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Elsevier, Value in Health, 7(16), p. A499, 2013

DOI: 10.1016/j.jval.2013.08.1124

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The cost effectiveness of peginterferon alfa and ribavirin for the treatment of hepatitis C in children and young people

Journal article published in 2013 by Keith Cooper ORCID, L. Baxter, Emma Loveman, Debbie Hartwell, G. K. Frampton
This paper is available in a repository.
This paper is available in a repository.

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Abstract

OBJECTIVES: To assess the cost-effectiveness of peginterferon α-2a and peginterferon α-2b in combination with ribavirin compared to best supportive care (BSC), for the treatment of chronic hepatitis C virus (HCV) in children and young people aged 3 to 17 years. METHODS: A Markov state-transition economic model of chronic HCV in children and young people was developed that extrapolated the impact of sustained virological response (SVR) on life expectancy, quality-adjusted life expectancy and lifetime costs. The model was adapted from one previously developed for adults. A systematic review was conducted of the clinical effectiveness of the treatments, and the health related quality of life for patients with hepatitis C. Uncertainty was explored through probabilistic and deterministic sensitivity analyses. RESULTS: Seven studies were identified that were relatively small and of generally poor quality. Estimates of SVR were similar for for peginterferon α-2a (60%) and peginterferon α-2b (58%) was similar, whilst the SVR for no treatment was assumed to be zero. From this model, peginterferon alfa (α-2a or α-2b) in combination with ribavirin was more effective and cheaper than BSC. Sensitivity analyses suggest that the results were generally robust to all changes to the structural assumptions and input parameters. The model results were most sensitive to changes to the discount rate, time horizon, SVR and baseline fibrosis of the cohort. CONCLUSIONS: Treatment of children and young people with peginterferon alfa (α-2a or α-2b) and ribavirin may be an effective therapy. Peginterferon alfa (α-2a or α-2b) in combination with ribavirin is cost-effective compared with BSC. However, the available evidence is of poor quality. The views expressed in this paper are those of the authors and do not necessarily represent the views or policies of the UK HTA programme or Department of Health.