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Activated protein C for the treatment of severe sepsis.

机译:活化蛋白C用于治疗严重脓毒症。

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摘要

In 2001, the PROWESS (Recombinant Human Activated Protein C Worldwide Evaluation in Severe Sepsis) trial demonstrated a 6.1% absolute decrease in mortality in patients with severe sepsis. Recombinant human activated protein C was subsequently licensed for use by both the US Food and Drug Administration and the European Medicines Evaluation Agency. There has been some controversy over aspects of the original study protocol, and subsequent trials have raised concerns about both the efficacy and the side effect profile of recombinant human activated protein C. Significant doubt remains as to the role of recombinant human activated protein C in the management of severe sepsis, and this review aims to summarize the evidence both for and against its use.
机译:2001年,PROWESS(严重脓毒症的全球重组人类活化蛋白C评估)试验表明,患有严重脓毒症的患者死亡率绝对降低6.1%。重组人活化蛋白C随后获得了美国食品药品监督管理局和欧洲药品评估局的许可使用。原始研究方案的各个方面存在争议,随后的试验引起了人们对重组人活化蛋白C的功效和副作用的关注。对于重组人活化蛋白C在重组人C中的作用仍然存在重大疑问。严重脓毒症的治疗,本综述旨在总结支持和反对使用败血症的证据。

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