Pharmacokinetics of mefloquine combined with artesunate in children with acute falciparum malaria

被引:43
作者
Price, R
Simpson, JA
Teja-Isavatharm, P
Than, MM
Luxemburger, C
Heppner, DG
Chongsuphajaisiddhi, T
Nosten, F
White, NJ
机构
[1] Mahidol Univ, Fac Trop Med, Bangkok 10400, Thailand
[2] Shoklo Malaria Res Unit, Mae Sot, Tak Province, Thailand
[3] AFRIMS, Dept Immunol & Med, Bangkok, Thailand
[4] Univ London St Georges Hosp, Sch Med, Div Infect Dis, London, England
[5] John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Trop Med, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
D O I
10.1128/AAC.43.2.341
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Combining artemisinin or a derivative with mefloquine increases cure rates in falciparum malaria patients, reduces transmission, and may slow the development of resistance. The combination of artesunate, given for 3 days, and mefloquine is now the treatment of choice for uncomplicated multidrug-resistant falciparum malaria acquired on the western or eastern borders of Thailand, To optimize mefloquine administration in this combination, a prospective study of mefloquine pharmacokinetics was conducted with 120 children (3 to 15 years old) with acute uncomplicated falciparum malaria, who were divided into four age and sex-matched groups. The patients all received artesunate (4 mg/kg of body weight/day orally for 3 days and mefloquine as either (i) a single dose (25 mg/kg) on day 2 with food, (ii) a split dose (15 mg/kg on day 2 and 10 mg/kg on day 3) with food, (iii) a single dose (25 mg/kg) on day 0 without food, or (iv) a single dose (25 mg/kg) on day 2 without food. Delaying administration of mefloquine until day 2 was associated with a mean (95% confidence interval) increase in estimated oral bioavailability of 72% (36 to 109%). On day 2 coadministration with food did not increase mefloquine absorption significantly, and there were no significant differences between patients receiving split- and single-dose administration. In combination with artesunate, mefloquine administration should be delayed until the second or third day after presentation.
引用
收藏
页码:341 / 346
页数:6
相关论文
共 23 条
[1]  
[Anonymous], 1990, Trans R Soc Trop Med Hyg, V84 Suppl 2, P1
[2]   Food increases the bioavailability of mefloquine [J].
Crevoisier, C ;
Handschin, J ;
Barre, J ;
Roumenov, D ;
Kleinbloesem, C .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 53 (02) :135-139
[3]  
CREVOISIER C, 1992, 13TH P INT C TROP ME, P268
[4]   QUANTITATION OF FANSIMEF COMPONENTS (MEFLOQUINE + SULFADOXINE + PYRIMETHAMINE) IN HUMAN PLASMA BY 2 HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHODS [J].
EDSTEIN, MD ;
LIKA, ID ;
CHONGSUPHAJAISIDDHI, T ;
SABCHAREON, A ;
WEBSTER, HK .
THERAPEUTIC DRUG MONITORING, 1991, 13 (02) :146-151
[5]   DIVIDED-DOSE KINETICS OF MEFLOQUINE IN MAN [J].
FRANSSEN, G ;
ROUVEIX, B ;
LEBRAS, J ;
BAUCHET, J ;
VERDIER, F ;
MICHON, C ;
BRICAIRE, F .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1989, 28 (02) :179-184
[6]   CLINICAL PHARMACOKINETICS OF MEFLOQUINE [J].
KARBWANG, J ;
WHITE, NJ .
CLINICAL PHARMACOKINETICS, 1990, 19 (04) :264-279
[7]  
KARBWANG J, 1994, B WORLD HEALTH ORGAN, V72, P83
[8]   RANDOMIZED TRIAL OF ARTESUNATE AND MEFLOQUINE ALONE AND IN SEQUENCE FOR ACUTE UNCOMPLICATED FALCIPARUM-MALARIA [J].
LOOAREESUWAN, S ;
VIRAVAN, C ;
VANIJANONTA, S ;
WILAIRATANA, P ;
SUNTHARASAMAI, P ;
CHAROENLARP, P ;
ARNOLD, K ;
KYLE, D ;
CANFIELD, C ;
WEBSTER, K .
LANCET, 1992, 339 (8797) :821-824
[9]   The epidemiology of malaria in a Karen population on the western border of Thailand [J].
Luxemburger, C ;
Thwai, KL ;
White, NJ ;
Webster, HK ;
Kyle, DE ;
Maelankirri, L ;
Chongsuphajaisiddhi, T ;
Nosten, F .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1996, 90 (02) :105-111
[10]  
Na Bangchang K, 1993, Southeast Asian J Trop Med Public Health, V24, P221