4.7 Article

Critical Illness-induced Corticosteroid Insufficiency: What It Is Not and What It Could Be

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 107, 期 7, 页码 2057-2064

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgac201

关键词

CIRCI; sepsis; critical illness; adrenal; hypercortisolemia

资金

  1. Research FoundationFlanders (FWO) [G091918N]
  2. Methusalem Program of the Flemish Government (KU Leuven) [METH/14/06]
  3. European Research Council Advanced Grant from the European Union's Horizon 2020 research and innovation program [AdvG-2017-785809]
  4. European Respiratory Society (ERS Gold Medal in ARDS)

向作者/读者索取更多资源

Critical illnesses increase cortisol levels and can lead to adrenal crisis if not adequately treated. Prolonged dependence on vital organ support in critically ill patients can result in central adrenal insufficiency, which may contribute to lingering vasopressor need and encephalopathy.
Critical illnesses are hallmarked by increased systemic cortisol availability, a vital part of the stress response. Acute stress may trigger a life-threatening adrenal crisis when a disease of the hypothalamic-pituitary-adrenal (HPA) axis is present and not adequately treated with stress doses of hydrocortisone. Stress doses of hydrocortisone are also used to reduce high vasopressor need in patients suffering from septic shock, in the absence of adrenal insufficiency. Research performed over the last 10 years focusing on the HPA axis during critical illness has led to the insight that neither of these conditions can be labeled critical illness-induced corticosteroid insufficiency or CIRCI. Instead, these data suggested using the term CIRCI for a condition that may develop in prolonged critically ill patients. Indeed, when patients remain dependent on vital organ support for weeks, they are at risk of acquiring central adrenal insufficiency. The sustained increase in systemic glucocorticoid availability, mainly brought about by suppressed circulating cortisol-binding proteins and suppressed hepatic/renal cortisol metabolism, exerts negative feedback inhibition at the hypothalamus/pituitary, while high levels of other glucocorticoid receptor ligands, such as bile acids, and drugs, such as opioids, may further suppress adrenocorticotropic hormone (ACTH) secretion. The adrenal cortex, depleted from ACTH-mediated trophic signaling for weeks, may become structurally and functionally impaired, resulting in insufficient cortisol production. Such a central HPA axis suppression may be maladaptive by contributing to lingering vasopressor need and encephalopathy, hence preventing recovery. Here, we review this concept of CIRCI and we advise on how to recognize and treat this poorly understood condition.

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