The status of diagnostic testing following referral from universal newborn hearing screening

Sue Windmill1, Ian M Windmill

  • 1Kosair Children's Hospital, Louisville, Kentucky 40292, USA.

Insights

Most Kentucky centers fail to meet infant hearing screening guidelines. Few infants receive genetic evaluations or amplification services, impacting early intervention for hearing loss.

Area of Science:

  • Pediatric Audiology
  • Early Hearing Detection and Intervention (EHDI)

Background:

  • The Joint Committee on Infant Hearing (JCIH) 2000 position statement outlines critical guidelines for Early Hearing Detection and Intervention (EHDI) programs.
  • These guidelines specify a comprehensive audiologic test battery for infants who do not pass newborn hearing screening.

Purpose of the Study:

  • To evaluate adherence to JCIH guidelines by follow-up diagnostic testing centers for infants in Kentucky.
  • To assess the provision of genetic evaluations and amplification services for infants with identified hearing loss.

Main Methods:

  • Reviewed services offered by 42 centers in Kentucky providing diagnostic testing for infants failing newborn hearing screening.
  • Compared services against the recommended audiologic test battery outlined by the JCIH, including electrophysiologic measures (ABR, bone-conducted ABR), OAEs, high-frequency tympanometry, and acoustic reflexes.

Main Results:

  • Only 3 out of 42 (7%) centers in Kentucky fully comply with the JCIH diagnostic test battery guidelines.
  • Fewer than 50% of infants diagnosed with hearing loss are referred for audiology-led genetic evaluations.
  • Only 19 out of 42 (45%) listed sites offer amplification services for infants with hearing loss.

Conclusions:

  • Significant gaps exist in Kentucky's EHDI program, with most centers not adhering to recommended diagnostic protocols.
  • Inadequate referral for genetic evaluations and limited access to amplification services hinder comprehensive care for infants with hearing loss.

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