Hyperaldosteronism Flashcards
Aetiology of hyperaldosteronism
Bilateral idiopathic adrenal hyperplasia is the most common cause of primary hyperaldosteronism
Excess aldosterone may be secondary to an adrenal adenoma (Conn’s syndrome, 70%)
Hyperplasia of the adrenal cortex (30%)
Rare: Glucocorticoid-suppressible hyperaldosteronism (1-3%) or an aldosterone producing adrenal carcinoma
Excess aldosterone results in Increased sodium and water retention causing hypertension, increased renal potassium loss and hypokalaemia and suppression of renin due to NaCl retention
Risk factor for hyperaldosteronism
Age 20-70
Family history of PA
Family history of early onset of hypertension and/or stroke
Symptoms and signs of hyperaldosteronism
Usually asymptomatic
Nocturia, Polyuria (nephrogenic DI secondary to hypokalaemia)
Lethargy
Mood disturbance (irritability, anxiety, depression)
Difficulty concentrating
Paraesthesia’s, muscle cramp
Muscle weakness
Palpitations
Headache
Sign: hypertension
Investigations for hyperaldosteronism
Urine potassium: high
Aldosterone/renin ratio: raised (done after stopping anti-HTN for 2 weeks)
U&Es: Hypokalaemia
HR-CT: visualise any adrenal masses
Bialteral adrenal vein catheterisation and sampling: distinguish between Conn’s syndrome and bilateral adrenal hyperplasia
Fludrocortisone suppression test: failure of aldosterone suppression
Salt loading: failure of aldosterone suppression
Postural test: aldosterone and renin levels increase (Bilateral adrenal hyperplasia)
Management for unilateral adrenal masses causing hyperaldosteronism
Unilateral laparoscopic adrenalectomy
1. Aldosterone antagonists e.g. amiloride, spironolactone, epleronone
2. Stop K+ supplementation immediately before surgery
3. Discontinue aldosterone antagonists
Post-op fluids without KCl
Adrenal lesion ≥ 2.5cm → immediate unilateral laparoscopic adrenalectomy
Management for bilateral adrenal masses causing hyperaldosteronism
- Aldosterone antagonists e.g. amiloride 2.5-15mg orally once daily in 2 divided doses, spironolactone, eplerenone
- Laparoscopic adrenalectomy
Complications of hyperaldosteronism
Complications of hypertension
- Stroke
- Myocardial Infarction
- Heart Failure
- Atrial fibrillation
- Impaired renal function
Perioperative complications (e.g., bleeding, infection, wound hernia, cardiovascular events)
Aldosterone antagonist- or mineralocorticoid receptor antagonist-induced hyperkalaemia
Prognosis for hyperaldosteronism
Surgery either cures hypertension (50%) or will make it more amenable to anti-hypertensive therapy in those who are not cured (usually elderly or those with long-standing HTN)
Recurrence of PA in those apparently cured after 12 months is uncommon
Hypertension is improved and control achieved in the majority undergoing aldosterone antagonist treatment, but this is not as dramatic as surgical treatment
Hypertension in familial hyperaldosteronism type I (FH-I) is frequently of early onset and may be severe enough to cause early death, usually from haemorrhagic stroke, unless specifically treated, but treatment with glucocorticoids is usually highly effective