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Unveiling cognitive disengagement syndrome: A hidden challenge in children with epilepsy
Cansu Mercan Isik1, Dilek Cebeci2
1Department of Child and Adolescent Psychiatry, Cumhuriyet University Faculty of Medicine, Sivas, Turkey.
Insights
Cognitive disengagement syndrome (CDS) affects 76% of children with epilepsy, significantly higher than controls. Seizure control and age are key factors associated with CDS in pediatric epilepsy patients.
Area of Science:
- Pediatric Neurology
- Child Psychiatry
- Neurodevelopmental Disorders
Background:
- Epilepsy in children is often associated with comorbidities.
- Cognitive disengagement syndrome (CDS) and attention deficit hyperactivity disorder (ADHD) are potential concerns in this population.
Purpose of the Study:
- To determine the prevalence of CDS and ADHD in children with epilepsy.
- To identify factors associated with these conditions in pediatric epilepsy patients.
Main Methods:
- A case-control study involving 62 children with epilepsy (aged 6-18) and 51 healthy controls.
- Data collection included sociodemographics, epilepsy characteristics, medication use, and psychiatric evaluations using structured interviews and scales.
Main Results:
- 76% of children with epilepsy exhibited CDS, compared to 26% of controls (p < 0.01).
- Patients with epilepsy showed higher scores on attention and disruptive behavior scales.
- Lack of seizure control and age over 12 were linked to higher CDS prevalence. Age, number, and duration of antiseizure medications predicted specific behavioral scores.
Conclusions:
- This is the first study to investigate CDS and ADHD prevalence in children with epilepsy.
- Findings underscore the need for research into the mechanisms of CDS in epilepsy and the development of targeted interventions.
Background:
In our study, we aimed to investigate the prevalence of cognitive disengagement syndrome (CDS) and attention deficit hyperactivity disorder (ADHD) in children with epilepsy and to identify the associated factors.
Method:
The study included 62 patients with epilepsy aged 6-18 and 51 healthy controls. Sociodemographic data, epilepsy characteristics, and medication usage were collected. Psychiatric evaluations used various structured interviews and scales.
Results:
The mean ages for patients and controls were 9.7 and 9.9 years, respectively. CDS was present in 76 % of patients with epilepsy compared to 26 % of controls (p < 0.01). Patients with epilepsy scored higher on Barkley Child Attention Scale (BCAS) and Turgay DSM-IV Disruptive Behavior Disorders Symptom Screening Scale (T-DSM-IV-S). CDS prevalence was higher in patients without seizure control and those over age 12. Linear regressions demonstrated that age predicted BCAS-sluggish scores (R2: 0.284, p < 0.001) and T-DSM-IV-S hyperactivity scores (R2: 0.065, p: 0.023). The number of antiseizure medications (R2: 0.065, p: 0.023) and the duration of antiseizure medication usage (R2: 0.079, p: 0.014) predicted T-DSM-IV-S oppositional scores.
Conclusion:
Our study is the first study in this field. Our study findings highlight the need for further research to understand the pathophysiological mechanisms underlying CDS in epilepsy and to develop targeted interventions.
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