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Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
High night-to-night variability in childhood obstructive sleep apnea severity
Lena Xiao1, Mystica Terrance2, Chun Ting Au3
1Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada; University of Toronto, Toronto, Canada; Department of Pediatrics, British Columbia Children's Hospital, Vancouver, Canada; University of British Columbia, Vancouver, Canada.
Polysomnography (PSG) shows poor reliability for diagnosing moderate-severe obstructive sleep apnea (OSA) in children. A single night
Area of Science:
- Pediatric Sleep Medicine
- Respiratory Medicine
- Clinical Diagnostics
Background:
- Overnight polysomnography (PSG) is the standard diagnostic tool for childhood obstructive sleep apnea (OSA).
- Night-to-night variability in PSG results is known in adults but poorly understood in pediatric populations.
- This study addresses the test-retest reliability of PSG in children diagnosed with moderate-to-severe OSA.
Purpose of the Study:
- To evaluate the test-retest reliability of polysomnography (PSG) in children with moderate-to-severe obstructive sleep apnea (OSA).
- To determine if a single PSG is sufficient for accurate diagnosis and management of pediatric OSA.
Main Methods:
- Secondary analysis of baseline and repeat PSG data from two pediatric clinical trials.
- Included children aged 4-18 years with moderate-to-severe OSA.
- Compared diagnostic PSG results obtained approximately 48 days apart.
Main Results:
- Twenty-seven children were analyzed (median age 8 years).
- A significant proportion (26%) showed mild or no OSA on repeat PSG.
- Poor correlation was found for key OSA metrics: apnea-hypopnea index (ICC 0.27), oxygen desaturation index (ICC 0.10), and hypoxic burden (ICC 0.45).
Conclusions:
- Polysomnography demonstrates poor test-retest reliability in children with moderate-to-severe OSA.
- Relying solely on a single night of PSG may lead to misdiagnosis or inadequate treatment planning for pediatric OSA.
- Further research into optimizing diagnostic protocols for pediatric OSA is warranted.
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