Systematic review with meta-analysis: the effects of rifaximin in hepatic encephalopathy

161 Citations (Scopus)

Abstract

BACKGROUND: Rifaximin is recommended for prevention of hepatic encephalopathy (HE). The effects of rifaximin on overt and minimal HE are debated.

AIM: To perform a systematic review and meta-analysis of randomised controlled trials (RCTs) on rifaximin for HE.

METHODS: We performed electronic and manual searches, gathered information from the U.S. Food and Drug Administration Home Page, and obtained unpublished information on trial design and outcome measures from authors and pharmaceutical companies. Meta-analyses were performed and results presented as risk ratios (RR) with 95% confidence intervals (CI) and the number needed to treat. Subgroup, sensitivity, regression and sequential analyses were performed to evaluate the risk of bias and sources of heterogeneity.

RESULTS: We included 19 RCTs with 1370 patients. Outcomes were recalculated based on unpublished information of 11 trials. Overall, rifaximin had a beneficial effect on secondary prevention of HE (RR: 1.32; 95% CI 1.06-1.65), but not in a sensitivity analysis on rifaximin after TIPSS (RR: 1.27; 95% CI 1.00-1.53). Rifaximin increased the proportion of patients who recovered from HE (RR: 0.59; 95% CI: 0.46-0.76) and reduced mortality (RR: 0.68, 95% CI 0.48-0.97). The results were robust to adjustments for bias control. No small study effects were identified. The sequential analyses only confirmed the results of the analysis on HE recovery.

CONCLUSIONS: Rifaximin has a beneficial effect on hepatic encephalopathy and may reduce mortality. The combined evidence suggests that rifaximin may be considered in the evidence-based management of hepatic encephalopathy.

Original languageEnglish
JournalAlimentary Pharmacology and Therapeutics
Volume40
Issue number2
Pages (from-to)123-32
Number of pages10
ISSN0269-2813
DOIs
Publication statusPublished - Jul 2014

Keywords

  • Bias (Epidemiology)
  • Hepatic Encephalopathy
  • Humans
  • Odds Ratio
  • Protective Agents
  • Randomized Controlled Trials as Topic
  • Rifamycins
  • Secondary Prevention

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