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Functional Impacts of Aminoglycoside Treatment on Speech Perception and Extended High-Frequency Hearing Loss in a Pediatric Cystic Fibrosis Cohort

  • Chelsea M. Blankenship
  • , Lisa L. Hunter
  • , M. Patrick Feeney
  • , Madison Cox
  • , Lindsey Bittinger
  • , Angela C. Garinis
  • , Li Lin
  • , Gary McPhail
  • , John P. Clancy

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose The purpose of this study is to better understand the prevalence of ototoxicity-related hearing loss and its functional impact on communication in a pediatric and young adult cohort with cystic fibrosis (CF) and individuals without CF (controls). Method We did an observational, cross-sectional investigation of hearing function in children, teens, and young adults with CF (n = 57, M = 15.0 years) who received intravenous aminoglycoside antibiotics and age- and gender-matched controls (n = 61, M = 14.6 years). Participants completed standard and extended high-frequency audiometry, middle ear measures, speech perception tests, and a hearing and balance questionnaire. Results Individuals with CF were 3-4 times more likely to report issues with hearing, balance, and tinnitus and performed significantly poorer on speech perception tasks compared to controls. A higher prevalence of hearing loss was observed in individuals with CF (57%) compared to controls (37%). CF and control groups had similar proportions of slight and mild hearing losses; however, individuals with CF were 7.6 times more likely to have moderate and greater degrees of hearing loss. Older participants displayed higher average extended high-frequency thresholds, with no effect of age on average standard frequency thresholds. Although middle ear dysfunction has not previously been reported to be more prevalent in CF, this study showed that 16% had conductive or mixed hearing loss and higher rates of previous otitis media and pressure equalization tube surgeries compared to controls. Conclusions Individuals with CF have a higher prevalence of conductive, mixed, and sensorineural hearing loss; poorer speech-in-noise performance; and higher rates of multiple symptoms associated with otologic disorders (tinnitus, hearing difficulty, dizziness, imbalance, and otitis media) compared to controls. Accordingly, children with CF should be asked about these symptoms and receive baseline hearing assessment(s) prior to treatment with potentially ototoxic medications and at regular intervals thereafter in order to provide otologic and audiologic treatment for hearing- and ear-related problems to improve communication functioning.

Original languageEnglish (US)
Pages (from-to)834-853
Number of pages20
JournalAmerican journal of audiology
Volume30
Issue number3
DOIs
StatePublished - Oct 11 2021

Funding

This research was supported by National Institute on Deafness and Other Communication Disorders Grant R01DC010202 (multiprincipal investigators: Doug Keefe, Lisa L. Hunter, and Patrick Feeney), Clinical and Translational Science Award Program Grant 5UL1TR001425-04 (Center for Clinical and Translational Science Training at the University of Cincinnati), and the Cincinnati Children’s Hospital Medical Center Research Foundation Place Outcomes Research Award (multiprinciple investigators: Lisa L. Hunter and John P. Clancy). The content of this article is solely the responsibility of the authors and does not reflect the official views of the National Institutes of Health, the Department of Veterans Affairs, or Cincinnati Children’s Hospital Medical Center. Portions of this study were presented at the World Congress of Audiology 2018, North American Cystic Fibrosis Conference 2019, and the Association for Research in Otolaryngology 2020. We also thank our participants, their families, and the Summer Under-graduate Research Foundation scholars. This research was supported by National Institute on Deafness and Other Communication Disorders Grant R01DC010202 (multiprincipal investigators: Doug Keefe, Lisa L. Hunter, and Patrick Feeney), Clinical and Translational Science Award Program Grant 5UL1TR001425-04 (Center for Clinical and Translational Science Training at the University of Cincinnati), and the Cincinnati Children’s Hospital Medical Center Research Foundation Place Outcomes Research Award (multiprinciple investigators: Lisa L. Hunter and John P. Clancy). The content of this article is solely the responsibility of the authors and does not reflect the official views of the National Institutes of Health, the Department of Veterans Affairs, or Cincinnati Children’s Hospital Medical Center. Portions of this study were presented at the World Congress of Audiology 2018, North American Cystic Fibrosis Conference 2019, and the Association for Research in Otolaryngology 2020. We also thank our participants, their families, and the Summer Undergraduate Research Foundation scholars.

FundersFunder number
Department of Veterans Affairs, or Cincinnati Children’s Hospital Medical Center
Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of Health
National Institute on Deafness and Other Communication Disorders R01DC012546 Xue Zhong Liu National Institute on Deafness and Other Communication Disorders R01DC012115 Xue Zhong Liu National Institute on Deafness and Other Communication Disorders R01DC014427 Ulrich Müller Peter G Barr-Gillespie National Institute on Deafnessand Other Communication Disorders R01DC005965 Ulrich Müller National Institute on Deafness and Other Communication Disorders5UL1TR001425-04, R01DC010202
Cincinnati Children's Hospital Medical Center
Department of Emergency Medicine University, Cincinnati Medical Center Cincinnati

    ASJC Scopus subject areas

    • Speech and Hearing

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