Hayashi Manabu, Abe Kazumichi, Fujita Masashi, Okai Ken, Takahashi Atsushi, Ohira Hiromasa
Department of Gastroenterology, Fukushima Medical University School of Medicine, Japan.
Intern Med. 2018 Sep 1;57(17):2451-2458. doi: 10.2169/internalmedicine.0629-17. Epub 2018 Mar 30.
Objective Hyponatremia is closely associated with the pathophysiology of cirrhosis. However, the association between the serum sodium level and the response to tolvaptan is unclear. This study evaluated the factors related to the tolvaptan response and the prognosis in cirrhosis patients with ascites and hyponatremia. Methods We retrospectively reviewed the clinical records of cirrhosis patients hospitalized for treatment with tolvaptan. The associations of patient baseline characteristics with the tolvaptan response after one week and of the characteristics after one-month tolvaptan treatment with the prognosis were analyzed. Results We analyzed 83 cirrhosis patients with ascites, including 34 patients with hyponatremia. The response rates to tolvaptan in patients with serum sodium <130 mEq/L, 130-135 mEq/L, and >135 mEq/L were 20%, 66%, and 58%, respectively (p=0.22). The serum sodium level was associated with the response to tolvaptan [odds ratio=1.18; 95% confidence interval (CI) =1.02-1.37; p=0.029]. In patients with hyponatremia, the serum sodium level after 1-month tolvaptan treatment was increased compared to baseline (132 mEq/L vs. 136 mEq/L, p=0.006), and an increasing serum sodium level was associated with a lower risk of mortality (hazard ratio=0.85; 95% CI=0.75-0.97; p=0.016). The survival rate was higher in patients with an increase in the serum sodium level after 1 month than in patients with a decreased serum sodium level (p=0.023). Conclusion Tolvaptan treatment was effective in cirrhosis patients with ascites and hyponatremia, but a low serum sodium level was associated with non-responsiveness to tolvaptan. An increased serum sodium level after one-month tolvaptan treatment may positively influence the mortality risk in cirrhosis patients with hyponatremia.
目的 低钠血症与肝硬化的病理生理学密切相关。然而,血清钠水平与托伐普坦反应之间的关联尚不清楚。本研究评估了腹水和低钠血症肝硬化患者中与托伐普坦反应及预后相关的因素。方法 我们回顾性分析了因托伐普坦治疗而住院的肝硬化患者的临床记录。分析了患者基线特征与一周后托伐普坦反应之间的关联,以及托伐普坦治疗一个月后的特征与预后之间的关联。结果 我们分析了83例腹水肝硬化患者,其中34例为低钠血症患者。血清钠<130 mEq/L、130 - 135 mEq/L和>135 mEq/L的患者对托伐普坦的反应率分别为20%、66%和58%(p = 0.22)。血清钠水平与托伐普坦反应相关[比值比 = 1.18;95%置信区间(CI)= 1.02 - 1.37;p = 0.029]。在低钠血症患者中,托伐普坦治疗1个月后的血清钠水平较基线升高(132 mEq/L对136 mEq/L,p = 0.006),血清钠水平升高与较低的死亡风险相关(风险比 = 0.85;95% CI = 0.75 - 0.97;p = 0.016)。1个月后血清钠水平升高的患者生存率高于血清钠水平降低的患者(p = 0.023)。结论 托伐普坦治疗对腹水和低钠血症的肝硬化患者有效,但血清钠水平低与对托伐普坦无反应相关。托伐普坦治疗1个月后血清钠水平升高可能对低钠血症肝硬化患者的死亡风险产生积极影响。