Suppr超能文献

利福昔明预防肝性脑病的疗效与安全性:一项荟萃分析。

Efficacy and safety of rifaximin for the prophylaxis of hepatic encephalopathy: A meta-analysis.

作者信息

Huang Ji, Cheng Cong, Li Yong, Liu Yongqi, Liu Youshun

机构信息

Department of Traditional Chinese Medicine, Ganzhou People's Hospital, Ganzhou, China.

Department of Infectious Disease, Successful Hospital Affiliated to Xiamen University, Xiamen, China.

出版信息

Medicine (Baltimore). 2025 Jan 31;104(5):e39905. doi: 10.1097/MD.0000000000039905.

Abstract

BACKGROUND AND AIM

The efficacy of rifaximin in the prevention of overt hepatic encephalopathy (HE) has not been established. The aim of this study was to access the efficacy and safety of rifaximin in the prophylaxis of HE.

METHODS

We conducted a meta-analysis search of the Cochrane Library, PubMed, ClinicalTrials.gov, Web of Science, and EMBASE as of March 2022. We pooled data by random-effects DerSimonian-Laird models to calculate hazard ratios (relative risks, RRs) for mortality, incidence of HE, and adverse events.

RESULTS

Fourteen randomized controlled trials were included in the study. Rifaximin helped prevent HE (RR = -0.47, 95% confidence interval [CI]: -0.68 to -0.26) in patients with cirrhosis, but did not reduce mortality (RR = 0.03, 95% CI: -0.32 to 0.39) or increase the occurrence of adverse events (RR = -0.08, 95% CI: 0.22-0.07). Subgroup analysis showed that rifaximin was effective in both the primary (RR = 1.17, 95% CI: 1.06-1.29) and secondary (RR = 1.17, 95% CI: 1.06-1.29) prevention of HE. Moreover, subgroup analysis found that rifaximin helped prevent HE in alcohol-related (RR = -0.59, 95% CI: -0.87 to -0.32) or virus-associated (RR = -0.41, 95% CI: -0.71 to -0.11), and underwent transjugular intrahepatic portosystemic shunt (RR = -0.51, 95% CI: -0.76 to -0.27) or non-transjugular intrahepatic portosystemic shunt (RR = -0.35, 95% CI: -0.66 to -0.05) cirrhotic patients. Subgroup analyzed by the intervention, rifaximin versus placebo (RR = -0.43, 95% CI: -0.73 to -0.14) and rifaximin+lactulose versus lactulose (RR = -0.57, 95% CI: -0.68 to -0.26) were statistically significant prevention of HE, rather than rifaximin versus lactulose (RR = -0.44, 95% CI: -1.0 to 0.11).

CONCLUSIONS

Rifaximin is beneficial for primary and secondary prevention of HE, but it does not reduce mortality or increase the incidence of adverse events in patients with end-stage cirrhosis caused by virus or alcohol.

摘要

背景与目的

利福昔明在预防显性肝性脑病(HE)方面的疗效尚未确定。本研究旨在评估利福昔明预防HE的有效性和安全性。

方法

截至2022年3月,我们对Cochrane图书馆、PubMed、ClinicalTrials.gov、科学网和EMBASE进行了荟萃分析检索。我们采用随机效应DerSimonian-Laird模型汇总数据,以计算死亡率、HE发病率和不良事件的风险比(相对风险,RRs)。

结果

该研究纳入了14项随机对照试验。利福昔明有助于预防肝硬化患者发生HE(RR = -0.47,95%置信区间[CI]:-0.68至-0.26),但未降低死亡率(RR = 0.03,95% CI:-0.32至0.39)或增加不良事件的发生(RR = -0.08,95% CI:0.22 - 0.07)。亚组分析表明,利福昔明在HE的一级预防(RR = 1.17,95% CI:1.06 - 1.29)和二级预防(RR = 1.17,95% CI:1.06 - 1.29)中均有效。此外,亚组分析发现,利福昔明有助于预防酒精相关(RR = -0.59,95% CI:-0.87至-0.32)或病毒相关(RR = -0.41,95% CI:-0.71至-0.11)的肝硬化患者发生HE,以及接受经颈静脉肝内门体分流术(RR = -0.51,95% CI:-0.76至-0.27)或非经颈静脉肝内门体分流术(RR = -0.35,95% CI:-0.66至-0.05)的肝硬化患者发生HE。按干预措施进行亚组分析,利福昔明与安慰剂(RR = -0.43,95% CI:-0.73至-0.14)以及利福昔明 + 乳果糖与乳果糖(RR = -0.57,95% CI:-0.68至-0.26)预防HE具有统计学意义,而利福昔明与乳果糖(RR = -0.44,95% CI:-1.0至0.11)无统计学意义。

结论

利福昔明对HE的一级和二级预防有益,但它不会降低由病毒或酒精引起的终末期肝硬化患者的死亡率或增加不良事件的发生率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f93/11789876/09b4adaaf197/medi-104-e39905-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验