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dc.contributor.authorNamutangula, Beatrice
dc.contributor.authorNdeezi, Grace
dc.contributor.authorByarugaba, Justus S. Justus S.
dc.contributor.authorTumwine, James K
dc.date.accessioned2013-02-14T14:53:04Z
dc.date.available2013-02-14T14:53:04Z
dc.date.issued2007-10-24
dc.identifier.citationNamutangula, B., Ndeezi, G., Byarugaba, J. S. & Tumwine, J. K. (2007). Mannitol as adjunct therapy for childhood cerebral malaria in Uganda: a randomized clinical trial. Malaria Journal 2007, 6:138en_US
dc.identifier.issnhttp://www.malariajournal.com/content/6/1/138
dc.identifier.issn
dc.identifier.urihttp://dx.doi.org/10.1186/1475-2875-6-138
dc.identifier.urihttp://hdl.handle.net/10570/1072
dc.description© 2007 Namutangula et al; licensee BioMed Central Ltd. This article is available from: http://www.malariajournal.com/content/6/1/138en_US
dc.description.abstractBackground: Several reports have suggested that raised intracranial pressure (ICP) is a major contributor to death among children with cerebral malaria. Mannitol, an osmotic diuretic, effectively lowers ICP and is used to treat post-traumatic raised ICP. It is not clear whether intravenous mannitol given to children with cerebral malaria improves clinical outcome. The objective of this study was to determine the effect of mannitol as adjunct therapy on the clinical outcome of children with cerebral malaria. Methods: This randomized double-blind placebo controlled clinical trial was carried out at the Emergency Paediatric ward of Mulago Hospital, Uganda's national referral and teaching hospital. One hundred and fifty six children aged 6 to 60 months with cerebral malaria were randomized to either one dose of mannitol 1 g/kg or placebo, in addition to intravenous quinine. Main outcome measures included coma recovery time; time to sit unsupported, begin oral intake; duration of hospitalization; death and adverse effects. Results: Time to regain consciousness (p = 0.11), sit unsupported (p = 0.81), time to start oral intake (p = 0.13) and total coma duration (p = 0.07) were similar in both groups. There was no significant difference in the mortality between the placebo (13/80 or 16.3%) and mannitol (10/76 or 13.2%) groups: RR = 1.2 (CI 0.5–2.7). No adverse effects were observed after administration of mannitol. Conclusion: Mannitol had no significant impact on clinical outcome of cerebral malaria. It is difficult to recommend intravenous mannitol as adjunct therapy for childhood cerebral malaria.en_US
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.subjectCerebral malaria Ugandaen_US
dc.titleMannitol as adjunct therapy for childhood cerebral malaria in Uganda: a randomized clinical trialen_US
dc.typeJournal article, peer revieweden_US


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