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Treatment options for hyponatremia in heart failure.

Abstract
Hyponatremia is independently associated with adverse outcomes in patients with congestive heart failure (CHF). The primary cause of hyponatremia in CHF is the inappropriate secretion of the antidiuretic hormone arginine vasopressin (AVP). The binding of AVP to V(2) receptors in the renal collecting duct promotes water retention, a process that can lead to dilutional hyponatremia as well as increased ventricular preload. Conventional treatment of hyponatremia in CHF is largely based on water restriction, which is neither effective nor well-tolerated. V(2)- and dual V(1a)/V(2)-receptor antagonists offer physiologically based treatment for dilutional hyponatremia. Clinical trials in patients with hyponatremia including those with CHF using both selective and nonselective vasopressin antagonists have demonstrated the effectiveness and safety of these agents in correcting this common electrolyte abnormality.
AuthorsSteven R Goldsmith
JournalCongestive heart failure (Greenwich, Conn.) (Congest Heart Fail) Vol. 16 Suppl 1 Pg. S15-8 (Jul 2010) ISSN: 1751-7133 [Electronic] United States
PMID20653706 (Publication Type: Journal Article, Review)
Chemical References
  • Antidiuretic Hormone Receptor Antagonists
  • Benzazepines
  • Biomarkers
  • Tolvaptan
Topics
  • Antidiuretic Hormone Receptor Antagonists
  • Benzazepines (therapeutic use)
  • Biomarkers
  • Blood Volume (physiology)
  • Heart Failure (complications, drug therapy, physiopathology)
  • Humans
  • Hyponatremia (drug therapy, etiology)
  • Inappropriate ADH Syndrome (drug therapy, etiology)
  • Signal Transduction
  • Tolvaptan

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