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Artemisinin resistance – modelling the potential human and economic costs
BACKGROUND: Artemisinin combination therapy is recommended as first-line treatment for falciparum malaria across the endemic world and is increasingly relied upon for treating vivax malaria where chloroquine is failing. Artemisinin resistance was first detected in western Cambodia in 2007, and is no...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254187/ https://www.ncbi.nlm.nih.gov/pubmed/25418416 http://dx.doi.org/10.1186/1475-2875-13-452 |
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author | Lubell, Yoel Dondorp, Arjen Guérin, Philippe J Drake, Tom Meek, Sylvia Ashley, Elizabeth Day, Nicholas PJ White, Nicholas J White, Lisa J |
author_facet | Lubell, Yoel Dondorp, Arjen Guérin, Philippe J Drake, Tom Meek, Sylvia Ashley, Elizabeth Day, Nicholas PJ White, Nicholas J White, Lisa J |
author_sort | Lubell, Yoel |
collection | PubMed |
description | BACKGROUND: Artemisinin combination therapy is recommended as first-line treatment for falciparum malaria across the endemic world and is increasingly relied upon for treating vivax malaria where chloroquine is failing. Artemisinin resistance was first detected in western Cambodia in 2007, and is now confirmed in the Greater Mekong region, raising the spectre of a malaria resurgence that could undo a decade of progress in control, and threaten the feasibility of elimination. The magnitude of this threat has not been quantified. METHODS: This analysis compares the health and economic consequences of two future scenarios occurring once artemisinin-based treatments are available with high coverage. In the first scenario, artemisinin combination therapy (ACT) is largely effective in the management of uncomplicated malaria and severe malaria is treated with artesunate, while in the second scenario ACT are failing at a rate of 30%, and treatment of severe malaria reverts to quinine. The model is applied to all malaria-endemic countries using their specific estimates for malaria incidence, transmission intensity and GDP. The model describes the direct medical costs for repeated diagnosis and retreatment of clinical failures as well as admission costs for severe malaria. For productivity losses, the conservative friction costing method is used, which assumes a limited economic impact for individuals that are no longer economically active until they are replaced from the unemployment pool. RESULTS: Using conservative assumptions and parameter estimates, the model projects an excess of 116,000 deaths annually in the scenario of widespread artemisinin resistance. The predicted medical costs for retreatment of clinical failures and for management of severe malaria exceed US$32 million per year. Productivity losses resulting from excess morbidity and mortality were estimated at US$385 million for each year during which failing ACT remained in use as first-line treatment. CONCLUSIONS: These ‘ballpark’ figures for the magnitude of the health and economic threat posed by artemisinin resistance add weight to the call for urgent action to detect the emergence of resistance as early as possible and contain its spread from known locations in the Mekong region to elsewhere in the endemic world. |
format | Online Article Text |
id | pubmed-4254187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42541872014-12-04 Artemisinin resistance – modelling the potential human and economic costs Lubell, Yoel Dondorp, Arjen Guérin, Philippe J Drake, Tom Meek, Sylvia Ashley, Elizabeth Day, Nicholas PJ White, Nicholas J White, Lisa J Malar J Research BACKGROUND: Artemisinin combination therapy is recommended as first-line treatment for falciparum malaria across the endemic world and is increasingly relied upon for treating vivax malaria where chloroquine is failing. Artemisinin resistance was first detected in western Cambodia in 2007, and is now confirmed in the Greater Mekong region, raising the spectre of a malaria resurgence that could undo a decade of progress in control, and threaten the feasibility of elimination. The magnitude of this threat has not been quantified. METHODS: This analysis compares the health and economic consequences of two future scenarios occurring once artemisinin-based treatments are available with high coverage. In the first scenario, artemisinin combination therapy (ACT) is largely effective in the management of uncomplicated malaria and severe malaria is treated with artesunate, while in the second scenario ACT are failing at a rate of 30%, and treatment of severe malaria reverts to quinine. The model is applied to all malaria-endemic countries using their specific estimates for malaria incidence, transmission intensity and GDP. The model describes the direct medical costs for repeated diagnosis and retreatment of clinical failures as well as admission costs for severe malaria. For productivity losses, the conservative friction costing method is used, which assumes a limited economic impact for individuals that are no longer economically active until they are replaced from the unemployment pool. RESULTS: Using conservative assumptions and parameter estimates, the model projects an excess of 116,000 deaths annually in the scenario of widespread artemisinin resistance. The predicted medical costs for retreatment of clinical failures and for management of severe malaria exceed US$32 million per year. Productivity losses resulting from excess morbidity and mortality were estimated at US$385 million for each year during which failing ACT remained in use as first-line treatment. CONCLUSIONS: These ‘ballpark’ figures for the magnitude of the health and economic threat posed by artemisinin resistance add weight to the call for urgent action to detect the emergence of resistance as early as possible and contain its spread from known locations in the Mekong region to elsewhere in the endemic world. BioMed Central 2014-11-23 /pmc/articles/PMC4254187/ /pubmed/25418416 http://dx.doi.org/10.1186/1475-2875-13-452 Text en © Lubell et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lubell, Yoel Dondorp, Arjen Guérin, Philippe J Drake, Tom Meek, Sylvia Ashley, Elizabeth Day, Nicholas PJ White, Nicholas J White, Lisa J Artemisinin resistance – modelling the potential human and economic costs |
title | Artemisinin resistance – modelling the potential human and economic costs |
title_full | Artemisinin resistance – modelling the potential human and economic costs |
title_fullStr | Artemisinin resistance – modelling the potential human and economic costs |
title_full_unstemmed | Artemisinin resistance – modelling the potential human and economic costs |
title_short | Artemisinin resistance – modelling the potential human and economic costs |
title_sort | artemisinin resistance – modelling the potential human and economic costs |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254187/ https://www.ncbi.nlm.nih.gov/pubmed/25418416 http://dx.doi.org/10.1186/1475-2875-13-452 |
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