Department of Medicine I, University Hospital Bonn, Bonn.
Center for Infectiology Berlin (CIB), Berlin.
J Clin Gastroenterol. 2020 Feb;54(2):192-199. doi: 10.1097/MCG.0000000000001189.
International guidelines recommend prioritized treatment initiation in hepatitis C virus (HCV)-infected patients with advanced liver disease. We aimed to evaluate whether the widespread usage of direct acting antivirals (DAAs) has led to a decrease in late presentation for care.
Data derived from the multicenter German Hepatitis C Cohort (GECCO) was analyzed. Treatment naive HCV-infected patients initiating DAA-based treatment between January 2014 and September 2017 were included. Advanced liver disease was defined by aspartate aminotransferase to platelet ratio index score ≥1.5, METAVIR≥F3, or FibroScan ≥9.5 kPa. Period prevalence and risk factors for late presentation were evaluated.
Six hundred fifty-three HCV-monoinfected and 210 HIV/HCV-coinfected patients (mean age, 48.6±12.7 y; 65.5% male) were included. Overall 32.5% of patients had advanced liver disease. In 2014 39.4% of patients presented with advanced liver disease, decreasing to 30.1%, 34.4%, and 26.4% in the years 2015, 2016, and 2017 (P=0.057), respectively. Patients with and without advanced liver disease differed in age (P<0.0001), CD4 ≤350/µL (P=0.027), genotype (P=0.005), transmission route (P=0.047), body mass index (P<0.001), and time since diagnosis (P=0.007). In the multivariable binary logistic regression analysis GT3, age above 45 years and being diagnosed >2 years ago were positively and HCV transmission through men who have sex with men was negatively associated with advanced liver disease.
Overall 32.5% of patients presented with advanced liver disease. We observed a trend toward a lower proportion of patients starting treatment late.GT3, age, years since HCV diagnosis and HCV transmission route were identified as risk factors for presentation with advanced liver disease.
国际指南建议对患有晚期肝病的丙型肝炎病毒(HCV)感染患者优先开始治疗。我们旨在评估直接作用抗病毒药物(DAA)的广泛应用是否导致就诊时间延迟。
分析了多中心德国丙型肝炎队列(GECCO)的数据。纳入了 2014 年 1 月至 2017 年 9 月期间开始 DAA 治疗的初治 HCV 感染患者。晚期肝病定义为天冬氨酸氨基转移酶与血小板比值指数评分≥1.5、METAVIR≥F3 或 FibroScan≥9.5kPa。评估了晚期就诊的现患率和危险因素。
共纳入 653 例 HCV 单感染和 210 例 HIV/HCV 合并感染患者(平均年龄 48.6±12.7 岁;65.5%为男性)。总体上,32.5%的患者有晚期肝病。2014 年,39.4%的患者有晚期肝病,2015 年、2016 年和 2017 年分别降至 30.1%、34.4%和 26.4%(P=0.057)。有和无晚期肝病的患者在年龄(P<0.0001)、CD4<350/µL(P=0.027)、基因型(P=0.005)、传播途径(P=0.047)、体重指数(P<0.001)和诊断后时间(P=0.007)方面存在差异。在多变量二项逻辑回归分析中,GT3、年龄>45 岁和诊断>2 年前被确定为与晚期肝病相关的阳性因素,而通过男男性接触传播与晚期肝病呈负相关。
总体上,32.5%的患者有晚期肝病。我们观察到就诊时间延迟的患者比例呈下降趋势。GT3、年龄、诊断后时间和 HCV 传播途径是出现晚期肝病的危险因素。