Talisuna Ambrose O, Nalunkuma-Kazibwe Anne, Bakyaita Nathan, Langi Peter, Mutabingwa Theonest K, Watkins William W, Van Marck Eric, D'Alessandro Umberto, Egwang Thomas G
Ministry of Health, Kampala, Uganda.
Trop Med Int Health. 2004 Feb;9(2):222-9. doi: 10.1046/j.1365-3156.2003.01187.x.
The rapid development of falciparum resistance to sulphadoxine-pyrimethamine (SP) in East and Central Africa has raised concerns as to the efficacy of combining it with another drug. In 2002, we assessed the efficacy of SP alone and combined with amodiaquine (AQ/SP) or chloroquine (CQ/SP) in Ugandan children with uncomplicated falciparum malaria. At day 14, adequate clinical response was 100% (84/84) for AQ/SP, 93% (92/101) for CQ/SP and 91% (73/80) for SP. At day 28, parasitological failure (RI-RIII) occurred in 16% (13/80) of children treated with AQ/SP, in 48% (48/100) of those treated with CQ/SP and in 61% (48/79) of those treated with SP alone. Compared with the AQ/SP arm, the odds for parasitological failure at day 28 were five times higher (95% CI, 2-10) in the CQ/SP group and sevenfold higher (95% CI, 3-17) in that of SP alone. CQ/SP does not offer any significant added benefit over SP alone while AQ/SP is an efficacious low-cost combination. These findings have important policy implications for Uganda and other resource-constrained African countries faced with the problematic choice of a new first-line antimalarial treatment in a context of high CQ resistance.
在东非和中非,恶性疟原虫对磺胺多辛-乙胺嘧啶(SP)的耐药性迅速发展,这引发了人们对将其与另一种药物联合使用疗效的担忧。2002年,我们评估了单独使用SP以及将其与阿莫地喹(AQ/SP)或氯喹(CQ/SP)联合使用对患有非复杂性恶性疟的乌干达儿童的疗效。在第14天,AQ/SP组的充分临床反应率为100%(84/84),CQ/SP组为93%(92/101),SP组为91%(73/80)。在第28天,接受AQ/SP治疗的儿童中有16%(13/80)出现寄生虫学失败(RI - RIII),接受CQ/SP治疗的儿童中有48%(48/100)出现,单独接受SP治疗的儿童中有61%(48/79)出现。与AQ/SP组相比,CQ/SP组在第28天出现寄生虫学失败的几率高五倍(95%置信区间,2 - 10),单独使用SP组则高七倍(95%置信区间,3 - 17)。与单独使用SP相比,CQ/SP没有任何显著的额外益处,而AQ/SP是一种有效的低成本联合用药。这些发现对乌干达以及其他资源有限的非洲国家具有重要的政策意义,这些国家在氯喹耐药率高的情况下面临选择新的一线抗疟治疗方案的难题。