| Literature DB >> 26454241 |
Hui-Leng Tan1, Leila Kheirandish-Gozal2, François Abel3, David Gozal4.
Abstract
Children with craniofacial syndromes are at risk of sleep disordered breathing, the most common being obstructive sleep apnea. Midface hypoplasia in children with craniosynostosis and glossoptosis in children with Pierre Robin syndrome are well recognized risk factors, but the etiology is often multifactorial and many children have multilevel airway obstruction. We examine the published evidence and explore the current management strategies in these complex patients. Some treatment modalities are similar to those used in otherwise healthy children such as adenotonsillectomy, positive pressure ventilation and in the refractory cases, tracheostomy. However, there are some distinct approaches such as nasopharyngeal airways, tongue lip adhesion, mandibular distraction osteogenesis in children with Pierre Robin sequence, and midface advancement in children with craniosynostoses. Clinicians should have a low threshold for referral for evaluation of sleep-disordered-breathing in these patients.Entities:
Keywords: Cleft lip and palate; Craniofacial anomalies; Craniosynostoses; Sleep disordered breathing
Mesh:
Year: 2015 PMID: 26454241 PMCID: PMC5374513 DOI: 10.1016/j.smrv.2015.05.010
Source DB: PubMed Journal: Sleep Med Rev ISSN: 1087-0792 Impact factor: 11.609