Abstract

Background: Rifaximin is commonly used for hepatic encephalopathy (HE). However, the effects of long-term treatment for Japanese people are limited. Therefore, this study aimed to investigate the effects and safety of long-term treatment with rifaximin on HE. Methods: A total of 215 patients with cirrhosis administered with rifaximin developed overt or covert HE, which was diagnosed by an attending physician for >12 months. Laboratory data were extracted at pretreatment and 3, 6, and 12 months after rifaximin administration. The long-term effect of rifaximin was evaluated, and the incidence of overt HE during 12 months and adverse events was extracted. Results: Ammonia levels were significantly improved after 3 months of rifaximin administration and were continued until 12 months. There were no serious adverse events after rifaximin administration. The number of overt HE incidents was 9, 14, and 27 patients within 3, 6, and 12 months, respectively. Liver enzymes, renal function, and electrolytes did not change after rifaximin administration. Prothrombin activity is a significant risk factor for the occurrence of overt HE. The serum albumin, prothrombin activity, and albumin–bilirubin (ALBI) scores were statistically improved after 3 and 6 months of rifaximin administration. Moreover, the same results were obtained in patients with Child–Pugh C. Conclusions: The long-term rifaximin treatment was effective and safe for patients with HE, including Child–Pugh C.

Highlights

  • Hepatic encephalopathy (HE) is a common complication of patients with liver cirrhosis, causing neuropsychological and neuromuscular dysfunctions in various degrees

  • In 116 (54.0%) patients, rifaximin was added to lactulose

  • The complications of cirrhosis were associated with esophageal varices (119 patients), portosystemic shunting (PSS) (107 patients), splenomegaly (160 patients), ascites (79 patients), and HCC (74 patients)

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Summary

Introduction

Hepatic encephalopathy (HE) is a common complication of patients with liver cirrhosis, causing neuropsychological and neuromuscular dysfunctions in various degrees. The prognosis of liver cirrhosis reportedly worsens when overt HE occurs, with a mortality rate within 1 year of 64% and within 5 years of 85%. Covert HE occurs in 80% of patients with liver cirrhosis, and covert HE, as well as overt HE, can impair the prognosis and increase the risk of hospitalization [5]. Methods: A total of 215 patients with cirrhosis administered with rifaximin developed overt or covert HE, which was diagnosed by an attending physician for >12 months. The long-term effect of rifaximin was evaluated, and the incidence of overt HE during 12 months and adverse events was extracted. The serum albumin, prothrombin activity, and albumin–bilirubin (ALBI) scores were statistically improved after 3 and 6 months of rifaximin administration. The same results were obtained in patients with Child–Pugh C

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