Adagu S I, Okoyeh J N, Lege-Oguntoye L, Ogala W N, Ogunrinde G O, Faji J T, Sani A H
Department of Pharmacology, Ahmadu Bello University, Zaria, Nigeria.
J Trop Med Hyg. 1995 Oct;98(5):296-8.
The efficacy in vivo of a 3-day oral regimen of quinine (30 mg/kg/day) was assessed in 34 children with falciparum malaria in an area of northern Nigeria with previously documented low-grade parasite resistance to chloroquine and sulphadoxine-pyrimethamine (SDX/PYR). By day 4, all 34 children were free of parasites. Mean parasite clearance time and fever clearance time were 2.7 and 1.7 days, respectively. However, on day 14, 5 (14.7%) children were again parasitaemic and 4 of them were clinically ill. They were again treated successfully with a standard course of oral chloroquine. No adverse drug effects were recorded. Of the 34 children, 9 parasite isolates were successfully cultured in vitro. EC50 and EC99 were 14.0 and 126.0 pmol per well respectively, indicating decreased parasite sensitivity but no resistance in vitro. In conclusion, the 3-day course of quinine was found to be an effective alternative to standard chloroquine treatment in the study area.
在尼日利亚北部一个先前记录显示疟原虫对氯喹和磺胺多辛-乙胺嘧啶(SDX/PYR)存在低度耐药性的地区,对34名患恶性疟的儿童评估了为期3天的口服奎宁方案(30毫克/千克/天)的体内疗效。到第4天,所有34名儿童的疟原虫均消失。平均疟原虫清除时间和发热清除时间分别为2.7天和1.7天。然而,在第14天,5名(14.7%)儿童再次出现疟原虫血症,其中4名出现临床症状。他们再次接受标准疗程的口服氯喹治疗,治疗成功。未记录到药物不良反应。34名儿童中,9株疟原虫分离株成功进行了体外培养。半数有效浓度(EC50)和99%有效浓度(EC99)分别为每孔14.0皮摩尔和126.0皮摩尔,表明疟原虫敏感性降低,但体外未出现耐药性。总之,在研究地区,发现为期3天的奎宁疗程是标准氯喹治疗的有效替代方案。