Trial reportNeurology2017
Pretreatment behavior and subsequent medication effects in childhood absence epilepsy.
Trial report in Neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00088452 (Childhood Absence Epilepsy Rx PK-PD-Pharmacogenetics Study), which is not on this map. Cited by 19 papers, 5 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Childhood Absence Epilepsy Rx PK-PD-Pharmacogenetics Study
Who cites it
19 citing papers in PubMed, 5 syntheses or guidelines pooled it, 39 citations in OpenAlex.
- Antiseizure medications for idiopathic generalized epilepsies: a systematic review and network meta-analysis.Journal of neurology · 2023Pooled it
- Ethosuximide, sodium valproate or lamotrigine for absence seizures in children and adolescents.The Cochrane database of systematic reviews · 2021Pooled it
- Towards a Better Understanding of Cognitive Deficits in Absence Epilepsy: a Systematic Review and Meta-Analysis.Neuropsychology review · 2019Pooled it
- Historical trend toward improved long-term outcome in childhood absence epilepsy.Epilepsy research · 2019Pooled it
- Ethosuximide, sodium valproate or lamotrigine for absence seizures in children and adolescents.The Cochrane database of systematic reviews · 2019Pooled it
- An innovative ethosuximide granule formulation designed for pediatric use: Comparative pharmacokinetics, safety, tolerability, and palatability profile versus reference syrup.Pharmacology research & perspectives · 2023Trial
- Sleep spindle deficits in childhood absence epilepsy improve with antiseizure treatment and disease resolution.bioRxiv : the preprint server for biology · 2026Article
- Interruption of rat absence seizures by auditory stimulation.bioRxiv : the preprint server for biology · 2025Article
- A 6-year-old with childhood absence epilepsy and motor hyperactivity.Epilepsy & behavior reports · 2024Article
- Thalamocortical circuits in generalized epilepsy: Pathophysiologic mechanisms and therapeutic targets.Neurobiology of disease · 2023Review
- Article
- Therapeutic Options for Childhood Absence Epilepsy.Pediatric reports · 2021Review
- Article
- Absence Seizures in Children: Usual and the Unusual.Indian journal of pediatrics · 2020Review
- Clinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizures.Brain : a journal of neurology · 2020Review
- HPO-Shuffle: an associated gene prioritization strategy and its application in drug repurposing for the treatment of canine epilepsy.Bioscience reports · 2019Article
- Driving status of patients with generalized spike-wave on EEG but no clinical seizures.Epilepsy & behavior : E&B · 2019Review
- A Practical Guide to Treatment of Childhood Absence Epilepsy.Paediatric drugs · 2019Review
- Article
Corrections and comments
- Commented on by
Authors and funding
12 authors at 2 institutions in 1 country.
Funding
Abstract
objectiveTo characterize pretreatment behavioral problems and differential effects of initial therapy in children with childhood absence epilepsy (CAE).
methodsThe Child Behavior Checklist (CBCL) was administered at baseline, week 16-20, and month 12 visits of a randomized double-blind trial of ethosuximide, lamotrigine, and valproate. Total problems score was the primary outcome measure.
resultsA total of 382 participants at baseline, 310 participants at the week 16-20 visit, and 168 participants at the month 12 visit had CBCL data. At baseline, 8% (95% confidence interval [CI] 6%-11%) of children with CAE had elevated total problems scores (mean 52.9 ± 10.91). At week 16-20, participants taking valproic acid had significantly higher total problems (51.7 [98.3% CI 48.6-54.7]), externalizing problems (51.4 [98.3% CI 48.5-54.3]), attention problems (57.8 [98.3% CI 55.6-60.0]), and attention-deficit/hyperactivity problems (55.8 [98.3% CI 54.1-57.6]) scores compared to participants taking ethosuximide (46.5 [98.3% CI 43.4-49.6]; 45.8 [98.3% CI 42.9-48.7]; 54.6 [98.3% CI 52.4-56.9]; 53.0 [98.3% CI 51.3-54.8]). Lack of seizure freedom and elevated week 16-20 Conner Continuous Performance Test confidence index were associated with worse total problems scores. At month 12, participants taking valproic acid had significantly higher attention problems scores (57.9 [98.3% CI 55.6-60.3]) compared to participants taking ethosuximide (54.5 [95% CI 52.1-56.9]).
conclusionsPretreatment and ongoing behavioral problems exist in CAE. Valproic acid is associated with worse behavioral outcomes than ethosuximide or lamotrigine, further reinforcing ethosuximide as the preferred initial therapy for CAE. CLINICALTRIALSGOV IDENTIFIER: NCT00088452. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that for children with CAE, valproic acid is associated with worse behavioral outcomes than ethosuximide or lamotrigine.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.