Addison's disease

Hypocortisolism / Adrenal Insufficiency



Background

  • Classified on problem site: hypothalamic-pituitary-adrenal axis
  • Normal adrenal=
    • Mineralocorticoids - zona glomerulosa
    • Gluccortisoids - zona fasciculata
    • Sex hormones - zona reticularis
  • Secondary = pit. cannot produce enough ACTH or adrenals not responding to ACTH
  • Tertiary = little/ineffective CRH from hypothalamus

Aetiology

Hypo-cortisol caused by:

  • Long-term steroid treatment
  • Adrenocortical disease (Addison's disease), autoimmune, infections (tuberculosis, HIV), haemorrhage, metastatic deposits
  • Pituitary or hypothalamic disease (tumour, trauma, infection, or ischaemia)

For primary:

  • 90% autoimmune
  • F > M, 30-50 yo

Clinical

  • Insidious: Wt loss, fatigue ± ↓BP (NB postural)
  • Occasionally skin pigmentation (MSH)
  • If pituitary- no skin pigmentation or hypokalaemia (mineralocorticoids okay)
  • Diagnosed with low Serum/plasma cortisol (particularly early morning)
  • May have transient hypocortisolism (< 400nmol/l) in sepsis
  • Confirm with a short ACTH test
  • Beware those on chronic steroid therapy unless morning cortisol > 200 nmol/l

Labs


Addisonian crisis

  • Altered consciousness, ↓BP, ↓Glucose
  • Usually a Hx of recent nausea, vomiting
  • Beware and treat for underlying trigger (sepsis, trauma, SCS)
  • Baseline bloods and save serum before treatment for later cortisol level measurement
  • ± CXR then:
  • Hydrocortisone 200mg IV
  • Correct dehydration, hyponatraemia and hypoglycaemia:
    • 2 litres saline in first 3 hours
  • Closely monitor glucose if unresponsive or intubated


Content by Dr Íomhar O' Sullivan. Last review Dr Simon Walsh 11/03/2022, Dr ÍOS 5/01/25.