Ginès Pere, Wong Florence, Watson Hugh, Milutinovic Slobodan, del Arbol Luis Ruiz, Olteanu Dan
Hospital Clínic, University of Barcelona, Institut d'Investigacions Biomèdiques August Pi-Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Barcelona, Catalunya, Spain.
Hepatology. 2008 Jul;48(1):204-13. doi: 10.1002/hep.22293.
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 < or =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.
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.
肝硬化患者的低钠血症与显著的发病率和死亡率相关,且使腹水管理复杂化。血管加压素受体拮抗剂通过增加肾脏无溶质自由水排泄来提高血清钠浓度,但它们对腹水管理的影响尚未得到评估。我们的目的是研究高度选择性血管加压素V(2)受体拮抗剂萨特普坦对肝硬化低钠血症患者腹水管理和血清钠的影响。总共110例患有肝硬化、腹水和低钠血症(血清钠≤130 mmol/L)的患者被纳入一项多中心、双盲、随机、对照研究,比较三种固定剂量的萨特普坦(每日一次5 mg、12.5 mg或25 mg)与安慰剂。治疗持续时间为14天,所有患者均接受每日100 mg的螺内酯治疗。萨特普坦治疗与腹水控制改善相关,表现为体重减轻(第14天的平均变化,安慰剂组为+0.49 kg[±4.99],5 mg、12.5 mg和25 mg剂量组分别为+0.15 kg[±4.23]、-1.59 kg[±4.60]和-1.68 kg[±4.98];总体剂量-效应关系P = 0.05)以及腹围相应减小。这种对腹水的有益作用与血清钠改善相关(从基线到第5天的平均变化,安慰剂组为1.3±4.2、5 mg、12.5 mg和25 mg/天萨特普坦组分别为4.5±3.5、4.5±4.8和6.6±4.3 mmol/L;与安慰剂相比,所有组P<0.01)。与接受安慰剂治疗的患者相比,接受萨特普坦治疗的患者口渴明显更常见,而其他不良事件的发生率在各组之间相似。
V(2)受体拮抗剂萨特普坦可改善肝硬化、腹水和低钠血症患者在利尿剂治疗下的腹水控制并增加血清钠。