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Published on: April 11, 2019
Measurable outcomes for pediatric epileptic encephalopathy: a single-center experience with corticosteroid therapy
Jacqueline S Gofshteyn1, Kevin Gurcharran K1, Belinda O Marquis1
1Division of Child Neurology, Department of Pediatrics, Weill Cornell Medicine.
Insights
Corticosteroids show promise in treating pediatric epileptic encephalopathy, with significant seizure reduction and improved sleep patterns observed. Dexamethasone specifically demonstrated better cognitive improvements in parents' reports.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Pharmacology
Background:
- Corticosteroids are used for refractory childhood epilepsy, but effectiveness is unclear due to population heterogeneity and varied outcomes.
- Standardized outcome measures are lacking for assessing corticosteroid efficacy in pediatric epileptic encephalopathy.
Purpose of the Study:
- To identify measurement domains and estimate effect sizes for corticosteroids in treating pediatric epileptic encephalopathy.
- To characterize population heterogeneity and identify outcomes needing better measurement tools.
Main Methods:
- Retrospective single-center cohort study of children with epileptic encephalopathy (excluding infantile spasms).
- Standardized oral dexamethasone or IV methylprednisolone treatment.
- Novel ordinal scales assessed long-term video electroencephalography (EEG) for seizure burden, epileptiform activity, organization, and sleep architecture.
- Parental reports of cognitive function were abstracted from medical records.
Main Results:
- 46% of 35 children had >50% seizure reduction post-treatment.
- Significant reduction in tonic seizures (2.6-fold decrease) observed in a subset.
- Improved sleep spindle formation (37% to 63%, p=0.04) and parental-reported cognitive improvements (43%) were noted.
- Dexamethasone showed superior cognitive improvement rates (58%) compared to methylprednisolone (25%, p=0.03).
Conclusions:
- Corticosteroids can reduce seizures and improve EEG sleep architecture in pediatric epileptic encephalopathy.
- Cognitive improvements, particularly with dexamethasone, warrant further investigation with standardized tools.
- Future large studies should focus on seizure reduction, EEG organization, sleep architecture, and cognitive outcomes.
Abstract:
Corticosteroids are commonly used to treat refractory epilepsy in children, but the heterogeneity of the population and lack of standardized outcome measures have limited understanding of their effectiveness. We conducted a single-center study of corticosteroids for epileptic encephalopathy to (a) identify domains for measurement and estimate potential effect sizes, (b) characterize heterogeneity, and (c) identify outcomes that may need better tools for measurement. In this retrospective single-center cohort study, children with epileptic encephalopathy (excluding infantile spasms) were treated with a standardized course of oral dexamethasone or IV methylprednisolone. Long-term video electroencephalography (EEG) was assessed via novel ordinal scales for five features: seizure semiology/burden, epileptiform activity, slowing, organization, and sleep architecture. We abstracted parental assessment of functional domains (i.e., cognition) from the medical records. Pre-treatment and post-treatment EEG features, functional domains, and treatment regimens were compared. Thirty-five children with refractory epilepsy were included. Overall, 16/35 (46%) of individuals had a >50% reduction in seizure frequency from the pre-treatment EEG to the initial post-treatment EEG. In particular, tonic seizures (in a subset of 23 children) were reduced (24-hour tonic seizure count pre-treatment was 8 [4-13] and 3 [1-5] post-treatment EEG#1, p=0.04). For follow-up post-treatment EEGs, there was: (1) better formation of sleep spindles (37% normal pre-treatment to 63% normal post-treatment; p=0.04); and (2) improvement in parental reported cognition (in 43%). Improved cognition was the only outcome that differed between the dexamethasone and methylprednisolone treated groups (58% for dexamethasone [n=11/19] vs. 25% for methylprednisolone [n=4/16]; p=0.03). Large studies should be powered to detect reductions in seizures (particularly tonic as we identified a 2.6-fold reduction), improved EEG organization, and improved sleep architecture (21 percentage points). Cognitive improvements following steroid treatment, reported by parents, should be quantified and fully characterized in future work.
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