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Rationale and design of the multicenter, randomized, double-blind, placebo-controlled study to evaluate the Efficacy of Vasopressin antagonism in Heart Failure: Outcome Study with Tolvaptan (EVEREST)

Gheorghiade, M. (författare)
Orlandi, C. (författare)
Burnett, J. C. (författare)
visa fler...
Demets, D. (författare)
Grinfeld, L. (författare)
Maggioni, A. (författare)
Swedberg, Karl, 1944 (författare)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
Udelson, J. E. (författare)
Zannad, F. (författare)
Zimmer, C. (författare)
Konstam, M. A. (författare)
visa färre...
 (creator_code:org_t)
2005
2005
Engelska.
Ingår i: Journal of cardiac failure. - 1071-9164. ; 11:4, s. 260-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Hospitalizations for worsening heart failure due to fluid overload (congestion) are common. Agents that treat congestion without causing electrolyte abnormalities or worsening renal function are needed. Tolvaptan is an oral vasopressin (V 2 ) antagonist that decreases body weight and increases urine volume without inducing renal dysfunction or hypokalemia. The Efficacy of Vasopressin antagonism in Heart Failure Outcome Study with Tolvaptan (EVEREST) trial is evaluating mortality, morbidity, and patient-assessed global clinical status in patients treated with tolvaptan compared with standard care. METHODS AND RESULTS: Patients are eligible for inclusion if they have a reduced left ventricular ejection fraction and are hospitalized for worsening heart failure with evidence of systemic congestion. Patients are randomized 1:1 to tolvaptan 30 mg/day or matching placebo for a minimum of 60 days. Time to all-cause mortality and time to cardiovascular mortality or heart failure hospitalization are the coprimary end points. Patient-assessed global clinical status and quality of life are also evaluated. EVEREST will be continued until 1065 deaths occur. As of April 18, 2005, 2260 patients have been enrolled. CONCLUSION: Tolvaptan has been shown to reduce body weight in patients with worsening heart failure without inducing renal dysfunction or causing hypokalemia. The results of EVEREST will determine whether these effects translate into improved clinical outcomes.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Benzazepines/*therapeutic use
Body Weight/drug effects
Double-Blind Method
Follow-Up Studies
Heart Failure
Congestive/*drug therapy
Hospitalization
Humans
Hypokalemia/prevention & control
Placebos
Quality of Life
Receptors
Vasopressin/*antagonists & inhibitors
*Research Design
Stroke Volume/drug effects
Survival Rate
Treatment Outcome
Urination/drug effects
Ventricular Dysfunction
Left/drug therapy

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