Adrenal glands produce steroids- glucocorticoids and mineralocorticoids & androgens; therefore in adrenal insufficiency there are low levels of steroids & androgens
Presentation: generalised weakness, low Na+, high K+, hypotensive, hypoglycaemia
Diagnosis: low cortisol following ACTH bolus (short synACTHen test)
Management: hydrocortisone (glucocorticoid) and fludrocortisone (mineralocorticoid)
History
Global weakness with infective symptoms
Loss of consciousness - syncope/ presyncope
Background: long term steroids or autoimmune conditions
Examination
Dehydrated
Hypotension with postural drop
Investigations
HypoNatraemia , HyperKalaemia (or upper limits of normal)
Diagnostic framework:
Random cortisol: if > 150 unlikely
Morning short synACTHen test
If cortisol fails to rise, diagnose adrenal insufficiency
ACTH
Low: pituitary issue
High: adrenal issue
Differentials: Sepsis , Hypothermia , Hypothyroid coma
Classification: (aetiology)
Primary (adrenal issue)
Addison's Disease: autoimmune adrenal destruction
Adrenal metastasis (1%),
Adrenal haemorrhage, adrenalectomy
Secondary (pituitary issue)
Iatrogenic suppression with chronic steroids (e.g. PMR )
Pituitary tumours or surgery
Sheehan's Syndrome
Acute
Stabilise patient
Double basal steroids
If unwell/ unsure of dose- Hydrocortisone 200mg IV stat + 100mg QID (plenty)
Long term
Investigate underlying cause: ACTH & focused imaging.
Debate about the utility of morning/ random cortisol and if high whether it can rule out adrenal insufficiency.
Written in 2025