Long-term effects of increased adoption of artemisinin combination therapies in Burkina Faso

Zupko, R.; Nguyen, T. D.; Some, A. F.; Tran, T. N.-A.; Gerardin, J.; Dudas, P.; Giang, D. D. H.; Wesolowski, A.; Ouedraogo, J.-B.; Boni, M. F.

Artemisinin combination therapies (ACTs) are the WHO-recommended first-line therapies for uncomplicated Plasmodium falciparum malaria. The emergence and spread of artemisinin-resistant genotypes is a major global public health concern. To explore how the increased adoption of ACTs may affect the high-burden high-impact malaria setting of Burkina Faso, we added spatial structure to a validated individual-based stochastic model of P. falciparum transmission and evaluated long-term effects of increased ACT use. We explored how de novo emergence of artemisinin-resistant genotypes may occur under scenarios in which private-market drugs are eliminated or multiple first-line therapies (MFT) are deployed. We found that elimination of private market drugs would reduce the long-run treatment failures. An MFT policy with equal deployment of artemether-lumefantrine (AL) and dihydroartemisinin-piperaquine (DHA-PPQ) may accelerate near-term drug resistance and treatment failure rates, due to early failure and substantially reduced treatment efficacy resulting from piperaquine-resistant genotypes. A rebalanced MFT approach (90% AL, 10% DHA-PPQ) results in better long-term outcomes than using AL alone but may be difficult to implement in practice.