Hiramine Yasunari, Uto Hirofumi, Mawatari Seiichi, Kanmura Shuji, Imamura Yasushi, Hiwaki Takuya, Saishoji Akiko, Yada Takazumi, Inada Yukiko, Sakamoto Hidemori, Higashi Hirofumi, Kubozono Osamu, Maenohara Shigeho, Ido Akio
Department of Internal Medicine, Kagoshima Kouseiren Hospital, Kagoshima, Japan.
Center for Digestive and Liver Diseases, Miyazaki Medical Center Hospital, Miyazaki, Japan.
Hepatol Res. 2019 Jul;49(7):765-777. doi: 10.1111/hepr.13337. Epub 2019 Apr 30.
Despite accumulating evidence concerning the efficacy of tolvaptan in the treatment of body fluid retention or hyponatremia, the effect of tolvaptan on the prognosis of patients with hepatic ascites has not been fully investigated.
A total of 628 patients with hepatic ascites who were treated with diuretics (furosemide, spironolactone, or tolvaptan) between 2007 and 2017 were enrolled and divided into two groups: those who received tolvaptan (original tolvaptan group, n = 278) and those who did not (original control group, n = 350). The cumulative survival rates between the groups were compared and the factors associated with survival in patients with hepatic ascites were identified using a Cox regression analysis. In addition, propensity score matching was applied in patients who started conventional diuretics for new-onset hepatic ascites after September 2013 (pre-matching tolvaptan group, n = 177; pre-matching control group, n = 63), and the cumulative survival rates were compared between the post-matching tolvaptan and control groups.
The survival rate was significantly higher in the tolvaptan group than the control group (P = 0.005), and tolvaptan therapy was identified as an independent factor associated with survival (hazard ratio 0.721 for death relative to control, P < 0.001). The propensity score-matched comparison also showed a significantly higher survival rate in the tolvaptan group (n = 51) than in the control group (n = 51) (P = 0.009).
This study suggests that tolvaptan might improve the prognosis of patients with hepatic ascites.
尽管关于托伐普坦治疗体液潴留或低钠血症疗效的证据不断积累,但托伐普坦对肝腹水患者预后的影响尚未得到充分研究。
纳入2007年至2017年间接受利尿剂(呋塞米、螺内酯或托伐普坦)治疗的628例肝腹水患者,分为两组:接受托伐普坦治疗的患者(原托伐普坦组,n = 278)和未接受托伐普坦治疗的患者(原对照组,n = 350)。比较两组的累积生存率,并使用Cox回归分析确定与肝腹水患者生存相关的因素。此外,对2013年9月后开始使用常规利尿剂治疗新发肝腹水的患者应用倾向评分匹配法(匹配前托伐普坦组,n = 177;匹配前对照组,n = 63),比较匹配后托伐普坦组和对照组的累积生存率。
托伐普坦组的生存率显著高于对照组(P = 0.005),托伐普坦治疗被确定为与生存相关的独立因素(相对于对照组,死亡风险比为0.721,P < 0.001)。倾向评分匹配比较也显示托伐普坦组(n = 51)的生存率显著高于对照组(n = 51)(P = 0.009)。
本研究表明托伐普坦可能改善肝腹水患者的预后。