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Health economic analysis of antiviral drugs in the global polio eradication endgame

BACKGROUND: Pollio antiviral drugs (PAVDs) may provide a critical tool in the eradication endgame by stopping poliovirus infections in immunodeficient individuals who may not clear the virus without therapeutic intervention. Although prolonged/chronic poliovirus excreters are rare, they represent a...

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Autores principales: Badizadegan, Kamran, Kalkowska, Dominika A., Thompson, Kimberly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680042/
https://www.ncbi.nlm.nih.gov/pubmed/37577803
http://dx.doi.org/10.1177/0272989X231191127
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author Badizadegan, Kamran
Kalkowska, Dominika A.
Thompson, Kimberly M.
author_facet Badizadegan, Kamran
Kalkowska, Dominika A.
Thompson, Kimberly M.
author_sort Badizadegan, Kamran
collection PubMed
description BACKGROUND: Pollio antiviral drugs (PAVDs) may provide a critical tool in the eradication endgame by stopping poliovirus infections in immunodeficient individuals who may not clear the virus without therapeutic intervention. Although prolonged/chronic poliovirus excreters are rare, they represent a source of poliovirus reintroduction into general population. Prior studies that assumed successful cessation of all oral poliovirus vaccine (OPV) use estimated the potential upper bound of the incremental net benefits (INBs) of resource investments in research and development of PAVDs. However, delays in polio eradication, OPV cessation, and the development of PAVDs necessitate an updated economic analysis to reevaluate the costs and benefits of further investments in PAVDs. METHODS: Using a global integrated model of polio transmission, immunity, vaccine dynamics, risks, and economics, we explore the risks of reintroduction of polio transmission due to immunodeficiency-related vaccine derived poliovirus (iVDPV) excreters and reevaluate the upper bound of the INBs of PAVDs. RESULTS: Under the current conditions, for which the use of OPV will likely continue for the foreseeable future, even with successful eradication of type 1 WPV by the end of 2023 and continued use of Sabin OPV for outbreak response, we estimate upper bound INB of 60 million US$2019. With >100 million US$2019 already invested in PAVD development and with the introduction of novel OPVs that are less likely to revert to neurovirulence, our analysis suggests the expected INBs of PAVDs would not offset their costs. CONCLUSIONS: While PAVDs could play an important role in the polio endgame, their expected economic benefits drop with ongoing OPV use and poliovirus transmissions. However, stakeholders may pursue development of PAVDs as a desired product regardless of their economic benefits.
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spelling pubmed-106800422023-11-27 Health economic analysis of antiviral drugs in the global polio eradication endgame Badizadegan, Kamran Kalkowska, Dominika A. Thompson, Kimberly M. Med Decis Making Article BACKGROUND: Pollio antiviral drugs (PAVDs) may provide a critical tool in the eradication endgame by stopping poliovirus infections in immunodeficient individuals who may not clear the virus without therapeutic intervention. Although prolonged/chronic poliovirus excreters are rare, they represent a source of poliovirus reintroduction into general population. Prior studies that assumed successful cessation of all oral poliovirus vaccine (OPV) use estimated the potential upper bound of the incremental net benefits (INBs) of resource investments in research and development of PAVDs. However, delays in polio eradication, OPV cessation, and the development of PAVDs necessitate an updated economic analysis to reevaluate the costs and benefits of further investments in PAVDs. METHODS: Using a global integrated model of polio transmission, immunity, vaccine dynamics, risks, and economics, we explore the risks of reintroduction of polio transmission due to immunodeficiency-related vaccine derived poliovirus (iVDPV) excreters and reevaluate the upper bound of the INBs of PAVDs. RESULTS: Under the current conditions, for which the use of OPV will likely continue for the foreseeable future, even with successful eradication of type 1 WPV by the end of 2023 and continued use of Sabin OPV for outbreak response, we estimate upper bound INB of 60 million US$2019. With >100 million US$2019 already invested in PAVD development and with the introduction of novel OPVs that are less likely to revert to neurovirulence, our analysis suggests the expected INBs of PAVDs would not offset their costs. CONCLUSIONS: While PAVDs could play an important role in the polio endgame, their expected economic benefits drop with ongoing OPV use and poliovirus transmissions. However, stakeholders may pursue development of PAVDs as a desired product regardless of their economic benefits. 2023 2023-08-14 /pmc/articles/PMC10680042/ /pubmed/37577803 http://dx.doi.org/10.1177/0272989X231191127 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Badizadegan, Kamran
Kalkowska, Dominika A.
Thompson, Kimberly M.
Health economic analysis of antiviral drugs in the global polio eradication endgame
title Health economic analysis of antiviral drugs in the global polio eradication endgame
title_full Health economic analysis of antiviral drugs in the global polio eradication endgame
title_fullStr Health economic analysis of antiviral drugs in the global polio eradication endgame
title_full_unstemmed Health economic analysis of antiviral drugs in the global polio eradication endgame
title_short Health economic analysis of antiviral drugs in the global polio eradication endgame
title_sort health economic analysis of antiviral drugs in the global polio eradication endgame
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680042/
https://www.ncbi.nlm.nih.gov/pubmed/37577803
http://dx.doi.org/10.1177/0272989X231191127
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