- Critical illness-related corticosteroid insufficiency
Critical illness-related corticosteroid insufficiency (CIRCI) is a form of adrenal insufficiency in critically ill patients who have blood corticosteroid levels which are inadequate for the severe stress response they experience. Combined with decreased glucocorticoid receptor sensitivity and tissue response to corticosteroids, this adrenal insufficiency constitutes a negative prognostic factor for intensive care patients.
The hypothalamic-pituitary-adrenal axis (HPA axis), in which the hypothalamus and pituitary gland control adrenal secretions, undergoes profound changes during critical illness. Both very high and very low levels of cortisol have been linked to a poor outcome in intensive care patients. It has been suggested that high levels could represent severe stress, whereas low levels are due to blunted cortisol production and response.
CIRCI can be suspected in patients with low blood pressure despite resuscitation with intravenous fluids and vasopressor drugs. The Surviving Sepsis Campaign guidelines advocate intravenous hydrocortisone only in adults with septic shock and refractory hypotension. The exact definition of this condition, the best ways to test for corticoid insufficiency in critically ill patients, and the therapeutic use of (usually low doses) of corticosteroids remains a subject of debate.
The best known feature that suggests a possible underlying adrenal insufficiency is low blood pressure despite resuscitation with intravenous fluids, requiring vasopressor drugs. These patients typically display tachycardia and other signs of hyperdynamic shock. Other symptoms include fever, purpura fulminans, and gastrointestinal or neurological disturbances. All these features are relatively non-specific in intensive care patients.
In some patients a specific reason for adrenal insufficiency can be suspected, such as prior intake of corticosteroids that suppressed the HPA axis, or use of enzyme inducing drugs such as phenytoin. Treatment with imidazole drugs such as etomidate, ketoconazole and miconazole can also suppress the HPA axis, as well as drugs used specifically for this purpose, such as metyrapone.
Several blood test abnormalities can suggest corticosteroid insufficiency, such as hypoglycaemia, hyponatremia, hyperkalemia, hypercalcemia, neutropenia, eosinophilia, hyperprolactinemia and hypothyroidism.
The exact diagnostic tests and cut-off values to diagnose critical illness-related corticosteroid insufficiency are not agreed upon. This also applies to the distinction between absolute and relative adrenal insufficiency, a reason why the term critical illness–related corticosteroid insufficiency is preferred to relative adrenal insufficiency. The variation in cortisol levels according to disease type and severity, as well as variation within the same patient, hampers the establishment of a clear threshold below which CIRCI occurs. Moreover, in patients whose adrenals are already maximally stimulated, a stimulation test would not be informative. Furthermore, a short test might not adequately assess response to the chronic stress of critical illness.
Both random total cortisol levels, total cortisol levels or increment after ACTH stimulation tests, free cortisol levels, or a combination of these have been proposed as diagnostic tests. Other stimulation tests for adrenal insufficiency which are used in non-critical patients, such as the test using metyrapone or a test which employs insulin to induce hypoglycemia, are not preferred for CIRCI. Both a metyrapone-induced decrease in cortisol and hypoglycemia are potentially harmful to intensive care patients. The exact dose of ACTH remains a matter of debate. In the CORTICUS study, ACTH stimulation testing predicted mortality whereas baseline cortisol levels did not. However, possible benefits of corticosteroid therapy do not seem to be completely predicted by ACTH stimulation testing. For these reasons, guidelines currently do not recommend that ACTH stimulation testing should guide the decision whether or not to administer corticosteroids. Cortisol immunoassays on the other hand have been shown to be prone to both over- and underestimation.
In adults with septic shock and refractory hypotension despite resuscitation with intravenous fluids and vasopressors, hydrocortisone is the preferred corticosteroid. It can be divided in several doses or administered as a continuous infusion. Fludrocortisone is optional in CIRCI, and dexamethasone is not recommended. Little evidence is available to judge when and how corticosteroid therapy should be stopped; guidelines recommend tapering corticosteroids when vasopressors are no longer needed.
Corticosteroid treatment has also been suggested as an early treatment option in patient with acute respiratory distress syndrome. Steroids have not been shown beneficial for sepsis alone. Historically, higher doses of steroids were given, but these have been suggested to be harmful compared to the lower doses which are advocated today.
In the CORTICUS study, hydrocortisone hastened the reversal of septic shock, but did not influence mortality, with an increased occurrence of septic shock relapse and hypernatremia. The latter findings tempered enthusiasm for the broad use of hydrocortisone in septic shock. Prior to this study, several other smaller studies showed beneficial effects of long courses of low doses of corticoid. Several factors (such as lack of statistical power due to slow recruitment) could have led a false-negative finding on mortality in the CORTICUS study; thus, more research is needed.
In acute states of severe stress, cortisol secretion by the adrenal gland increases up to sixfold, parallel to the severity of the condition. This is partly due to an increased secretion of corticotropin-releasing hormone (CRH) and adrenocorticotropic hormone (ACTH). Several cytokines have been also shown to interfere with the HPA axis at multiple levels. There is also an increase in the number and affinity of glucocorticoid receptors. Levels of corticosteroid-binding globulin (CBG) and albumin, which normally bind cortisol, are decreased, resulting in increased levels of free cortisol. Furthermore, anaesthesia drugs like etomidate could interfere with the HPA axis. The secretion also loses its normal diurnal pattern of morning peak levels and evening and night time troughs. Nevertheless, secretion remains pulsatile and there is a marked variation in blood samples from the same individual.
High blood levels of cortisol during critical illness could theoretically be protective because of several reasons. They modulate metabolism (for example, by inducing high blood sugar levels, thereby providing energy to the body). They also suppress excessive immune system activation and exert supporting effects on the circulatory system. Increased susceptibility to infections, hyperglycemia (in patients already prone to stress hyperglycemia), gastrointestinal bleeding, electrolyte disturbances and steroid-induced myopathy (in patients already prone to critical illness polyneuropathy) are possible harmful effects.
In the chronic phase of severe illness, cortisol levels decrease slowly and return to normal when the patient recovers. ACTH levels are however low, and CBG levels increase.
- ^ a b c d e Marik PE, Pastores SM, Annane D et al. (June 2008). "Recommendations for the diagnosis and management of corticosteroid insufficiency in critically ill adult patients: consensus statements from an international task force by the American College of Critical Care Medicine". Crit. Care Med. 36 (6): 1937–49. doi:10.1097/CCM.0b013e31817603ba. PMID 18496365. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?doi=10.1097/CCM.0b013e31817603ba.
- ^ Rothwell PM, Lawler PG (January 1995). "Prediction of outcome in intensive care patients using endocrine parameters". Crit. Care Med. 23 (1): 78–83. doi:10.1097/00003246-199501000-00015. PMID 8001391. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=23&issue=1&spage=78.
- ^ Annane D, Sébille V, Troché G, Raphaël JC, Gajdos P, Bellissant E (February 2000). "A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotropin". JAMA 283 (8): 1038–45. doi:10.1001/jama.283.8.1038. PMID 10697064. http://jama.ama-assn.org/cgi/pmidlookup?view=long&pmid=10697064.
- ^ a b c d e f g h Dellinger RP, Levy MM, Carlet JM et al. (January 2008). "Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock: 2008". Crit. Care Med. 36 (1): 296–327. doi:10.1097/01.CCM.0000298158.12101.41. PMID 18158437. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?doi=10.1097/01.CCM.0000298158.12101.41.
- ^ a b c d e f g h i j k l m n o Mesotten D, Vanhorebeek I, Van den Berghe G (September 2008). "The altered adrenal axis and treatment with glucocorticoids during critical illness". Nat Clin Pract Endocrinol Metab 4 (9): 496–505. doi:10.1038/ncpendmet0921. PMID 18695699.
- ^ Lamberts SW, Bons EG, Bruining HA, de Jong FH (January 1987). "Differential effects of the imidazole derivatives etomidate, ketoconazole and miconazole and of metyrapone on the secretion of cortisol and its precursors by human adrenocortical cells". J. Pharmacol. Exp. Ther. 240 (1): 259–64. PMID 3027305. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=3027305.
- ^ Widmer IE, Puder JJ, König C et al. (August 2005). "Cortisol response in relation to the severity of stress and illness". J. Clin. Endocrinol. Metab. 90 (8): 4579–86. doi:10.1210/jc.2005-0354. PMID 15886236. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=15886236.
- ^ Lipiner-Friedman D, Sprung CL, Laterre PF et al. (April 2007). "Adrenal function in sepsis: the retrospective Corticus cohort study". Crit. Care Med. 35 (4): 1012–8. doi:10.1097/01.CCM.0000259465.92018.6E. PMID 17334243. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?doi=10.1097/01.CCM.0000259465.92018.6E.
- ^ a b Sprung CL, Annane D, Keh D et al. (January 2008). "Hydrocortisone therapy for patients with septic shock". N. Engl. J. Med. 358 (2): 111–24. doi:10.1056/NEJMoa071366. PMID 18184957. http://content.nejm.org/cgi/pmidlookup?view=short&pmid=18184957&promo=ONFLNS19.
- ^ a b Annane D, Sébille V, Charpentier C et al. (August 2002). "Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock". JAMA 288 (7): 862–71. doi:10.1001/jama.288.7.862. PMID 12186604. http://jama.ama-assn.org/cgi/pmidlookup?view=long&pmid=12186604.
- ^ Lefering R, Neugebauer EA (July 1995). "Steroid controversy in sepsis and septic shock: a meta-analysis". Crit. Care Med. 23 (7): 1294–303. doi:10.1097/00003246-199507000-00021. PMID 7600840. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=23&issue=7&spage=1294.
- ^ Minneci PC, Deans KJ, Banks SM, Eichacker PQ, Natanson C (July 2004). "Meta-analysis: the effect of steroids on survival and shock during sepsis depends on the dose". Ann. Intern. Med. 141 (1): 47–56. PMID 15238370.
- ^ Annane D, Bellissant E, Bollaert PE, Briegel J, Keh D, Kupfer Y (August 2004). "Corticosteroids for severe sepsis and septic shock: a systematic review and meta-analysis". BMJ 329 (7464): 480. doi:10.1136/bmj.38181.482222.55. PMC 515196. PMID 15289273. http://bmj.com/cgi/pmidlookup?view=long&pmid=15289273.
- ^ Briegel J, Forst H, Haller M et al. (April 1999). "Stress doses of hydrocortisone reverse hyperdynamic septic shock: a prospective, randomized, double-blind, single-center study". Crit. Care Med. 27 (4): 723–32. PMID 10321661. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=27&issue=4&spage=723.
- ^ Bollaert PE, Charpentier C, Levy B, Debouverie M, Audibert G, Larcan A (April 1998). "Reversal of late septic shock with supraphysiologic doses of hydrocortisone". Crit. Care Med. 26 (4): 645–50. doi:10.1097/00003246-199804000-00010. PMID 9559600. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=26&issue=4&spage=645.
- ^ Oppert M, Schindler R, Husung C et al. (November 2005). "Low-dose hydrocortisone improves shock reversal and reduces cytokine levels in early hyperdynamic septic shock". Crit. Care Med. 33 (11): 2457–64. doi:10.1097/01.CCM.0000186370.78639.23. PMID 16276166. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=33&issue=11&spage=2457.
- ^ Yildiz O, Doganay M, Aygen B, Güven M, Keleştimur F, Tutuû A (June 2002). "Physiological-dose steroid therapy in sepsis ISRCTN36253388". Crit Care 6 (3): 251–9. doi:10.1186/cc1498. PMC 125315. PMID 12133187. http://ccforum.com/content/6/3/251.
- ^ Keh D, Boehnke T, Weber-Cartens S et al. (February 2003). "Immunologic and hemodynamic effects of "low-dose" hydrocortisone in septic shock: a double-blind, randomized, placebo-controlled, crossover study". Am. J. Respir. Crit. Care Med. 167 (4): 512–20. doi:10.1164/rccm.200205-446OC. PMID 12426230. http://ajrccm.atsjournals.org/cgi/pmidlookup?view=long&pmid=12426230.
- ^ a b Hamrahian AH, Oseni TS, Arafah BM (April 2004). "Measurements of serum free cortisol in critically ill patients". N. Engl. J. Med. 350 (16): 1629–38. doi:10.1056/NEJMoa020266. PMID 15084695. http://content.nejm.org/cgi/pmidlookup?view=short&pmid=15084695&promo=ONFLNS19.
- ^ a b Marik PE, Zaloga GP (November 2002). "Adrenal insufficiency in the critically ill: a new look at an old problem". Chest 122 (5): 1784–96. doi:10.1378/chest.122.5.1784. PMID 12426284. http://www.chestjournal.org/cgi/pmidlookup?view=long&pmid=12426284.
- ^ Duthie DJ, Fraser R, Nimmo WS (February 1985). "Effect of induction of anaesthesia with etomidate on corticosteroid synthesis in man". Br J Anaesth 57 (2): 156–9. doi:10.1093/bja/57.2.156. PMID 2982387. http://bja.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=2982387.
- ^ Cooper MS, Stewart PM (February 2003). "Corticosteroid insufficiency in acutely ill patients". N. Engl. J. Med. 348 (8): 727–34. doi:10.1056/NEJMra020529. PMID 12594318. http://content.nejm.org/cgi/pmidlookup?view=short&pmid=12594318&promo=ONFLNS19.
- ^ Venkatesh B, Mortimer RH, Couchman B, Hall J (April 2005). "Evaluation of random plasma cortisol and the low dose corticotropin test as indicators of adrenal secretory capacity in critically ill patients: a prospective study". Anaesth Intensive Care 33 (2): 201–9. PMID 15960402.
- ^ Van den Berghe G, de Zegher F, Bouillon R (June 1998). "Clinical review 95: Acute and prolonged critical illness as different neuroendocrine paradigms". J. Clin. Endocrinol. Metab. 83 (6): 1827–34. doi:10.1210/jc.83.6.1827. PMID 9626104. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=9626104.
- ^ Arlt W, Hammer F, Sanning P et al. (July 2006). "Dissociation of serum dehydroepiandrosterone and dehydroepiandrosterone sulfate in septic shock". J. Clin. Endocrinol. Metab. 91 (7): 2548–54. doi:10.1210/jc.2005-2258. PMID 16608898. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=16608898.
- ^ Marx C, Petros S, Bornstein SR et al. (May 2003). "Adrenocortical hormones in survivors and nonsurvivors of severe sepsis: diverse time course of dehydroepiandrosterone, dehydroepiandrosterone-sulfate, and cortisol". Crit. Care Med. 31 (5): 1382–8. doi:10.1097/01.CCM.0000063282.83188.3D. PMID 12771606. http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=31&issue=5&spage=1382.
- ^ Vermes I, Beishuizen A (December 2001). "The hypothalamic-pituitary-adrenal response to critical illness". Best Pract. Res. Clin. Endocrinol. Metab. 15 (4): 495–511. doi:10.1053/beem.2001.0166. PMID 11800520.
Health science · Medicine · Medical specialities · Intensive care medicine / Critical care medicine and Respiratory therapy General terms ConditionsOrgan system failureComplications Diagnosis Life supporting treatments Drugs ICU scoring systems Organisations Related specialties
Wikimedia Foundation. 2010.
Look at other dictionaries:
Critical illness polyneuropathy — (CIP) and critical illness myopathy (CIM) are overlapping syndromes of widespread muscle weakness and neurological dysfunction that can develop in critically ill patients receiving intensive care. CIP and CIM have similar symptoms and… … Wikipedia
Critical care nursing — is the field of nursing with a focus on the utmost care of the critically ill or unstable patients. Critical care nurses can be found working in a wide variety of environments and specialties, such as emergency departments and the intensive care… … Wikipedia
Critical Care Air Transport Team — (CCATT) dates from 1996, when the United States Air Force formally established what has proved to be one of the latest milestones in the history of military medicine. The CCATT is a three person, highly specialized medical asset that can create… … Wikipedia
Adrenal insufficiency — Infobox Disease Name = PAGENAME Caption = Adrenal gland DiseasesDB = ICD10 = ICD10|E|27|1|e|20 ICD10|E|27|4|e|20 ICD9 = ICD9|255.4 ICDO = OMIM = MedlinePlus = eMedicineSubj = emerg eMedicineTopic = 16 MeshID = D000309 Adrenal insufficiency is a… … Wikipedia
Sepsis — Infobox Disease Name = Sepsis Caption = DiseasesDB = 11960 ICD10 = ICD10|A|40| |a|30 ICD10|A|41|0|a|30 ICD9 = ICD9|995.91 ICDO = OMIM = MedlinePlus = 000666 eMedicineSubj = eMedicineTopic = MeshID = D018805 Sepsis is a serious medical condition… … Wikipedia
Shock (circulatory) — Acute shock redirects here. For the psychological condition, see Acute stress reaction. Shock ICD 10 many incl. R57 ICD 9 785 DiseasesDB … Wikipedia
Distributive shock — is defined by hypotension and generalized tissular hypoxia. This form of relative hypovolemia is the result of blood vessel dilation. Septic shock is the major cause, but there are other examples as well. Examples Examples of this form of… … Wikipedia
Multiple organ dysfunction syndrome — Classification and external resources ICD 9 995.92 eMedicine med/3372 … Wikipedia
Mechanical ventilation — In architecture and climate control, mechanical or forced ventilation is the use of powered equipment, e.g. fans and blowers, to move air see ventilation (architecture). Mechanical ventilation Intervention … Wikipedia
Nosocomial infection — Classification and external resources Contaminated surfaces increase cross transmission ICD 10 Y … Wikipedia