Pentoxifylline as an adjunct therapy in children with cerebral malaria
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Published on: July 17, 2014
Bertrand Lell1, Carsten Köhler, Betty Wamola
1KEMRI Centre for Geographic Medicine Research (Coast), Kilifi, Kenya. bertrand.lell@uni-tuebingen.de
Insights
Pentoxifylline (PTX) did not significantly alter mortality in African children with cerebral malaria. While TNF levels were lower in the PTX group, the study noted unexpectedly high mortality rates.
Area of Science:
- Pediatric infectious diseases
- Pharmacology and pharmacokinetics
- Malariology
Background:
- Severe malaria, particularly cerebral malaria, poses a significant threat to children in endemic regions.
- Pentoxifylline (PTX) has demonstrated potential in modulating disease processes relevant to malaria pathogenesis.
- Previous research indicated PTX could shorten coma duration in pediatric cerebral malaria.
Purpose of the Study:
- To evaluate the pharmacokinetics, safety, and efficacy of Pentoxifylline (PTX) in African children diagnosed with cerebral malaria.
- To assess the impact of PTX on clinical outcomes and biological markers in this patient population.
Main Methods:
- A pilot study involving ten children with cerebral malaria receiving quinine plus a continuous infusion of PTX (10 mg/kg/24 hours for 72 hours).
- A control group of five children received quinine with normal saline.
- Measurements included plasma PTX and tumor necrosis factor (TNF) levels, Blantyre Coma Score, parasitemia, hematology, and vital signs.
Main Results:
- Mortality was 40% in the PTX group versus 20% in the control group, a difference that was not statistically significant (p = 0.60).
- Laboratory parameters and clinical data showed no significant differences between the groups.
- Children treated with PTX exhibited lower levels of tumor necrosis factor (TNF).
Conclusions:
- The study's small sample size precludes definitive conclusions regarding PTX efficacy.
- An unexpectedly high mortality rate was observed in the Pentoxifylline (PTX) treatment group.
- Further investigation with larger cohorts is warranted to ascertain the safety and efficacy of PTX in pediatric cerebral malaria.
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.
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