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周效磺胺-乙胺嘧啶用于治疗加蓬儿童的恶性疟原虫疟疾

Sulfadoxine-pyrimethamine for the treatment of Plasmodium falciparum malaria in Gabonese children.

作者信息

Deloron P, Mayombo J, Le Cardinal A, Mezui-Me-Ndong J, Bruzi-Baert C, Lekoulou F, Elissa N

机构信息

International Centre for Medical Research, Franceville, Gabon.

出版信息

Trans R Soc Trop Med Hyg. 2000 Mar-Apr;94(2):188-90. doi: 10.1016/s0035-9203(00)90272-4.

Abstract

Chloroquine can no longer be recommended as the first-line treatment for falciparum malaria in several parts of Africa, given the increasing resistance of Plasmodium falciparum to this drug. The sulfadoxine-pyrimethamine combination (SP) is obviously an alternative candidate, that has already been selected as first-line antimalarial treatment by a few African countries. However, the extent of resistance to SP appears to be highly variable within Africa. Therefore, we investigated the efficacy of SP to treat uncomplicated malaria attacks in children from south-east Gabon. Sixty-six children presenting with a P. falciparum malaria attack were given a standard regimen of SP, and were followed at Days 3, 7, 14, and 21. No RIII response was observed, but relatively high prevalences of RII (18.2%) and RI (12.1%) were present. Moreover, analysis of the clinical outcome according to CDC criteria showed that initial clinical response was lacking in 8.5% of children, and that clinical failure occurred in 9.1%.

摘要

鉴于恶性疟原虫对氯喹的耐药性不断增加,在非洲的几个地区,氯喹已不再被推荐作为恶性疟的一线治疗药物。磺胺多辛-乙胺嘧啶合剂(SP)显然是一个替代选择,已经有一些非洲国家将其选作一线抗疟治疗药物。然而,在非洲,对SP的耐药程度似乎差异很大。因此,我们调查了SP治疗加蓬东南部儿童单纯性疟疾发作的疗效。66名出现恶性疟原虫疟疾发作的儿童接受了标准的SP治疗方案,并在第3、7、14和21天进行随访。未观察到RIII反应,但存在相对较高的RII(18.2%)和RI(12.1%)患病率。此外,根据美国疾病控制与预防中心(CDC)标准对临床结果进行分析显示,8.5%的儿童缺乏初始临床反应,9.1%的儿童出现临床失败。

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