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Sleep disordered breathing in bronchopulmonary dysplasia
Luis E Ortiz1, Sharon A McGrath-Morrow1, Laura M Sterni1
1Johns Hopkins Medical Institutions, Baltimore, Maryland.
Bronchopulmonary dysplasia (BPD) is linked to sleep disordered breathing (SDB) in children. Severity of BPD, smoke exposure, and race impact SDB, which improves with age but remains elevated.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Neonatology
Background:
- Limited data exist on the impact of bronchopulmonary dysplasia (BPD) on sleep disordered breathing (SDB).
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease affecting premature infants.
- Sleep disordered breathing (SDB) encompasses conditions like sleep apnea and hypoventilation during sleep.
Purpose of the Study:
- To investigate the association between bronchopulmonary dysplasia (BPD) severity and the likelihood of sleep disordered breathing (SDB) in early childhood.
- To explore demographic factors influencing the development of SDB in children with BPD.
Main Methods:
- Retrospective analysis of patient data and overnight polysomnogram (PSG) results from a BPD registry (2008-2015).
- Utilized multiple linear regression to assess the relationship between PSG findings and patient variables.
- Included 140 children with BPD who underwent at least one sleep study.
Main Results:
- Elevated respiratory disturbance index (RDI) observed in the BPD population (mean 9.9 events/hr).
- Increased severity of respiratory disease correlated with more central events.
- Secondhand smoke exposure was linked to lower oxygen saturation nadirs and more desaturation events.
- Racial differences noted: non-white subjects had higher obstructive apnea-hypopnea index (OAHI), while white subjects had more central events.
Conclusions:
- The study population with BPD exhibited elevated RDI compared to non-preterm norms.
- BPD severity, environmental smoke exposure, and race are potential factors exacerbating SDB.
- While RDI improved with age, it remained elevated by age 4, indicating a persistent risk for SDB sequelae in this population.
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