肝脏 ›› 2025, Vol. 30 ›› Issue (1): 37-41.

• 肝功能衰竭 • 上一篇    下一篇

利福昔明治疗肝衰竭及其并发症的疗效分析

张莉, 卞兆连, 田李均, 刘一村, 陈伟杰, 薛红   

  1. 226001 江苏 南通大学医学院,南通市第三人民医院/南通大学附属南通第三医院(张莉,刘一村,陈伟杰);南通大学附属南通第三医院/南通市第三人民医院消化内科(卞兆连), 重症医学科(田李均), 肝病科(薛红)
  • 收稿日期:2023-11-30 出版日期:2025-01-31 发布日期:2025-03-10
  • 通讯作者: 薛红,Email:xuehong1981@126.com

An analysis on the treatment effect of rifaximin on liver failure and its complications

ZHANG Li1, BIAN Zhao-lian2, TIAN Li-jun3, LIU Yi-cun1, CHEN Wei-jie1, XUE Hong4   

  1. 1. Nantong University School of Medicine, Jiangsu 226001, China;
    2. Nantong University Affiliated Nantong Third Hospital/Nantong Third People's Hospital, Department of Gastroenterology, Nantong University Affiliated Nantong Third Hospital/Nantong Third People's Hospital, Jiangsu 226006, China;
    3. Department of Intensive Care Medicine, Nantong 226006;
    4. Department of Hepatology, Nantong University Affiliated Nantong Third Hospital/Nantong Third People's Hospital, Jiangsu 226006, China
  • Received:2023-11-30 Online:2025-01-31 Published:2025-03-10
  • Contact: XUE Hong, Email:xuehong1981@126.com

摘要: 目的 探讨利福昔明对肝衰竭(liver failure, LF)及其并发症的影响及疗效评估。 方法 回顾性地收集并分析2020年1月—2022年10月在南通市第三人民医院诊治的75例肝衰竭患者的临床资料。在内科综合治疗及部分人工肝支持的基础上,根据有无使用利福昔明治疗将患者分成利福昔明组和对照组,利福昔明组在对照组基础上给予利福昔明400 mg,每日3次,疗程3个月。记录两组患者入院时并发症(感染、肝性脑病、腹水)的发生情况以及随访期间并发症的好转情况;根据随访90 d时患者的生存状态,绘制Kaplan-Meier生存曲线比较两组患者90 d的生存率。 结果 两组间年龄、性别、人工肝、CTP评分及MELD评分等差异无统计学意义(P>0.05);经过3个月的规律治疗,利福昔明组的感染好转率高于对照组(77.8% vs. 44.4%,P=0.020)、肝性脑病(Hepatic encephalopathy, HE)好转率高于对照组(88.9% vs. 37.5%,P=0.013)、腹水好转率高于对照组(62.5% vs. 31.2%,P=0.038),差异均有统计学意义(P<0.05);Kaplan-Meier分析显示利福昔明组的肝衰竭患者90 d生存率[36.0% (9/25)]高于对照组率[16.0% (8/50)](P<0.05)。 结论 在LF患者中,利福昔明治疗显著改善感染、HE以及腹水的并发症,有利于延长肝衰竭患者的生存期,证明了利福昔明在肝衰竭及其并发症的治疗中具有一定的可行性。

关键词: 利福昔明, 肝衰竭, 并发症, 肠道菌群, 疗效

Abstract: Objective To investigate the treatment effect of rifaximin on liver failure (LF) and its complications. Methods The clinical data of 75 patients with liver failure treated at the Third People's Hospital of Nantong City from January 2020 to October 2022 were retrospectively analyzed. On the basis of comprehensive medical treatment and partial artificial liver support, patients were divided into a rifaximin group and a control group according to the presence or absence of rifaximin treatment. The patients in rifaximin group were given rifaximin 400 mg three times daily for 3 months on top of the treatment of control group. The occurrence of complications (i.e., infection, hepatic encephalopathy, ascites) at the time of admission and the improvement of complications during the follow-up period were recorded in both groups; Kaplan-Meier survival curves were plotted to compare the 90-day survival rates of the two groups according to the survival status of patients at 90 days of follow-up. Methods There were no statistically significant differences in age, sex, artificial liver, Child-Turcotte-Pugh (CTP) score and Model for End-Stage Liver Disease (MELD) score between the two groups (P>0.05); after 3 months of regular treatment, the rate of improvement of infection was higher in the rifaximin group than in the control group (77.8% vs. 44.4%, P=0.020), and the rate of improvement of hepatic encephalopathy (HE) was higher than that in the (88.9% vs. 37.5%, P=0.013) and ascites (62.5% vs. 31.2%, P=0.038), all statistically significant (P<0.05); Kaplan-Meier analysis showed that the 90-day survival rate of patients with liver failure in the rifaximin group [36.0% (9/25)] was higher than that in the control group [16.0% (8/50)] (P<0.05). Conclusion In patients with liver failure, rifaximin treatment significantly improved the complications of infection, Hepatic Encephalopathy (HE), and ascites, and helped prolong the survival of patients, demonstrating the feasibility of rifaximin in the treatment of liver failure and its complications.    

Key words: Rifaximin, Liver failure, Complications, Intestinal microbiota, Efficacy