Management and outcomes of obstructive sleep apnea in children with Robin sequence, a cross-sectional study

Manouk J S van Lieshout1,2, Koen F M Joosten3,4, Maarten J Koudstaal5,3

  • 1Department of Oral and Maxillofacial Surgery, Erasmus Medical Center, Sophia Children's Hospital, Room D-210,, 3000 CA, Rotterdam,, The Netherlands. m.vanlieshout@erasmusmc.nl.

Insights

Children with Robin sequence needing respiratory support require ongoing monitoring for obstructive sleep apnea (OSA) until adulthood. Those treated with prone positioning alone are less likely to develop later airway issues.

Area of Science:

  • Pediatric Pulmonology
  • Sleep Medicine
  • Craniofacial Anomalies

Background:

  • Obstructive sleep apnea (OSA) is a significant concern in children with Robin sequence (RS).
  • Understanding the prevalence and course of OSA in RS is crucial for timely intervention.
  • Early management strategies may influence long-term respiratory outcomes.

Purpose of the Study:

  • To determine the prevalence and course of obstructive sleep apnea (OSA) in children with Robin sequence (RS) aged 1-18 years.
  • To evaluate the management of OSA in this pediatric population.
  • To identify risk factors for persistent or developing OSA in children with RS.

Main Methods:

  • Cross-sectional study involving 63 children aged 1-18 years with RS.
  • Data collection on baseline characteristics and management strategies.
  • Polysomnography used for OSA evaluation.

Main Results:

  • Respiratory support was more frequently needed in non-isolated RS cases (p < 0.05).
  • In the prone positioning group (n=32), only one child had OSA.
  • In the respiratory support group (n=31), 42% had respiratory problems, with 10 requiring ongoing support.

Conclusions:

  • Nearly 25% of children with RS experience respiratory problems between ages 1 and 18.
  • Children with RS managed with prone positioning as infants are unlikely to develop later obstructive airway issues.
  • Children requiring early respiratory support are at higher risk for persistent or recurrent OSA beyond age 1.
Abstract

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