Dihydroartemisinin-Piperaquine vs. Artemether-Lumefantrine for First-Line Treatment of Uncomplicated Malaria in African Children: A Cost-Effectiveness Analysis

被引:15
作者
Pfeil, Johannes [1 ,2 ,3 ]
Borrmann, Steffen [4 ,5 ]
Tozan, Yesim [6 ,7 ]
机构
[1] Univ Hosp, Ctr Childhood & Adolescent Med, Heidelberg, Germany
[2] Univ Hosp, Dept Infect Dis, Heidelberg, Germany
[3] German Ctr Infect Res DZIF, Heidelberg, Germany
[4] Kenyan Med Res Inst KEMRI, Kilifi, Kenya
[5] Univ Tubingen, Inst Trop Med, Tubingen, Germany
[6] NYU, Steinhardt Sch Culture Educ & Human Dev, New York, NY USA
[7] Heidelberg Univ, Inst Publ Hlth, Heidelberg, Germany
来源
PLOS ONE | 2014年 / 9卷 / 04期
关键词
PLASMODIUM-FALCIPARUM; COMBINATION THERAPY; NON-INFERIORITY; ARTESUNATE; EFFICACY; BURDEN;
D O I
10.1371/journal.pone.0095681
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Recent multi-centre trials showed that dihydroartemisinin-piperaquine (DP) was as efficacious and safe as artemether-lumefantrine (AL) for treatment of young children with uncomplicated P. falciparum malaria across diverse transmission settings in Africa. Longitudinal follow-up of patients in these trials supported previous findings that DP had a longer post-treatment prophylactic effect than AL, reducing the risk of reinfection and conferring additional health benefits to patients, particularly in areas with moderate to high malaria transmission. Methods: We developed a Markov model to assess the cost-effectiveness of DP versus AL for first-line treatment of uncomplicated malaria in young children from the provider perspective, taking into consideration the post-treatment prophylactic effects of the drugs as reported by a recent multi-centre trial in Africa and using the maximum manufacturer drug prices for artemisinin-based combination therapies set by the Global Fund in 2013. We estimated the price per course of treatment threshold above which DP would cease to be a cost-saving alternative to AL as a first-line antimalarial drug. Results: First-line treatment with DP compared to AL averted 0.03 DALYs (95% CI: 0.006-0.07) and 0.001 deaths (95% CI: 0.00-0.002) and saved $0.96 (95% CI: 0.33-2.46) per child over one year. The results of the threshold analysis showed that DP remained cost-saving over AL for any DP cost below $1.23 per course of treatment. Conclusions: DP is superior to AL from both the clinical and economic perspectives for treatment of uncomplicated P. falciparum malaria in young children. A paediatric dispersible formulation of DP is under development and should facilitate a targeted deployment of this antimalarial drug. The use of DP as first-line antimalarial drug in paediatric malaria patients in moderate to high transmission areas of Africa merits serious consideration by health policymakers.
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