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1.
Epilepsia ; 37(9): 822-32, 1996 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8814094

RESUMO

PURPOSE: The main purpose of this prospective study was to analyze whether 1 year of treatment was as effective as 3 years with respect to remission rate in children with idiopathic epilepsy. METHODS: Treatment for epileptic seizures was started in 207 children aged 2-16 years. They were randomized to treatment for 1 or 3 years. At the end of the predetermined treatment period, 161 children had been seizure-free for 6 months and the treatment could be gradually withdrawn. RESULTS: The overall remission rate in our group of patients was significantly higher (71%) in the group treated for 3 years than in the group treated for 1 year (53%). However, comparison of remission rates between patients with different seizure types showed statistically significant differences in outcome depending on duration of treatment only in children with complex partial seizures (CPS). CONCLUSIONS: Our results show that 1 year of treatment can be recommended in children with benign partial epilepsy with rolandic spikes (BECT) and in children with simple partial seizures (SPS) but is clearly insufficient in children with CPS. A proper seizure classification is one important tool, although not sufficient, in offering recommendations concerning the duration of treatment in children with idiopathic epilepsy.


Assuntos
Anticonvulsivantes/uso terapêutico , Epilepsia/tratamento farmacológico , Adolescente , Criança , Pré-Escolar , Epilepsias Parciais/tratamento farmacológico , Epilepsia Parcial Complexa/tratamento farmacológico , Feminino , Seguimentos , Humanos , Masculino , Prognóstico , Estudos Prospectivos , Recidiva , Fatores de Tempo , Resultado do Tratamento
2.
Acta Paediatr ; 82(1): 66-70, 1993 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-8453225

RESUMO

Epileptic seizures caused by tumors in children have been regarded as uncommon. We have studied 99 consecutive cases of brain tumors during the period 1980-1987. In 20 cases the tumor was localized to one of the hemipheres and 10 of the cases had seizures, in 9 as the only initial symptom. Details of the clinical picture and the course are presented. Delay from initial symptoms to correct diagnosis was considerable in 4 cases--more than six years. The factors mainly responsible for this delay were: initial EEG normal or soon normalized, misinterpretation of computerized tomography and seizure freedom with or without antiepileptic drug treatment. We conclude that regional slowing in the EEG is a common, although not obligatory, finding. Computerized tomography should be performed in all children with newly presented epilepsy of partial type, except for those with benign partial epilepsy with centro-temporal spikes.


Assuntos
Neoplasias Encefálicas/complicações , Epilepsia/etiologia , Adolescente , Astrocitoma/complicações , Astrocitoma/diagnóstico , Neoplasias Encefálicas/diagnóstico , Criança , Pré-Escolar , Eletroencefalografia , Feminino , Humanos , Masculino , Oligodendroglioma/diagnóstico , Estudos Retrospectivos , Fatores de Tempo , Tomografia Computadorizada por Raios X
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