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Published on: December 6, 2016
Pediatric Obstructive Sleep Apnea: Consensus, Controversy, and Craniofacial Considerations
Ravi K Garg1,2, Ahmed M Afifi1,2, Catharine B Garland1,2
1Madison, Wis.; and Cairo, Egypt.
Insights
Pediatric obstructive sleep apnea (POSA) affects children
Area of Science:
- Pediatric Sleep Medicine
- Craniofacial Anomalies
- Respiratory Disorders
Background:
- Pediatric obstructive sleep apnea (POSA) involves upper airway obstruction during sleep, leading to neurodevelopmental and cardiometabolic issues.
- POSA is prevalent in healthy children and more common in those with craniofacial anomalies, where bone structure can contribute to obstruction.
- Traditional symptoms like snoring are unreliable; polysomnography is the diagnostic standard.
Purpose of the Study:
- To review current theories on the pathophysiology of pediatric sleep apnea.
- To summarize diagnostic standards and management strategies for POSA.
- To discuss emerging treatments, including orthodontic and craniofacial interventions for refractory cases and children with craniofacial anomalies.
Main Methods:
- Comprehensive review of existing literature on pediatric obstructive sleep apnea.
- Inclusion of data from both healthy children and those with craniofacial anomalies.
- Focus on pathophysiology, diagnosis, and a broad spectrum of treatment options.
Main Results:
- Adenotonsillectomy is effective for most children, but 20% have treatment-refractory POSA.
- Positive airway pressure, medical therapy, orthodontics, and surgery are alternatives for refractory cases.
- Craniofacial interventions like rapid maxillary and distraction osteotomies show therapeutic value for children with skeletal growth impairment.
Conclusions:
- Effective management of pediatric obstructive sleep apnea requires understanding its diverse causes, from soft tissue to skeletal factors.
- While adenotonsillectomy is a primary treatment, alternative and combined interventions are crucial for refractory cases and those with craniofacial differences.
- Further investigation into orthodontic and craniofacial treatments is warranted to improve respiratory outcomes in affected children.
Abstract:
Pediatric obstructive sleep apnea, characterized by partial or complete obstruction of the upper airway during sleep, is associated with multiple adverse neurodevelopmental and cardiometabolic consequences. It is common in healthy children and occurs with a higher incidence among infants and children with craniofacial anomalies. Although soft-tissue hypertrophy is the most common cause, interplay between soft tissue and bone structure in children with craniofacial differences may also contribute to upper airway obstruction. Snoring and work of breathing are poor predictors of obstructive sleep apnea, and the gold standard for diagnosis is overnight polysomnography. Most healthy children respond favorably to adenotonsillectomy as first-line treatment, but 20 percent of children have obstructive sleep apnea refractory to adenotonsillectomy and may benefit from positive airway pressure, medical therapy, orthodontics, craniofacial surgery, or combined interventions. For children with impairment of facial skeletal growth or craniofacial anomalies, rapid maxillary expansion, midface distraction, and mandibular distraction have all been demonstrated to have therapeutic value and may significantly improve a child's respiratory status. This Special Topic article reviews current theories regarding the underlying pathophysiology of pediatric sleep apnea, summarizes standards for diagnosis and management, and discusses treatments in need of further investigation, including orthodontic and craniofacial interventions. To provide an overview of the spectrum of disease and treatment options available, a deliberately broad approach is taken that incorporates data for both healthy children and children with craniofacial anomalies.
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