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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.
Objective:
To characterize polysomnographic (PSG) findings of children with sickle cell disease (SCD) suspected of having sleep disordered breathing (SDB).
Methods:
Families of 100 consecutively referred children with SCD completed the Children's Sleep Habit Questionnaire during a routine visit to identify concerns regarding sleep habits and sleep behavior. Of these, 48 children were identified as displaying behaviors suspicious of SDB. Nineteen agreed to an overnight PSG. The results from the PSGs of the SCD with obstructive sleep apnea syndrome (OSAS) group (SCD-OSAS; group 1) were compared with the results of 10 age, sex, and ethnicity-matched patients identified as OSAS with no medical comorbidities (uncomplicated OSAS; group 2).
Results:
SDB was identified in 79% of the SCD group. As compared with the uncomplicated OSAS group, the SCD with OSAS group displayed nocturnal desaturation with lower nadir values, of longer duration, with a 4-fold increased risk for oxygen desaturation below 85%, higher percentage of total sleep time with end-tidal carbon dioxide (ET CO2) values >50 mm Hg, with a 3.7-fold increased risk for spending more than 25% of total sleep time with ET CO2 more than 50 mm Hg and higher peak ET CO2 with a 7-fold increase for peak ET CO2 above 53 mm Hg.
Conclusions:
Children with SCD suspicious of SDB may have not only a higher incidence of OSAS, but also more severe nocturnal desaturation and hypercapnia as compared with children with uncomplicated OSAS.
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