Endocrine: Adrenal Insufficiency
Adrenal Insufficiency
Definitions
- Adrenal Insufficiency: Insufficient Hormone Production within the Adrenal Gland
- Types:
- Primary (Addison Disease): From Disease within the Adrenal Gland
- Secondary: From Decreased ACTH Secretion by the Pituitary Gland
- Tertiary: From Decreased CRH Secretion by the Hypothalamus
Causes
- Primary Adrenal Insufficiency (Addison Disease)
- Autoimmune (Most Common Primary Cause – 70-90%)
- Tuberculosis (Was Previously the Most Common Cause Before Vaccination)
- Fungal Infections
- HIV/AIDS
- Metastatic Cancer
- Adrenal Hemorrhage/Infarction
- Can Be Caused by Infection (Pseudomonas, Meningococcemia, etc.)
- Waterhouse-Friderichsen Syndrome
- Adrenal Hemorrhage After Meningococcal Infection
- Presents as Adrenal Insufficiency After Meningitis
- Medications (Ketoconazole, Fluconazole, Rifampin, etc.)
- Secondary Adrenal Insufficiency
- Pituitary Adenoma
- Pituitary Surgery
- Pituitary Radiation
- Infection
- Pituitary Infarction – Sheehan Syndrome
- Pituitary Apoplexy
- Tertiary Adrenal Insufficiency
- Abrupt Steroid Withdrawal – Most Common Cause of Adrenal Insufficiency Overall
- Tumor
- Radiation
- Infection
- Stroke
- Traumatic Brain Injury
Waterhouse-Friderichsen Syndrome; Adrenal Excision 1
Presentation
- Addisonian/Adrenal Crisis: Hypotension/Shock Refractory to IV Fluids & Vasopressors
- Hypotension Itself is the Most Common First Sign
- Anorexia
- Abdominal Pain
- Nausea & Vomiting
- Fatigue & Lethargy
- Confusion
- Weight Loss
- Muscle Pain
- Hypoglycemia
- Symptoms Specific to Primary Adrenal Insufficiency:
- Skin Hyperpigmentation – ACTH Converted to MSH (Melanocyte-Stimulating Hormone)
- Mineralocorticoid Deficiency – Salt Craving, Postural Hypotension, Hyponatremia & Hyperkalemia
Diagnosis
- Standard Test for Diagnosis: ACTH Stimulation Test
- Treatment for Adrenal Crisis Should Be Started Before Diagnosis is Established
- Determine Type (If Necessary):
- First: Measure Basal ACTH
- High ACTH: Primary Adrenal Insufficiency
- Low ACTH: CRH Stimulation Test
- CRH Stimulation Test:
- Absent/Low ACTH Response: Secondary Adrenal Insufficiency
- Exaggerated ACTH Response: Tertiary Adrenal Insufficiency
- First: Measure Basal ACTH
Tests
- ACTH Stimulation Test
- Given Cosyntropin (Synthetic ACTH) 250 mcg & Serum Cortisol is Measured After 30-60 Minutes
- Normal Cortisol Response: ≥ 18-20 mcg/dL
- Can Be Done at Any Time of the Day – Response in Adrenal Insufficiency Will Remain Low Regardless of Time of Day
- Given Cosyntropin (Synthetic ACTH) 250 mcg & Serum Cortisol is Measured After 30-60 Minutes
- Morning Serum Cortisol
- Normal: 10-20 mcg/dL
- Low: < 3-5 mcg/dL
- *High Specificity, Low Sensitivity
- Morning Salivary Cortisol
- Normal: > 5.8 ng/mL
- Low: < 1.8 ng/mL
- Afternoon Cortisol Levels Have Wide Variability & Do Not Help in Diagnosis
Treatment
- Treatment: IV Fluids & Steroids
- Standard Glucocorticoid: Hydrocortisone
- IV Dose: 100 mg Bolus & 50 mg Every 6 Hours or 200 mg Infusion Over 24 Hours
- Duration of Action: Short Acting (8-12 Hours)
- Has Glucocorticoid & Some Mineralocorticoid Effect
- Other Steroids if Hydrocortisone Unavailable:
- Prednisone PO
- Duration of Action: Intermediate Acting (12-36 Hours)
- Prednisolone PO
- Duration of Action: Intermediate Acting (12-36 Hours)
- Dexamethasone IV
- Dose: 4 mg Every 12 Hours
- Duration of Action: Long Acting (36-72 Hours)
- Does Not Interfere with ACTH Stimulation Test
- No Mineralocorticoid Effect – Can Trigger an Adrenal Crisis in Primary Adrenal Insufficiency if Not Concurrently Given Fludrocortisone
- Prednisone PO
- When Resolved: Can Wean/Taper Rapidly Over 48 Hours
References
- Hale AJ, LaSalvia M, Kirby JE, Kimball A, Baden R. Fatal purpura fulminans and Waterhouse-Friderichsen syndrome from fulminant Streptococcus pneumoniae sepsis in an asplenic young adult. IDCases. 2016 Aug 16;6:1-4. (License: CC BY-NC-ND-4.0)