A systematic review and meta-analysis on the efficacy of fecal microbiome transplantation in patients with severe alcohol-associated hepatitis

医学 粪便细菌疗法 微生物群 移植 荟萃分析 肝移植 粪便 重症监护医学 内科学 生物信息学 微生物学 抗生素 生物 艰难梭菌
作者
Evance Pakuwal,Jin Lin Tan,Richard Woodman,Amanda J. Page,Andrea M. Stringer,Mohamed Asif Chinnaratha
出处
期刊:European Journal of Gastroenterology & Hepatology [Lippincott Williams & Wilkins]
卷期号:37 (11): 1260-1268 被引量:2
标识
DOI:10.1097/meg.0000000000003003
摘要

Background Severe alcohol-associated hepatitis (sAH) has a high short-term mortality, with limited treatment options. Fecal microbiota transplantation (FMT) has shown benefits in small, uncontrolled studies. Aim Perform a systematic review and meta-analysis to provide updated evidence on the efficacy and safety of FMT in sAH patients. Method Electronic databases were searched till 4 December 2023 for studies comparing FMT with standard of care (SOC) in sAH patients. Sensitivity analysis (leave-one-out method) and subgroup analyses were performed. Pooled risk ratio (RR) was used to compare the survival outcomes. Results Eight studies with 444 patients (FMT: 218; SOC: 226) met the eligibility criteria and were included in this meta-analysis. The 28- and 90-day survival range was higher in the FMT group (75–100% and 53–87%) compared to the SOC group (48–80% and 25–56%). The random-effects model showed a statistically significant increase in survival in the FMT arm at 28 days [RR (95% confidence interval) 2.30 (1.24–4.28), P = 0.01] and 90 days [2.53 (1.34–4.77), P < 0.001]. However, there was no statistically significant change in survival at the 6-month [1.89 (0.89–4.05), P = 0.10] and the 12-month time [1.86 (0.68–5.08), P = 0.23]. Sensitivity analysis showed no major changes in the overall effect sizes, and subgroup analysis showed that the survival benefit was restricted only to the retrospective studies. No serious treatment-related adverse events were reported. Conclusion FMT is a safe and efficacious treatment option that improves short-term survival in sAH patients, without major adverse events. A multicentre randomized controlled trial with an adequate sample size is required to confirm these findings.
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