Volume 44, Issue 3 pp. 87-91

Post-natal hearing loss in universal neonatal hearing screening communities: Current limitations and future directions

Nicole Hutt

Nicole Hutt

SWISH, Sydney Children's Hospital, Randwick, New South Wales, Australia

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Christine Rhodes

Christine Rhodes

SWISH, Sydney Children's Hospital, Randwick, New South Wales, Australia

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First published: 27 February 2008
Citations: 23
Mrs Christine Rhodes, SWISH, Sydney Children's Hospital, Randwick, NSW 2031, Australia. Fax: +02 9382 0072; email: [email protected]

Abstract

Abstract:  Universal hearing screening has dramatically improved outcomes for babies born with detectable hearing abnormalities; yet there are some infants who develop significant hearing problems after passing a neonatal screen. There is much conjecture as to the number and the characteristics of infants with post-natal hearing losses; yet evidence suggests that many children may be affected, and that a large proportion have no discoverable cause. Currently, screening programmes use lists of risk factors to enrol babies into surveillance programmes. This practice is problematic because audiological follow-ups are expensive and under-utilised, and parental disclosure is often inaccurate. The large databases from universal neonatal programmes could inform the development of effective, evidence-based practice and policy for the detection and intervention of children who develop post-natal hearing losses.

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