Abstract

PurposeLong-term effects on patient health-related quality of life (HRQoL) after direct-acting antiviral (DAA) treatment for hepatitis C virus (HCV) are unknown. We assessed the impact of DAA-mediated HCV clearance on HRQoL from DAA initiation to 1 year after confirmed sustained virological response at 24 weeks post-treatment (SVR24).MethodsHRQoL was evaluated using the eight-item Short Form Health Survey (SF-8). Chronic HCV-infected patients were treated for 12 weeks with sofosbuvir-based DAAs. SF-8 was administered at baseline, treatment cessation, SVR24, and 1-year post-SVR24.ResultsA total of 109 chronic HCV-infected patients were enrolled. The average SF-8 scores were higher than the Japanese national standard values for bodily pain (BP) and mental health at baseline and for general health at 1-year post-SVR24. None of the SF-8 scores differed significantly between baseline and 1-year post-SVR24. Regarding age, sex, liver status, and treatment regimen, the SF-8 scores at 1-year post-SVR24 were affected by only age; individuals aged < 65 years had significantly higher physical component score (PCS), physical functioning, role physical, and BP scores than older individuals. In the multivariable analysis, only age of ≥ 65 years was significantly associated with influencing PCS at 1-year post-SVR24. However, no significant factors were identified for mental component score.ConclusionUpon long-term assessment, although more factors trended higher than national standard values at 1-year post-SVR24 than at baseline, there were no significant changes within factors. As PCS tended to be associated with age, patients aged ≥ 65 years should be carefully monitored for PCS.

Highlights

  • Hepatitis C virus (HCV) is a leading cause of hepatic cirrhosis, hepatocellular carcinoma, and end-stage liver disease [1, 2]

  • We found that more categories were higher than national standard values at 1-year post-clearance than at baseline, but there were no significant changes within categories

  • At baseline in this study, patients with chronic hepatitis C virus (HCV) infection had higher bodily pain (BP), VT, and mental health (MH) scores compared with the Japanese national standard values

Read more

Summary

Introduction

Hepatitis C virus (HCV) is a leading cause of hepatic cirrhosis, hepatocellular carcinoma, and end-stage liver disease [1, 2]. The introduction of interferon (IFN)-free direct-acting antiviral (DAA) regimens has changed the treatment of HCV infection. In 2014, the combined use of asunaprevir (an NS3/4A protease inhibitor) and daclatasvir (an NS5A inhibitor) became the first approved IFN-free treatment for genotype (GT) 1 HCV infection in Japan. Thereafter, sofosbuvir (SOF; an NS5B polymerase inhibitor) and ribavirin (RBV) [3] were indicated for GT2 HCV infection, and ledipasvir (LDV; an NS5A inhibitor)/SOF [4] were approved for use in patients with GT1 HCV infection. DAAs for HCV treatment were released one after another All these treatments show high efficacy and safety, with > 90% patients attaining a sustained virologic response (SVR), defined as the elimination of HCV at a particular timepoint after treatment completion, such as 24 weeks (SVR24)

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call