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Published on: September 20, 2024
Prednisone therapy in pediatric epilepsy
1Comprehensive Epilepsy Program, University of Alberta, Edmonton, Alberta, Canada.
Insights
Prednisone, a steroid, effectively treated intractable epilepsy in older children. Many patients achieved seizure freedom or significant reduction, with uncommon side effects, making it a viable alternative therapy.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
Background:
- Steroids are established treatments for West's syndrome.
- Limited data exists on steroid use for epilepsy in children over one year old.
Purpose of the Study:
- To evaluate the efficacy and safety of prednisone as an adjunctive treatment for intractable epilepsy in older children.
Main Methods:
- A study involving 28 children (18 months to 10 years) with intractable epilepsy.
- Prednisone (1 mg/kg/day for 12 weeks) was added to existing antiepileptic drugs.
- Seizure diaries and regular assessments monitored frequency and side effects over 1-5 years.
Main Results:
- 46% of patients became seizure-free, and 40% experienced a significant decrease in seizure frequency.
- Optimal results were observed in absence and Lennox-Gastaut syndrome groups.
- Adverse effects like weight gain and aggression were infrequent.
Conclusions:
- Prednisone is a safe and effective adjunctive therapy for intractable generalized epilepsy in older children.
- It offers a valuable alternative for patients unresponsive to conventional antiepileptic drugs.
Abstract:
Steroids are often an effective treatment for the West's syndrome. There have been few reports of steroid use in children with epilepsy outside the first year of life. I report my experience with prednisone for the treatment of older children with intractable epilepsy. Twenty-eight children (17 boys, 11 girls) aged 18 months to 10 years with intractable epilepsy were studied. Prednisone 1 mg/kg/day for 12 weeks (6 weeks daily and 6 weeks alternate therapy) was prescribed in addition to their regular antiepileptic medications. The parents kept seizure diaries, and the patients were regularly assessed for seizure frequency and side effects. The follow-up period was for 1 to 5 years. Thirteen patients (46%) became seizure free on prednisone and another 18 (40%) had a significant decrease in seizure frequency. Five patients (19%) had no change in seizure frequency. The best outcomes were seen in the absence group in which six out of seven patients became seizure free and in the Lennox-Gastaut syndrome group in which seven out of 10 became seizure free. Side effects were uncommon and included weight gain in five patients and aggression in four patients. Prednisone therapy is a safe and effective adjunctive treatment for epilepsy. It should be considered as an alternative treatment for older children with intractable generalized epilepsy who have failed conventional antiepileptic therapy.
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