PEDIATRICS Vol. 83 No. 3 March 1989, pp. 385-392
This Article
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kramer, S. J.
Right arrow Articles by Condon, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kramer, S. J.
Right arrow Articles by Condon, M.

Auditory Brainstem Responses and Clinical Follow-up of High-Risk Infants

Steven J. Kramer PhD1, Dianne R. Vertes PhD1, and Marie Condon MS, CED1

1 The Department of Otolaryngology, The University of Texas Medical Branch, Galveston

Auditory brainstem response (ABR) evaluations were performed on 667 high-risk infants from an infant special care unit. Of these infants, 82% passed the ABR. Those infants who failed the ABR were classified into two groups, those who failed at 30 dB hearing level and those who failed at 45 dB hearing level. All of the infants were encouraged to return for otologic/audiologic follow-up in 1, 3, or 6 months, depending on the initial ABR results. All of the infants with severe hearing impairments came from the group who failed at 45 dB hearing level. The incidence of severe sensorineural hearing impairment in this population was estimated to be 2.4%. For the group that failed at 30 dB hearing level, 80% of those who were abnormal at follow-up were considered to have conductive hearing disorders and 20% had mild sensorineural hearing impairments. In addition, infants enrolled in a parent-infant program for hearing impaired by 6 months of age were from the ABR program; however, several infants entered the parent-infant program at a relatively late age because they did not meet the high-risk criteria, they were from other hospitals, or they were not detected by the ABR program.

Key Words: auditory brainstem responses • hearing screening • otitis media • parent-infant program

Submitted on July 6, 1987
Accepted on April 5, 1988




This article has been cited by other articles:


Home page
Arch Otolaryngol Head Neck SurgHome page
M. G. Amatuzzi, C. Northrop, M. C. Liberman, A. Thornton, C. Halpin, B. Herrmann, L. E. Pinto, A. Saenz, A. Carranza, and R. D. Eavey
Selective Inner Hair Cell Loss in Premature Infants and Cochlea Pathological Patterns From Neonatal Intensive Care Unit Autopsies
Arch Otolaryngol Head Neck Surg, June 1, 2001; 127(6): 629 - 636.
[Abstract] [Full Text] [PDF]


Home page
CLIN PEDIATRHome page
E. S. Ruppert and K. Buhrer
Ohio's Infant Hearing Screening and Assessment Program: A Decade In Development
Clinical Pediatrics, January 1, 1992; 31(1): 19 - 22.
[Abstract] [PDF]