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Value appropriation in hepatitis C
BACKGROUND: In 2015, the Swedish government in an unprecedented move decided to allocate 150 million € to provide funding for new drugs for hepatitis C. This was triggered by the introduction of the first second generation of direct-acting antivirals (DAAs) promising higher cure rates and reduced si...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304061/ https://www.ncbi.nlm.nih.gov/pubmed/34855072 http://dx.doi.org/10.1007/s10198-021-01409-7 |
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author | Lindgren, Peter Löfvendahl, Sofia Brådvik, Gunnar Weiland, Ola Jönsson, Bengt |
author_facet | Lindgren, Peter Löfvendahl, Sofia Brådvik, Gunnar Weiland, Ola Jönsson, Bengt |
author_sort | Lindgren, Peter |
collection | PubMed |
description | BACKGROUND: In 2015, the Swedish government in an unprecedented move decided to allocate 150 million € to provide funding for new drugs for hepatitis C. This was triggered by the introduction of the first second generation of direct-acting antivirals (DAAs) promising higher cure rates and reduced side effects. The drugs were cost-effective but had a prohibitive budget impact. Subsequently, additional products have entered the market leading to reduction in prices and expansions of the eligible patient base. METHODS: We estimated the social surplus generated by the new DAAs in Stockholm, Sweden, for the years 2014–2019. The actual use and cost of the drugs was based on registry data. Effects on future health care costs, indirect costs and QALY gains were estimated using a Markov model based primarily on Swedish data and using previous generations of interferon-based therapies as the counterfactual. RESULTS: A considerable social surplus was generated, 15% of which was appropriated by the producers whose share fell rapidly over time as prices fell. Most of the consumer surplus was generated by QALY gains, although 10% was from reduced indirect costs. QALY gains increased less rapidly than the number of treated patients as the eligibility criteria was loosened. CONCLUSIONS: The transfer of funds from the government to the regions helped generate substantial surplus for both consumers and producers with indirect costs playing an important role. The funding model may serve as a model for the financing of innovative treatments in the future. |
format | Online Article Text |
id | pubmed-9304061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93040612022-07-23 Value appropriation in hepatitis C Lindgren, Peter Löfvendahl, Sofia Brådvik, Gunnar Weiland, Ola Jönsson, Bengt Eur J Health Econ Original Paper BACKGROUND: In 2015, the Swedish government in an unprecedented move decided to allocate 150 million € to provide funding for new drugs for hepatitis C. This was triggered by the introduction of the first second generation of direct-acting antivirals (DAAs) promising higher cure rates and reduced side effects. The drugs were cost-effective but had a prohibitive budget impact. Subsequently, additional products have entered the market leading to reduction in prices and expansions of the eligible patient base. METHODS: We estimated the social surplus generated by the new DAAs in Stockholm, Sweden, for the years 2014–2019. The actual use and cost of the drugs was based on registry data. Effects on future health care costs, indirect costs and QALY gains were estimated using a Markov model based primarily on Swedish data and using previous generations of interferon-based therapies as the counterfactual. RESULTS: A considerable social surplus was generated, 15% of which was appropriated by the producers whose share fell rapidly over time as prices fell. Most of the consumer surplus was generated by QALY gains, although 10% was from reduced indirect costs. QALY gains increased less rapidly than the number of treated patients as the eligibility criteria was loosened. CONCLUSIONS: The transfer of funds from the government to the regions helped generate substantial surplus for both consumers and producers with indirect costs playing an important role. The funding model may serve as a model for the financing of innovative treatments in the future. Springer Berlin Heidelberg 2021-12-02 2022 /pmc/articles/PMC9304061/ /pubmed/34855072 http://dx.doi.org/10.1007/s10198-021-01409-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Lindgren, Peter Löfvendahl, Sofia Brådvik, Gunnar Weiland, Ola Jönsson, Bengt Value appropriation in hepatitis C |
title | Value appropriation in hepatitis C |
title_full | Value appropriation in hepatitis C |
title_fullStr | Value appropriation in hepatitis C |
title_full_unstemmed | Value appropriation in hepatitis C |
title_short | Value appropriation in hepatitis C |
title_sort | value appropriation in hepatitis c |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304061/ https://www.ncbi.nlm.nih.gov/pubmed/34855072 http://dx.doi.org/10.1007/s10198-021-01409-7 |
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