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利福昔明治疗耐药性肝性脑病的附加治疗效果。

Add-on Therapeutic Effects of Rifaximin on Treatment-resistant Hepatic Encephalopathy.

机构信息

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Japan.

Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University, Japan.

出版信息

Intern Med. 2023 Apr 1;62(7):973-978. doi: 10.2169/internalmedicine.0212-22. Epub 2022 Sep 6.

Abstract

Objective Rifaximin is used to treat hepatic encephalopathy. However, whether or not rifaximin and lactulose combination therapy can enhance the treatment outcomes and reduce the hospitalization rate of patients with hepatic encephalopathy that are resistant to lactulose has yet to be determined. The present study investigated the hospitalization rate before and after rifaximin add-on therapy in patients resistant to lactulose. Methods A total of 36 patients who were resistant to lactulose with add-on rifaximin therapy were enrolled. Patients who were hospitalized and/or did not achieve normalization of ammonia levels under lactulose administration were defined as treatment-resistant. The primary outcome was the change in hospitalization rate due to hepatic encephalopathy at 24 weeks before and after rifaximin administration. Results Before rifaximin administration, 15 (41.6%) patients were hospitalized due to hepatic encephalopathy. After rifaximin administration, 8 (22.2%) patients were hospitalized due to hepatic encephalopathy. The hospitalization rates were significantly reduced after rifaximin administration (p=0.02). The median (interquartile range) ammonia levels upon rifaximin administration (baseline) and 8, 12, and 24 weeks after rifaximin administration were 124 (24-310) μg/dL, 78 (15-192) μg/dL, 67 (21-233) μg/dL, and 77 (28-200) μg/dL, respectively. Furthermore, the ammonia levels were significantly reduced by rifaximin add-on therapy (p=0.005, p=0.01, and p=0.01). Conclusion The addition of rifaximin to lactulose treatment in treatment-resistant patients decreases the hospitalization rate among patients with hepatic encephalopathy and may be used as an add-on treatment.

摘要

目的

利福昔明用于治疗肝性脑病。然而,利福昔明与乳果糖联合治疗是否能提高对乳果糖耐药的肝性脑病患者的治疗效果并降低其住院率,尚未确定。本研究旨在探讨对乳果糖耐药的患者加用利福昔明治疗前后的住院率。

方法

共纳入 36 例对乳果糖加用利福昔明治疗耐药的患者。给予乳果糖治疗后仍住院和/或血氨水平未恢复正常的患者定义为治疗耐药。主要结局为加用利福昔明治疗前后 24 周肝性脑病的住院率变化。

结果

在利福昔明治疗前,有 15 例(41.6%)患者因肝性脑病住院。在利福昔明治疗后,有 8 例(22.2%)患者因肝性脑病住院。加用利福昔明治疗后,住院率显著降低(p=0.02)。利福昔明治疗(基线)时及第 8、12、24 周时的中位(四分位距)血氨水平分别为 124(24-310)μg/dL、78(15-192)μg/dL、67(21-233)μg/dL 和 77(28-200)μg/dL。此外,加用利福昔明治疗后血氨水平显著降低(p=0.005、p=0.01 和 p=0.01)。

结论

在对乳果糖耐药的患者中加用利福昔明治疗可降低肝性脑病患者的住院率,可作为一种附加治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/877e/10125807/cde6045cc30b/1349-7235-62-0973-g001.jpg

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