Efficacy of sulfadoxine/pyrimethamine in the treatment of uncomplicated Plasmodium falciparum malaria in Republic of Congo

被引:22
作者
Nsimba, B [1 ]
Malonga, DA
Mouata, AM
Louya, F
Kiori, J
Malanda, M
Yocka, D
Oko-Ossho, J
Ebata-Mongo, S
Le Bras, J
机构
[1] Minist Hlth, Div Dis Control, Natl Malaria Control Program, POB 2846, Brazzaville, Rep Congo
[2] Makelekele Hosp, Dept Paediat, Brazzaville, Rep Congo
[3] Tie Tie Hosp, Dept Paediat, Pointe Noire, Rep Congo
[4] Jane Vialle Hlth Ctr, Brazzaville, Rep Congo
[5] Hop Bichat Claude Bernard, Natl Malaria Reference Ctr, F-75877 Paris 18, France
[6] Univ Paris 05, Parasitol Lab, Paris, France
关键词
D O I
10.4269/ajtmh.2004.70.133
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Congo is facing frequent failures of treatment of Plasmodium falciparum malaria with chloroquine (CQ), which is still recommended and used as a first-line drug. In Pointe-Noire and Brazzaville, the two largest cities that contain approximately 60% of the population of Congo, we compared the efficacy of CQ versus sulfadoxine/pyrimethamine (SP) for treatment of uncomplicated malaria in children 6-59 months old (mean = 33 months) using the standard World Health Organization (WHO) 14-day in vivo test in two phases between 1999 and 2002. Patients enrolled were randomly assigned to receive SP (25 mg/kg of sulfadoxine and 1.25 mg/kg of pyrimethamine) or CO (25 mg/kg). In the first phase of the study, 46 patients were assigned to the CQ (n = 23) or SP (n = 23) groups in Pointe-Noire and 52 children were assigned to the CQ (n = 26) or to SP (n = 26) groups in Brazzaville. Results were interpreted according to the WHO lot quality assurance sampling method, and treatment failure rates for SP versus CQ were < 25% versus > 25% in both cities. In the second phase of the study, we accurately determined the actual proportion of treatment failures for SP in Brazzaville. Thus, in 75 of the 80 children enrolled and followed-up until day 14, no clinical or parasitologic failure was recorded and no serious adverse reaction was observed. Since the CQ treatment failure rate exceeds the unacceptable upper limit, SP seems well to be an appropriate alternative for the first-line treatment of uncomplicated P. falciparum malaria, at least in the settings of the present study.
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页码:133 / 138
页数:6
相关论文
共 28 条
[11]  
Guiyedi V, 2001, B SOC PATHOL EXOT, V94, P253
[12]   Sensitivities of malaria in Zaire [J].
Hodes, RM ;
Wolday, D ;
Kibreab, T .
TROPICAL DOCTOR, 1997, 27 (03) :190-190
[13]  
LEBRAS J, 1985, LANCET, V2, P1071
[14]   Survival probability of drug resistant mutants in malaria parasites [J].
Mackinnon, MJ .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1997, 264 (1378) :53-59
[15]   SULFADOXINE PYRIMETHAMINE OR CHLOROQUINE CLINDAMYCIN TREATMENT OF GABONESE SCHOOL-CHILDREN INFECTED WITH CHLOROQUINE-RESISTANT MALARIA [J].
METZGER, W ;
MORDMULLER, B ;
GRANINGER, W ;
BIENZLE, U ;
KREMSNER, PG .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1995, 36 (04) :723-728
[16]  
MOUNT DL, 1989, B WORLD HEALTH ORGAN, V67, P295
[17]   Chemoresistance of Plasmodium falciparum in urban Yaounde (Cameroon).: Part One:: Monitoring in vitro and in vivo of Plasmodium falciparum resistance to chloroquine between 1994 and 1999 in Yaounde (Cameroon) [J].
Ringwald, P ;
Ekobo, AS ;
Keundjian, A ;
Mangamba, DK ;
Basco, LK .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2000, 5 (09) :612-619
[18]   Pyrimethamine/sulfadoxine for treating uncomplicated Plasmodium falciparum malaria in young children in Gabon [J].
SchmidtOtt, R ;
Luckner, D ;
Lehman, LG ;
Lell, B ;
Matousek, P ;
Greve, B ;
Kremsner, PG .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1997, 91 (05) :578-579
[19]   Amodiaquine, sulfadoxine/pyrimethamine, and combination therapy for treatment of uncomplicated falciparum malaria in Kampala, Uganda: a randomised trial [J].
Staedke, SG ;
Kamya, MR ;
Dorsey, G ;
Gasasira, A ;
Ndeezi, G ;
Charlebois, ED ;
Rosenthal, PJ .
LANCET, 2001, 358 (9279) :368-374
[20]  
STOTT GJ, 1995, B WORLD HEALTH ORGAN, V73, P369