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Predicting the presence of sleep-disordered breathing in children with Down syndrome
Joy Nehme1, Robert LaBerge2, Mary Pothos3
1Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Insights
Sleep-disordered breathing (SDB) is common in children with Down syndrome. Clinical symptoms do not predict SDB, but gastroesophageal reflux may be mistaken for it, necessitating ongoing SDB surveillance.
Area of Science:
- Pediatric Pulmonology
- Genetics and Genetic Diseases
- Sleep Medicine
Background:
- Sleep-disordered breathing (SDB) affects a significant portion of children with Down syndrome.
- Limited resources and specific risk factors necessitate efficient SDB evaluation strategies in this population.
Purpose of the Study:
- To identify clinical predictors of SDB in children with Down syndrome.
- To aid in prioritizing children with Down syndrome for SDB evaluation.
Main Methods:
- Retrospective cohort study of 119 children with Down syndrome undergoing polysomnography.
- Analysis of concurrent diagnoses, referral reasons, and sleep symptoms.
- Logistic regression models to identify predictors of SDB (Apnea-Hypopnea Index > 5 events/hour).
Main Results:
- SDB prevalence was 42.9% in the study cohort, peaking around age 8.
- Clinical sleep symptoms were not significantly associated with SDB.
- Gastroesophageal reflux showed an association with lower odds of obstructive SDB (OAHI > 5).
Conclusions:
- SDB is highly prevalent across all ages in children with Down syndrome.
- Clinical symptoms are unreliable predictors of SDB in this group.
- Gastroesophageal reflux may present similarly to SDB, underscoring the need for continuous SDB surveillance.
Objective:
Sleep-disordered breathing (SDB) is highly prevalent in children with Down syndrome. Given the scarcity of resources and the presence of risk factors for SDB in this population, the objective of this study is to identify the clinical predictors of SDB, which would assist prioritization of children with Down syndrome for SDB evaluation.
Methods:
A retrospective cohort study was conducted on children enrolled in the Down syndrome clinic at CHEO who underwent polysomnography in 2004-2014. Total apnea-hypopnea index (AHI) or obstructive AHI (OAHI) > 5 events/hour was considered clinically significant. Associations between SDB and concurrent diagnoses, referral reasons, and sleep symptoms assessed by questionnaire were examined using Pearson's chi-square test or Fisher's exact test as appropriate. Univariate and multivariate logistic regression analyses were used to examine the predictors of SDB.
Results:
SDB was present in 42.9% of 119 children, with its highest prevalence at age 8 years. Symptoms were not significantly associated with AHI > 5 events/hour or OAHI > 5 events/hour. Gastroesophageal reflux was associated with lower odds of OAHI > 5 events/hour on univariate testing (odds ratio 0.16, 95% CI 0.04-0.72; p = 0.02) and multivariate analysis (odds ratio 0.05, 95% CI 0.0006-0.50; p = 0.002).
Conclusions:
SDB is highly prevalent at all ages in children with Down syndrome. Symptoms did not predict SDB in this population, although gastroesophageal reflux may mimic SDB, which indicates that clinicians should continue to perform ongoing surveillance for SDB throughout the lifespan of children with Down syndrome.
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