Institute of Liver Studies and Transplantation, King's College Hospital, London, UK.
Liver Sciences, Faculty of Life Sciences and Medicine, 1st Floor James Black Centre, School of Immunology and Microbial Sciences, King's College London, London, UK.
Aliment Pharmacol Ther. 2019 Aug;50(4):435-441. doi: 10.1111/apt.15326. Epub 2019 Jun 6.
Rifaximin reduces the risk of overt hepatic encephalopathy (HE) and is associated with significant reductions in hospitalisations and 30-day readmissions.
To examine the outcomes of patients listed for liver transplantation with a diagnosis of HE on rifaximin compared to those naïve to the drug.
Patient records of those listed for liver transplantation over a 2-year period were retrospectively reviewed. Patients were included if they had at least two episodes of overt HE resulting in hospitalisation or were encephalopathic at the time of assessment.
Of the 622 patients listed for transplantation, 101 had HE. Sixty-six patients were treated with rifaximin and 35 were naïve at listing. The use of concurrent lactulose was not significantly different between groups. Median MELD score was similar (15 [14-16)] rifaximin-treated and 16 [14-18] rifaximin-naïve). Patients on the waiting list treated with rifaximin had reduced all-cause admissions, episodes of spontaneous bacterial peritonitis and variceal bleeding. Mean length of stay was 9 days (95% CI 6-12) in the rifaximin-treated group vs 14 (95% CI 7-21) in the rifaximin-naïve group. Multivariate regression analysis demonstrated that rifaximin was independently associated with an increase in average days to readmission (adjusted effect estimate 71, 95% CI 3-140 days) and reduced likelihood of requirement for prioritisation on the waiting list (odds ratio 0.29; 95% CI 0.89-0.93).
Rifaximin prescribed for HE in patients listed for liver transplantation improved outcomes with significant reduction in admissions related to spontaneous bacterial peritonitis, ascites and variceal bleeding.
利福昔明可降低显性肝性脑病(HE)的风险,并显著降低住院和 30 天再入院的风险。
研究接受利福昔明治疗的肝移植患者与未接受该药物治疗的患者的 HE 诊断结果。
回顾性分析了 2 年内接受肝移植患者的病历。如果患者有至少两次因显性 HE 导致住院的发作或在评估时处于脑病状态,则将其纳入研究。
在 622 名接受移植的患者中,有 101 例患有 HE。66 例患者接受了利福昔明治疗,35 例患者在列表中未接受治疗。两组患者同时使用乳果糖的情况无显著差异。中位 MELD 评分相似(利福昔明治疗组为 15 [14-16],利福昔明未治疗组为 16 [14-18])。在等待名单上接受利福昔明治疗的患者,全因入院、自发性细菌性腹膜炎和食管静脉曲张出血的发作减少。利福昔明治疗组的平均住院时间为 9 天(95%CI 6-12),而利福昔明未治疗组为 14 天(95%CI 7-21)。多变量回归分析表明,利福昔明与再入院平均天数的增加独立相关(调整后的效应估计值为 71,95%CI 3-140 天),并且降低了在等待名单上需要优先排序的可能性(比值比 0.29;95%CI 0.89-0.93)。
在接受肝移植的患者中,利福昔明用于治疗 HE 可改善患者的预后,显著减少与自发性细菌性腹膜炎、腹水和食管静脉曲张出血相关的入院次数。