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Bench-to-bedside review: Sepsis severe sepsis and septic shock – does the nature of the infecting organism matter?

机译:从病床到病床的回顾:败血症严重的败血症和败血性休克–感染生物的性质重要吗?

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摘要

International guidelines concerning the management of patients with sepsis, septic shock and multiple organ failure make no reference to the nature of the infecting organism. Indeed, most clinical signs of sepsis are nonspecific. In contrast, in vitro data suggest that there are mechanistic differences between bacterial, viral and fungal sepsis, and imply that pathogenetic differences may exist between subclasses such as Gram-negative and Gram-positive bacteria. These differences are reflected in different cytokine profiles and mortality rates associated with Gram-positive and Gram-negative sepsis in humans. They also suggest that putative anti-mediator therapies may act differently according to the nature of an infecting organism. Data from some clinical trials conducted in severe sepsis support this hypothesis. It is likely that potential new therapies targeting, for example, Toll-like receptor pathways will require knowledge of the infecting organism. The advent of new technologies that accelerate the identification of infectious agents and their antimicrobial sensitivities may allow better tailored anti-mediator therapies and administration of antibiotics with narrow spectra and known efficacy.
机译:关于败血症,败血性休克和多器官功能衰竭患者的治疗的国际指导方针未提及感染生物的性质。实际上,大多数败血症的临床体征是非特异性的。相反,体外数据表明细菌性,病毒性和真菌性脓毒症之间存在机制差异,这意味着亚类(如革兰氏阴性菌和革兰氏阳性菌)之间可能存在致病性差异。这些差异反映在与人革兰氏阳性和革兰氏阴性败血症相关的不同细胞因子谱和死亡率上。他们还建议,根据感染生物的性质,假定的抗介体疗法可能会发挥不同的作用。在严重脓毒症中进行的一些临床试验数据支持了这一假设。针对例如Toll样受体途径的潜在新疗法可能需要了解感染生物。加速识别传染原及其抗菌敏感性的新技术的出现可能允许更好地量身定做抗介体疗法,并以窄光谱和已知功效施用抗生素。

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