Literature DB >> 26725891

Why do I treat my patients with mild hepatitis C?

Vincenza Calvaruso1, Antonio Craxì1.   

Abstract

The major advances achieved in the treatment of HCV by the development of new direct-acting antiviral agents (DAAs) allow treatment of almost the entire spectrum of patients with chornic infection. As a result of the exceedingly high cost of DAAs in many countries, IFN-free DAA regimens are mostly reserved to patients with advanced fibrosis or cirrhosis. Hence, treatment of patients with milder liver disease is often deferred. This could ultimately result in an increased burden of advanced liver disease and in increased long-term costs of management. Moreover, studies performed during the 'interferon era' and the early data on interferon-free regimens show that patients without severe fibrosis achieve higher rates of sustained virological response with less treatment-related adverse events. Unfortunately, there is no univocal way to predict the progression of liver fibrosis and therefore to identify the patients with early disease who would require urgent HCV treatment. Many studies have also demonstrated that treatment-induced HCV clearance reduces all-cause mortality regardless of the stage of liver fibrosis, pointing to an effect on extrahepatic manifestations of HCV infection. Last but not least, pharmacoeconomic studies show that DAA treatment of patients with mild HCV disease is cost-effective even at high prices of drugs, thus suggesting the opprtunity to treat regardless of the stage of liver disease.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  antiviral agents; chronic hepatitis C; costs; extrahepatic manifestations

Mesh:

Substances:

Year:  2016        PMID: 26725891     DOI: 10.1111/liv.13011

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  6 in total

1.  Disparities in Initiation of Direct-Acting Antiviral Agents for Hepatitis C Virus Infection in an Insured Population.

Authors:  Julia L Marcus; Leo B Hurley; Scott Chamberland; Jamila H Champsi; Laura C Gittleman; Daniel G Korn; Jennifer B Lai; Jennifer O Lam; Mary Pat Pauly; Charles P Quesenberry; Joanna Ready; Varun Saxena; Suk I Seo; David J Witt; Michael J Silverberg
Journal:  Public Health Rep       Date:  2018-05-11       Impact factor: 2.792

2.  How hepatitis C patients manage the treatment process of pegylated interferon and ribavirin therapy: a qualitative study.

Authors:  Shu-Mei Tsai; Jung-Ta Kao; Yun-Fang Tsai
Journal:  BMC Health Serv Res       Date:  2016-07-11       Impact factor: 2.655

3.  Future complications of chronic hepatitis C in a low-risk area: projections from the hepatitis c study in Northern Norway.

Authors:  H Kileng; L Bernfort; T Gutteberg; O S Moen; M G Kristiansen; E J Paulssen; L K Berg; J Florholmen; R Goll
Journal:  BMC Infect Dis       Date:  2017-09-16       Impact factor: 3.090

4.  Comment on Nuño Solinís R, et al. "Value of Treating All Stages of Chronic Hepatitis C: A Comprehensive Review of Clinical and Economic Evidence".

Authors:  Patrice Cacoub
Journal:  Infect Dis Ther       Date:  2017-03-29

Review 5.  Hepatitis C virus cure with direct acting antivirals: Clinical, economic, societal and patient value for China.

Authors:  Qing Xie; Jian-Wei Xuan; Hong Tang; Xiao-Guang Ye; Peng Xu; I-Heng Lee; Shan-Lian Hu
Journal:  World J Hepatol       Date:  2019-05-27

Review 6.  Hepatitis C virus: A critical approach to who really needs treatment.

Authors:  Elias Kouroumalis; Argyro Voumvouraki
Journal:  World J Hepatol       Date:  2022-01-27
  6 in total

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