Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation.


Journal

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology
ISSN: 1537-4505
Titre abrégé: Otol Neurotol
Pays: United States
ID NLM: 100961504

Informations de publication

Date de publication:
01 06 2023
Historique:
pmc-release: 01 06 2024
medline: 15 5 2023
pubmed: 11 5 2023
entrez: 11 5 2023
Statut: ppublish

Résumé

To determine the relationship between hearing loss etiology, cochlear implant (CI) programming levels, and speech perception performance in a large clinical cohort of pediatric CI recipients. Retrospective chart review. Tertiary care hospitals. A total of 136 pediatric CI recipients (218 ears) were included in this study. All patients had diagnoses of either enlarged vestibular aqueduct (EVA) or GJB2 (Connexin-26) mutation confirmed via radiographic data and/or genetic reports. All patients received audiologic care at either Boston Children's Hospital or Massachusetts Eye and Ear in Boston, MA, between the years 1999 and 2020. Electrode impedances and programming levels for each active electrode and speech perception scores were evaluated as a function of etiology (EVA or GJB2 mutation). Children with EVA had significantly higher impedances and programming levels (thresholds and upper stimulation levels) than the children with GJB2 mutation. Speech perception scores did not differ as a function of etiology in this sample; rather, they were positively correlated with duration of CI experience (time since implantation). Differences in electrode impedances and CI programming levels suggest that the electrode-neuron interface varies systematically as a function of hearing loss etiology in pediatric CI recipients with EVA and those with GJB2 mutation. Time with the CI was a better predictor of speech perception scores than etiology, suggesting that children can adapt to CI stimulation with experience.

Identifiants

pubmed: 37167444
doi: 10.1097/MAO.0000000000003879
pii: 00129492-202306000-00005
pmc: PMC10176457
mid: NIHMS1882237
doi:

Substances chimiques

Connexins 0
GJB2 protein, human 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e273-e280

Subventions

Organisme : NIDCD NIH HHS
ID : R01 DC012142
Pays : United States
Organisme : NIDCD NIH HHS
ID : T32 DC005361
Pays : United States

Informations de copyright

Copyright © 2023, Otology & Neurotology, Inc.

Déclaration de conflit d'intérêts

The authors disclose no conflicts of interest.

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Auteurs

Kelly N Jahn (KN)

Department of Speech, Language, and Hearing, University of Texas at Dallas, Richardson, Texas.

Charlotte Morse-Fortier (C)

Audiology Division, Massachusetts Eye and Ear.

David Faller (D)

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital.

Michael S Cohen (MS)

Department of Otolaryngology-Head and Neck Surgery, Harvard Medical School, Boston, Massachusetts.

Elizabeth Doney (E)

Audiology Division, Massachusetts Eye and Ear.

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