In Vivo Efficacy and Parasite Clearance of Artesunate plus Sulfadoxine-Pyrimethamine Versus Artemether-Lumefantrine in Mali

被引:15
|
作者
Niare, Karamoko [1 ]
Dara, Antoine [7 ]
Sagara, Issaka [1 ]
Sissoko, Mahaniadou S. [1 ]
Guindo, Cheick Oumar [1 ,2 ]
Cisse, Nana H. [1 ]
Coulibaly, Cheick Oumar
Ringwald, Pascal [3 ]
Benoit-Vical, Francoise [4 ]
Berry, Antoine [5 ,6 ]
Djimde, Abdoulaye A. [1 ]
Doumbo, Ogobara K. [1 ]
机构
[1] USTTB, MRTC, DEAP, POB 1805, Bamako, Mali
[2] World Hlth Org Off, Bamako, Mali
[3] WHO, Global Malaria Programme, Drug Resistance & Containment, CH-1211 Geneva, Switzerland
[4] CNRS, LCC, Toulouse, France
[5] Ctr Hosp Univ CHU Toulouse, Serv Parasitol Mycol, Toulouse, France
[6] Univ Toulouse, CPTP, Toulouse, France
[7] Univ Maryland, Sch Med, Inst Global Hlth, Div Malaria Res, Baltimore, MD 21201 USA
来源
关键词
PLASMODIUM-FALCIPARUM MALARIA; INTERMITTENT PREVENTIVE TREATMENT; SUB-SAHARAN AFRICA; ARTEMISININ RESISTANCE; CLINICAL MALARIA; DRUG-RESISTANCE; SAFETY; TRIAL; SELECTION; IMPACT;
D O I
10.4269/ajtmh.15-0503
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Although artemisinin resistance has yet to be reported in Africa, surveillance of the efficacy of artemisinin-based combination therapies (ACTs) is warranted. Here, the efficacy of artesunate + sulfadoxine-pyrimethamine (AS+SP) and artemether-lumefantrine (AL) was evaluated in Mali. Randomized open-label comparative in vivo assay of AS+SP versus AL were carried out using the 28-day follow-up World Health Organization protocol. Patients with uncomplicated falciparum malaria and at least 6 months of age were recruited between October 2010 and January 2014. A subset of these patients was selected to measure Plasmodium falciparum clearance time. Polymerase chain reaction corrected adequate clinical and parasitological responses were 100% for AS+SP and 98.2% for AL with no significant difference (P = 0.06). The reinfection rates were comparable (P = 0.63) with 8.0% for AS+SP and 12.6% for AL. Individuals under 8 years were more susceptible to treatment failure (relative risk = 1.9; 95% confidence interval = 1.2, 3.3). Median parasite clearance half-life was 1.7 hours (interquartile range [IQR] = 1.3-2.2) for AS+SP and 1.9 hours (IQR = 1.5-2.5) for AL with no statistically significant difference (P = 0.24). Efficacy of AS+SP and AL was high. This study provides baseline information on parasite clearance half-lives after ACT treatment, particularly AS+SP, in Mali.
引用
收藏
页码:634 / 639
页数:6
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