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多器官功能衰竭。“两次打击”模型的有效性如何?

Multiple organ failure. How valid is the "two hit" model?

作者信息

Saadia R, Schein M

机构信息

Department of Surgery, Baragwanath Hospital, Johannesburg, South Africa.

出版信息

J Accid Emerg Med. 1999 May;16(3):163-6; discussion 166-7. doi: 10.1136/emj.16.3.163.

Abstract

Inflammatory "one hit" and "two hit" models have recently been proposed to account for the development of multiple organ failure (MOF) in trauma and critically ill surgical patients when no source of infection can be found. In the "one hit" model, the initial insult is so massive that a systemic inflammatory response syndrome is triggered and leads rapidly to MOF. In the "two hit" scenario, initially less severely injured patients eventually develop MOF as a result of a reactivation of their inflammatory response caused by an adverse and often minor intercurrent event. At first sight, the theory is attractive because it seems to fit commonly observed clinical patterns. Indeed, injured patients often respond to initial resuscitation but, after an insult of some sort, develop organ dysfunction and die. The "two hit" model is furthermore mirrored at the cellular level. Inflammatory cells are indeed susceptible of being primed by an initial stimulus and reactivated subsequently by a relatively innocuous insult. However, in the absence of clinical and biological corroboration based on cytokine secretion patterns, these models should not be accepted uncritically.

摘要

最近有人提出炎症“一次打击”和“二次打击”模型,以解释在创伤和危重症外科患者中,在找不到感染源的情况下多器官功能衰竭(MOF)的发生机制。在“一次打击”模型中,初始损伤非常严重,以至于引发全身炎症反应综合征并迅速导致MOF。在“二次打击”情况下,最初受伤较轻的患者最终会因由不良且通常轻微的并发事件引起的炎症反应重新激活而发展为MOF。乍一看,该理论很有吸引力,因为它似乎符合常见的临床模式。的确,受伤患者通常对初始复苏有反应,但在遭受某种损伤后,会出现器官功能障碍并死亡。“二次打击”模型在细胞水平上也有体现。炎症细胞确实容易受到初始刺激的启动,随后被相对无害的损伤重新激活。然而,在缺乏基于细胞因子分泌模式的临床和生物学确证的情况下,这些模型不应被不加批判地接受。

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