Volume 49, Issue 12 pp. 1406-1413
Original Article

Real-world effects of long-term rifaximin treatment for Japanese patients with hepatic encephalopathy

Hiroyuki Suzuki

Hiroyuki Suzuki

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Hitomi Sezaki

Corresponding Author

Hitomi Sezaki

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

Correspondence: Dr Hitomi Sezaki, Department of Hepatology, Toranomon Hospital, 2-2-2 Toranomon, Minato-ku, Tokyo, 105-0001, Japan. Email: [email protected]Search for more papers by this author
Fumitaka Suzuki

Fumitaka Suzuki

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Kayoko Kasuya

Kayoko Kasuya

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Tomoya Sano

Tomoya Sano

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Shunichiro Fujiyama

Shunichiro Fujiyama

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Yusuke Kawamura

Yusuke Kawamura

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Tetsuya Hosaka

Tetsuya Hosaka

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Norio Akuta

Norio Akuta

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Satoshi Saitoh

Satoshi Saitoh

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Masahiro Kobayashi

Masahiro Kobayashi

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Yasuji Arase

Yasuji Arase

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Kenji Ikeda

Kenji Ikeda

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Yoshiyuki Suzuki

Yoshiyuki Suzuki

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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Hiromitsu Kumada

Hiromitsu Kumada

Department of Hepatology, Toranomon Hospital, Tokyo, Japan

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First published: 26 July 2019
Citations: 12
Conflict of interest: Hiromitsu Kumada received honoraria for lectures from MSD, Bristol-Myers Squibb, Gilead Sciences, AbbVie, Glaxo Smith Klein, and Dainippon Sumitomo Pharma. Fumitaka Suzuki received honoraria for lectures from Bristol-Myers Squibb and AbbVie. Yoshiyuki Suzuki received honoraria for lectures from Bristol-Myers Squibb and AbbVie. Kenji Ikeda received honoraria for lectures from Dainippon Sumitomo Pharma and Eisai. Norio Akuta received honoraria for lectures from Bristol-Myers Squibb and AbbVie. The other authors have no conflict of interest.
Financial support: None declared.

Abstract

Aim

Rifaximin (RFX) improves hepatic encephalopathy (HE). However, information on long-term treatment with RFX is limited. In this study, we aimed to investigate the effect of long-term treatment with RFX on HE and liver function. Moreover, we investigated factors associated with the recurrence of HE under RFX treatment.

Methods

In this retrospective cohort study, we consecutively enrolled 65 patients with HE who initiated RFX treatment (1200 mg/day) in our hospital from January 2017 to June 2018. We evaluated liver function test results, including blood ammonia levels, and the recurrence rate of HE after RFX treatment.

Results

The median follow-up duration was 41.6 weeks (range, 1.4–96.7 weeks). The blood ammonia level significantly declined from 157 to 86 μg/dL at 4 weeks after RFX treatment (P < 0.01), and the effect was prolonged. Furthermore, Child–Pugh score decreased in 51% (26/51) of the patients at 12 weeks during RFX treatment. The recurrence rate of HE after RFX treatment was 26.2% (17/65), and presence of ascites at baseline was identified as the only independent risk factor for HE recurrence (hazard ratio 4.71; 95% confidence interval, 1.27–17.5; P = 0.02). The cumulative recurrence rate of HE was significantly lower in patients without ascites than in patients with ascites at baseline (13.8% vs. 50.8%, P = 0.001).

Conclusions

Long-term treatment with RFX was beneficial for HE and liver function in patients with HE. Furthermore, the recurrence rate of HE was low in RFX-treated patients without ascites. Thus, long-term treatment with RFX could be effective for the management of Japanese patients with HE.

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