3.9 Article

Analysis of Obstructive Sleep Apnoea in Craniofacial Microsomia Based on Polysomnography

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SAGE PUBLICATIONS INC
DOI: 10.1177/10556656231221654

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hemifacial microsomia; airway obstruction; retrospective study

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This study investigated the prevalence of obstructive sleep apnoea (OSA) in patients with craniofacial microsomia (CFM) and its relationship with the severity of CFM. The results showed that CFM patients, particularly those with type II and type III, have a higher incidence of OSA. However, the incidence of OSA does not correlate positively with the severity of CFM, with type III patients having certain particularities.
Objective: This study aimed to investigate the prevalence of obstructive sleep apnoea (OSA) in patients with craniofacial microsomia (CFM) through polysomnography (PSG) and the relationship with the severity of CFM. Methods: This study reviewed patients of CFM with pre-operative PSG data between January 2005 and September 2023. Patients were grouped according to the Pruzansky-Kaban classification. OSA was diagnosed and severity was assessed by the obstructive apnea-hypopnea index. The Pediatric Sleep Questionnaire was used to investigate OSA-related signs and symptoms. The chi 2 test and Fisher's exact test were used to compare between groups. Univariate logistic regression was used to identify risk factors associated with OSA. A p-value less than 0.05 was considered statistically significant. Results: A total of 121 patients with CFM were included in the study with 3 bilateral and 118 unilateral patients. In total, 86 patients (71.07%) were diagnosed with OSA. The prevalence of OSA in type IIa, type IIb and type III was 72.97%, 78.33%, and 47.62%. There was no statistically significant difference in the prevalence of OSA between type IIa and type IIb (p > .05). The difference in the prevalence of OSA between type III and type II was statistically significant (p < .05). Snoring was the most common symptom among the patients of CFM with OSA. Conclusions: Patients with CFM have a higher incidence of OSA based on PSG in type II and type III patients. The incidence of OSA did not correlate positively with the severity of CFM, with type III patients having certain particularities.

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