Efficacy and safety of intermittent preventive treatment for malaria in schoolchildren: a systematic review

被引:22
作者
Matangila, Junior R. [1 ,2 ]
Mitashi, Patrick [1 ]
da Luz, Raquel A. Inocencio [2 ]
Lutumba, Pascal T. [1 ]
Van Geertruyden, Jean-Pierre [2 ]
机构
[1] Univ Kinshasa, Dept Med Tropicale, Fac Med, Kinshasa XI, DEM REP CONGO
[2] Univ Antwerp, Epidemiol Global Hlth Inst, B-2610 Antwerp, Belgium
关键词
Intermittent preventive treatment; Efficacy; Safety; Schoolchildren; Review; SULFADOXINE-PYRIMETHAMINE; CLINICAL MALARIA; BED NETS; CHILDREN; ANEMIA; IMPACT; TRANSMISSION; MORBIDITY; BURDEN; RESISTANCE;
D O I
10.1186/s12936-015-0988-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Intermittent preventive treatment (IPT) is a proven malaria control strategy in infants and pregnancy. School-aged children represent 26 % of the African population, and an increasing percentage of them are scholarized. Malaria is causing 50 % of deaths in this age group and malaria control efforts may shift the malaria burden to older age groups. Schools have been suggested as a platform for health interventions delivery (deworming, iron-folic acid, nutrients supplementation, (boost-) immunization) and as a possible delivery system for IPT in schoolchildren (IPTsc). However, the current evidence on the efficacy and safety of IPTsc is limited and the optimal therapeutic regimen remains controversial. Methods: A systematic search for studies reporting efficacy and safety of IPT in schoolchildren was conducted using PubMed, Web of Science, Clinicaltrials and WHO/ICTRP database, and abstracts from congresses with the following key words: intermittent, preventive treatment AND malaria OR Plasmodium falciparum AND schoolchildren NOT infant NOT pregnancy. Results: Five studies were identified. Most IPTsc regimes demonstrated substantial protection against malaria parasitaemia, with dihydroartemisinin-piperaquine (DP) given monthly having the highest protective effect (PE) (94 %; 95 % CI 93-96). Contrarily, SP did not provide any PE against parasitaemia. However, no IPT regimen provided a PE above 50 % in regard to anaemia, and highest protection was provided by SP+ amodiaquine (AQ) given four-monthly (50 %; 95 % CI 41-53). The best protection against clinical malaria was observed in children monthly treated with DP (97 %; 95 % CI 87-98). However, there was no protection when the drug was given three-monthly. No severe adverse events were associated with the drugs used for IPTsc. Conclusion: IPTsc may reduce the malaria-related burden in schoolchildren. However, more studies assessing efficacy of IPT in particular against malaria-related anaemia and clinical malaria in schoolchildren must be conducted.
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