Diferencia entre revisiones de «Adrenal crisis»

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==Background==
==Background==
[[File:Gray1120-adrenal glands.png|thumb|Posterior view of the adrenal glands (colored) in relation to the viscera and large vessels of the abdomen (thoracic vertebra removed).]]
*'''Life-threatening emergency''' resulting from acute cortisol deficiency
[[File:HPA axis combined.jpg|thumb|Types of adrenal insufficiency (primary, secondary, and tertiary) compared to normal physiology.]]
*'''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>
*Adrenal insufficiency occurs when the adrenal glands fail to supply the physiologic demands of the body for glucocorticoids (cortisol) and/or mineralocorticoids (aldosterone).
*Most common cause: stress event in patient with chronic adrenal insufficiency on glucocorticoid replacement who does NOT increase dose ("stress dosing")
*Divided into primary adrenal insufficiency or secondary adrenal insufficiency
*Can also occur as first presentation of undiagnosed adrenal insufficiency
*Adrenal crisis is the acute, life-threatening presentation of adrenal insufficiency<ref>Hahner S, Loeffler M, Bleicken B, et al. Epidemiology of adrenal crisis in chronic adrenal insufficiency: the need for new prevention strategies. Eur J Endocrinol. 2010;162(3):597-602. doi:10.1530/EJE-09-0884</ref>
**8-47% of patients with primary adrenal insufficiency will have at least one adrenal crisis in their lives
**Consider in any patient with unexplained [[hypotension]] (especially in those with [[HIV]] or taking exogenous steroids)
**Generally caused by mineralocorticoid deficiency, not glucocorticoid deficiency
***This is the reason crises occur much more frequently with primary adrenal insufficiency


===Causes of 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
**Metastases
**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)
**[[sepsis|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 [[steroid]] therapy


==Clinical Features==
==Clinical Features==
[[File:AdrenalCrisis.jpg|thumb|Forty-nine year-old with an adrenal crisis. Appearance, showing lack of facial hair, dehydration, Queen Anne’s sign (panel A), pale skin, muscular and weight loss, and loss of body hair (panel B)..]]
*Refractory hypotension/[[shock]] — does NOT respond to IV fluids or vasopressors until cortisol replaced
*Adrenal Crisis<ref>Rao RH, Vagnucci AH, Amico JA. Bilateral massive adrenal hemorrhage: early recognition and treatment. Ann Intern Med. 1989;110(3):227-235. doi:10.7326/0003-4819-110-3-227</ref>
*Weakness, fatigue, lethargy → obtundation → coma
**[[Hypotension]] (refractory to fluids/pressors)(90%)
*Nausea, vomiting, abdominal pain (may mimic [[acute abdomen]])
**[[Abdominal tenderness]] (86%)
*Fever or hypothermia
**[[Fever]] (66%)
*Hypoglycemia (especially in children; cortisol is counterregulatory)
**[[AMS|Confusion/delirium/lethargy]](42%)
*Dehydration (cortisol deficiency + aldosterone deficiency in primary AI)
**[[Hypoglycemia]]
*In chronic primary AI: hyperpigmentation (increased ACTH → MSH), vitiligo, salt craving
**Low bicarbonate, non-anion gap [[metabolic acidosis]] (due to decreased acid secretion in kidneys from aldosterone deficiency)<ref>Izumi Y et al. Renal tubular acidosis complicated with hyponatremia due to cortisol insufficiency. Oxf Med Case Reports. 2015 Nov; 2015(11): 360–363.</ref>


*Primary Adrenal Insufficiency<ref>Bancos I, Hahner S, Tomlinson J, Arlt W. Diagnosis and management of adrenal insufficiency. Lancet Diabetes Endocrinol. 2015;3(3):216-226. doi:10.1016/S2213-8587(14)70142-1</ref>
===Classic Lab Pattern===
**[[Anorexia]] (100%)
*Hyponatremia (most common electrolyte abnormality)
**[[Weakness|Weakness/fatigue]] (84-100%)
*Hyperkalemia (primary AI only — aldosterone deficiency; absent in secondary/tertiary)
**Hyperpigmentation (41-94%)
*Hypoglycemia
**[[Hypotension]] (41-94%)
*Eosinophilia (cortisol normally suppresses eosinophils)
**[[Hyponatremia]] (57-88%)
*Metabolic acidosis, elevated BUN (dehydration)
**[[Hyperkalemia]] (30-85%)
**Azotemia (55%)
**[[Dehydration]]
 
*Secondary Adrenal Insufficiency
**Similar to primary adrenal insufficiency
**No hyperpigmentation
**No hyperkalemia
**Hypotension less common


==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==
==Evaluation==
*'''Labs'''
*'''Random cortisol level''' (draw BEFORE giving steroids if possible, but '''do NOT delay treatment'''):
**CBC - [[eosinophilia]]<ref>Nutman TB. Evaluation and differential diagnosis of marked, persistent eosinophilia. Immunol Allergy Clin North Am. 2007 Aug; 27(3): 529–549.</ref>
**Cortisol <3 mcg/dL: diagnostic of adrenal insufficiency
**Chemistry
**Cortisol 3-18 mcg/dL in acutely stressed patient: suspicious (should be elevated in stress)
**Random cortisol, renin, and ACTH levels
**Cortisol >18 mcg/dL in acute illness: effectively rules out AI
***Do not wait for levels before starting treatment
*ACTH level (distinguish primary vs secondary):
**[[ACTH (cosyntropin) stimulation test]]
**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.


*'''Imaging'''
===Key Principles===
**Consider CXR to identify infectious triggers
*'''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)


==Management==
===Taper===
''Begin treatment immediately in any suspected case (prognosis related to rapidity of treatment)''
*Once stable: taper to maintenance over 2-4 days
*Treat underlying cause, if known
*Maintenance: hydrocortisone 15-25 mg/day (divided doses)
*[[IVF]] - D5NS 2-3L (corrects fluid deficit and hypoglycemia)
*Primary AI also needs fludrocortisone 0.05-0.1 mg PO daily (mineralocorticoid replacement)
*[[Steroids]]
**[[Hydrocortisone]] - 2mg/kg up to 100mg IV bolus
***Drug of choice if K+>6 (provides glucocorticoid and mineralocorticoid effects)
**[[Dexamethasone]] - 4mg IV bolus
***Consider in hemodynamically stable patients if ACTH stimulation test will be performed (will not interfere with the test)
***Along with methylprednisolone, dexamethasone has negligible mineralocorticoid effect, so '''choose hydrocortisone in'''<ref>Wilson TA et al. Adrenal Hypoplasia Medication. eMedicine. Feb 11, 2013. http://emedicine.medscape.com/article/918967-medication.</ref>:
****[[Hypotension]]
****[[Hyponatremia]] or [[hyperkalemia]]
**Comparable steroid dosages
***[[Hydrocortisone]] (50-75mg/m2 or 1-2mg/kg)
***[[Methylprednisolone]] are 10-15mg/m2
***[[Dexamethasone]] 1-1.5mg/m2
*[[Vasopressors]]
**Administer after steroid therapy in patients unresponsive to fluid resuscitation


===Stress-Dose Steroids in Illness===
===Prevention===
''To aid in mounting stress response in those with adrenal insufficiency lacking endogenous cortisol''
*Medical alert bracelet for all patients with adrenal insufficiency
{| {{table}}
*Sick day rules: double or triple oral glucocorticoid dose during illness
| align="center" style="background:#f0f0f0;"|'''Illness Type'''
*Injectable hydrocortisone at home for emergencies (patient education)
| align="center" style="background:#f0f0f0;"|'''Steroid Administration'''
*Stress dosing prior to surgery: hydrocortisone 100 mg IV before induction
|-
| Minor, with fever < 38°C||Double dose of chronic maintenance steroids
|-
| Severe, with fever > 38°C||Triple dose of chronic maintenance steroids
|-
| Vomiting, listless, or hypotensive||[[Hydrocortisone]] at 1-2mg/kg (as above in adrenal crisis)
|}


==Disposition==
==Disposition==
*'''Admission'''
*'''ICU admission''' for hemodynamic instability or altered mental status
**Admit all patients with acute adrenal insufficiency, especially if new diagnosis for the patient
*Monitored bed for less severe presentations
**Patients with adrenal crisis should receive ICU admission
*Endocrinology consultation
*'''Discharge'''
*Serial electrolytes, glucose monitoring
**Consult endocrinology if discharge considered for mild cases w/ normal lab values
*Patient and family education on stress dosing before discharge
 
== Calculators ==
{{Steroid_Conversion_Calculator}}


==See Also==
==See Also==
*[[Congenital Adrenal Hyperplasia]]
*[[Adrenal insufficiency]]
*[[Addison's disease]]
*[[Myxedema coma]]
 
*[[Sepsis]]
==External Links==
*[[Shock]]
*[http://www.emdocs.net/core-em-adrenal-crisis/ emDocs - Adrenal Crisis]
*[[Hyponatremia]]


==References==
==References==
<references/>
<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:Endocrinology]]
[[Category:Endocrinology]]
[[Category:Critical Care]]

Revisión actual - 09:56 22 mar 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