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
相关论文
共 50 条
  • [1] Population Pharmacokinetics of Dihydroartemisinin and Piperaquine in Pregnant and Nonpregnant Women with Uncomplicated Malaria
    Tarning, Joel
    Rijken, Marcus J.
    McGready, Rose
    Phyo, Aung Pyae
    Hanpithakpong, Warunee
    Day, Nicholas P. J.
    White, Nicholas J.
    Nosten, Francois
    Lindegardh, Niklas
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (04) : 1997 - 2007
  • [2] Pharmacokinetics of Piperaquine in Pregnant Women in Sudan with Uncomplicated Plasmodium falciparum Malaria
    Adam, Ishag
    Tarning, Joel
    Lindegardh, Niklas
    Mahgoub, Hyder
    McGready, Rose
    Nosten, Francois
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2012, 87 (01): : 35 - 40
  • [3] Efficacy and pharmacokinetics of artekin (dihydroartemisinin and piperaquine) for the treatment of uncomplicated falciparum malaria in Vietnam
    Edstein, Michael D.
    Dao, Nguyen V.
    Ngoa, Nguyen D.
    Hue, Nguyen D.
    Thuy, Le T.
    The, Nguyen D.
    Thanh, Nguyen X.
    Dai, Bui
    Travers, Thomas
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2007, 77 (05): : 28 - 28
  • [4] Population Pharmacokinetics of Lumefantrine in Pregnant and Nonpregnant Women With Uncomplicated Plasmodium falciparum Malaria in Uganda
    Kloprogge, F.
    Piola, P.
    Dhorda, M.
    Muwanga, S.
    Turyakira, E.
    Apinan, S.
    Lindegardh, N.
    Nosten, F.
    Day, N. P. J.
    White, N. J.
    Guerin, P. J.
    Tarning, J.
    CPT-PHARMACOMETRICS & SYSTEMS PHARMACOLOGY, 2013, 2 (11):
  • [5] Population pharmacokinetics of Artemether and dihydroartemisinin in pregnant women with uncomplicated Plasmodium falciparum malaria in Uganda
    Tarning, Joel
    Kloprogge, Frank
    Piola, Patrice
    Dhorda, Mehul
    Muwanga, Sulaiman
    Turyakira, Eleanor
    Nuengchamnong, Nitra
    Nosten, Francois
    Day, Nicholas P. J.
    White, Nicholas J.
    Guerin, Philippe J.
    Lindegardh, Niklas
    MALARIA JOURNAL, 2012, 11
  • [6] Population pharmacokinetics of Artemether and dihydroartemisinin in pregnant women with uncomplicated Plasmodium falciparum malaria in Uganda
    Joel Tarning
    Frank Kloprogge
    Patrice Piola
    Mehul Dhorda
    Sulaiman Muwanga
    Eleanor Turyakira
    Nitra Nuengchamnong
    François Nosten
    Nicholas PJ Day
    Nicholas J White
    Philippe J Guerin
    Niklas Lindegardh
    Malaria Journal, 11
  • [8] Pharmacokinetics of dihydroartemisinin following oral artesunate treatment of pregnant women with acute uncomplicated falciparum malaria
    McGready, R
    Stepniewska, K
    Ward, SA
    Cho, T
    Gilveray, G
    Looareesuwan, S
    White, NJ
    Nosten, F
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 62 (05) : 367 - 371
  • [9] Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria
    Zani, Babalwa
    Gathu, Michael
    Donegan, Sarah
    Olliaro, Piero L.
    Sinclair, David
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2014, (01):
  • [10] Pharmacokinetics of dihydroartemisinin following oral artesunate treatment of pregnant women with acute uncomplicated falciparum malaria
    R. McGready
    K. Stepniewska
    S. A. Ward
    T. Cho
    G. Gilveray
    S. Looareesuwan
    N. J. White
    F. Nosten
    European Journal of Clinical Pharmacology, 2006, 62 : 367 - 371