Seasonal intermittent preventive treatment with artesunate and sulfadoxine-pyrimethamine for prevention of malaria in Senegalese children:: a randomised, placebo-controlled, double-blind trial

被引:164
作者
Cissé, B
Sokhna, C
Boulanger, D
Milet, J
Bâ, EH
Richardson, K
Hallett, R
Sutherland, C
Simondon, K
Simondon, F
Alexander, N
Gaye, O
Targett, G
Lines, J
Greenwood, B
Trape, JF
机构
[1] London Sch Hyg & Trop Med, London WC1B 3DP, England
[2] Inst Rech Dev, Dakar, Senegal
[3] Univ Cheikh Anta Diop Dakar, Dakar, Senegal
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0140-6736(06)68264-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In the Sahel and sub-Sahelian regions of Africa, malaria transmission is highly seasonal. During a short period of high malaria transmission, mortality and morbidity are high in children under age 5 years. We assessed the efficacy of seasonal intermittent preventive treatment-a lull dose of antimalarial treatment given at defined times without previous testing for malaria infection. Methods We did a randomised, placebo-controlled, double-blind trial of the effect of intermittent preventive treatment on morbidity from malaria in three health-care centres in Niakhar, a rural area of Senegal. 1136 children aged 2-59 months received either one dose of artesunate plus one dose of sulfadoxine-pyrimethamine or two placebos on three occasions during the malaria transmission season. The primary outcome was a first or single episode of clinical malaria detected through active or passive case detection. Primary analysis was by intention-to-treat. This study is registered with ClinicalTrials.gov, number NCT00132561. Findings During 13 weeks of follow-up, the intervention led to an 86% (95% CI 80-90) reduction in the occurrence of clinical episodes of malaria. With passive case detection, protective efficacy against malaria was 86% (77-92), and when detected actively was 86% (78-91). The incidence of malaria in children on active drugs was 308 episodes per 1000 person-years at risk, whereas in those on placebo it was 2250 episodes per 1000 person-years at risk. 13 children were not included in the intention-to-treat analysis, which was restricted to children who received a first dose of antimalarial or placebo. There was an increase in vomiting in children who received the active drugs, but generally the intervention was well tolerated. Interpretation Intermittent preventive treatment could be highly effective for prevention of malaria in children under 5 years of age living in areas of seasonal malaria infection.
引用
收藏
页码:659 / 667
页数:9
相关论文
共 37 条
[1]  
ALLEN SJ, 1990, J TROP MED HYG, V93, P313
[2]   SEASONAL-VARIATION OF PEDIATRIC DISEASES IN THE GAMBIA, WEST-AFRICA [J].
BREWSTER, DR ;
GREENWOOD, BM .
ANNALS OF TROPICAL PAEDIATRICS, 1993, 13 (02) :133-146
[3]   Decline of infant and child mortality rates in rural Senegal over a 37-year period (1963-1999) [J].
Delaunay, V ;
Etard, JF ;
Préziosi, MP ;
Marra, A ;
Simondon, F .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2001, 30 (06) :1286-1293
[4]   Randomized, controlled trial of daily iron supplementation and intermittent sulfadoxine-pyrimethamine for the treatment of mild childhood anemia in western Kenya [J].
Desai, MR ;
Mei, JV ;
Kariuki, SK ;
Wannemuehler, KA ;
Phillips-Howard, PA ;
Nahlen, BL ;
Kager, PA ;
Vulule, JM ;
ter Kuile, FO .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (04) :658-666
[5]  
DICKO A, 2004, AM J TROP MED HYG S, V71, P6
[6]   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
[7]   Childhood mortality and probable causes of death using verbal autopsy in Niakhar, Senegal, 1989-2000 [J].
Etard, JF ;
Le Hesran, JY ;
Diallo, A ;
Diallo, JP ;
Ndiaye, JL ;
Delaunay, V .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2004, 33 (06) :1286-1292
[8]  
Geerligs PDP, 2003, B WORLD HEALTH ORGAN, V81, P205
[9]  
Greenwood B, 2004, AM J TROP MED HYG, V70, P1
[10]  
GREENWOOD BM, 1988, LANCET, V1, P1121