Annane Djillali, Pastores Stephen M, Arlt Wiebke, Balk Robert A, Beishuizen Albertus, Briegel Josef, Carcillo Joseph, Christ-Crain Mirjam, Cooper Mark S, Marik Paul E, Meduri Gianfranco Umberto, Olsen Keith M, Rochwerg Bram, Rodgers Sophia C, Russell James A, Van den Berghe Greet
General ICU Department, Raymond Poincaré hospital (APHP), Health Science Centre Simone Veil, Université Versailles SQY-Paris Saclay.
Department of Anesthesiology and Critical Care Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States of America.
Crit Care Med. 2017 Dec;45(12):2089-2098. doi: 10.1097/CCM.0000000000002724.
To provide a narrative review of the latest concepts and understanding of the pathophysiology of critical illness-related corticosteroid insufficiency (CIRCI).
A multi-specialty task force of international experts in critical care medicine and endocrinology and members of the Society of Critical Care Medicine and the European Society of Intensive Care Medicine.
Medline, Database of Abstracts of Reviews of Effects (DARE), Cochrane Central Register of Controlled Trials (CENTRAL) and the Cochrane Database of Systematic Reviews.
Three major pathophysiologic events were considered to constitute CIRCI: dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis, altered cortisol metabolism, and tissue resistance to glucocorticoids. The dysregulation of the HPA axis is complex, involving multidirectional crosstalk between the CRH/ACTH pathways, autonomic nervous system, vasopressinergic system, and immune system. Recent studies have demonstrated that plasma clearance of cortisol is markedly reduced during critical illness, explained by suppressed expression and activity of the primary cortisol-metabolizing enzymes in the liver and kidney. Despite the elevated cortisol levels during critical illness, tissue resistance to glucocorticoids is believed to occur due to insufficient glucocorticoid alpha-mediated anti-inflammatory activity.
Novel insights into the pathophysiology of CIRCI add to the limitations of the current diagnostic tools to identify at-risk patients and may also impact how corticosteroids are used in patients with CIRCI.
对危重症相关皮质类固醇功能不全(CIRCI)病理生理学的最新概念和理解进行叙述性综述。
由重症医学和内分泌学领域的国际专家组成的多专业特别工作组,以及危重症医学会和欧洲重症监护医学会的成员。
医学文献数据库(Medline)、循证医学数据库(DARE)、Cochrane系统评价中心对照试验注册库(CENTRAL)和Cochrane系统评价数据库。
三个主要病理生理事件被认为构成CIRCI:下丘脑 - 垂体 - 肾上腺(HPA)轴调节异常、皮质醇代谢改变以及组织对糖皮质激素的抵抗。HPA轴调节异常很复杂,涉及促肾上腺皮质激素释放激素(CRH)/促肾上腺皮质激素(ACTH)途径、自主神经系统、血管加压素能系统和免疫系统之间的多向相互作用。最近的研究表明,危重症期间皮质醇的血浆清除率显著降低,这是由于肝脏和肾脏中主要皮质醇代谢酶的表达和活性受到抑制。尽管危重症期间皮质醇水平升高,但由于糖皮质激素α介导的抗炎活性不足,仍认为会发生组织对糖皮质激素的抵抗。
对CIRCI病理生理学的新见解增加了当前用于识别高危患者的诊断工具的局限性,也可能影响CIRCI患者使用皮质类固醇的方式。