Tolvaptan, an oral vasopressin antagonist, in the treatment of hyponatremia in cirrhosis

被引:100
作者
Cardenas, Andres [1 ,2 ]
Gines, Pere [2 ,3 ]
Marotta, Paul [4 ]
Czerwiec, Frank [5 ]
Oyuang, John [5 ]
Guevara, Monica [2 ,3 ]
Afdhal, Nezam H. [6 ]
机构
[1] Univ Barcelona, Hosp Clin, Inst Malalties Digest & Metab, GI Unit, Barcelona 08036, Catalunya, Spain
[2] CIBEREHD, IDIBAPS, Barcelona, Catalunya, Spain
[3] Univ Barcelona, Hosp Clin, Inst Malalties Digest & Metab, Liver Unit, Barcelona 08036, Spain
[4] London Hlth Sci Ctr, London, ON, Canada
[5] Otsuka Pharmaceut Dev & Commercializat Inc, Rockville, MD USA
[6] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Ctr Liver, Boston, MA 02215 USA
关键词
Cirrhosis; Dilutional hyponatremia; Ascites; Chronic liver disease; Edema; Vaptans; Antidiuretic hormone; Arginine vasopressin; V-2 RECEPTOR ANTAGONIST; SERUM SODIUM; DOUBLE-BLIND; TRIAL; ASCITES; PATHOGENESIS; MULTICENTER; FAILURE;
D O I
10.1016/j.jhep.2011.08.020
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Tolvaptan is a vasopressin V2-receptor antagonist that improves serum sodium concentration by increasing renal solute-free water excretion. Specific data on the safety and efficacy of tolvaptan in patients with cirrhosis and hyponatremia has not been exclusively evaluated. Methods: This sub-analysis of the Study of Ascending Levels of Tolvaptan trials examined cirrhotic patients with hyponatremia who received 15 mg oral tolvaptan (n = 63; increased to 30 or 60 mg if needed) or placebo (n = 57) once-daily for 30 days. At baseline, 44% had mild hyponatremia (serum sodium 130-134 mmol/L), 56% had marked hyponatremia (serum sodium <130 mmol/L), 85% had cirrhosis due to alcohol and/or hepatitis B/C, and 80% were Child-Pugh class B/C. Results: Tolvaptan was effective in raising serum sodium. Average daily area under the curve for serum sodium was significantly greater in the tolvaptan group from baseline to day 4 (p<0.0001) and day 30 (p<0.0001). This superiority was maintained after stratification by baseline hyponatremia (mild and marked), estimated glomerular filtration rate (<= 60 ml/min and >60 ml/min), or serum creatinine levels (<1.5 mg/dl and >= 1.5 mg/dl). Hyponatremia recurred 7 days after discontinuation of tolvaptan. Mean mental component summary scores of the SF-12 health survey improved from baseline to day 30 in the tolvaptan group but not the placebo group (4.68 vs. 0.08, p = 0.02). Major side effects due to tolvaptan were dry mouth and thirst. Gastrointestinal bleeding occurred in 10% and 2% of patients in the tolvaptan and placebo group, respectively (p = 0.11). Adverse event rates, withdrawals, and deaths were similar in both groups. Conclusions: One month of tolvaptan therapy improved serum sodium levels and patient-reported health status in cirrhotic patients with hyponatremia. Hyponatremia recurred in tolvaptan-treated patients after discontinuation. (C) 2011 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:571 / 578
页数:8
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