口服Paritaprevir/Ritonavir/Ombitasvir+Dasabuvir或Daclatasvir/Asunaprevir治疗慢性丙型肝炎基因1b:来自台湾的真实世界数据

Shou-Wu Lee
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引用次数: 0

摘要

背景:乙型丙型肝炎病毒(HCV)基因型在台湾占主导地位。我们在此报告一名慢性HCV基因型1b感染患者的真实数据,该患者接受口服Pro-D或DAC/ASV治疗。方法:回顾性收集2015年10月至2017年1月接受DAAs治疗的慢性丙型肝炎基因型1b感染患者的数据。DAAs方案包括12周的Pro-D和24周的DCV+ASV。记录治疗12周时ALT、胆红素、EOTVR、SVR的疗效和安全性。结果81例患者中,Pro-D组60例,DCV/ASV组21例,EOTVR率为98.3%,SVR12率为90.5%。在DCV/ASV治疗的第三个月,ALT升高,在Pro-D治疗的第二周,胆红素升高。结论:本研究发现SVR12分别为90.5% ~ 98.3%和90.5%。治疗期间肝功能参数升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatments of Chronic Hepatitis C Genotype 1b with Oral Paritaprevir/Ritonavir/Ombitasvir+Dasabuvir or Daclatasvir/Asunaprevir: A Real-World Data from Taiwan
Background: Hepatitis C Virus (HCV) genotype 1b is predominant in Taiwan. We report here using real-world data on a chronic HCV genotype 1b-infected patient given treatments of oral Pro-D or DAC/ASV. Methods: Data from subjects with chronic hepatitis C genotype 1b-infection undergoing DAAs therapy was retrospectively collected from October 2015 to January 2017. The DAAs regimens included a 12-week Pro-D and 24-week DCV+ASV. The therapeutic effectiveness and safety, including ALT, bilirubin, EOTVR and SVR at 12 weeks were all recorded. Results: Among all 81 subjects, 60 and 21 cases belonged to the Pro-D group and DCV/ASV group, with the rate of EOTVR and SVR12 being 98.3% and 90.5% respectively. Elevation of ALT was noted at the third month of DCV/ASV treatment, and increasing bilirubin was found at the secondary weeks of Pro-D treatment. Conclusion: Our study found SVR12 were 90.5% to 98.3% and 90.5%. Elevated liver function parameters were noted during the therapeutic period.
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