Critical illness-related corticosteroid insufficiency (CIRCI): A narrative review from a multispecialty task force of the Society of Critical Care Medicine (SCCM) and the European Society of Intensive Care Medicine (ESICM) Journal Article


Authors: Annane, D.; Pastores, S. M.; Arlt, W.; Balk, R. A.; Beishuizen, A.; Briegel, J.; Carcillo, J.; Christ-Crain, M.; Cooper, M. S.; Marik, P. E.; Meduri, G. U.; Olsen, K. M.; Rochwerg, B.; Rodgers, S. C.; Russell, J. A.; Van Den Berghe, G.
Article Title: Critical illness-related corticosteroid insufficiency (CIRCI): A narrative review from a multispecialty task force of the Society of Critical Care Medicine (SCCM) and the European Society of Intensive Care Medicine (ESICM)
Abstract: OBJECTIVE: To provide a narrative review of the latest concepts and understanding of the pathophysiology of critical illness-related corticosteroid insufficiency (CIRCI). PARTICIPANTS: 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. DATA SOURCES: Medline, Database of Abstracts of Reviews of Effects (DARE), Cochrane Central Register of Controlled Trials (CENTRAL) and the Cochrane Database of Systematic Reviews. RESULTS: 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. CONCLUSIONS: 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.
Keywords: signal transduction; pathophysiology; metabolism; hypothalamus hypophysis system; physiology; intensive care; cytokine; cytokines; severity of illness index; advisory committees; hydrocortisone; critical care; critical illness; glucocorticoid receptor; receptors, glucocorticoid; neuroendocrine cells; adrenal insufficiency; neurosecretory cell; systemic inflammatory response syndrome; hypophysis adrenal system; hypothalamo-hypophyseal system; pituitary-adrenal system; glucocorticoid receptor alpha; advisory committee; humans; human
Journal Title: Critical Care Medicine
Volume: 45
Issue: 12
ISSN: 0090-3493
Publisher: Lippincott Williams & Wilkins  
Date Published: 2017-12-01
Start Page: 2089
End Page: 2098
Language: English
DOI: 10.1097/ccm.0000000000002724
PUBMED: 28938251
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 1 February 2018 -- Source: Scopus
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  1. Stephen Pastores
    248 Pastores