利福昔明
医学
酒精性肝炎
内科学
随机对照试验
炎症
胃肠病学
肝性脑病
全身炎症
酒精性肝病
肝硬化
免疫学
抗生素
生物
微生物学
作者
Nina Kimer,Mads Meldgaard,O Hamberg,Thit Mynster Kronborg,Allan M. Lund,Holger Jon Møller,Flemming Bendtsen,Henriette Ytting
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2022-03-14
卷期号:17 (3): e0264278-e0264278
被引量:20
标识
DOI:10.1371/journal.pone.0264278
摘要
Background and aims Alcoholic hepatitis (AH) is characterized by acute liver failure, neurocognitive impairment and renal failure. Severe inflammatory reactions are also known to occur in AH. Inflammation and bacterial translocation in the gut are thought to have major impact on disease development and progression. The mortality rate for AH is close to 50%. We aimed to assess the efficacy of rifaximin in treating AH and its impact on inflammation and metabolism. Methods The trial was approved by relevant authorities (EudraCT no: 2014-02264-33, Scientific Ethics Committee, jr. no: H-1-2014-056). Primary outcomes were changes in metabolic and inflammatory markers. Secondary outcomes were portal hypertension, kidney and neurocognitive function. Results Thirty-two patients were randomized to standard medical therapy (SMT) or SMT plus rifaximin, allocation was concealed. Four patients in the SMT group and five patients in the SMT + rifaximin group died due to AH and liver failure. No adverse events related to the study medication were observed. We found no significant differences in amino acids or inflammation markers (IL-2, IL-6, IL-8, IL-10, TNF-α, interferon-γ) between the groups after 28 and 90 days. Conclusion Rifaximin does not alter inflammation or metabolism in patients with AH.
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