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Response to sequential treatment schedules in childhood epilepsy: risk for development of refractory epilepsy
J Ramos-Lizana1, P Aguilera-López, J Aguirre-Rodríguez
1Pediatric Neurology Unit, Department of Pediatrics, Torrecárdenas Hospital, Almería, Spain. jramoslizana@telefonica.net
Insights
Many children with epilepsy achieve seizure control with sequential treatments, and only a small percentage develop refractory epilepsy. This study highlights the effectiveness of ongoing therapeutic adjustments in pediatric epilepsy management.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Therapeutics
Background:
- Epilepsy is a common neurological disorder in children.
- Identifying effective treatment strategies is crucial for long-term outcomes.
- Understanding the risk of refractory epilepsy informs clinical practice.
Purpose of the Study:
- To evaluate treatment response in children with epilepsy undergoing sequential drug regimens.
- To determine the incidence and risk factors for developing refractory epilepsy in pediatric patients.
- To analyze the long-term seizure control rates in childhood epilepsy.
Main Methods:
- Prospective follow-up of 343 children diagnosed with epilepsy before age 14.
- Defined seizure control as a 2-year seizure-free period.
- Defined refractory epilepsy as failure of >2 drugs with persistent seizures for ≥18 months.
Main Results:
- Seventy percent of patients achieved seizure control by 5 years, and 86% by 10 years.
- Fifty-nine percent were controlled with the first antiepileptic drug.
- Among those who failed initial treatments, subsequent regimens led to control in 39% (after first failure), 23% (after second), and 12% (after third).
- The cumulative risk of developing refractory epilepsy was 8% at 6 years and 12% at 10 years.
Conclusions:
- A substantial number of children with epilepsy can achieve seizure control through sequential treatment adjustments.
- The development of refractory epilepsy is relatively uncommon in the pediatric population studied.
- These findings support the continued use of trial-and-error with multiple antiepileptic drugs in managing childhood epilepsy.
Purpose:
To investigate response to sequential treatment schedules and risk of development of refractory epilepsy in childhood.
Methods:
All children younger than 14 years with two or more unprovoked seizures seen at our hospital between 1994 and 2004 were included and prospectively followed. "Seizure control" was defined as a 2-year seizure-free interval without further recurrences except those related to attempts of medication withdrawal and "refractory epilepsy" as failure of >2 drugs plus >1 seizure/month for > or =18 months.
Results:
343 Patients were included, 191 males and 152 females. Mean age at diagnosis was 4y 10 mo (SD 3 year 10 month). Mean follow-up period was 76.2 mo (SD 35.2). The probability of achieving "seizure control" was 70% and 86% at 5 and 10 years. 59% of patients were "controlled" with the first drug used. Among patients failing the first, second and third therapeutic regimen due to lack of efficacy, 39%, 23% and 12% respectively were finally "controlled" with subsequent treatment schedules Risk of development of refractory epilepsy was 8% and 12% at 6 and 10 years.
Conclusion:
After failing a first drug, a significant proportion of children can still be controlled with subsequent therapeutic schedules. Only a small proportion develops refractory epilepsy.
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