Severity of obstructive sleep apnea in children with sickle cell disease

Joseph Kaleyias1, Navid Mostofi, Mitzie Grant

  • 1Sections of Neurology and Sleep Medicine, St Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA, USA.

Insights

Children with sickle cell disease (SCD) and suspected sleep disordered breathing (SDB) show a higher incidence and severity of obstructive sleep apnea syndrome (OSAS), including significant nocturnal desaturation and hypercapnia.

Area of Science:

  • Pediatric Pulmonology
  • Sleep Medicine
  • Hematology

Background:

  • Sleep disordered breathing (SDB) is a concern in children with sickle cell disease (SCD).
  • Polysomnography (PSG) is crucial for diagnosing SDB and its severity.

Purpose of the Study:

  • To characterize polysomnographic (PSG) findings in children with SCD who exhibit symptoms suggestive of SDB.
  • To compare PSG results between children with SCD and obstructive sleep apnea syndrome (OSAS) and those with uncomplicated OSAS.

Main Methods:

  • 100 children with SCD completed a sleep habit questionnaire; 48 showed SDB suspicion.
  • 19 children with SCD underwent overnight PSG.
  • PSG results were compared between the SCD-OSAS group and an age, sex, and ethnicity-matched uncomplicated OSAS group.

Main Results:

  • SDB was identified in 79% of the SCD group.
  • The SCD-OSAS group experienced more severe nocturnal desaturation (lower nadir, longer duration, increased risk of SpO2 <85%) compared to the uncomplicated OSAS group.
  • The SCD-OSAS group showed significantly higher end-tidal carbon dioxide (ET CO2) levels, indicating increased hypercapnia.

Conclusions:

  • Children with SCD and suspected SDB have a higher prevalence of OSAS.
  • These children present with more severe nocturnal desaturation and hypercapnia than those with uncomplicated OSAS.
Abstract

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