hypoadrenal (Addisonian) crisis; acute adrenal insufficiency
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Introduction
Hypoadrenal (Addisonian) crisis occurs secondary inadequate release of glucocorticoids & mineralocorticoids from the adrenal cortex.
Etiology
- acute adrenal hemorrhage
- precipitating factors in patient's with Addison's disease
- infection, especially gastroenteritis with vomiting, diarrhea, dehydration
- injury
- surgery
- less commonly
- exercise & emotional upset less frequently
- minor medical procedures such as vaccinations or infusions
- immunotherapy or chemotherapy
- abrupt discontinuation of glucocorticoid therapy
- risk factors
- older age
- history of prior adrenal crises[2]
- autoimmune polyglandular syndromes
- type 1 diabetes mellitus
- asthma
- cardiac disease[2]
Clinical manifestations
- hypotension, shock
- acute abdominal symptoms
- delirium, obtundation, or both
- hyponatremia, hyperkalemia, hypoglycemia
- pyrexia
- some patients may have multiple episodes[2]
Laboratory
- chem 7
- serum Na+: hyponatremia
- serum K+: hyperkalemia
- serum Cl- allows calculation of anion gap
- serum bicarbonate: low due to metabolic acidosis
- serum glucose: hypoglycemia
- serum cortisol
- eosinophil count may be elevated (eosinophilia)
Management
- volume expansion with intravenous saline
- hydrocortisone 100 mg IV every 8 hours
- marked resolution of hypotension within 1 hour
- improvement in clinical symptoms within 2 hours[2]
- parenteral administration of hydrocortisone at home may prevent progression of an early adrenal crisis[2]
- subcutaneous administration of hydrocortisone is an alternative to intramuscular injection (off-label)[2]