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Understanding SIADH: Causes and Treatment
Apr 19, 2025
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Learn with Med Nuggets: SIADH
What is SIADH?
Syndrome of Inappropriate Antidiuretic Hormone Secretion.
ADH (Vasopressin)
:
Hormone made in the hypothalamus.
Stored and released by the posterior pituitary gland.
Regulates water balance by causing reabsorption in kidney's distal convoluted tubule and collecting duct cells.
SIADH
:
Condition where body makes too much ADH.
Leads to increased water retention, diluting solutes (e.g., sodium).
Inhibits aldosterone release and stimulates ANP & BNP release.
Pathophysiology
Aldosterone
: Normally causes sodium retention and hydrogen ion excretion; inhibited in SIADH.
ANP & BNP
: Released by atria and ventricles when stretched; promote sodium and water excretion.
Results in euvolemic hyponatremia.
Etiology
Causes
:
Ectopic ADH production outside pituitary, e.g., in lungs.
CNS disorders, trauma.
Medications (e.g., SSRIs, Carbamazepine, Cyclophosphamide).
Mnemonic
: Lung or brain issues can cause SIADH.
Clinical Importance
Dangers
: Low sodium levels can cause cerebral edema.
Symptoms
: Headaches, confusion, hallucinations, coma, death.
Diagnosis
Laboratory findings diagnostic of SIADH:
Low serum sodium level.
Serum osmolality < 275.
Urine osmolality > 100.
Urine sodium > 40.
Normal renal, adrenal, and thyroid function.
Treatment
Initial steps
:
Treat underlying cause (e.g., stop causative drug).
Restrict fluid intake.
Medications
:
Loop diuretics for volume overload.
Demeclocycline (ADH inhibitor).
Vaptans (e.g., Tolvaptan) - ADH receptor antagonists.
Severe cases
:
Acute symptomatic hyponatremia: Use hypertonic saline cautiously.
Chronic hyponatremia: Correct sodium slowly (8 mEq/L/day) to avoid osmotic demyelination syndrome.
Conclusion
Understanding and managing SIADH is crucial to prevent serious complications.
Always consider the underlying causes and treat accordingly.
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