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dc.contributor.authorLell, Bertrand
dc.contributor.authorKöhler, Carsten
dc.contributor.authorWamola, Betty
dc.contributor.authorOlola, Christopher HO
dc.contributor.authorKivaya, Esther
dc.contributor.authorKokwaro, Gilbert
dc.contributor.authorWypij, David
dc.contributor.authorMithwani, Sadik
dc.contributor.authorTaylor, Terrie E
dc.contributor.authorKremsner, Peter G
dc.contributor.authorNewton, Charles RJC
dc.date.accessioned2013-03-19T15:58:35Z
dc.date.available2013-03-19T15:58:35Z
dc.date.issued2010-12-21
dc.identifier.citationMalaria Journal. 2010 Dec 21;9(1):368
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/21176151
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/14719
dc.description.abstractAbstract Background Pentoxifylline (PTX) affects many processes that may contribute to the pathogenesis of severe malaria and it has been shown to reduce the duration of coma in children with cerebral malaria. This pilot study was performed to assess pharmacokinetics, safety and efficacy of PTX in African children with cerebral malaria. Methods Ten children admitted to the high dependency unit of the Kilifi District Hospital in Kenya with cerebral malaria (Blantyre coma score of 2 or less) received quinine plus a continuous infusion of 10 mg/kg/24 hours PTX for 72 hours. Five children were recruited as controls and received normal saline instead of PTX. Plasma samples were taken for PTX and tumour necrosis factor (TNF) levels. Blantyre Coma Score, parasitemia, hematology and vital signs were assessed 4 hourly. Results One child (20%) in the control group died, compared to four children (40%) in the PTX group. This difference was not significant (p = 0.60). Laboratory parameters and clinical data were comparable between groups. TNF levels were lower in children receiving PTX. Conclusions The small sample size does not permit definitive conclusions, but the mortality rate was unexpectedly high in the PTX group.
dc.titlePentoxifylline as an adjunct therapy in children with cerebral malaria
dc.typeJournal Article
dc.date.updated2013-03-19T15:58:36Z
dc.description.versionPeer Reviewed
dc.language.rfc3066en
dc.rights.holderBertrand Lell et al.; licensee BioMed Central Ltd.


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