Treatment for Low Cortisol Levels (Hypocortisolism)
The treatment for hypocortisolism (low cortisol levels) consists primarily of hydrocortisone replacement at 15-20 mg daily in divided doses, with the morning dose being 10-15 mg (2/3 of total dose) and the afternoon dose being 5-10 mg (1/3 of total dose). 1
Diagnosis Before Treatment
Before initiating treatment, proper diagnosis is essential:
- Hypocortisolism should be confirmed with laboratory testing:
- ACTH stimulation test (gold standard): A delta total serum cortisol of <9 μg/dL after ACTH administration or random total cortisol <10 μg/dL indicates adrenal insufficiency 2
- Measure 21-hydroxylase autoantibodies to check for primary adrenal insufficiency 1
- Low-normal or subnormal plasma cortisol plus elevated ACTH indicates primary adrenal insufficiency (Addison's disease) 2
- Low-normal cortisol with low ACTH suggests secondary hypocortisolism 2
Treatment Protocol
For Primary Adrenal Insufficiency:
Glucocorticoid replacement:
- Hydrocortisone 15-20 mg total daily dose in divided doses 1
- Morning dose: 10-15 mg (2/3 of total dose)
- Afternoon dose: 5-10 mg (1/3 of total dose)
Mineralocorticoid replacement:
For Secondary Adrenal Insufficiency:
- Glucocorticoid replacement only:
Dose Adjustments for Special Situations
Stress Dosing:
Mild illness (fever, minor infection):
- Double or triple the daily hydrocortisone dose 1
Moderate symptoms:
- Increase to 2-3 times maintenance dose (30-50 mg total hydrocortisone or prednisone 20 mg daily)
- Taper back to maintenance over 5-10 days 1
Severe illness or adrenal crisis:
- Immediate IV hydrocortisone 100 mg or dexamethasone 4 mg
- At least 2L of normal saline IV 1
Pregnancy:
- Hydrocortisone requirements may increase, particularly in the third trimester
- Parenteral hydrocortisone should be planned for during delivery 1
Patient Education and Safety Measures
- Provide a medical alert bracelet/necklace and steroid card with emergency instructions 1
- Educate on stress dosing and when to seek emergency care
- Teach self-administration of injectable hydrocortisone for emergencies 1
Monitoring and Follow-up
Review patients at least annually:
- Assess weight, blood pressure, and serum electrolytes
- Monitor for development of autoimmune disorders, particularly hypothyroidism 1
Bone mineral density assessment every 3-5 years
Consider calcium and vitamin D supplementation 1
Titrate hydrocortisone to the lowest effective dose that maintains well-being
Adjust based on clinical symptoms rather than laboratory values alone 1
Important Cautions and Pitfalls
- Drug-induced secondary adrenal insufficiency requires gradual dose reduction when discontinuing treatment 4
- Avoid abrupt discontinuation of glucocorticoid therapy, which can precipitate adrenal crisis 5
- Patients with comorbidities such as asthma and diabetes have a higher risk of adrenal crisis 1
- Long-term use of hydrocortisone at doses ≥20 mg can lead to secondary adrenal insufficiency 1
- Monitor for side effects of glucocorticoid therapy, including hypertension, hyperglycemia, and osteoporosis 5, 4
- Patients on immunosuppressant doses should avoid exposure to chickenpox or measles 4
By following this treatment protocol and monitoring plan, patients with hypocortisolism can achieve adequate cortisol replacement while minimizing the risk of complications from both under-replacement and over-replacement.