
Obstructive sleep apnea (OSA) is prevalent in children with sickle cell disease (SCD). Therefore, this study compared the demographic, clinical, and polysomnographic characteristics of children with and without SCD. This retrospective chart review included children with SCD (n = 89) and without SCD (n = 192) ages 1–18 years referred for polysomnography (PSG) for OSA. Children with SCD referred for PSG are at risk for severe OSA. Compared with the non‐SCD group, most children were African American with lower rates of obesity and lower AHIs but more extended periods of nocturnal hypoxemia. The likelihood of severe OSA decreased with increasing age for the SCD group.
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