Pharmacokinetics of Dihydroartemisinin and Piperaquine in Pregnant and Nonpregnant Women with Uncomplicated Falciparum Malaria

被引:57
|
作者
Rijken, Marcus J. [1 ]
McGready, Rose [1 ,2 ,3 ]
Phyo, Aung Phae [1 ]
Lindegardh, Niklas [2 ,3 ]
Tarning, Joel [2 ,3 ]
Laochan, Natthapon [1 ]
Than, Hla Hla [1 ]
Mu, Oh [1 ]
Win, Aye Kyi [1 ]
Singhasivanon, Pratap
White, Nicholas [2 ,3 ]
Nosten, Francois [1 ,2 ,3 ]
机构
[1] Shoklo Malaria Res Unit, Tak 63110, Thailand
[2] Mahidol Univ, Fac Trop Med, Mahidol Oxford Trop Med Res Unit, Bangkok, Thailand
[3] Churchill Hosp, Ctr Trop Med, Oxford OX3 7LJ, England
基金
英国惠康基金; 比尔及梅琳达.盖茨基金会;
关键词
POPULATION PHARMACOKINETICS; ARTEMETHER-LUMEFANTRINE; ARTESUNATE; CHILDREN; EFFICACY; INFECTIONS; THAILAND; BORDER; VIVAX; AREA;
D O I
10.1128/AAC.05067-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dihydroartemisinin-piperaquine is a fixed-dose artemisinin-based combination treatment. Some antimalarials have altered pharmacokinetics in pregnancy. Pregnant women in the 2nd or 3rd trimester and matched nonpregnant women with uncomplicated falciparum malaria were treated with a total of 6.4 mg/kg of body weight dihydroartemisinin and 51.2 mg/kg piperaquine once daily for 3 days. Venous blood samples were drawn at prespecified time points over 9 weeks. Plasma dihydroartemisinin and piperaquine concentrations were analyzed by liquid chromatography-mass spectrometry. Piperaquine and dihydroartemisinin pharmacokinetics were well described. There were no significant differences in total piperaquine exposure (P = 0.80) or drug exposure during the terminal elimination phase (72 h to infinity) (P = 0.64) between the two groups. The apparent volume of distribution of piperaquine was significantly smaller (602 liters/kg versus 877 liters/kg) in pregnant women than in nonpregnant women (P = 0.0057), and the terminal elimination half-life was significantly shorter (17.8 days versus 25.6 days; P = 0.0023). Dihydroartemisinin exposure after the first dose was significantly lower (844 h x ng/ml versus 1,220 h x ng/ml, P = 0.0021) in pregnant women, but there were no significant differences in total dihydroartemisinin exposure or maximum concentrations between the two groups. There were no significant differences in any pharmacokinetic parameters between the second and third trimester. These results obtained through noncompartmental analysis suggest that in the treatment of falciparum malaria, there are no clinically important differences in the pharmacokinetics of dihydroartemisinin or piperaquine between pregnant and nonpregnant women. However, a more detailed analysis using population pharmacokinetic modeling is needed to fully investigate the differences found for some of the pharmacokinetic parameters, such as the terminal half-life.
引用
收藏
页码:5500 / 5506
页数:7
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