%0 Journal Article
%T A national study of choanal atresia in tertiary care centers in Canada - part I: clinical presentation.
%A Paradis J
%A Dzioba A
%A El-Hakim H
%A Hong P
%A Kozak FK
%A Nguyen LHP
%A Perera D
%A Propst EJ
%A Siu JM
%A Wojtera M
%A Husein M
%A  
%J J Otolaryngol Head Neck Surg
%V 50
%N 1
%D Jul 2021 12
%M 34253250
暂无%R 10.1186/s40463-021-00517-x
%X <B>BACKGROUND: </B>To evaluate the clinical presentation of choanal atresia (CA) in tertiary centers across Canada.<BR><B>METHODS: </B>Multi-centre case series involving six tertiary care pediatric hospitals across Canada. Retrospective chart review of patients born between 1980 and 2010 diagnosed with CA at a participating center.<BR><B>RESULTS: </B>The health charts of 215 patients (59.6% female) with CA were reviewed and included in this study. The mean age of patients at time of CA presentation was 0.4 months (range 0.1 to 7.2 months) for bilateral CA and 37.8 months (range 0.1 to 164.1 months) for unilateral cases. The most common presenting symptoms for bilateral CA in decreasing order were respiratory distress (96.4%), feeding difficulties (68.2%), and rhinorrhea (65.5%), and for unilateral cases in decreasing order were rhinorrhea (92.0%), feeding difficulties (24.7%), and respiratory distress (18.0%). For the majority of patients (73.2%), the obstruction comprised mixed bony and membranous tissue, with only 10.5% presenting with a purely membranous obstruction. Familial history of CA was confirmed in only 3.3% of cases. One half of patients with CA presented with one or more associated anomalies and 30.6% had a syndrome.<BR><B>CONCLUSIONS: </B>The present investigation is the first national multi-institutional study evaluating the clinical presentation of CA over three decades. The present cohort of CA patients presented with a breadth of co-morbidities with highly variable presentations, with bilateral cases being more severely affected than unilateral cases. Further investigation into hereditary linkages to CA development is warranted.