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

Author:

Hsieh Yung-YuORCID,Chen Wei-MingORCID,Chang Kao-Chi,Chang Te-ShengORCID,Hung Chao-HungORCID,Yang Yao-HsuORCID,Tung Shui-Yi,Wei Kuo-LiangORCID,Shen Chen-Heng,Wu Cheng-Shyong,Ding Yuan-Jie,Hu Jing-Hong,Huang Yu-Ting,Lin Meng-HungORCID,Lu Chung-KuangORCID,Lin Yi-Hsiung,Lin Ming-ShyanORCID

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.

Funder

Chiayi Chang Gung Memorial Hospital

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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