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The airway in patients with craniofacial abnormalities
Author(s) -
Nargozian Charles
Publication year - 2004
Publication title -
pediatric anesthesia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.704
H-Index - 82
eISSN - 1460-9592
pISSN - 1155-5645
DOI - 10.1046/j.1460-9592.2003.01200.x
Subject(s) - medicine , craniofacial , treacher collins syndrome , craniofacial abnormality , anatomy , temporomandibular joint , supernumerary , hemifacial microsomia , dysostosis , surgery , orthodontics , congenital disease , psychiatry
Summary Airway management for patients with craniofacial disorders poses many challenges. The anaesthesiologist must be familiar with the normal bony and soft‐tissue anatomy in the airway and how anatomy is altered by various congenital disorders. Specific areas to assess include the oral cavity, anterior mandibular space, maxilla, temporomandibular joint and vertebral column. Congenital conditions that may alter normal anatomy and therefore anaesthetic management include cleft lip and palate with or without Pierre Robin syndrome, craniofacial dysostosis, mandibulofacial dysostosis/Treacher Collins syndrome, hemifacial microsomia, Klippel‐Feil syndrome, Beckwith‐Wiedemann syndrome, trisomy 21/Down's syndrome, Freeman–Sheldon/whistling face syndrome/craniocarpotarsal dysplasia, fibrodysplasia ossificans progressiva, mucopolysaccharidosis and vascular malformations.