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肯尼亚沿海学龄人群中恶性疟原虫对氯喹及三种二线抗疟药物的反应

Response of falciparum malaria to chloroquine and three second line antimalarial drugs in a Kenyan coastal school age population.

作者信息

Hagos B, Khan B, Ofulla A V, Kariuki D, Martin S K

机构信息

Department of Pharmacy, University of Nairobi, Kenya.

出版信息

East Afr Med J. 1993 Oct;70(10):620-3.

PMID:8187656
Abstract

Ambulatory rural school children in the Mombasa area with P. falciparum parasitaemia were examined and randomly assigned to treatment with one of three second-line antimalarials--amodiaquine, pyrimethamine/sulphadoxine (P/SD) and pyrimethamine/sulfalene (P/SL). Clinical signs and parasitaemia were followed daily for the first week and on days 14 and 28. WHO Mark II schizont inhibition tests were performed for all the above 3 drugs and chloroquine. The total number of cases was 73. The mean parasite density was 142.1 +/- 207; 102.7 +/- 166; 82.74 +/- 93 parasites per 300 WBC for amodiaquine, P/SD, and P/SL, respectively. In vitro tests showed a chloroquine resistance rate of 60% and no resistance to all of the second line drugs. Also, all children treated successfully cleared their parasitaemia with mean clearance rates of 2.05 +/- 0.57; 1.86 +/- 0.47; 2.05 +/- 0.50 days for amodiaquine, P/SD and P/SL, respectively. Even though, no difference in the effectiveness between the second line drugs used was found, reinfection rates as depicted by day 28 parasitaemia differed--amodiaquine 16%; P/SD 0%; and P/SL4.35%. This difference could be attributed to the difference in the pharmacokinetic properties of the drugs.

摘要

对蒙巴萨地区患有恶性疟原虫血症的农村流动学龄儿童进行了检查,并将他们随机分配接受三种二线抗疟药之一的治疗,即氨酚喹、乙胺嘧啶/磺胺多辛(P/SD)和乙胺嘧啶/磺胺林(P/SL)。在第一周以及第14天和第28天每天对临床症状和疟原虫血症进行跟踪。对上述3种药物以及氯喹进行了WHO Mark II裂殖体抑制试验。病例总数为73例。氨酚喹、P/SD和P/SL每300个白细胞中的平均寄生虫密度分别为142.1±207、102.7±166和82.74±93个寄生虫。体外试验显示氯喹耐药率为60%,对所有二线药物均无耐药。此外,所有接受治疗的儿童均成功清除了疟原虫血症,氨酚喹、P/SD和P/SL的平均清除率分别为2.05±0.57天、1.86±0.47天和2.05±0.50天。尽管所使用的二线药物之间在疗效上未发现差异,但第28天疟原虫血症所显示的再感染率有所不同——氨酚喹为16%;P/SD为0%;P/SL为4.35%。这种差异可能归因于药物的药代动力学特性不同。

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