Adrenal Disorder Drugs/Treatments Flashcards
Glucocorticoid Toxicities
Cushingoid Effects: 2+ weeks of treatment w/ CSC
- Hyperglycemia, Insulin resistance, iatrogenic DM
- Central obesity
- Muscle wasting, osteoporosis, thinning/bruising of skin
- Poor wound healing
- Impaired linear growth in children
Other toxicities:
- Androgenic effects- hirsuitism, acne, sweating
- Depression, anxiety, hypomania
- Increased intraocular pressure, glaucoma, cataracts
- Peptic Ulcers
- Immunosuppressive- opportunistic bacterial/fungal infections (candida)
- Insomnia
- Hypertension- some glucocorticoids with mineralocorticoid activities
Chronic Adrenal Insufficiency Treatments (Adison’s)
- Classic Replacement Therapy: hydrocortisone + fludrocortisone
- Hydrocortisone- 2-3x/day, oral, increase doses w/ stress
- Fludrocortisone- aldosterone replacement
- Prednisone (intermediate acting)
- Dexamethosone (long acting)
- Adequate tx: disappearance of hyperpigmentation and resolution of electrolyte abnormalities
- Early AM cortisol shoudn’t be suppressed but should be
Acute Adrenal Insufficiency Treatment
- Potentially life threatening, IV tx needed ASAP
- Large dose of parenteral hydrocortisone
- Correct fluid-electrolyte abnormalities
- Treat underlying cause- infection, hemorrhage, trauma
- Taper off hydrocortisone when pt. improves to avoid withdrawal, then treat like chronic adrenal insufficiency
Congenital Adrenal Hyperplasia (CAH)
- Dexamethasone admin. to mother during pregnancy if high risk
- Hydrocortisone replacement therapy (dose adjust for growth/bone maturation)
- Alternate day therapy w/ prednisone to increase ACTH suppression w/out growth inhibition
- Oral fludrocortisone + salt to maintain BP, PRA and electrolytes (aldosterone replacement)
Iatrogenic Cushing’s Syndrome Treatment
- Taper off CSC gradually
- May take 2-12 mo. for Hypothal-pit-adrenal axis to function then another 6-9 mo. for cortisol to normalize
CSC withdrawal Sx: Anorexia, N/V, weight loss, lethargy, headache, fever, joints and muscle pain, postural hypotension
Endogenous Cushing’s Syndrome/Disease Treatment
1st line: removal of ACTH or cortisol producing tumor
2nd line: radiotherapy, pharm, bilateral adrenalectomy
Ketoconazole & Metyrapone
Adrenal steroid biosynthesis inhibitors (cushing’s tx)
Cabergoline
DA Receptor agonist (inhibits PRL, inhibits ACTH)
- ACTH antagonist
Pasireotide
Somatostatin receptor agonist (ACTH antagonist)
Spironolactone & Eplerenone
- Mineralocorticoid Receptor Antagonists
- Normalize BP and K+ level in hyperaldosteronism
- Spironolactone can also antagonize androgen and progesterone receptors w/ side effects including gynecomastia (painful), decreased libido, impotence and menstrual irregularities (decreased estrogen conversion)
- Eplerenone: MC rec. specific- no sex hormone side effects
Pheochromocytoma Treatment
- Surgical resection of Pheo: stabilize BP and pulse first w/ alpha blockers then beta blockers b/c physical stimulation of pheo can cause release of stored catecholamines
Alpha-Blockers: Phenoxybenzamine, Prazosin, Terazosin, Doxazosin, alpha block for 1-2 weeks or until there’s hypotension and tachycardio
Beta Blockers: Atenolol, metoprolol, propanolol, 3 days tx after alpha block os complete
Metyrosine
Tyrosine hydroxylate inhibitor: blocks catecholamine synthesis
- management of pheo related hypertension