Efficacy of a 3-day artesunate-mefloquine combination in the treatment of uncomplicated falciparum malaria in Kanchanaburi province of Thailand

被引:1
|
作者
Congpuong, Kanungnit [1 ]
Saipomsud, Wittaya [2 ]
Chompoonuch, Chutatip [3 ]
Niemhom, Paitoon [4 ]
Vinayak, Sumiti [5 ]
Satimai, Wichai
机构
[1] Minist Publ Hlth, Dept Dis Control, Lab Reference Ctr, Bur Vector Borne Dis, Nonthaburi 11000, Thailand
[2] Vector Borne Dis Unit, Kanchanaburi 71150, Thailand
[3] Off Dis Prevent & Control, Ratchaburi 70000, Thailand
[4] Vector Borne Dis Ctr, Kanchanaburi 71000, Thailand
[5] CDC CCID NCZVED DPD Malaria Branch, Atlanta, GA 30341 USA
关键词
Artesunate-mefloquine combination; efficacy study; falciparum malaria; Kanchanaburi province; IN-VIVO;
D O I
10.2478/abm-2010-0036
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: In Kanchanaburi province located on the Thai-Myanmar border, Plasmodium falciparum parasites have developed significant resistance to commonly-used anti-malarials. For use against falciparum malaria, 2-day artesunate-mefloquine combination (MAS2) has recently been replaced by a 3-day artesunatc-mefloquine combination (MAS3) that is an artemisinin-based combination therapy regimen recommended by the WHO. Objective: Investigate the efficacy and safety of MAS3 in the treatment of uncomplicated falciparum malaria in patients of Kanchaburi province. Methods: The study was conducted at Bongtee sub-district, Sai Yok district, Kanchanaburi province between June and November 2009. Fifty-one uncomplicated falciparum malaria patients were enrolled. Inclusion, exclusion and study method followed the WHO protocol for assessment and monitoring of antimalarial drug efficacy for the treatment of uncomplicated falciparum malaria. Patients received a MAS3 and were followed for 42 days. Results: All patients clinically recovered, but four patients were again parasitaemic on day 21, ( I patient) 28 (2 patients) and 42 (1 patient), respectively. Molecular analyses suggested that all recurrences were caused by recrudescence. There were no severe adverse events, but complaints of headache, gastrointestinal upset, nausea, and vomiting. Delay in parasite clearance was found. Proportion of parasite clearance on day 1, 2, 3 and 7 were 17.7%, 62.7%, 80.4%, and 100%, respectively. Conclusion: MAS3 is comparable to MAS2, and meet the WHO efficacy criteria for use against falciparum malaria, but the effect on parasite clearance was inferior to that of MAS2. Close monitoring evaluation is required.
引用
收藏
页码:289 / 295
页数:7
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