Monitoring the post surgery inflammatory host response

F. Paruk, J. Chausse
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引用次数: 23

Abstract

The human response to surgery is meant to be protective and to promote healing. The cascade of events that ensue following tissue injury is highly complicated and involves an interplay of the metabolic, hemodynamic, hormonal and immunological systems. The release of biomolecules known as damage-associated molecular patterns (DAMPs) activates the pro-inflammatory innate and anti-inflammatory adaptive responses, which are designed to defend and contain the inflammatory process locally. The magnitude of tissue injury influences the scale of the inflammatory response. Further, patient factors as well as medical therapy influences this response. An imbalance between the pro-inflammatory and anti-inflammatory response or an exaggerated response may culminate with organ dysfunction, an increased susceptibility for infections or death. Cell mediated immunity (CMI) is often suppressed post surgery and patients are predisposed to the development of postoperative infections and complications. Mapping the immune response would be useful in terms of adjudging the patient’s response to surgery, alerting clinicians to the occurrence of complications thereby providing the opportunity to implement appropriate management timeously if necessary. There is a vast overlap in the surgical inflammatory response with that of the pathogen-associated molecular patterns (PAMPs) induced response that follows sepsis. This presents a challenge in the postoperative period in terms of distinguishing between infectious and non-infectious complications. Biomarkers have thus emerged as attractive contenders to map the immune response. Taking into account the complexity of the inflammatory response, it is unlikely that a single biomarker will ever be utilised to achieve this. In the era of personalised medicine, where our patient populations are quite heterogeneous, future directions point towards the use of multiple panels of novel biomarkers. Currently the procalcitonin (PCT) and C-reactive protein (CRP) are available for general use. This review explores the inflammatory response to surgery and the utility of CRP and PCT in the postoperative period. It highlights the importance of using biomarker kinetics coupled with the clinical response and the principle of individualised interpretation.
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监测术后炎症宿主反应
人类对手术的反应是为了保护和促进愈合。组织损伤后发生的一连串事件非常复杂,涉及代谢、血液动力学、激素和免疫系统的相互作用。被称为损伤相关分子模式(DAMP)的生物分子的释放激活了促炎先天和抗炎适应性反应,这些反应旨在局部防御和控制炎症过程。组织损伤的程度影响炎症反应的程度。此外,患者因素以及药物治疗会影响这种反应。促炎和抗炎反应之间的失衡或过度反应可能最终导致器官功能障碍、感染或死亡的易感性增加。细胞介导的免疫(CMI)通常在手术后受到抑制,患者容易发生术后感染和并发症。绘制免疫反应图有助于判断患者对手术的反应,提醒临床医生并发症的发生,从而在必要时及时实施适当的管理。手术炎症反应与败血症后病原体相关分子模式(PAMP)诱导的反应有很大的重叠。这对术后区分感染性和非感染性并发症提出了挑战。因此,生物标记物已成为绘制免疫反应图的有吸引力的竞争者。考虑到炎症反应的复杂性,不太可能使用单一的生物标志物来实现这一点。在个性化医学时代,我们的患者群体非常异质,未来的方向指向使用多种新型生物标志物。目前降钙素原(PCT)和C反应蛋白(CRP)可用于一般用途。这篇综述探讨了手术后的炎症反应以及CRP和PCT在术后的应用。它强调了使用生物标志物动力学与临床反应和个性化解释原则相结合的重要性。
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