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利福昔明在肝硬化重症患者预后中的作用

Role of Rifaximin in the Prognosis of Critically Ill Patients with Liver Cirrhosis.

作者信息

Bai Zhaohui, Li Congcong, Lai Yongjie, Hu Xiaojuan, Shi Luwen, Guan Xiaodong, Xu Yang

机构信息

Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.

Department of Respiratory and Critical Care Medicine, General Hospital of Northern Theater Command, Shenyang 110840, China.

出版信息

Antibiotics (Basel). 2025 Mar 10;14(3):287. doi: 10.3390/antibiotics14030287.

Abstract

: Critically ill patients with liver cirrhosis impose a substantial health burden on the world. Rifaximin is a potential treatment option for such patients. : We extracted critically ill patients with liver cirrhosis from the Medical Information Mart for Intensive Care (MIMIC) IV database. Based on study outcomes, the current study included prevention and treatment cohorts. A 1:1 propensity score matching (PSM) analysis was performed to match the characteristics of patients. The risk of ICU admission and intensive care unit (ICU), in-hospital, 90-day, and 180-day death were explored. Cox regression analyses were conducted, and hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated. Kaplan-Meier curves were further drawn to demonstrate the cumulative 90-day and 180-day survival rate. : Overall, 5381 critically ill patients with liver cirrhosis were included. In the prevention cohort, rifaximin could decrease the risk of ICU admission (HR = 0.427, 95%CI: 0.338-0.539, < 0.001). In the treatment cohort, rifaximin could decrease the risk of ICU (HR = 0.530, 95%CI: 0.311-0.902, = 0.019) and in-hospital death (HR = 0.119, 95%CI: 0.033-0.429, = 0.001) in critically ill patients with liver cirrhosis. However, rifaximin could not decrease the risk of 90-day (HR = 0.905, 95%CI: 0.658-1.245, = 0.541) and 180-day (HR = 1.043, 95%CI: 0.804-1.353, = 0.751) death in critically ill patients with liver cirrhosis. Kaplan-Meier curve analyses also showed that rifaximin could not significantly decrease the 90-day ( = 0.570) and 180-day ( = 0.800) cumulative mortality. : This study suggests that rifaximin can significantly decrease the risk of ICU admission and improve short-term survival but does not impact long-term survival in critically ill patients with liver cirrhosis.

摘要

肝硬化重症患者给全球带来了沉重的健康负担。利福昔明是这类患者的一种潜在治疗选择。

我们从重症监护医学信息数据库(MIMIC)IV中提取了肝硬化重症患者。根据研究结果,本研究包括预防队列和治疗队列。进行了1:1倾向评分匹配(PSM)分析以匹配患者特征。探讨了入住重症监护病房(ICU)的风险以及ICU、住院期间、90天和180天死亡风险。进行了Cox回归分析,并计算了风险比(HR)和95%置信区间(CI)。进一步绘制了Kaplan-Meier曲线以显示90天和180天的累积生存率。

总体而言,纳入了5381例肝硬化重症患者。在预防队列中,利福昔明可降低入住ICU的风险(HR = 0.427,95%CI:0.338 - 0.539,P < 0.001)。在治疗队列中,利福昔明可降低肝硬化重症患者入住ICU的风险(HR = 0.530,95%CI:0.311 - 0.902,P = 0.019)和住院死亡风险(HR = 0.119,95%CI:0.033 - 0.429,P = 0.001)。然而,利福昔明不能降低肝硬化重症患者90天(HR = 0.905,95%CI:0.658 - 1.245,P = 0.541)和180天(HR = 1.043,95%CI:0.804 - 1.353,P = 0.751)死亡的风险。Kaplan-Meier曲线分析还表明,利福昔明不能显著降低90天(P = 0.570)和180天(P = 0.800)的累积死亡率。

本研究表明,利福昔明可显著降低肝硬化重症患者入住ICU的风险并改善短期生存率,但对长期生存率无影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3652/11939653/9cbbc8f290b4/antibiotics-14-00287-g001.jpg

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