscored the modest progress in reducing sepsis-related mortality. This review will focus on novel therapeutics such as oxidative stress targets, cytokine modulation, endothelial cell modulation, etc., that are being conceptualized for the management of sepsis and septic shock.

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