Chloroquine pharmacokinetics in pregnant and nonpregnant women with vivax malaria.

Sue Jean Lee; Rose McGready; Christine Fernandez; Kasia Stepniewska; Moo Koo Paw; Samuel Jacher Viladpai-nguen; Kyaw Lay Thwai; Leopoldo Villegas; Pratap Singhasivanon; Brian M Greenwood ORCID logo; +2 more... Nicholas J White; François Nosten; (2008) Chloroquine pharmacokinetics in pregnant and nonpregnant women with vivax malaria. European journal of clinical pharmacology, 64 (10). pp. 987-992. ISSN 0031-6970 DOI: 10.1007/s00228-008-0500-z
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PURPOSE: We compared the pharmacokinetics of chloroquine in pregnant and nonpregnant women treated for Plasmodium vivax malaria. METHODS: Twelve pregnant women and 15 nonpregnant women of child-bearing age with acute P. vivax malaria were treated with 25 mg chloroquine base/kg over 3 days on the northwestern border of Thailand. Blood concentrations of chloroquine and desethylchloroquine were measured using hydrophilic interaction liquid chromatography coupled with fluorescence detection. Twenty-five women completed the pharmacokinetic study. RESULTS: Although increasing gestational age was associated with reduced chloroquine AUC0-->infinity, there was no significant difference overall in the pharmacokinetics of chloroquine between pregnant and nonpregnant women. Fever was associated with lower chloroquine AUC0-->infinity values. Desethylchloroquine area under the curve (AUC) values were not significantly affected by pregnancy. CONCLUSIONS: Pregnancy did not significantly affect blood concentrations of chloroquine or its metabolite, desethylchloroquine, in women with P. vivax malaria.

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