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. 1974 Feb;49(2):133-6.
doi: 10.1136/adc.49.2.133.

Upper respiratory tract in cystic fibrosis. Ear-nose-throat survey of 50 children

B Taylor, J N Evans, G A Hope

Upper respiratory tract in cystic fibrosis. Ear-nose-throat survey of 50 children

B Taylor et al. Arch Dis Child. 1974 Feb.

Abstract

An ear-nose-throat survey was carried out on 50 children aged 4 to 10 years with cystic fibrosis. 10% were shown to be transiently deaf, associated with eustachian tube dysfunction. There were no confirmed cases of secretory otitis media. 10 children (20%) were found to have nasal polyps or gave a history of polypectomy. Though a high incidence of middle ear problems in children with cystic fibrosis has been reported from the U.S.A., neither deafness nor secretory otitis media was found to be a problem in the group studied.

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