Outcomes in children with down syndrome and mild obstructive sleep apnea treated non-surgically

Javier J M Howard1, Kathleen M Sarber2,3, Wenwen Yu2,4

  • 1College of Medicine, University of Cincinnati, Cincinnati, Ohio, U.S.A.

The Laryngoscope
|October 12, 2019
PubMed

Insights

Single medication or oxygen therapy showed low effectiveness for mild obstructive sleep apnea (OSA) in children with Down syndrome (DS). Multimodality treatments may be necessary for this population.

Area of Science:

  • Pediatric Pulmonology
  • Sleep Medicine
  • Genetics

Background:

  • Mild obstructive sleep apnea (OSA) is common in children with Down syndrome (DS).
  • Standard treatments like nasal steroids, oral anti-leukotrienes, and oxygen are effective in healthy children but their efficacy in DS is unknown.
  • Non-surgical interventions are crucial for managing OSA in this vulnerable population.

Purpose of the Study:

  • To evaluate the effectiveness of single medication therapy, supplemental oxygen, or observation for mild OSA in children with Down syndrome.
  • To compare polysomnographic outcomes between different non-surgical treatment groups.
  • To determine the resolution rate of mild OSA in children with DS under these treatments.

Main Methods:

  • Retrospective review of children (<18 years) with DS and mild OSA (obstructive apnea-hypopnea index [oAHI] ≥1 to <5 events/hour) treated non-surgically from 2012-2017.
  • Analysis of demographic data, comorbidities, and pre- and post-treatment polysomnograms.
  • Assessment of oAHI, oxyhemoglobin saturation nadir, and % total sleep time in REM.

Main Results:

  • No significant changes in oAHI, oxygen saturation, or CO2 levels were observed across treatment groups (medication, oxygen, observation).
  • OSA resolution rates were low: 20% with medication, 7.7% with observation, and 0% with oxygen.
  • Treatment outcomes did not correlate with reported symptoms or baseline OSA severity.

Conclusions:

  • Single-agent therapies demonstrate limited efficacy in resolving mild OSA in children with Down syndrome.
  • Multimodality treatment approaches should be considered for managing mild OSA in this population.
  • Further prospective studies are needed to establish effective treatment strategies for children with DS and OSA.
Abstract

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