Evidence map›Paper›PMID 33385299›Full record

Trial reportHepatology international2021

Low-dose rifaximin prevents complications and improves survival in patients with decompensated liver cirrhosis.

Xin Zeng, Xia Sheng, Pei-Qin Wang, Hai-Guang Xin, Yi-Bin Guo, Yong Lin, Jia-Wei Zhong, Cheng-Zhi He, Jie Yin, Tao-Tao Liu and 12 more

2 registry-linked trialsAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Hepatology international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 29 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 5 pooled it
3.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02190357 phase4unknown statusnot on this map

Rifaximin Reduces the Complications of Decompensated Cirrhosis

TypeinterventionalSponsorShanghai Changzheng HospitalRan2014 to 2019Enrolled200ConditionsCirrhosisArmsRifaximin
NCT05786859 early_phase1unknown statusnot on this mapstarted 2023, after this paper: background citation

The Efficacy and Safety of Rifaximin In The Treatment of HBV Associated Acute-on-Chronic Liver Failure Patients With Mild to Moderate Hepatic Encephalopathy

TypeinterventionalSponsorSun Yat-sen UniversityRan2023 to 2025Enrolled124ConditionsLiver Failure, Acute on Chronic, Hepatic Encephalopathy, HBV, Hepatitis BArmsRifaximin 200 mg, Standard Treatment without Rifaximin
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 5 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  5. Efficacy and Safety of Rifaximin in the Prevention of Recurrent Episodes of Hepatic Encephalopathy: A Systematic Review and Meta-analysis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Pooled it
  6. Review
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  9. Interaction of inflammation and portal hypertension in cirrhosis progression.Nature reviews. Gastroenterology & hepatology · 2025
    Review
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  11. Microbial Approaches to Treat and Prevent Hepatic Encephalopathy.Gastroenterology clinics of North America · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 1 country.

Xin Zeng *Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Xia Sheng *Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Pei-Qin Wang *Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Hai-Guang XinDepartment of Infectious Disease, Changzheng Hospital, Second Military Medical University, Shanghai, 200003, China.
Yi-Bin GuoDepartment of Health Statistics, Second Military Medical University, Shanghai, 200433, China.
Yong LinDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Jia-Wei ZhongDepartment of Gastroenterology, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.
Cheng-Zhi HeDivision of Gastroenterology and Hepatology, Institute of Digestive Disease, Tongji Hospital, Tongji University School of Medicine, Shanghai, 200065, China.
Jie YinDepartment of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Tao-Tao LiuDepartment of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Wei-Juan MaDepartment of Gastroenterology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.
Xiao XiaoDivision of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and HepatologyState Key Laboratory for Oncogenes and Related GenesSchool of Medicine, Ministry of HealthRenji HospitalShanghai Jiao Tong University; Shanghai Institute of Digestive Disease, Shanghai, 200001, China.
Pei-Mei ShiDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Zong-Li YuanDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Ling YangDivision of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Xiong MaDivision of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and HepatologyState Key Laboratory for Oncogenes and Related GenesSchool of Medicine, Ministry of HealthRenji HospitalShanghai Jiao Tong University; Shanghai Institute of Digestive Disease, Shanghai, 200001, China.
Jian-Ming XuDepartment of Gastroenterology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.
Xi-Zhong ShenDepartment of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Chang-Qing YangDivision of Gastroenterology and Hepatology, Institute of Digestive Disease, Tongji Hospital, Tongji University School of Medicine, Shanghai, 200065, China.
Xuan ZhuDepartment of Gastroenterology, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.
Nong-Hua LvDepartment of Gastroenterology, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, China.
Wei-Fen XieDepartment of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China. weifenxie@medmail.com.cn.ORCID http://orcid.org/0000-0002-7137-112X
Second Military Medical University · CNNanchang University · CNSun Yat-sen University · CNAnhui Medical University · CNState Key Laboratory of Oncogene and Related Genes · CNTongji University · CNUnion Hospital · CN

Funding

the Emerging advanced technology joint research project from Shanghai Hospital Development Center SHDC12016103the Key Projects of Shanghai Science and Technology Committee 17411950800the National Natural Science Foundation of China 81530019the National Natural Science Foundation of China 81770600the Top-Level Clinical Discipline Project of Shanghai Pudong PWYgf2018-04
6 · The paper itself

Abstract

BACKGROUND AND

aimsRifaximin has been recommended as a prophylactic drug for hepatic encephalopathy (HE) and spontaneous bacterial peritonitis (SBP). This study aims to explore whether low-dose rifaximin can prevent overall complications and prolong survival in cirrhotic patients.

methodsIn this multi-centre randomized open-labelled prospective study, 200 patients with decompensated cirrhosis were randomly assigned at a ratio of 1:1. Patients in rifaximin group were administered 400 mg rifaximin twice daily for 6 months, and all other therapeutic strategies were kept unchanged in both groups as long as possible. The primary efficacy endpoints were the incidence of overall complications and liver transplantation-free survival. The secondary endspoints were the incidence of each major cirrhosis-related complication, as well as the Child-Pugh score and class.

resultsThe major baseline characteristics were similar in the two groups except for HE. The cumulative incidence and frequency of overall complications were significantly lower in rifaximin group than in the control group (p < 0.001). Though liver transplantation-free survival was not significantly different between the two groups, subgroup analysis showed rifaximin markedly prolonged liver transplantation-free survival in patients with Child-Pugh score ≥ 9 (p = 0.007). Moreover, rifaximin markedly reduced the episodes of ascites exacerbation (p < 0.001), HE (p < 0.001) and gastric variceal bleeding (EGVB, p = 0.031). The incidence of adverse events was similar in the two groups.

conclusionLow-dose rifaximin significantly decreases the occurrence of overall complications, leading to prolonged survival in patients with advanced stages of cirrhosis in this trail. Further study should be carried out to compare the effect of this low-dose rifaximin with normal dose (1200 mg/day) rifaximin in preventing cirrhosis-related complications. CLINICAL TRIAL NUMBER: NCT02190357.

Indexed as

Esophageal and Gastric VaricesLiver CirrhosisGastrointestinal HemorrhageHepatic EncephalopathyHumansPharmaceutical PreparationsProspective StudiesRifaximinPharmaceutical PreparationsRifaximinCirrhosis-related complicationsHepatic encephalopathyIntestinal endotoxaemiaLiver transplantation-free survivalMicrobiotaMulti-centre open-labelled studyOesophageal and gastric variceal bleedingPortal hypertensionRandomized prospective studySpontaneous bacterial peritonitis

Identifiers

PMID33385299
OpenAlexW3115250338

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.