Adrenal crisis: Difference between revisions

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==Background==
==Background==
*Consider in any pt w/ unexplained hypotension (esp if have HIV or take steroids)
*'''Life-threatening emergency''' resulting from acute cortisol deficiency
*Main factor causing adrenal crisis is mineralocorticoid, not glucocorticoid, deficiency
*'''Mortality up to 25%''' if untreated; rapidly fatal without intervention<ref>Hahner S, et al. Adrenal crisis: prevalence, prevention, and education. ''Endocr Connect''. 2015;4(2):R27-R35. PMID 25766587</ref>
**This is the reason crises occur much more frequently w/ primary adrenal insufficiency
*Most common cause: stress event in patient with chronic adrenal insufficiency on glucocorticoid replacement who does NOT increase dose ("stress dosing")
*Major clinical problem is hypotension
*Can also occur as first presentation of undiagnosed adrenal insufficiency
**Most commonly presents as shock


===Causes (Adrenal Insufficiency)===
===Causes of Adrenal Insufficiency===
*Primary adrenal insufficiency (decreased cortisol and aldosterone)
*Primary (adrenal gland destruction):
**Autoimmune (70%)
**Autoimmune adrenalitis (Addison disease — most common in developed countries)
**Adrenal hemorrhage
**Infections: TB (most common worldwide), CMV, HIV, fungal
***Coagulation disorders
**Bilateral adrenal hemorrhage (Waterhouse-Friderichsen syndrome [[meningococcemia]], anticoagulation, [[DIC]])
***[[Sepsis]] (Waterhouse-Friderichsen syndrome)
**Metastatic disease, bilateral adrenalectomy
**Meds
*Secondary (pituitary — ACTH deficiency):
**Infection ([[HIV]], [[TB]])
**Pituitary tumors, surgery, radiation, Sheehan syndrome
*** TB is most common worldwide cause primary adrenal insuffiency
*Tertiary (hypothalamic — MOST COMMON overall):
**[[Sarcoidosis]]/[[amyloidosis]]
**Chronic exogenous glucocorticoid use → HPA axis suppression
**Mets
**Even short courses >2 weeks can suppress HPA axis
**[[Congenital Adrenal Hyperplasia|CAH]]
**Abrupt discontinuation → adrenal crisis
*Secondary adrenal insufficiency (decreased ACTH -> decreased cortisol only)
**Withdrawal of steroid therapy
**Pituitary disease
**[[Head trauma]]
**Postpartum pituitary necrosis
**Infiltrative disorders of pituitary or hypothalamus


===Precipitants===
===Precipitants of Crisis===
*Increased demand
*Infection/sepsis (most common trigger)
**Infection
*Surgery, trauma, critical illness
**[[MI]]
*Non-compliance or abrupt withdrawal of chronic steroids
**Surgery
*GI illness with vomiting (unable to take oral steroids)
**Trauma
*Emotional stress, adrenal hemorrhage
*Decreased supply
**Discontinuation of steriod therapy


==Clinical Features==
==Clinical Features==
*[[Hypotension]]
*Refractory hypotension/[[shock]] — does NOT respond to IV fluids or vasopressors until cortisol replaced
**Refractory to fluids/presors
*Weakness, fatigue, lethargy → obtundation → coma
*[[Dehydration]]
*Nausea, vomiting, abdominal pain (may mimic [[acute abdomen]])
*[[Abdominal tenderness]]
*Fever or hypothermia
**Usually generalized
*Hypoglycemia (especially in children; cortisol is counterregulatory)
*[[Hyponatremia]]/[[hyperkalemia]]
*Dehydration (cortisol deficiency + aldosterone deficiency in primary AI)
** Hyperkalemia is not expected in Secondary Adrenal Insuffiency
*In chronic primary AI: hyperpigmentation (increased ACTH → MSH), vitiligo, salt craving
*[[Hypoglycemia]]
 
*Confusion/[[delirium]]/lethargy
===Classic Lab Pattern===
*[[Fever]]
*Hyponatremia (most common electrolyte abnormality)
**Usually caused by infection
*Hyperkalemia (primary AI only — aldosterone deficiency; absent in secondary/tertiary)
*Hypoglycemia
*Eosinophilia (cortisol normally suppresses eosinophils)
*Metabolic acidosis, elevated BUN (dehydration)


==Differential Diagnosis==
==Differential Diagnosis==
{{Shock DDX}}
*[[Sepsis]] / [[septic shock]] (most common misdiagnosis — and most common precipitant)
*[[Thyroid storm]] / [[myxedema coma]]
*[[Diabetic ketoacidosis]]
*[[Hypovolemic shock]]
*Acute abdomen (gastroenteritis, [[pancreatitis]])
*Drug withdrawal
*[[Pheochromocytoma]] crisis
 
==Evaluation==
*'''Random cortisol level''' (draw BEFORE giving steroids if possible, but '''do NOT delay treatment'''):
**Cortisol <3 mcg/dL: diagnostic of adrenal insufficiency
**Cortisol 3-18 mcg/dL in acutely stressed patient: suspicious (should be elevated in stress)
**Cortisol >18 mcg/dL in acute illness: effectively rules out AI
*ACTH level (distinguish primary vs secondary):
**High ACTH = primary AI; Low/normal ACTH = secondary/tertiary
*BMP: hyponatremia, hyperkalemia, hypoglycemia, metabolic acidosis
*CBC: eosinophilia, lymphocytosis
*'''Blood glucose''' (POC immediately)
*TSH (concurrent hypothyroidism in autoimmune polyendocrine syndrome)
*Infectious workup: blood cultures, UA, CXR, lactate (identify precipitant)
*'''ACTH stimulation test''' (cosyntropin test): NOT needed acutely — do NOT delay treatment for this test
 
==Management==
===Immediate===
*'''Hydrocortisone 100 mg IV bolus''' — '''give immediately if suspected''' (even before lab confirmation)
*Then hydrocortisone 50 mg IV q6-8h (or continuous infusion 200 mg/24h)
*If hydrocortisone unavailable: dexamethasone 4 mg IV (does not interfere with subsequent cortisol testing)
*IV fluids: aggressive NS resuscitation (patients are often 2-3L volume depleted)
**D5NS if hypoglycemic — correct hypoglycemia with D50W 25-50 mL IV
*Vasopressors if refractory hypotension (norepinephrine) — shock typically improves rapidly with steroids
*Treat precipitant: antibiotics for infection, etc.
 
===Key Principles===
*'''Do NOT delay steroids for diagnostic testing'''
*Hydrocortisone at stress doses provides both glucocorticoid AND mineralocorticoid activity (no need for separate fludrocortisone in acute phase)
*Hypotension refractory to fluids and vasopressors in a critically ill patient → think adrenal crisis
*Correct electrolytes (but hyperkalemia usually resolves with hydrocortisone and fluids)
 
===Taper===
*Once stable: taper to maintenance over 2-4 days
*Maintenance: hydrocortisone 15-25 mg/day (divided doses)
*Primary AI also needs fludrocortisone 0.05-0.1 mg PO daily (mineralocorticoid replacement)
 
===Prevention===
*Medical alert bracelet for all patients with adrenal insufficiency
*Sick day rules: double or triple oral glucocorticoid dose during illness
*Injectable hydrocortisone at home for emergencies (patient education)
*Stress dosing prior to surgery: hydrocortisone 100 mg IV before induction


==Diagnosis==
==Disposition==
*CBC - eosinophilia
*'''ICU admission''' for hemodynamic instability or altered mental status
*Chemistry
*Monitored bed for less severe presentations
*Random cortisol, renin, and ACTH levels
*Endocrinology consultation
**Do not wait for levels before starting treatment
*Serial electrolytes, glucose monitoring
*[[ACTH (cosyntropin) stimulation test]]
*Patient and family education on stress dosing before discharge


==Treatment==
== Calculators ==
;Begin treatment immediately in any suspected case (prognosis related to rapidity of treatment)
{{Steroid_Conversion_Calculator}}
#[[IVF]]
#*D5NS IV 2-3L (corrects fluid deficit and hypoglycemia)
#Steroids
#*[[Hydrocortisone]]
#**Drug of choice if K+>6 (provides glucocorticoid and mineralcorticoid effects)
#**2mg/kg up to 100mg IV bolus
#*[[Dexamethasone]]
#**Consider in stable patients if ACTH stim test will be performed (won't interfere w/ the test)
#**4mg IV bolus
#[[Vasopressors]]
#*Administered after steriod therapy in pts unresponsive to fluid resuscitation
#Treat underlying cause


==See Also==
==See Also==
*[[Congenital Adrenal Hyperplasia]]
*[[Adrenal insufficiency]]
*[[Addison's disease]]
*[[Myxedema coma]]
*[[Sepsis]]
*[[Shock]]
*[[Hyponatremia]]


==References==
==References==
*ACEP Critical Decisions in Emergency Medicine July 2012 issue
<references/>
*Bornstein SR, et al. Diagnosis and treatment of primary adrenal insufficiency: an Endocrine Society clinical practice guideline. ''J Clin Endocrinol Metab''. 2016;101(2):364-389. PMID 26760044
*Rushworth RL, et al. Adrenal crisis. ''N Engl J Med''. 2019;381(9):852-861. PMID 31461595
*Puar TH, et al. Adrenal crisis: still a deadly event in the 21st century. ''Am J Med''. 2016;129(3):339.e1-e9. PMID 26524708


[[Category:Endo]]
[[Category:Endocrinology]]
[[Category:Critical Care]]

Latest revision as of 09:56, 22 March 2026

Background

  • Life-threatening emergency resulting from acute cortisol deficiency
  • Mortality up to 25% if untreated; rapidly fatal without intervention[1]
  • Most common cause: stress event in patient with chronic adrenal insufficiency on glucocorticoid replacement who does NOT increase dose ("stress dosing")
  • Can also occur as first presentation of undiagnosed adrenal insufficiency

Causes of Adrenal Insufficiency

  • Primary (adrenal gland destruction):
    • Autoimmune adrenalitis (Addison disease — most common in developed countries)
    • Infections: TB (most common worldwide), CMV, HIV, fungal
    • Bilateral adrenal hemorrhage (Waterhouse-Friderichsen syndrome — meningococcemia, anticoagulation, DIC)
    • Metastatic disease, bilateral adrenalectomy
  • Secondary (pituitary — ACTH deficiency):
    • Pituitary tumors, surgery, radiation, Sheehan syndrome
  • Tertiary (hypothalamic — MOST COMMON overall):
    • Chronic exogenous glucocorticoid use → HPA axis suppression
    • Even short courses >2 weeks can suppress HPA axis
    • Abrupt discontinuation → adrenal crisis

Precipitants of Crisis

  • Infection/sepsis (most common trigger)
  • Surgery, trauma, critical illness
  • Non-compliance or abrupt withdrawal of chronic steroids
  • GI illness with vomiting (unable to take oral steroids)
  • Emotional stress, adrenal hemorrhage

Clinical Features

  • Refractory hypotension/shock — does NOT respond to IV fluids or vasopressors until cortisol replaced
  • Weakness, fatigue, lethargy → obtundation → coma
  • Nausea, vomiting, abdominal pain (may mimic acute abdomen)
  • Fever or hypothermia
  • Hypoglycemia (especially in children; cortisol is counterregulatory)
  • Dehydration (cortisol deficiency + aldosterone deficiency in primary AI)
  • In chronic primary AI: hyperpigmentation (increased ACTH → MSH), vitiligo, salt craving

Classic Lab Pattern

  • Hyponatremia (most common electrolyte abnormality)
  • Hyperkalemia (primary AI only — aldosterone deficiency; absent in secondary/tertiary)
  • Hypoglycemia
  • Eosinophilia (cortisol normally suppresses eosinophils)
  • Metabolic acidosis, elevated BUN (dehydration)

Differential Diagnosis

Evaluation

  • Random cortisol level (draw BEFORE giving steroids if possible, but do NOT delay treatment):
    • Cortisol <3 mcg/dL: diagnostic of adrenal insufficiency
    • Cortisol 3-18 mcg/dL in acutely stressed patient: suspicious (should be elevated in stress)
    • Cortisol >18 mcg/dL in acute illness: effectively rules out AI
  • ACTH level (distinguish primary vs secondary):
    • High ACTH = primary AI; Low/normal ACTH = secondary/tertiary
  • BMP: hyponatremia, hyperkalemia, hypoglycemia, metabolic acidosis
  • CBC: eosinophilia, lymphocytosis
  • Blood glucose (POC immediately)
  • TSH (concurrent hypothyroidism in autoimmune polyendocrine syndrome)
  • Infectious workup: blood cultures, UA, CXR, lactate (identify precipitant)
  • ACTH stimulation test (cosyntropin test): NOT needed acutely — do NOT delay treatment for this test

Management

Immediate

  • Hydrocortisone 100 mg IV bolusgive immediately if suspected (even before lab confirmation)
  • Then hydrocortisone 50 mg IV q6-8h (or continuous infusion 200 mg/24h)
  • If hydrocortisone unavailable: dexamethasone 4 mg IV (does not interfere with subsequent cortisol testing)
  • IV fluids: aggressive NS resuscitation (patients are often 2-3L volume depleted)
    • D5NS if hypoglycemic — correct hypoglycemia with D50W 25-50 mL IV
  • Vasopressors if refractory hypotension (norepinephrine) — shock typically improves rapidly with steroids
  • Treat precipitant: antibiotics for infection, etc.

Key Principles

  • Do NOT delay steroids for diagnostic testing
  • Hydrocortisone at stress doses provides both glucocorticoid AND mineralocorticoid activity (no need for separate fludrocortisone in acute phase)
  • Hypotension refractory to fluids and vasopressors in a critically ill patient → think adrenal crisis
  • Correct electrolytes (but hyperkalemia usually resolves with hydrocortisone and fluids)

Taper

  • Once stable: taper to maintenance over 2-4 days
  • Maintenance: hydrocortisone 15-25 mg/day (divided doses)
  • Primary AI also needs fludrocortisone 0.05-0.1 mg PO daily (mineralocorticoid replacement)

Prevention

  • Medical alert bracelet for all patients with adrenal insufficiency
  • Sick day rules: double or triple oral glucocorticoid dose during illness
  • Injectable hydrocortisone at home for emergencies (patient education)
  • Stress dosing prior to surgery: hydrocortisone 100 mg IV before induction

Disposition

  • ICU admission for hemodynamic instability or altered mental status
  • Monitored bed for less severe presentations
  • Endocrinology consultation
  • Serial electrolytes, glucose monitoring
  • Patient and family education on stress dosing before discharge

Calculators

Steroid Conversion Calculator

Steroid Conversion Calculator
Starting Steroid 5
Dose of Starting Steroid (mg) 10
Equivalent Doses
Hydrocortisone (mg)
Prednisone / Prednisolone (mg)
Methylprednisolone (mg)
Dexamethasone (mg)
Relative Potency Reference
Steroid Equivalent Dose (mg) Relative Anti-inflammatory Potency
Hydrocortisone 20 1
Prednisone / Prednisolone 5 4
Methylprednisolone 4 5
Triamcinolone 4 5
Dexamethasone 0.75 25-30
References
  • Liu D, et al. A practical guide to the monitoring and management of the complications of systemic corticosteroid therapy. Allergy Asthma Clin Immunol. 2013;9(1):30.
  • Czock D, et al. Pharmacokinetics and pharmacodynamics of systemically administered glucocorticoids. Clin Pharmacokinet. 2005;44(1):61-98.

See Also

References

  1. Hahner S, et al. Adrenal crisis: prevalence, prevention, and education. Endocr Connect. 2015;4(2):R27-R35. PMID 25766587
  • Bornstein SR, et al. Diagnosis and treatment of primary adrenal insufficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2016;101(2):364-389. PMID 26760044
  • Rushworth RL, et al. Adrenal crisis. N Engl J Med. 2019;381(9):852-861. PMID 31461595
  • Puar TH, et al. Adrenal crisis: still a deadly event in the 21st century. Am J Med. 2016;129(3):339.e1-e9. PMID 26524708