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Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis
The Affordable Medicines Facility for malaria (AMFm) was conceived as a global market-based mechanism to increase access to effective malaria treatment and prolong effectiveness of artemisinin. Although results from a pilot implementation suggested that the subsidy was effective in increasing access...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590492/ https://www.ncbi.nlm.nih.gov/pubmed/25994293 http://dx.doi.org/10.1098/rsif.2014.1356 |
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author | Klein, Eili Y. Smith, David L. Cohen, Justin M. Laxminarayan, Ramanan |
author_facet | Klein, Eili Y. Smith, David L. Cohen, Justin M. Laxminarayan, Ramanan |
author_sort | Klein, Eili Y. |
collection | PubMed |
description | The Affordable Medicines Facility for malaria (AMFm) was conceived as a global market-based mechanism to increase access to effective malaria treatment and prolong effectiveness of artemisinin. Although results from a pilot implementation suggested that the subsidy was effective in increasing access to high-quality artemisinin combination therapies (ACTs), the Global Fund has converted AMFm into a country-driven mechanism whereby individual countries could choose to fund the subsidy from within their country envelopes. Because the initial costs of the subsidy in the pilot countries was higher than expected, countries are also exploring alternatives to a universal subsidy, such as subsidizing only child doses. We examined the incremental cost-effectiveness of a child-targeted policy using an age-structured bioeconomic model of malaria from the provider perspective. Because the vast majority of malaria deaths occur in children, targeting children could potentially improve the cost-effectiveness of the subsidy, though it would avert significantly fewer deaths. However, the benefits of a child-targeted subsidy (i.e. deaths averted) are eroded as leakage (i.e. older individuals taking young child-targeted doses) increases, with few of the benefits of a universal subsidy gained (i.e. reductions in overall prevalence). Although potentially more cost-effective, a child-targeted subsidy must contain measures to reduce the possibility of leakage. |
format | Online Article Text |
id | pubmed-4590492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45904922015-10-13 Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis Klein, Eili Y. Smith, David L. Cohen, Justin M. Laxminarayan, Ramanan J R Soc Interface Research Articles The Affordable Medicines Facility for malaria (AMFm) was conceived as a global market-based mechanism to increase access to effective malaria treatment and prolong effectiveness of artemisinin. Although results from a pilot implementation suggested that the subsidy was effective in increasing access to high-quality artemisinin combination therapies (ACTs), the Global Fund has converted AMFm into a country-driven mechanism whereby individual countries could choose to fund the subsidy from within their country envelopes. Because the initial costs of the subsidy in the pilot countries was higher than expected, countries are also exploring alternatives to a universal subsidy, such as subsidizing only child doses. We examined the incremental cost-effectiveness of a child-targeted policy using an age-structured bioeconomic model of malaria from the provider perspective. Because the vast majority of malaria deaths occur in children, targeting children could potentially improve the cost-effectiveness of the subsidy, though it would avert significantly fewer deaths. However, the benefits of a child-targeted subsidy (i.e. deaths averted) are eroded as leakage (i.e. older individuals taking young child-targeted doses) increases, with few of the benefits of a universal subsidy gained (i.e. reductions in overall prevalence). Although potentially more cost-effective, a child-targeted subsidy must contain measures to reduce the possibility of leakage. The Royal Society 2015-06-06 /pmc/articles/PMC4590492/ /pubmed/25994293 http://dx.doi.org/10.1098/rsif.2014.1356 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Klein, Eili Y. Smith, David L. Cohen, Justin M. Laxminarayan, Ramanan Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title | Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title_full | Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title_fullStr | Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title_full_unstemmed | Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title_short | Bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
title_sort | bioeconomic analysis of child-targeted subsidies for artemisinin combination therapies: a cost-effectiveness analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590492/ https://www.ncbi.nlm.nih.gov/pubmed/25994293 http://dx.doi.org/10.1098/rsif.2014.1356 |
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