Publication:
Artemisinin resistance – modelling the potential human and economic costs

dc.contributor.authorYoel Lubellen_US
dc.contributor.authorArjen Dondorpen_US
dc.contributor.authorGuérin, Philippe Jen_US
dc.contributor.authorTom Drakeen_US
dc.contributor.authorSylvia Meeken_US
dc.contributor.authorElizabeth Ashleyen_US
dc.contributor.authorDay, Nicholas PJen_US
dc.contributor.authorWhite, Nicholas Jen_US
dc.contributor.authorWhite, Lisa Jen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Mahidol-Oxford Tropical Medicine Research Uniten_US
dc.date.accessioned2017-10-25T03:41:09Z
dc.date.available2017-10-25T03:41:09Z
dc.date.created2017-10-25
dc.date.issued2014
dc.description.abstractBackground: 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.en_US
dc.identifier.citationMalaria Journal. Vol.13, (2014), 452en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/2903
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.rights.holderBioMed Centralen_US
dc.subjectOpen Access articleen_US
dc.subjectMalariaen_US
dc.subjectArtemisininsen_US
dc.subjectAnti-malarial resistanceen_US
dc.subjectEconomicsen_US
dc.titleArtemisinin resistance – modelling the potential human and economic costsen_US
dc.typeResearch Articleen_US
dspace.entity.typePublication
mods.location.urlhttp://www.malariajournal.com/content/13/1/452

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