Efficacy of chloroquine, amodiaquine, sulphadoxine- pyrimethamine and combination therapy with artesunate in Mozambican children with non-complicated malaria

被引:70
作者
Abacassamo, F
Enosse, S
Aponte, JJ
Gómez-Olivé, FX
Quintó, L
Mabunda, S
Barreto, A
Magnussen, P
Ronn, AM
Thompson, R
Alonso, PL
机构
[1] Hosp Clin Barcelona, Ctr Int Hlth, IDIBAPS, Barcelona, Spain
[2] Ctr Invest Saude Manhica, Manhica, Mozambique
[3] Univ Eduardo Mondlane, Fac Med, Mondlane, Maputo, Mozambique
[4] Minist Saude, Inst Nacl Saude, Maputo, Mozambique
[5] Minist Saude, Direccao Nacl Saude, Natl Malaria Control Programme, Maputo, Mozambique
[6] Danish Bilharziasis Labs, Copenhagen, Denmark
[7] Univ Copenhagen, Dept Int Hlth, Ctr Med Parasitol, Copenhagen, Denmark
关键词
Plasmodium falciparum; antimalarials; first-line treatment; national policy; drug resistance; combination therapy;
D O I
10.1046/j.1365-3156.2003.01182.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
This paper reports a two-phase study in Manhica district, Mozambique: first we assessed the clinical efficacy and parasitological response of Plasmodium falciparum to chloroquine (CQ), sulphadoxine-pyrimethamine (SP) and amodiaquine (AQ), then we tested the safety and efficacy in the treatment of uncomplicated malaria, of three combinations: AQ + SP, artesunate (AR) + SP and AQ + AR. Based on the WHO (1996, WHO/MAL/96.1077) in vivo protocol, we conducted two open, randomized, clinical trials. Children aged 6-59 months with axillary body temperature greater than or equal to37.5 degreesC and non-complicated malaria were randomly allocated to treatment groups and followed up for 21 days (first and second trial) and 28 days (first trial). The therapeutic efficacy of AQ (91.6%) was better than that of SP (82.7%) and CQ (47.1%). After 14 days, 69% of the strains were parasitologically resistant to CQ, 21.4% to SP and 26% to AQ. Co-administration of AQ + SP, AR + SP and AQ + AR was safe and had 100% clinical efficacy at 14-day follow-up. The combination therapies affected rapid fever clearance time and reduced the incidence of gametocytaemia during follow-up.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 34 条
[1]   RANDOMIZED TRIAL OF EFFICACY OF SPF66 VACCINE AGAINST PLASMODIUM-FALCIPARUM MALARIA IN CHILDREN IN SOUTHERN TANZANIA [J].
ALONSO, PL ;
SMITH, T ;
SCHELLENBERG, JRMA ;
MASANJA, H ;
MWANKUSYE, S ;
URASSA, H ;
DEAZEVEDO, IB ;
CHONGELA, J ;
KOBERO, S ;
MENENDEZ, C ;
HURT, N ;
THOMAS, MC ;
LYIMO, E ;
WEISS, NA ;
HAYES, R ;
KITUA, AY ;
LOPEZ, MC ;
KILAMA, WL ;
TEUSCHER, T ;
TANNER, M .
LANCET, 1994, 344 (8931) :1175-1181
[2]  
[Anonymous], 1996, WHOMAL961077
[3]   Molecular basis of in vivo resistance to sulfadoxine-pyrimethamine in African adult patients infected with Plasmodium falciparum malaria parasites [J].
Basco, LK ;
Tahar, R ;
Ringwald, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (07) :1811-1814
[4]  
Bloland PB, 2000, B WORLD HEALTH ORGAN, V78, P1378
[5]   Amodiaquine remains effective for treating uncomplicated malaria in West and Central Africa [J].
Brasseur, P ;
Guiguemde, R ;
Diallo, S ;
Guiyedi, V ;
Kombila, A ;
Ringwald, P ;
Olliaro, P .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1999, 93 (06) :645-650
[6]  
DGEDGE M, 1998, AVALIACAO IN VIVO EF
[7]  
DGEDGE M, 1997, REV MED MOCAMBIQUE, V7, P12
[8]  
DILLEN JV, 1999, T ROY SOC TROP MED H, V93, P185
[9]   A randomized safety and tolerability trial of artesunate plus sulfadoxine-pyrimethamine versus sulfadoxine-pyrimethamine alone for the treatment of uncomplicated malaria in Gambian children [J].
Doherty, JF ;
Sadiq, AD ;
Bayo, L ;
Alloueche, A ;
Olliaro, P ;
Milligan, P ;
von Seidlein, L ;
Pinder, M .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1999, 93 (05) :543-546
[10]   Sulfadoxine/pyrimethamine alone or with amodiaquine or artesunate for treatment of uncomplicated malaria: a longitudinal randomised trial [J].
Dorsey, G ;
Njama, D ;
Kamya, MR ;
Cattamanchi, A ;
Kyabayinze, D ;
Staedke, SG ;
Gasasira, A ;
Rosenthal, PJ .
LANCET, 2002, 360 (9350) :2031-2038