Audiometric assessment of pediatric patients with cystic fibrosis

Abstract

BackgroundThe purpose of this study was to evaluate hearing impairment in pediatric patients with cystic fibrosis (CF). MethodsThis is a retrospective analysis of the AudGen database generated by Children's Hospital of Philadelphia. Audiograms were analyzed for type of hearing loss (HL), pure-tone-average (PTA), laterality, and change in hearing over time. Medical charts were reviewed to identify factors that influence development and progression of hearing loss. Results217 patients with CF were included in this study. 69 (31.8%) had hearing loss on initial audiogram. Chronic otitis media (OR: 2.4, 95% CI: 1.3–4.5, p<0.01), Eustachian tube dysfunction (OR: 2.4, 95% CI: 1.4–5.4, p<0.01), and otorrhea (OR: 6.3, 95% CI: 1.6–24.7, p<0.01) were positive predictors of HL. Children with a diagnosis of diabetes had more decline in hearing over time than those without diabetes (12.4±17.2dB worsening vs. −5.7±9.8dB improvement in PTA, p=0.014). ConclusionThis is the largest comprehensive analysis of all types of hearing loss in pediatric patients with CF. Our data suggest that children with more severe sinus disease may be at lower risk for inflammatory middle ear disease and subsequent hearing loss. Patients who develop complications of CF such as diabetes should be monitored frequently, and the use of ototoxic drugs should be limited if possible.