Health disparities in pediatric cochlear implantation: An audiologic perspective

Erin Kirkham, Chana Sacks, Fuad Baroody, Juned Siddique, Mary Ellen Nevins, Audie Woolley, Dana Suskind*

*Corresponding author for this work

Research output: Contribution to journalArticle

21 Scopus citations

Abstract

Objectives: A national survey of pediatric cochlear implantation (PCI) audiologists was conducted with three aims: (1) to determine if PCI audiologists perceive within their clinical practice a negative effect of low socioeconomic status (SES) on postimplant speech and language outcomes; (2) to understand their perceptions of the underlying factors leading to outcome disparities; and (3) to elicit suggestions for improving outcomes in disadvantaged populations. We hypothesized that audiologists would perceive reduced speech and language outcomes within their lower SES patient population, and that this noted disparity would be related to parental adherence (compliance) and access to habilitation. Design: A survey containing 22 quantitative and open-ended questions was electronically mailed to a data base of 234 PCI audiologists. Forty-four percent (N = 103 of 234) responded to the survey, with the majority (98 of 103) answering all questions. Quantitative responses were analyzed using the Stata 9 statistical package with significance at p < 0.05. Qualitative responses were analyzed using standardized codebook and content analysis. Transcripts were read and coded for the main ideas expressed in each response. The codes were then analyzed for patterns and organized into subthemes that were then grouped into themes. Results: Seventy-eight percent (N = 76 of 98) of respondents perceived an effect of SES on postimplant speech and language outcomes. Qualitative responses uniformly demonstrated audiologists' perception that lower SES patient populations were more likely to experience reduced speech and language outcomes. Two major themes emerged in audiologists' explanations of SES-related disparities: internal factors of parental influence (i.e., parental self-efficacy, adherence, and habilitation carryover), and external factors (i.e., inadequate therapy and lack of available resources). Three primary suggestions were offered for reducing the disparity: improvement in cochlear implant services (92%), increased emphasis on parental education and intervention (87%), and the development of stricter candidacy requirements (15%). Conclusions: This study offers evidence to show that PCI audiologists note an SES-related disparity in the field of PCI. Respondents suggest the need for a broad and culturally sensitive effort to both increase access to qualified healthcare professionals and develop approaches that will aid parents in the at-home habilitation process.

Original languageEnglish (US)
Pages (from-to)515-525
Number of pages11
JournalEar and hearing
Volume30
Issue number5
DOIs
StatePublished - Oct 2009

ASJC Scopus subject areas

  • Otorhinolaryngology
  • Speech and Hearing

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    Kirkham, E., Sacks, C., Baroody, F., Siddique, J., Nevins, M. E., Woolley, A., & Suskind, D. (2009). Health disparities in pediatric cochlear implantation: An audiologic perspective. Ear and hearing, 30(5), 515-525. https://doi.org/10.1097/AUD.0b013e3181aec5e0