Abstract:A cohort of hundred children with febrile convulsions, in the age group of 3 months to 5 years were followed up prospectively for one year to study the natural course of the illness, and to determine if specific factors would increase the risk of recurrence of febrile convulsions. The risk factors studied were age of onset under one year, long duration of convulsion (more than 15 minutes), family history of febrile convulsion or epilepsy and combination of two or all of the above factors. Four groups of childr… Show more
“…Pavlidou et al [3] in their study have shown that young age plays a major role in susceptibility of FS, and if there is an individual temperature threshold level above which a [6] showed that children with recurrent seizures were younger at age of onset and had more often family history of FS; and on the whole age less than 16 months at the moment of first convulsion and existence of family history of epilepsy or FS increases the recurrence of FS. Another study in which risk factors of FS were studied including 1) age of onset under one year, 2) long duration of convulsion (more than 15 minutes) and 3) family history of epilepsy or convulsion) showed that although all the groups with risk factors had a trend towards a higher recurrence rate in comparison to controls, difference observed clinically was not statistically significant [7]. In our study, a significant correlation is present between FS and age less than 12 months.…”
To evaluate the risk factors for recurrence in febrile seizures, a prospective study was conducted in children with first time febrile seizures. Factors recorded include 1) family history of febrile seizures, 2) family history of epilepsy, 3) type of febrile seizures (focal or generalized), 4) developmental status and neurological examination of the patient 5) patients' age and temperature. For each patient an electroencephalography (EEG) was recorded within 2 weeks of seizures and EEGs having epileptiform waves were considered abnormal. Patients were followed from March 2003 until February 2005 for seizure recurrence. Of 98 children included in the study, 68 (60.4%) were boys and 38 (39.4%) girls. Sixty patients were in the age group of 1?3 years (62.5%) and 80 in age group of 6 months ? 3 years (83.3%). Recurrence of febrile seizures was seen in 34 cases (35.4%). Recurrence rate in children less than 12 months of age was 45%, in children aged 1?3 years it was 28% and in children older than 3 years 25%. There was a significant correlation between age less than 12 months and recurrence of febrile seizures (P < 0.05). In patients with a positive family history, recurrence rate was 38.9% and in those with negative family history it was 22% (P < 0.05). Abnormal EEG was seen in 16% of girls and 34% boys. In conclusion, recurrence of febrile seizures is more frequent during the first year after initial seizure, with age less than 12 months and in patients with a positive family history for febrile seizures.
“…Pavlidou et al [3] in their study have shown that young age plays a major role in susceptibility of FS, and if there is an individual temperature threshold level above which a [6] showed that children with recurrent seizures were younger at age of onset and had more often family history of FS; and on the whole age less than 16 months at the moment of first convulsion and existence of family history of epilepsy or FS increases the recurrence of FS. Another study in which risk factors of FS were studied including 1) age of onset under one year, 2) long duration of convulsion (more than 15 minutes) and 3) family history of epilepsy or convulsion) showed that although all the groups with risk factors had a trend towards a higher recurrence rate in comparison to controls, difference observed clinically was not statistically significant [7]. In our study, a significant correlation is present between FS and age less than 12 months.…”
To evaluate the risk factors for recurrence in febrile seizures, a prospective study was conducted in children with first time febrile seizures. Factors recorded include 1) family history of febrile seizures, 2) family history of epilepsy, 3) type of febrile seizures (focal or generalized), 4) developmental status and neurological examination of the patient 5) patients' age and temperature. For each patient an electroencephalography (EEG) was recorded within 2 weeks of seizures and EEGs having epileptiform waves were considered abnormal. Patients were followed from March 2003 until February 2005 for seizure recurrence. Of 98 children included in the study, 68 (60.4%) were boys and 38 (39.4%) girls. Sixty patients were in the age group of 1?3 years (62.5%) and 80 in age group of 6 months ? 3 years (83.3%). Recurrence of febrile seizures was seen in 34 cases (35.4%). Recurrence rate in children less than 12 months of age was 45%, in children aged 1?3 years it was 28% and in children older than 3 years 25%. There was a significant correlation between age less than 12 months and recurrence of febrile seizures (P < 0.05). In patients with a positive family history, recurrence rate was 38.9% and in those with negative family history it was 22% (P < 0.05). Abnormal EEG was seen in 16% of girls and 34% boys. In conclusion, recurrence of febrile seizures is more frequent during the first year after initial seizure, with age less than 12 months and in patients with a positive family history for febrile seizures.
“…Among the studies (Table 3) comparing use of phenobarbital and placebo, in five ones 4,6,[13][14][15] phenobarbital reduced the recurrence risk for febrile seizures. But in 3 studies 4,13-15 , the relative reduced risk was not significant.…”
Section: Discussionmentioning
confidence: 99%
“…There are studies demonstrating a relation between the number of febrile seizures, mainly the complex ones, and the risk for epilepsy [2][3] . Besides, recurrent convulsions may be deleterious to intellectual development 4 . The prevention of febrile seizures might be benefi-cial, but the long-term management is controversial [5][6][7] .…”
-Convulsions triggered by fever are the most common type of seizures in childhood, and 20% to 30% of them have recurrence. The prophylactic treatment is still controversial, so we performed a systematic review to find out the effectiveness of continuous phenobarbital and intermittent diazepam compared to placebo for febrile seizure recurrence. Method: Only randomized, double-blind, placebo-controlled trials were analyzed. The recurrence of febrile seizure was assessed for each drug. Results: Ten eligible clinical trials were included. Febrile seizure recurrence was smaller in children treated with diazepam or phenobarbital than in placebo group. Prophylaxis with either phenobarbital or diazepam reduces recurrences of febrile seizures. The studies were clinical, methodological, and statistically heterogeneous. Conclusion: The effectiveness of phenobarbital and diazepam could not be demonstrated because clinical trials were heterogeneous, and the recommendation for treatment recurrence should rely upon the experience of the assistant physician yet.KEY WORDS: prophylactic treatment, febrile seizures, intermittent diazepam, continuous phenobarbital.Diazepam intermitente e fenobarbital contínuo para tratamento da recorrência de convulsões febris: uma revisão sistemática com metanálise RESUMO -As convulsões desencadeadas por febre são muito comuns na infância e 20% a 30% delas apresentam recorrência. O tratamento profilático, no entanto, ainda é controverso, motivo porque realizamos uma revisão sistemática para avaliar a eficácia do tratamento da recidiva de convulsão febril com diazepam e fenobarbital comparados a placebo. Método: Analisamos somente estudos randomizados, duplo-cegos, controlados, utilizando fenobarbital contínuo ou diazepam intermitente versus placebo. Resultados: Dez ensaios clínicos foram incluídos. A recorrência de convulsão febril foi menor no grupo das crianças tratadas com diazepam ou fenobarbital em relação ao controle. Tanto diazepam quanto fenobarbital reduziram as recorrências da convulsão febril. Os estudos foram clínica, metodológica e estatisticamente heterogêneos. Conclusão: A eficácia do fenobarbital e diazepam não pôde ser demonstrada nesta metanálise por causa da heterogeneidade dos ensaios clínicos, e a recomendação para tratamento de recorrência deve basear-se na experiência clínica de cada médico. PALAVRAS-CHAVE: tratamento profilático, convulsões febris, diazepam intermitente, fenobarbital contínuo.
“…In addition, it has been used widely prophylactically to prevent recurrence of febrile seizures. Some studies have found that long‐term phenobarbital therapy reduces recurrence after simple or atypical febrile convulsions (Wolf et al., 1977; Camfield et al., 1980; Bacon et al., 1981; Mamelle et al., 1984; Thilothammal et al., 1993), whereas others have found no significant difference when compared to placebo or intermittent diazepam (Knudsen & Vestermark, 1978; Mckinlay & Newton, 1989). Two meta‐analytic reviews concluded that, despite a statistically significant benefit in seizure rate reduction, the heterogeneity of participating studies and side effects did not allow any recommendation for using phenobarbital as long‐term prophylaxis (Rantala et al., 1997; Masuko et al., 2003).…”
Summary
Phenobarbital (phenobarbitone) was first used as an antiepileptic drug 100 years ago, in 1912. This article tells the story of the discovery of its antiepileptic action, its early development, and the subsequent course of its clinical use over the 100‐year period. The side effects, pharmacokinetics, and misuse of barbiturates are considered, along with the more recent clinical trials and the drug’s current clinical utilization. The introduction of controlled drug regulations, the comparative cost of phenobarbital, and its inclusion on the World Health Organization (WHO) essential drug list are discussed. It is one of the few drugs on the formulary in 1912 that is still listed today, and remarkably its efficacy in epilepsy has not been significantly bettered. The current recommendation by the WHO is that phenobarbital should be offered as the first option for therapy for convulsive epilepsy in adults and children if availability can be ensured. This is rated as a strong recommendation because of the proven efficacy and low cost of phenobarbital, and despite its perceived side‐effect profile and the practical problems of access. Whether this recommendation puts “a hierarchy on the brain,” as has been suggested, is arguable. Much still needs to be learned about the drug’s effects, and the issues raised by phenobarbital have lessons for all antiepileptic drug therapy.
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