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1.
Am J Trop Med Hyg ; 48(2): 193-7, 1993 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-8447522

RESUMO

To examine the effect of iron chelation against human malaria, 37 Zambians with asymptomatic Plasmodium falciparum infections were randomly assigned to 72-hr infusions of desferrioxamine B or placebo. Mean concentrations of ring forms decreased significantly with desferrioxamine B (P < 0.001) but not with a placebo. Over seven days of observation, mean parasite concentrations remained at the initial levels in six individuals originally given placebo, but decreased promptly with administration of desferrioxamine B (P = 0.001). Mean parasitemia was significantly lower for up to four weeks in 16 subjects treated with desferrioxamine B when compared with the eight who had received placebo only (P = 0.027). We conclude that iron chelation has antiplasmodial activity and may offer a new therapeutic strategy for falciparum malaria.


Assuntos
Desferroxamina/uso terapêutico , Malária Falciparum/tratamento farmacológico , Adulto , Animais , Desferroxamina/administração & dosagem , Desferroxamina/farmacologia , Feminino , Humanos , Bombas de Infusão , Malária Falciparum/sangue , Masculino , Plasmodium falciparum/efeitos dos fármacos
2.
Trans R Soc Trop Med Hyg ; 92(2): 214-8, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9764337

RESUMO

To examine the effect of iron chelation on mortality in cerebral malaria, we enrolled 352 children in a trial of deferoxamine in addition to standard quinine therapy at 2 centres in Zambia, one rural and one urban. Entrance criteria included age < 6 years, Plasmodium falciparum parasitaemia, normal cerebral spinal fluid, and unrousable coma. Deferoxamine (100 mg/kg/d infused for a total of 72 h) or placebo was added to a 7 d regimen of quinine that included a loading dose. Mortality overall was 18.3% (32/175) in the deferoxamine group and 10.7% (19/177) in the placebo group (adjusted odds ratio 1.8; 95% confidence interval 0.9-3.6; P = 0.074). At the rural study site, mortality was 15.4% (18/117) with deferoxamine compared to 12.7% (15/118) with placebo (P = 0.78, adjusted for covariates). At the urban site, mortality was 24.1% (14/58) with deferoxamine and 6.8% (4/59) with placebo (P = 0.061, adjusted for covariates). Among survivors, there was a non-significant trend to faster recovery from coma in the deferoxamine group (adjusted odds ratio 1.2; 95% confidence interval 0.97-1.6; P = 0.089). Hepatomegaly was significantly associated with higher mortality, while splenomegaly was associated with lower mortality. This study did not provide evidence for a beneficial effect on mortality in children with cerebral malaria when deferoxamine was added to quinine, given in a regimen that included a loading dose.


Assuntos
Antídotos/uso terapêutico , Antimaláricos/uso terapêutico , Desferroxamina/uso terapêutico , Quelantes de Ferro/uso terapêutico , Malária Cerebral/tratamento farmacológico , Malária Cerebral/mortalidade , Parasitemia/tratamento farmacológico , Parasitemia/mortalidade , Quinina/uso terapêutico , Criança , Pré-Escolar , Coma/tratamento farmacológico , Método Duplo-Cego , Quimioterapia Combinada , Feminino , Febre/tratamento farmacológico , Humanos , Lactente , Masculino , Estudos Prospectivos , Taxa de Sobrevida , Resultado do Tratamento , Zâmbia/epidemiologia
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