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Published on: December 6, 2016
Pediatric Obstructive Sleep Apnea and Sickle Cell Disease: Demographic and Polysomnographic Features
Claire A Abijay1, W Craig Kemper1, An Pham1,2
1Children's Medical Center Dallas, Dallas, Texas, USA.
Insights
Children with sickle cell disease (SCD) are at risk for severe obstructive sleep apnea (OSA). While they have lower obesity rates and apnea-hypopnea index (AHI), they experience more nocturnal hypoxemia.
Area of Science:
- Pediatric Pulmonology
- Hematology
- Sleep Medicine
Background:
- Obstructive sleep apnea (OSA) is a common comorbidity in children with sickle cell disease (SCD).
- Understanding the specific characteristics of OSA in this population is crucial for effective management.
Purpose of the Study:
- To compare the demographic, clinical, and polysomnographic features of children with and without SCD undergoing polysomnography (PSG) for OSA.
- To identify risk factors for severe OSA in children with SCD.
Main Methods:
- Retrospective chart review of children aged 1-18 years referred for PSG.
- Comparison of two groups: children with SCD (n=89) and without SCD (n=192).
- Analysis of demographic data, clinical history, and polysomnographic parameters including apnea-hypopnea index (AHI) and oxygen saturation.
Main Results:
- Children with SCD were predominantly African American (95% vs. 28%) with lower BMI z-scores and obesity rates (13% vs. 52%) compared to the non-SCD group.
- The SCD group had a lower mean AHI (13.6 vs. 22.4) but a higher percentage of sleep time with oxygen saturation below 90% (10.5% vs. 3.5%).
- Severe OSA was diagnosed in 43% of children with SCD, and the likelihood of severe OSA decreased with increasing age in this group.
Conclusions:
- Children with SCD referred for PSG are at significant risk for severe OSA, characterized by nocturnal hypoxemia despite lower AHIs.
- Demographic and clinical differences exist between children with and without SCD concerning OSA.
- Age is a factor influencing the severity of OSA in children with SCD.
Objective:
Obstructive sleep apnea (OSA) is prevalent in children with sickle cell disease (SCD). We compared the demographic, clinical, and polysomnographic characteristics of children with and without SCD.
Methods:
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.
Results:
Children with SCD were predominantly African American when compared to the non-SCD group (95% vs. 28%, p < 0.001). The non-SCD group had a higher BMI z-score (1.3 vs. 0.1, p < 0.001) and a higher percentage of patients classified as obese (52% vs. 13%, p < 0.001). In children with SCD, 43% had severe OSA and 5.6% had no OSA. In the non-SCD group, 67% had severe OSA and 4.7% had no OSA. The SCD compared to the non-SCD group had a lower mean apnea-hypopnea index (AHI) (13.6 vs. 22.4, p = 0.006) but a higher percent sleep time below 90% oxygen saturation (10.5% vs. 3.5%, p < 0.001). Predicted probability for severe OSA in children with SCD decreased with increasing age (OR = 0.81, 95% CI: 0.70-0.93).
Conclusion:
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 longer periods of nocturnal hypoxemia. Likelihood for severe OSA decreased with increasing age for the SCD group.
Level Of Evidence:
3, retrospective comparative study Laryngoscope, 133:1766-1772, 2023.
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