Critical illness-related corticosteroid insufficiency

Other names| CIRCI

Critical illness-related corticosteroid insufficiency  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.[1]

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.[2] It has been suggested that high levels could represent severe stress, whereas low levels are due to blunted cortisol production and response.[3]

CIRCI can be suspected in patients with low blood pressure despite resuscitation with intravenous fluids and vasopressor drugs.[4] The Surviving Sepsis Campaign guidelines advocate intravenous hydrocortisone only in adults with septic shock and refractory hypotension.[4] 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.[5]

## Contents

* 1 Signs and symptoms
* 2 Physiology
* 3 Diagnosis
* 4 Treatment
* 5 See also
* 6 References

## Signs and symptoms

The best known feature that suggests a possible underlying adrenal insufficiency is low blood pressure despite resuscitation with intravenous fluids, requiring vasopressor drugs.[4] These patients typically display tachycardia and other signs of hyperdynamic shock.[5] Other symptoms include fever, purpura fulminans, and gastrointestinal or neurological disturbances.[5] All these features are relatively non-specific in intensive care patients.[5]

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.[5] 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.[6]

Several blood test abnormalities can suggest corticosteroid insufficiency, such as hypoglycemia, hyponatremia, hyperkalemia, hypercalcemia, neutropenia, eosinophilia, hyperprolactinemia, and hypothyroidism.[5]

## Physiology

In acute states of severe stress, cortisol secretion by the adrenal gland increases up to sixfold, parallel to the severity of the condition.[7] 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.[8] There is also an increase in the number and affinity of glucocorticoid receptors.[5] Levels of corticosteroid-binding globulin (CBG) and albumin, which normally bind cortisol, are decreased, resulting in increased levels of free cortisol.[7] Furthermore, anaesthesia drugs like etomidate could interfere with the HPA axis.[9] The secretion also loses its normal diurnal pattern of morning peak levels and evening and night time troughs.[10] Nevertheless, secretion remains pulsatile and there is a marked variation in blood samples from the same individual.[11]

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.[8][12] 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.[5]

Blood levels of dehydroepiandrosterone increase, and levels of dehydroepiandrosterone sulfate decrease in response to critical illness.[13][14][15]

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.[5]

## Diagnosis

The exact diagnostic tests and cut-off values to diagnose critical illness-related corticosteroid insufficiency are not agreed upon.[1] 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.[5] 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.[5] Moreover, in patients whose adrenal glands are already maximally stimulated, a stimulation test would not be informative.[5] Furthermore, a short test might not adequately assess response to the chronic stress of critical illness.[5]

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.[5] 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.[16] In the CORTICUS study, ACTH stimulation testing predicted mortality whereas baseline cortisol levels did not.[17] However, possible benefits of corticosteroid therapy do not seem to be completely predicted by ACTH stimulation testing.[18][19] For these reasons, guidelines currently do not recommend that ACTH stimulation testing should guide the decision whether or not to administer corticosteroids.[1][4] Cortisol immunoassays on the other hand have been shown to be prone to both over- and underestimation.[4]

## Treatment

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.[1] Fludrocortisone is optional in CIRCI, and dexamethasone is not recommended.[4] Little evidence is available to judge when and how corticosteroid therapy should be stopped; guidelines recommend tapering corticosteroids when vasopressors are no longer needed.[1][4]

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.[20] Historically, higher doses of steroids were given, but these have been suggested to be harmful compared to the lower doses which are advocated today.[21]

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.[18] The latter findings tempered enthusiasm for the broad use of hydrocortisone in septic shock.[4] Prior to this study, several other smaller studies showed beneficial effects of long courses of low doses of corticoid.[19][22][23][24][25][26][27] 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.[5]

## See also

* Adrenal insufficiency
* Addison's disease
* Cortisol
* Hypothalamic–pituitary–adrenal axis
* Glucocorticoids

## References

1. ↑ 1.0 1.1 1.2 1.3 1.4 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.
2. ↑ "Prediction of outcome in intensive care patients using endocrine parameters". Crit. Care Med. 23 (1): 78–83. January 1995. doi:10.1097/00003246-199501000-00015. PMID 8001391.
3. ↑ "A 3-level prognostic classification in septic shock based on cortisol levels and cortisol response to corticotropin". JAMA 283 (8): 1038–45. February 2000. doi:10.1001/jama.283.8.1038. PMID 10697064.
4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 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.
5. ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 5.11 5.12 5.13 5.14 "The altered adrenal axis and treatment with glucocorticoids during critical illness". Nat Clin Pract Endocrinol Metab 4 (9): 496–505. September 2008. doi:10.1038/ncpendmet0921. PMID 18695699.
6. ↑ "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. January 1987. PMID 3027305. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=3027305.
7. ↑ 7.0 7.1 "Measurements of serum free cortisol in critically ill patients". N. Engl. J. Med. 350 (16): 1629–38. April 2004. doi:10.1056/NEJMoa020266. PMID 15084695.
8. ↑ 8.0 8.1 "Adrenal insufficiency in the critically ill: a new look at an old problem". Chest 122 (5): 1784–96. November 2002. doi:10.1378/chest.122.5.1784. PMID 12426284. http://www.chestjournal.org/cgi/pmidlookup?view=long&pmid=12426284.
9. ↑ "Effect of induction of anaesthesia with etomidate on corticosteroid synthesis in man". Br J Anaesth 57 (2): 156–9. February 1985. doi:10.1093/bja/57.2.156. PMID 2982387. http://bja.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=2982387.
10. ↑ "Corticosteroid insufficiency in acutely ill patients". N. Engl. J. Med. 348 (8): 727–34. February 2003. doi:10.1056/NEJMra020529. PMID 12594318.
11. ↑ "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. April 2005. doi:10.1177/0310057X0503300208. PMID 15960402.
12. ↑ "Clinical review 95: Acute and prolonged critical illness as different neuroendocrine paradigms". J. Clin. Endocrinol. Metab. 83 (6): 1827–34. June 1998. doi:10.1210/jc.83.6.1827. PMID 9626104. http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=9626104.
13. ↑ 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.
14. ↑ 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.
15. ↑ "The hypothalamic-pituitary-adrenal response to critical illness". Best Pract. Res. Clin. Endocrinol. Metab. 15 (4): 495–511. December 2001. doi:10.1053/beem.2001.0166. PMID 11800520.
16. ↑ 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.
17. ↑ 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.
18. ↑ 18.0 18.1 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.
19. ↑ 19.0 19.1 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.
20. ↑ "Steroid controversy in sepsis and septic shock: a meta-analysis". Crit. Care Med. 23 (7): 1294–303. July 1995. doi:10.1097/00003246-199507000-00021. PMID 7600840.
21. ↑ "Meta-analysis: the effect of steroids on survival and shock during sepsis depends on the dose". Ann. Intern. Med. 141 (1): 47–56. July 2004. doi:10.7326/0003-4819-141-1-200407060-00014. PMID 15238370.
22. ↑ "Corticosteroids for severe sepsis and septic shock: a systematic review and meta-analysis". BMJ 329 (7464): 480. August 2004. doi:10.1136/bmj.38181.482222.55. PMID 15289273.
23. ↑ 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. doi:10.1097/00003246-199904000-00025. PMID 10321661.
24. ↑ "Reversal of late septic shock with supraphysiologic doses of hydrocortisone". Crit. Care Med. 26 (4): 645–50. April 1998. doi:10.1097/00003246-199804000-00010. PMID 9559600.
25. ↑ 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.
26. ↑ "Physiological-dose steroid therapy in sepsis ISRCTN36253388". Crit Care 6 (3): 251–9. June 2002. doi:10.1186/cc1498. PMID 12133187.
27. ↑ 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.

* v
* t
* e

Intensive care medicine

* Health science
* Medicine
* Medical specialities
* Respiratory therapy

General terms|

* Intensive care unit (ICU)
* Neonatal intensive care unit (NICU)
* Pediatric intensive care unit (PICU)
* Coronary care unit (CCU)
* Critical illness insurance

Conditions|

| Organ system failure|

Shock sequence
SIRS
Sepsis
Severe sepsis
Septic shock
Multiple organ dysfunction syndrome

Other shock
Cardiogenic shock
Distributive shock
Anaphylaxis
Obstructive shock
Neurogenic shock
Spinal shock
Vasodilatory shock

Organ failure
Acute renal failure
Acute respiratory distress syndrome
Acute liver failure
Respiratory failure
Multiple organ dysfunction syndrome

* Neonatal infection
* Polytrauma
* Coma

|

Complications|

* Critical illness polyneuropathy / myopathy
* Critical illness–related corticosteroid insufficiency
* Decubitus ulcers
* Fungemia
* Stress hyperglycemia
* Stress ulcer

Iatrogenesis|

* Methicillin-resistant Staphylococcus aureus
* Oxygen toxicity
* Refeeding syndrome
* Ventilator-associated lung injury
* Ventilator-associated pneumonia
* Dialytrauma

Diagnosis|

* Arterial blood gas
* Catheter
* Arterial line
* Central venous catheter
* Pulmonary artery catheter
* Blood cultures
* Screening cultures

Life-supporting treatments|

* Airway management
* Chest tube
* Dialysis
* Enteral feeding
* Goal-directed therapy
* Induced coma
* Mechanical ventilation
* Therapeutic hypothermia
* Total parenteral nutrition
* Tracheal intubation

Drugs|

* Analgesics
* Antibiotics
* Antithrombotics
* Inotropes
* Intravenous fluids
* Neuromuscular-blocking drugs
* Recombinant activated protein C
* Sedatives
* Stress ulcer prevention drugs
* Vasopressors

ICU scoring systems|

* APACHE II
* Glasgow Coma Scale
* PIM2
* SAPS II
* SAPS III
* SOFA

Physiology|

* Hemodynamics
* Hypotension
* Level of consciousness
* Acid–base imbalance
* Water-electrolyte imbalance

Organisations|

* Society of Critical Care Medicine
* Surviving Sepsis Campaign
* European Society of Paediatric and Neonatal Intensive Care

Related specialties|

* Anesthesiology
* Cardiology
* Internal medicine
* Neurology
* Pediatrics
* Pulmonology
* Surgery
* Traumatology

0.00

(0 votes)

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Medicine:Critical_illness-related_corticosteroid_insufficiency&oldid=866869"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template