Skip to main navigation Skip to search Skip to main content

Unilateral craniofacial microsomia: Unrecognized cause of pediatric obstructive sleep apnea

  • Caroline Szpalski
  • , Meredith Vandegrift
  • , Parit A. Patel
  • , Geoffrey Appelboom
  • , Mark Fisher
  • , Jeffrey Marcus
  • , Joseph G. McCarthy
  • , Pradip R. Shetye
  • , Stephen M. Warren

Research output: Contribution to journalArticlepeer-review

Abstract

Bilateral craniofacial microsomia causes obstructive sleep apnea (OSA). We hypothesize that unilateral craniofacial microsomia (UCFM) is an underappreciated cause of OSA. The records of all pediatric UCFM patients from 1990 to 2010 were reviewed; only complete records were included in the study. UCFM patients with OSA (apnea hypopnea index >1/hr) were compared to UCFM patients without OSA. Univariate and multivariate Fisher and χ2 tests were performed. Of the 62 UCFM patients, 7 (11.3%) had OSA. All OSA patients had Pruzansky IIB or III mandibles. OSA patients presented with snoring (71.4%), failure to thrive (FTT) (57.1%), and chronic respiratory infections (42.8%). Snoring (P < 0.001), Goldenhar syndrome (P = 0.001), and FTT (P = 0.004) were significantly associated with OSA, but race, obesity, clefts, respiratory anomalies, adenotonsillar hypertrophy, and laterality were not. The prevalence of OSAin UCFMpatients is up to 10 times greater than in the general population. Snoring, Goldenhar syndrome, and FTT are significantly associated with the presence of OSA.

Original languageEnglish (US)
Pages (from-to)1277-1282
Number of pages6
JournalJournal of Craniofacial Surgery
Volume26
Issue number4
DOIs
StatePublished - Jun 1 2015
Externally publishedYes

Keywords

  • Apnea
  • Craniofacial syndromes
  • Hemifacial microsomia
  • Pediatric obstructive sleep apnea
  • Sleep disordered breathing
  • Unilateral craniofacial microsomia

ASJC Scopus subject areas

  • Surgery
  • Otorhinolaryngology

Fingerprint

Dive into the research topics of 'Unilateral craniofacial microsomia: Unrecognized cause of pediatric obstructive sleep apnea'. Together they form a unique fingerprint.

Cite this