RECOGNITION AND ASSESSMENT
Most common cause is secondary adrenal failure (hypothalamic-pituitary disease with inadequate ACTH or long-term corticosteroid therapy), where mineralocorticoid production is generally preserved
Symptoms and signs
- Lethargy
- Nausea
- Weight loss
- Hypoglycaemia
Indicators of severe adrenal insufficiency
- Hyponatraemia
- Hypoglycaemia
- Hypotension – systolic BP <90 mmHg, diastolic BP <50 mmHg
- Tachycardia – with no obvious cause
Primary adrenal failure
- Hypotension (postural/sustained)
- Pigmentation (palmar/buccal/scars/pressure areas)
- Vitiligo
Secondary adrenal failure
- Pallor
- Loss of pubic/axillary hair (because of co-existing secondary hypogonadism)
Risk factors
Primary adrenal failure
- Auto-immune disease (diabetes/hypothyroidism/pernicious anaemia)
- TB
- Metastases, especially from carcinoma of lung
Secondary adrenal failure
- Withdrawal of oral (or potent topical or inhaled) corticosteroids
- Pituitary surgery/radiotherapy
INVESTIGATIONS
- FBC
- U&E
- Blood glucose
Check for severe adrenal insufficiency
Guidance tool
Adrenal failure suspected
- Send gold top blood bottles for markers of pituitary function:
- Cortisol
- FSH/LH
- testosterone (males)
- TSH/FT4
- growth hormone (GH)
- insulin-like growth factor 1 (IGF-1)
- prolactin
- If adrenal insufficiency strongly suspected, send EDTA (purple) top blood bottle for adrenocorticotropic hormone (ACTH)
Results in primary adrenal failure only
- Hyperkalaemia
- Raised urea
IMMEDIATE TREATMENT
- If severely ill:
- hydrocortisone 100 mg as slow IV bolus, followed by 100 mg by slow IV bolus 6-hrly
- sodium chloride 0.9% 1 L by IV infusion over 30–60 min, followed by 3–4 L IV over next 24 hr
- If hypoglycaemic, give simultaneous infusion of:
- glucose 20% 100 mL by IV infusion over 30 min, followed by glucose 10% 1 L by IV infusion over 12 hr. Monitor blood glucose and change to glucose 20% if 10% inadequate
- glucagon is unhelpful in this situation
SUBSEQUENT MANAGEMENT
- Admit to endocrinology ward
- When improving and tolerating oral fluid:
- hydrocortisone 20 mg oral 8-hrly
- refer to endocrinology team for advice on maintenance dosage (usually 20 mg in morning and 10 mg in afternoon – no later than 1800 hr)
- if diagnosis in doubt, seek advice from endocrinology team about substituting dexamethasone 1 mg oral 8-hrly for hydrocortisone and perform SST within three days. If on oral hydrocortisone (maintenance dose 20 mg in morning and 10 mg in afternoon), afternoon dose can be omitted and SST carried out between 0800–0900 next day
- after the test and while awaiting result, revert to maintenance dose
- In primary adrenal failure:
- add fludrocortisone 50–100 microgram oral daily
- request adrenal autoantibodies
- arrange chest and abdominal X-rays
- if TB suspected, request CT scan of adrenals
- If secondary adrenal failure suspected, refer to endocrinology team
MONITORING
- U&E daily
- Lying and standing BP twice daily, looking for orthostatic hypotension
DISCHARGE AND FOLLOW-UP
- Patients must carry ‘Steroid card’ and wear ‘Medic Alert bracelet’
- Patients must understand need for:
- lifelong hydrocortisone
- doubling the daily dose for the duration of any intercurrent illness
- parenteral hydrocortisone if vomiting (supply with ampoule of hydrocortisone 100 mg to keep in fridge for use by paramedics in emergency)
- Refer to endocrinology for follow-up
© 2022 The Bedside Clinical Guidelines Partnership.
Created by University Hospital North Midlands and Keele University School of Computing and Mathematics.
Research and development team: James Mitchell, Ed de Quincey, Charles Pantin, Naveed Mustfa