Diferencia entre revisiones de «Adrenal crisis»

Sin resumen de edición
(Embed Steroid_Conversion_Calculator on clinical page)
 
(No se muestran 69 ediciones intermedias de 14 usuarios)
Línea 1: Línea 1:
==Diagnosis==
==Background==
*'''Life-threatening emergency''' resulting from acute cortisol 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>
*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


* Major factor precipitating adrenal crisis is mineralocorticoid, not glucocorticoid, deficiency
===Precipitants of Crisis===
* Major clinical problem is hypotension
*Infection/sepsis (most common trigger)
* Most commonly presents as shock
*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 Manifestations==
==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)


* Hypotension
==Differential Diagnosis==
* Refractory to fluids
*[[Sepsis]] / [[septic shock]] (most common misdiagnosis — and most common precipitant)
* Volume depletion
*[[Thyroid storm]] / [[myxedema coma]]
* Abdominal tenderness
*[[Diabetic ketoacidosis]]
* Usually generalized
*[[Hypovolemic shock]]
* Fever
*Acute abdomen (gastroenteritis, [[pancreatitis]])
* Usually caused by infection (source must be identified and treated)
*Drug withdrawal
*[[Pheochromocytoma]] crisis


Lab tests
==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


* Hyperkalemia
==Management==
* Hyponatremia
===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.


fever, hypoTN (refractory to fluids), hyperpigmentation by increased ACTH
===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)


- cushingoid look by chronic steroid use
===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)


- think about in kids with congenital adrenal hyperplasia (CAH) who present with shock
===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


==Workup==
== Calculators ==
{{Steroid_Conversion_Calculator}}


==See Also==
*[[Adrenal insufficiency]]
*[[Myxedema coma]]
*[[Sepsis]]
*[[Shock]]
*[[Hyponatremia]]


* Chemistry/glucose
==References==
* Guides therapy
<references/>
* Cortisol level
*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
* Confirms diagnosis
*Rushworth RL, et al. Adrenal crisis. ''N Engl J Med''. 2019;381(9):852-861. PMID 31461595
* Renin, ACTH
*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
* For evaluating differential diagnosis if cortisol level normal 


Treatment==
[[Category:Endocrinology]]
 
[[Category:Critical Care]]
 
* Do not wait for lab results to start treatment
* Fluids
* Infuse 2-3L of NS or D5NS (to correct hypoglycemia)
* Avoid hypotonic fluids (may worsen hyponatremia)
* Glucocorticoids
* Patient without previous diagnosis of adrenal insufficiency
* Dexamethasone 4mg IV bolus is preferred tx
* Patient with known primary adrenal insufficiency w/ potassium > 6
* Hydrocortisone 100mg IV bolus (preferred due to its mineralcorticoid activity)
* Mineralocorticoids are not indicated in acute management
* Treat underlying cause
== ==
 
 
==Source ==
 
 
7/2/09 PANI (Adapted from Mistry), UpToDate
 
 
 
 
[[Category:Endo]]

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