Gastroenterology and Hepatology, AZ Maria Middelares, Gent, Belgium.
Gastroenterology, UZ Antwerpen, Edegem, Belgium.
Acta Gastroenterol Belg. 2022 Jul-Sep;85(3):433-437. doi: 10.51821/85.3.9524. Epub 2022 Jun 30.
Advanced liver disease frequently culminates in hepatic encephalopathy (HE), which can be classified as covert or overt HE, with subtle or clinically obvious changes respectively. 30-40% of patients with cirrhosis develop overt HE, which negatively affects the patients' quality of life. Next to lactulose, rifaximin-α has been prescribed as a second line therapy to treat and reduce the risk of recurrence of overt HE. In this study, we aimed to evaluate the effect of rifaximin-α therapy, both on the number of occurring infections and on the evolution in hospital admissions of patients with overt HE.
A total of 66 cirrhotic patients, treated for at least 6 months with rifaximin-α at AZ Maria Middelares, between October 1st 2014 and January 1st 2020, were included in the study analysis. Medical records of all patients were evaluated over a period of 6 months prior and after initiation of rifaximin-α therapy.
Data analysis revealed that the included cirrhotic patients were severely ill, with a mean model for end-stage liver disease (MELD) score of 21, and a median Child Pugh score of 11. Among these patients, rifaximin-α treatment significantly downgraded the total number of infections, with a main effect on respiratory infections. Furthermore, rifaximin-α therapy led to a significant decrease in HE-related, as well as in other liver-related hospital admissions.
This study confirms the potential value of rifaximin-aα in reducing the number of developing infections and hospital admissions in a severely ill cirrhotic patient population.
晚期肝病常导致肝性脑病(HE),可分为隐性或显性 HE,分别有细微或明显的临床变化。40%的肝硬化患者会发展为显性 HE,这会降低患者的生活质量。除乳果糖外,利福昔明-α已被开为二线治疗药物,用于治疗和降低显性 HE 复发的风险。本研究旨在评估利福昔明-α治疗对显性 HE 患者感染次数和住院次数演变的影响。
共纳入 2014 年 10 月 1 日至 2020 年 1 月 1 日期间在 AZ Maria Middelares 接受利福昔明-α治疗至少 6 个月的 66 例肝硬化患者,对所有患者的病历进行了 6 个月的回顾性分析。
数据分析显示,纳入的肝硬化患者病情严重,平均终末期肝病模型(MELD)评分 21 分,Child-Pugh 评分中位数为 11 分。在这些患者中,利福昔明-α治疗显著降低了总感染次数,主要影响呼吸系统感染。此外,利福昔明-α治疗还显著降低了与 HE 相关的以及其他与肝脏相关的住院次数。
本研究证实了利福昔明-α在降低严重肝硬化患者感染次数和住院次数方面的潜在价值。