Kogiso Tomomi, Sagawa Takaomi, Kodama Kazuhisa, Taniai Makiko, Tokushige Katsutoshi
Department of Internal Medicine, Institute of Gastroenterology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
BMC Pharmacol Toxicol. 2018 Dec 18;19(1):87. doi: 10.1186/s40360-018-0277-3.
The vasopressin V2-receptor antagonist tolvaptan is used to treat cirrhotic patients with ascites. We investigated the outcome of long-term treatment.
This was a single-center retrospective study. Overall, 170 cirrhotic patients (95 males, median age 63 years) were enrolled and received tolvaptan orally after hospitalization for ascites, which included treatment with conventional diuretics. We compared patients who withdrew tolvaptan treatment after < 1 year (n = 90) with patients who continued treatment for ≥1 year (n = 37). In continuously treated patients, the pretreatment and post-treatment (1 year) blood biochemistry values were assessed.
Overall, 37 patients received treatment for ≥1 year and showed a higher response after tolvaptan therapy. The reduction in body weight was 2.0 (- 3.4-17.2) kg compared to discontinued cases, which had a body weight reduction of 1.1 (- 6.2-7.5) kg after 1 week. The group that received treatment for ≥1 year had a significantly lower rate of the complication gastroesophageal varices and also showed better liver function. In patients with continued treatment, serum levels of albumin was significantly higher without renal disturbance after 1 year of treatment. The prothrombin time/international normalized ratio and ammonia level were also significantly improved. Multivariate analyses showed that a change in body weight reduction and serum levels of albumin were predictive factors of continued administration.
Long-term tolvaptan treatment increased serum levels of albumin, decreased ammonia levels, and preserved renal function after 1 year of treatment. A reduction in body weight after 1 week was associated with a favorable outcome of tolvaptan therapy.
血管加压素V2受体拮抗剂托伐普坦用于治疗肝硬化腹水患者。我们研究了长期治疗的结果。
这是一项单中心回顾性研究。总共纳入了170例肝硬化患者(95例男性,中位年龄63岁),他们因腹水住院后口服托伐普坦,其中包括使用传统利尿剂治疗。我们将治疗时间<1年即停用托伐普坦的患者(n = 90)与持续治疗≥1年的患者(n = 37)进行了比较。在持续治疗的患者中,评估了治疗前和治疗后(1年)的血液生化值。
总体而言,37例患者接受了≥1年的治疗,托伐普坦治疗后显示出更高的反应。与停药病例相比,体重减轻了2.0(-3.4-17.2)kg,停药病例在1周后体重减轻了1.1(-6.2-7.5)kg。接受≥1年治疗的组胃食管静脉曲张并发症的发生率显著更低,肝功能也更好。在持续治疗的患者中,治疗1年后血清白蛋白水平显著升高,且无肾功能障碍。凝血酶原时间/国际标准化比值和氨水平也显著改善。多变量分析显示,体重减轻的变化和血清白蛋白水平是持续给药的预测因素。
长期托伐普坦治疗在治疗1年后可提高血清白蛋白水平,降低氨水平,并保留肾功能。1周后体重减轻与托伐普坦治疗的良好结果相关。