Pentoxifylline as an adjunct therapy in children with cerebral malaria
<p>Abstract</p> <p>Background</p> <p>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 ph...
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doaj-a0585fc8aba84accb02381d8c1b9e56c2020-11-25T01:30:48ZengBMCMalaria Journal1475-28752010-12-019136810.1186/1475-2875-9-368Pentoxifylline as an adjunct therapy in children with cerebral malariaKokwaro GilbertKivaya EstherOlola Christopher HOWamola BettyKöhler CarstenLell BertrandWypij DavidMithwani SadikTaylor Terrie EKremsner Peter GNewton Charles RJC<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>The small sample size does not permit definitive conclusions, but the mortality rate was unexpectedly high in the PTX group.</p> http://www.malariajournal.com/content/9/1/368 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kokwaro Gilbert Kivaya Esther Olola Christopher HO Wamola Betty Köhler Carsten Lell Bertrand Wypij David Mithwani Sadik Taylor Terrie E Kremsner Peter G Newton Charles RJC |
spellingShingle |
Kokwaro Gilbert Kivaya Esther Olola Christopher HO Wamola Betty Köhler Carsten Lell Bertrand Wypij David Mithwani Sadik Taylor Terrie E Kremsner Peter G Newton Charles RJC Pentoxifylline as an adjunct therapy in children with cerebral malaria Malaria Journal |
author_facet |
Kokwaro Gilbert Kivaya Esther Olola Christopher HO Wamola Betty Köhler Carsten Lell Bertrand Wypij David Mithwani Sadik Taylor Terrie E Kremsner Peter G Newton Charles RJC |
author_sort |
Kokwaro Gilbert |
title |
Pentoxifylline as an adjunct therapy in children with cerebral malaria |
title_short |
Pentoxifylline as an adjunct therapy in children with cerebral malaria |
title_full |
Pentoxifylline as an adjunct therapy in children with cerebral malaria |
title_fullStr |
Pentoxifylline as an adjunct therapy in children with cerebral malaria |
title_full_unstemmed |
Pentoxifylline as an adjunct therapy in children with cerebral malaria |
title_sort |
pentoxifylline as an adjunct therapy in children with cerebral malaria |
publisher |
BMC |
series |
Malaria Journal |
issn |
1475-2875 |
publishDate |
2010-12-01 |
description |
<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Methods</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusions</p> <p>The small sample size does not permit definitive conclusions, but the mortality rate was unexpectedly high in the PTX group.</p> |
url |
http://www.malariajournal.com/content/9/1/368 |
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