Pharmacokinetics of oral artesunate in children with moderately severe Plasmodium falciparum malaria

被引:50
作者
Bethell, DB
TejaIsavadharm, P
Cao, XTP
Pham, TTT
Ta, TTM
Tran, TNT
Nguyen, TTH
Phuong, PT
Kyle, D
Day, NPJ
White, NJ
机构
[1] CHO QUAN HOSP, WELLCOME TRUST CLIN RES UNIT, CTR TROP DIS, Ho Chi Minh City OX3 9DU, VIETNAM
[2] JOHN RADCLIFFE HOSP, NUFFIELD DEPT CLIN MED, CTR TROP MED, OXFORD, ENGLAND
[3] AFRIMS, DEPT IMMUNOL, BANGKOK, THAILAND
[4] DONG NAI PAEDIAT CTR, BIEN HOA, DONG NAI, VIETNAM
[5] CHO QUAN HOSP, CTR TROP DIS, Ho Chi Minh City, VIETNAM
基金
英国惠康基金;
关键词
malaria; Plasmodium falciparum; chemotherapy; pharmacokinetics; artesunate; children; Viet Nam;
D O I
10.1016/S0035-9203(97)90222-4
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The pharmacokinetic properties of oral artesunate (3 mg/kg) were determined in 10 Vietnamese children, aged from 6 to 15 years, with acute falciparum malaria of moderate severity. Plasma concentrations were measured using a bioassay and expressed in terms of antimalarial activity equivalent to dihydroartemisinin, the principal biologically active metabolite. Oral artesunate was absorbed rapidly with a mean time to peak plasma bioactivity of 1.7 h (95% confidence interval [95% CI] 0.8-2.6). There was wide variation in peak plasma concentrations with a mean value equivalent to 664 ng of dihydroartemisinin/mL (95% CI 387-9410, range 179-1395) and a four-fold variation in the area under the plasma concentration-time curves. Elimination from plasma was rapid with a mean (95% CI) half-life of 1.0 h (95% CI 0.8-1.4). Plasma antimalarial levels were below the limit of detection in all cases by 12 h, despite the relatively high dose of artesunate used. Oral artesunate is rapidly absorbed and rapidly eliminated in children with moderately severe malaria but there is considerable variation between individuals.
引用
收藏
页码:195 / 198
页数:4
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