Home video clips compared to polygraphy for obstructive sleep apnea diagnosis in children with autism spectrum

Gianna Cox1, Sherri Lynne Katz2, Vid Bijelić3

  • 1Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Sleep Medicine
|August 17, 2025
PubMed

Insights

Video clips using the Monash score (MS) show high sensitivity for detecting obstructive sleep apnea (OSA) in children with autism spectrum disorder (ASD). This tool may help screen for OSA when polysomnography is challenging.

Area of Science:

  • Pediatric Sleep Medicine
  • Autism Spectrum Disorder Research
  • Diagnostic Tool Development

Background:

  • Children with autism spectrum disorder (ASD) have a higher prevalence of obstructive sleep apnea (OSA) compared to neurotypical children.
  • Polysomnography (PSG), the gold standard for OSA diagnosis, is often challenging for children with ASD.
  • More accessible screening tools are needed for OSA in this population.

Purpose of the Study:

  • To evaluate the diagnostic characteristics of video clips for identifying OSA in children with ASD.
  • To compare the effectiveness of video-based screening with other established tools.

Main Methods:

  • Recruited children aged 4-18 years with ASD referred for PSG.
  • Parents recorded 2-minute home video clips, scored using the Monash score (MS).
  • Compared MS with Pediatric Sleep Questionnaire (PSQ), home polygraphy (PG) metrics (oAHI, ODI3), and McGill Oximetry Score (MOS) for moderate-severe OSA.

Main Results:

  • The Monash score (MS) demonstrated 100% sensitivity and 63.6% specificity for moderate-severe OSA.
  • MS outperformed the PSQ and MOS, with an AUC of 78.4.
  • While MS showed high sensitivity, its specificity was lower, and it did not outperform ODI3.

Conclusions:

  • The Monash score (MS) shows promise as a sensitive screening tool for OSA in children with ASD.
  • MS may serve as a viable alternative to more challenging diagnostic methods like PSG.
  • Further validation studies are required to confirm the utility of MS in clinical practice.
Abstract

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