尼日利亚北部恶性疟原虫对氯喹和磺胺嘧啶-乙胺嘧啶低度耐药地区3天口服奎宁方案的疗效

S I Adagu, J N Okoyeh, L Lege-Oguntoye, W N Ogala, G O Ogunrinde, J T Faji, A H Sani
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引用次数: 0

摘要

对尼日利亚北部地区34名恶性疟疾儿童进行了为期3天的口服奎宁(30 mg/kg/天)的体内疗效评估,该地区以前记录的寄生虫对氯喹和磺胺嘧啶-乙胺嘧啶(SDX/PYR)具有低级别耐药性。到第4天,所有34名儿童都没有寄生虫。平均寄生虫清除时间为2.7 d,发热清除时间为1.7 d。然而,在第14天,5例(14.7%)患儿再次出现寄生虫病,其中4例临床发病。他们再次用标准疗程的口服氯喹成功治疗。无不良药物反应记录。34例患儿中,9株寄生虫分离株体外培养成功。EC50和EC99分别为14.0和126.0 pmol /孔,表明寄生虫敏感性降低,但体外无抗性。总之,在研究地区,3天疗程的奎宁是标准氯喹治疗的有效替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of a 3-day oral regimen of quinine in an area of northern Nigeria with low-grade resistance of Plasmodium falciparum to chloroquine and sulphadoxine-pyrimethamine.

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.

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