Effects of satavaptan, a selective vasopressin V2 receptor antagonist, on ascites and serum sodium in cirrhosis with hyponatremia:: A randomized trial

被引:139
作者
Gines, Pere [1 ]
Wong, Florence [2 ]
Watson, Hugh [3 ]
Milutinovic, Slobodan [4 ]
del Arbol, Luis Ruiz [5 ]
Olteanu, Dan [6 ]
机构
[1] Univ Barcelona, Hosp Clin, Liver Unit, IDIBAPS,CIBEREHD, Barcelona, Catalunya, Spain
[2] Toronto Gen Hosp, Dept Med, Toronto, ON, Canada
[3] Sanofi Aventis Res & Dev, Chilly Mazarin, France
[4] Univ Zagreb, Gen Hosp Sveti Duh, Zagreb, Croatia
[5] Hosp Ramon & Cajal, Dept Gastroenterol, Hepat Hemodynam Unit, E-28034 Madrid, Spain
[6] Univ Hosp, Bucharest, Romania
关键词
D O I
10.1002/hep.22293
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hyponatremia in cirrhosis is associated with significant morbidity and mortality and complicates ascites management. Vasopressin receptor antagonists improve serum sodium concentration by increasing renal solute-free water excretion, but their effects on the management of ascites have not been assessed. Our aim was to investigate the effects of satavaptan, a highly selective vasopressin V-2 receptor antagonist, on ascites management and serum sodium in hyponatremic patients with cirrhosis. A total of 110 patients with cirrhosis, ascites, and hyponatremia (serum sodium <= 130 mmol/L) were included in a multicenter, double-blind, randomized, controlled study comparing three fixed doses of satavaptan (5 mg, 12.5 mg, or 25 mg once daily) versus placebo. Duration of treatment was 14 days and all patients received spironolactone at 100 mg/day. Satavaptan treatment was associated with improved control of ascites, as indicated by a reduction in body weight (mean change at Day 14 was +0.49 kg [+/-4.99] for placebo versus +0.15 kg [+/-4.23], -1-59 kg [+/-4.60] and -1.68 kg [+/-4.98] for the 5 mg, 12.5 mg, and 25 mg doses, respectively, P = 0.05 for a dose-effect relationship overall) and a parallel reduction in abdominal girth. This beneficial effect on ascites was associated with improvements in serum sodium (mean change from baseline to day 5 was 1.3 +/- 4.2, 4.5 +/- 3.5, 4.5 +/- 4.8, and 6.6 +/- 4.3 mmol/L for the placebo group and the groups on satavaptan at 5 mg, 12.5 mg, and 25 mg/day, respectively; P < 0.01 for all compared to placebo). Thirst was significantly more common in patients treated with satavaptan compared to those treated with placebo, whereas the frequency of other adverse events was similar among groups. Conclusion: The V-2 receptor antagonist satavaptan improves the control of ascites and increases serum sodium in patients with cirrhosis, ascites, and hyponatremia under diuretic treatment.
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页码:204 / 213
页数:10
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