Vasopressin and vasopressin antagonists in heart failure and hyponatremia

Dimitrios Farmakis, Gerasimos Filippatos*, Dimitrios T. Kremastinos, Mihai Gheorghiade

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

12 Scopus citations

Abstract

Increased synthesis of arginine vasopressin (AVP) plays a critical role in fluid retention and hyponatremia in patients with heart failure. The AVP receptor antagonists constitute a new class of agents that are promising in the management of hyponatremia and congestion. Three of these agents-conviaptan, tolvaptan, and lixivaptan-have been studied in clinical settings. All are effective in inducing aquaresis (ie, electrolyte-free water excretion) and normalizing serum sodium concentration. They are well tolerated without causing electrolyte disorders, hypotension, or renal impairment. Conivaptan has been approved by the US Food and Drug Administration for short-term intravenous treatment of euvolemic hyponatremia of variable etiology but has not been adequately studied in heart failure. The addition of tolvaptan to standard therapy in hospitalized patients with heart failure has led to symptomatic improvement and decreased body weight, but there is no long-term clinical benefit. Early data on lixivaptan in heart failure suggest a dose-dependent aquaresis effect, and larger studies are under way.

Original languageEnglish (US)
Pages (from-to)91-96
Number of pages6
JournalCurrent heart failure reports
Volume5
Issue number2
DOIs
StatePublished - 2008

Funding

Athens, Hellenic Cardiological Society, Otsuka, Medtronic, Roche Diagnostics, and BRAHMS. Dr. Kremastinos has received research grants from Sigma Tau.

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)
  • Emergency Medicine

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