Sleep Problems and Quality of Life in Children with Epilepsy Without Neurodevelopmental Disorders

Kotaro Yazaki1, Satoru Sakuma1, Yuuto Shirokihara2

  • 1Department of Pediatrics, Graduate School of Medicine, Osaka Metropolitan University, Osaka 545-8585, Japan.

PubMed

Insights

Sleep problems may not significantly impact the quality of life (QoL) in children with epilepsy (CWE) without neurodevelopmental disorders. Parents may not accurately assess CWE

Area of Science:

  • Pediatric Neurology
  • Sleep Medicine
  • Quality of Life Research

Background:

  • Sleep problems are known to affect the quality of life (QoL) and treatment outcomes in children with epilepsy (CWE).
  • This study focuses on CWE without neurodevelopmental disorders to isolate the impact of sleep on QoL.
  • Investigating discrepancies between child and parent QoL reports is crucial for accurate assessment.

Purpose of the Study:

  • To analyze sleep problems and their impact on QoL in children with epilepsy (CWE) without neurodevelopmental disorders.
  • To compare QoL and sleep issues between CWE and a control group of healthy children.
  • To examine the agreement between self-reported and parent-proxy reported QoL in CWE.

Main Methods:

  • Thirty-two CWE (grades 2-6) and 21 healthy controls completed the Kinder Lebensqualität Fragebogen (KINDL-R).
  • Parents of participants completed the KINDL-R and the Japanese Sleep Questionnaire for Elementary Schoolers (JSQ-ES).
  • Exclusion criteria included neurodevelopmental disorders, inability to complete questionnaires, and current use of sleeping medication.

Main Results:

  • No significant differences in sleep problem scores (JSQ-ES) were found between the epilepsy and control groups.
  • In the epilepsy group, no significant differences in QoL (KINDL-R) were observed between children with and without sleep problems.
  • Child and parent QoL reports showed poor agreement in the epilepsy group, unlike the control group.

Conclusions:

  • Sleep problems may not significantly affect the QoL of children with epilepsy who do not have neurodevelopmental disorders.
  • Parental assessment of QoL in children with epilepsy may not always align with the child's self-perception.
  • Utilizing both child self-reports and parent proxy reports is essential for a comprehensive understanding of QoL in CWE.

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