Pentoxifylline as a Supportive Agent in the Treatment of Cerebral Malaria in

In an open, randomized, controlled therapeutic trial, 56 children with cerebral malaria (eM) were randomly assigned to receive standard Quinine regimen with or without pentoxifylline (10 mgjkgjday by continuous intravenous infusion). Pentoxifylline exerted an inhibitory effect on the synthesis of tumor necrosis factor (TNF), a possible mediator of CM. The 26 children who received pentoxifylline had significantly shorter comas than controls (median, 6 vs. 46 h; P <.001). Pentoxifylline recipients showed a trend toward a lower mortality, with a borderline signifi-cant difference (P =.055). The better outcome in the pentoxifylline group was associated with a decline in TNF serum levels on the third day of treatment in a few subjects that was not seen in controls. While alternative or concurrent mechanisms of action may beof some relevance, larger double-blind trials are needed to determine whether pentoxifylline has a therapeutic role in CM. Most mortality associated with Plasmodium falciparum in-fection is caused by cerebral malaria (CM) [I]. Even with the best chemotherapeutic regimens and the most appropriate management ofassociated disorders, CM has a mortality rate of 5%-38 % [2, 3] in children, with occasional neurologic se-quelae in survivors [4]