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[Liposteroid therapy for refractory epileptic spasms]
Kuriko Kagitani Shimono1, Katsumi Imai, Rie Idoguchi
1Department of Developmental Medicine (Pediatrics), Osaka University Graduate School of Medicine, Suita, Osaka. kuriko@ped.med.osaka-u.ac.jp
No to Hattatsu = Brain and Development
|November 25, 2003
Summary
Liposteroid therapy showed limited efficacy for refractory epileptic spasms in 6 patients, with significant adverse effects observed. Modifications to the treatment regimen are recommended for this epilepsy treatment.
Area of Science:
- Neurology
- Pediatric Neurology
Background:
- Refractory epileptic spasms often require alternative treatments when standard therapies fail.
- Adrenocorticotropic hormone (ACTH) is a common treatment, but liposteroid is suggested as a safer alternative.
Observation:
- Intravenous liposteroid was administered to six patients with refractory epileptic spasms.
- Observed outcomes included transient spasm resolution, reappearance of spasms, and EEG improvement in one patient.
- Adverse effects such as behavioral changes, appetite loss, and increased tonic seizures were noted.
Findings:
- Liposteroid demonstrated a limited effect on refractory epileptic spasms, with only one patient experiencing complete resolution.
- Significant adverse effects were observed in multiple patients, necessitating discontinuation in one case.
- No serious adverse events like infection or brain shrinkage were reported.
Implications:
- Liposteroid may not be a consistently effective or safe alternative to ACTH for refractory epileptic spasms.
- The current liposteroid regimen requires modification to improve efficacy and reduce adverse effects.
- Further research is needed to optimize liposteroid therapy for pediatric epilepsy management.