The puzzle of sepsis: fitting the pieces of the inflammatory response with treatment.

Jane Cunneen, Martina Cartwright
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引用次数: 41

Abstract

Sepsis is a complex syndrome characterized by simultaneous activation of inflammation and coagulation in response to microbial insult. These events manifest as systemic inflammatory response syndrome (SIRS)/sepsis symptoms through release of proinflammatory cytokines, procoagulants, and adhesion molecules from immune cells and/or damaged endothelium.Conventional treatments have focused on source control, antimicrobials, vasopressors, and fluid resuscitation; however, a new treatment paradigm exists: that of treating the host response to infection with adjunct therapies including early goal directed therapy, drotrecogin alfa (activated), and immunonutrition. The multimechanistic drotrecogin alfa (activated) has been shown to reduce mortality in the severely septic patient when combined with traditional treatment. Therapies targeting improved oxygen and blood flow and reduction of apoptosis and free radicals are under investigation. Early sepsis diagnosis through detection of pro calcitonin, C reactive protein, sublingual CO2, and genetic factors may be beneficial. Ultimately, intervention timing may be the most important factor in reducing severe sepsis mortality.

败血症的难题:将炎症反应的碎片与治疗相匹配。
脓毒症是一种复杂的综合征,其特征是对微生物损伤的反应同时激活炎症和凝血。这些事件表现为系统性炎症反应综合征(SIRS)/败血症症状,通过免疫细胞和/或受损的内皮细胞释放促炎细胞因子、促凝剂和粘附分子。常规治疗侧重于源头控制、抗菌剂、血管加压剂和液体复苏;然而,存在一种新的治疗模式:用辅助治疗治疗宿主对感染的反应,包括早期目标导向治疗、原trecogin α(活化)和免疫营养。多机制甲羟孕酮(活化)已被证明与传统治疗联合使用可降低严重脓毒症患者的死亡率。针对改善氧和血流量以及减少细胞凋亡和自由基的治疗正在研究中。通过检测降钙素原、C反应蛋白、舌下CO2和遗传因素,早期诊断败血症可能是有益的。最终,干预时机可能是降低严重败血症死亡率的最重要因素。
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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