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直接作用抗病毒药物可减少丙型肝炎病毒相关肝硬化患者食管静脉曲张的新发。

Direct-Acting Antivirals Reduce the De Novo Development of Esophageal Varices in Patients with Hepatitis C Virus Related Liver Cirrhosis.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Chang Gung Memorial Hospital, Chiayi 613016, Taiwan.

College of Medicine, Chang Gung University, Taoyuan 333323, Taiwan.

出版信息

Viruses. 2023 Jan 16;15(1):252. doi: 10.3390/v15010252.

Abstract

The real-world benefits of direct-acting antiviral (DAA)-induced sustained virologic response (SVR) on the de novo occurrence and progression of esophageal varices (EV) remain unclear in patients with hepatitis C virus (HCV)-related liver cirrhosis (LC). This is a retrospective cohort study evaluating all patients with Child-Pugh class A HCV-related LC during 2013 to 2020 in the Chang Gung Medical System. A total of 215 patients fit the inclusion criteria and were enrolled. Of them, 132 (61.4%) patients achieved DAA induced-SVR and 83 (38.6%) did not receive anti-viral treatment. During a median follow-up of 18.4 (interquartile range, 10.1−30.9) months, the 2-year incidence of de novo EV occurrence was 8 (7.0%) in the SVR group and 7 (12.7%) in the treatment-naïve group. Compared to the treatment-naïve group, the SVR group was associated with a significantly lower incidence of EV occurrence (adjusted hazard ratio [aHR]: 0.47, p = 0.030) and a significantly lower incidence of EV progression (aHR: 0.55, p = 0.033). The risk of EV progression was strongly correlated with the presence of baseline EV (p < 0.001). To the best of our knowledge, this is the first study to demonstrate that DAA-induced SVR is associated with decreased risk of de novo EV occurrence and progression in the real world.

摘要

直接作用抗病毒药物(DAA)诱导的持续病毒学应答(SVR)对丙型肝炎病毒(HCV)相关肝硬化(LC)患者新发食管静脉曲张(EV)的发生和进展的实际获益尚不清楚。这是一项回顾性队列研究,评估了 2013 年至 2020 年期间在长庚医疗系统中丙型肝炎相关 A 级 Child-Pugh 肝硬化的所有患者。共有 215 名患者符合纳入标准并被纳入研究。其中,132 名(61.4%)患者实现了 DAA 诱导的 SVR,83 名(38.6%)未接受抗病毒治疗。在中位随访 18.4 个月(四分位间距,10.1-30.9)期间,SVR 组的 2 年新发 EV 发生率为 8 例(7.0%),治疗初治组为 7 例(12.7%)。与治疗初治组相比,SVR 组新发 EV 发生率显著降低(校正风险比[aHR]:0.47,p = 0.030),EV 进展发生率显著降低(aHR:0.55,p = 0.033)。EV 进展的风险与基线 EV 的存在密切相关(p < 0.001)。据我们所知,这是第一项证明 DAA 诱导的 SVR 与降低真实世界中新发 EV 发生和进展风险相关的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7096/9860555/188c5a5f15b9/viruses-15-00252-g001.jpg

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