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dc.contributor.authorNdibazza, Juliet
dc.contributor.authorMpairwe, Harriet
dc.contributor.authorWebb, Emily L.
dc.contributor.authorMawa, Patrice A.
dc.contributor.authorNampijja, Margaret
dc.contributor.authorMuhang, Lawrence
dc.contributor.authorKihembo, Macklyn
dc.contributor.authorLule, Swaib A.
dc.contributor.authorRutebarika, Diana
dc.contributor.authorApule, Barbara
dc.contributor.authorAkello, Florence
dc.contributor.authorAkurut, Hellen
dc.contributor.authorOduru, Gloria
dc.contributor.authorNaniima, Peter
dc.contributor.authorKizito, Dennison
dc.contributor.authorKizza, Moses
dc.contributor.authorKizindo, Robert
dc.contributor.authorTweyongere, Robert
dc.contributor.authorAlcock, Katherine J.
dc.contributor.authorMuwanga, Moses
dc.contributor.authorElliott, Alison M.
dc.date.accessioned2019-02-14T12:20:18Z
dc.date.available2019-02-14T12:20:18Z
dc.date.issued2012
dc.identifier.citationNdibazza, J. et al. (2012). Impact of Anthelminthic Treatment in Pregnancy and Childhood on Immunisations, Infections and Eczema in Childhood: A Randomised Controlled Trial. Uganda Martyrs University, Nkozi: Uganda Martyrs University.en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12280/1368
dc.description.abstractBackground: Helminth infections may modulate immune responses to unrelated pathogens and allergens; these effects may commence prenatally. We addressed the hypothesis that anthelminthic treatment in pregnancy and early childhood would improve responses to immunisation and modulate disease incidence in early childhood with both beneficial and detrimental effects. A randomised, double-blind, placebo-controlled trial was conducted in Entebbe, Uganda[ISRCTN32849447]. In three independent randomisations, 2507 pregnant women were allocated to receive single-dose albendazole or placebo, and praziquantel or placebo; 2016 of their offspring were randomised to receive quarterly singledose albendazole or placebo from age 15 months to 5 years. Primary outcomes were post-immunisation recall responses to BCG and tetanus antigens, and incidence of malaria, diarrhoea, and pneumonia; incidence of eczema was an important secondary outcome. Analysis was by intention-to-treat. Of 2345 live births, 1622 (69%) children remained in follow-up at age 5 years. 68% of mothers at enrolment, and 11% of five-year-olds, had helminth infections. Maternal hookworm and Schistosoma mansoni were effectively treated by albendazole and praziquantel, respectively; and childhood hookworm and Ascaris by quarterly albendazole. Incidence rates of malaria, diarrhoea, pneumonia, and eczema were 34, 65, 10 and 5 per 100 py, respectively. Albendazole during pregnancy caused an increased rate of eczema in the children (HR 1.58 (95% CI 1.15–2.17), p = 0.005). Quarterly albendazole during childhood was associated with reduced incidence of clinical malaria (HR 0.85 (95% CI 0.73–0.98), p = 0.03). There were no consistent effects of the interventions on any other outcome. Routine use of albendazole in pregnancy may not always be beneficial, even in tropical developing countries.By contrast, regular albendazole treatment in preschool children may have an additional benefit for malaria control wherehelminths and malaria are co-endemic. Given the low helminth prevalence in our children, the effect of albendazole on malaria is likely to be direct.en_US
dc.language.isoenen_US
dc.publisherUganda Martyrs Universityen_US
dc.subjectAnthelminthic Treatmenten_US
dc.subjectPregnancy & Childhooden_US
dc.subjectImmunisationsen_US
dc.subjectInfections & Eczemaen_US
dc.titleImpact of Anthelminthic Treatment in Pregnancy and Childhood on Immunisations, Infections and Eczema in Childhood: A Randomised Controlled Trialen_US
dc.typeArticleen_US


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