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Upper airway resistance syndrome in children: a clinical review

C Guilleminault1, A Khramtsov

  • 1Stanford University Sleep Disorders Clinic, CA 94305-5547, USA.

Insights

Upper airway resistant syndrome (UARS) is more prevalent in children than obstructive sleep apnea syndrome (OSAS). Diagnosis may require esophageal pressure monitoring, and craniofacial anomalies suggest orthodontic intervention for airway expansion.

Area of Science:

  • Pediatric Sleep Medicine
  • Respiratory Physiology
  • Craniofacial Orthodontics

Background:

  • Upper airway resistant syndrome (UARS) is more common in children than obstructive sleep apnea syndrome (OSAS).
  • Symptoms of UARS vary with age and family history of sleep-disordered breathing.
  • Enlarged tonsils and adenoids may coexist with mild craniofacial skeletal anomalies.

Purpose of the Study:

  • To highlight the prevalence and diagnostic challenges of UARS in children.
  • To emphasize the role of craniofacial structure in pediatric sleep-disordered breathing.
  • To advocate for early orthodontic assessment in affected children.

Main Methods:

  • Polygraphic recording with nasal cannula/pressure transducer to detect flow limitation.
  • Esophageal pressure monitoring for definitive diagnosis when other methods are inconclusive.
  • Maxillomandibular examination for craniofacial skeletal assessment.

Main Results:

  • UARS presents differently in children compared to adults.
  • Abnormal breathing may manifest as tachypnea without oxygen desaturation.
  • Flow limitation during sleep is a key indicator, often confirmed by esophageal manometry.
  • Craniofacial anomalies are frequently observed in children with UARS.

Conclusions:

  • UARS is a significant pediatric sleep disorder requiring specific diagnostic approaches.
  • Esophageal pressure monitoring is crucial for confirming UARS.
  • Orthodontic evaluation and treatment, including oral cavity expansion, are recommended for children with sleep-disordered breathing and craniofacial anomalies.

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