Observational pilot study of reported symptoms of obstructive sleep apnoea in children with epilepsy

Don S Urquhart1,2, Olaniyi O Kehinde3, Ailsa E Mclellan2,3

  • 1Department of Paediatric Respiratory and Sleep Medicine, Royal Hospital for Sick Children, Edinburgh, UK.

Insights

Children with epilepsy (CWE) show higher symptoms of obstructive sleep apnoea (OSA) and excessive daytime sleepiness (EDS) than typically developing children. Antiepileptic drugs may influence these findings, but do not fully explain them.

Area of Science:

  • Pediatric Neurology
  • Sleep Medicine
  • Clinical Research

Background:

  • Children with epilepsy (CWE) often experience sleep disturbances.
  • Previous research suggests a potential link between epilepsy and increased rates of obstructive sleep apnoea (OSA).

Purpose of the Study:

  • To compare symptoms of obstructive sleep apnoea (OSA) and excessive daytime sleepiness (EDS) in children with epilepsy (CWE) versus typically developing children.
  • To investigate potential contributing factors, such as antiepileptic drug (AED) use.

Main Methods:

  • Utilized the Pediatric Sleep Questionnaire's Sleep-Related Breathing Disorder scale (PSQ-SRBD) to assess OSA symptoms (score ≤0.33 indicates high likelihood).
  • Employed the Epworth Sleepiness Scale (ESS) to evaluate EDS (score ≥10 is abnormal).
  • Compared results between 33 CWE and 42 typically developing children.

Main Results:

  • 55% of CWE exhibited symptoms suggestive of OSA (PSQ-SRBD score ≥0.33) compared to 7% of controls (p<0.001).
  • 30% of CWE reported abnormal daytime sleepiness (ESS score ≥10) versus 5% of controls (p=0.003).
  • Higher PSQ-SRBD and ESS scores were observed in CWE taking antiepileptic drugs (AEDs), though elevated scores were also present in CWE not on AEDs compared to controls.

Conclusions:

  • Children with epilepsy demonstrate significantly higher rates of symptoms indicative of OSA and EDS compared to their typically developing peers.
  • While AEDs may be a confounding factor, they do not solely account for the observed associations.
  • Further research, including polysomnography, is recommended to confirm OSA diagnosis in this population.
Abstract