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A comparison of automated auditory brainstem responses and transiently evoked otoacoustic emissions for universal newborn hearing screening

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dc.contributor.author Korres, SG en
dc.contributor.author Balatsouras, DG en
dc.contributor.author Lyra, C en
dc.contributor.author Kandiloros, D en
dc.contributor.author Ferekidis, E en
dc.date.accessioned 2014-03-01T01:55:30Z
dc.date.available 2014-03-01T01:55:30Z
dc.date.issued 2006 en
dc.identifier.issn 1234-1010 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/27762
dc.subject hearing screening en
dc.subject screening en
dc.subject hearing en
dc.subject transiently evoked otoacoustic emissions en
dc.subject auditory brainstem responses en
dc.subject.classification Medicine, Research & Experimental en
dc.subject.other IDENTIFICATION en
dc.subject.other INTERVENTION en
dc.subject.other IMPAIRMENT en
dc.title A comparison of automated auditory brainstem responses and transiently evoked otoacoustic emissions for universal newborn hearing screening en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2006 en
heal.abstract Background: The aim of this study was to compare the performance of automated auditory brainstem responses (a-ABR) and automated transiently evoked otoacoustic emissions (a-TEOAEs). Material/Methods: A prospective, case-control study in a group of newborns was performed in a maternity hospital carrying out universal newborn hearing screening. Two groups of full-term newborns were examined. The first group included 50 newborns (100 ears) who underwent: 1) a-TEOAEs, 2) a-ABR, and 3) transiently evoked otoacoustic emissions (TEOAEs). The second group consisted of the same number of newborns who underwent identical testing, but in a different order: 1) a-ABR, 2) a-TEOAEs, and 3) TEOAEs. All a-TEOAE and a-ABR testing was performed using the AccuScreen device and all standard TEOAE testing was performed using the ILO88. The pass-fail results of each method were recorded and compared. Results: a-ABR yielded lower referral rates than the otoacoustic emission tests, but the differences were not statistically significant. Comparison between the two groups of study showed higher "pass" rates in the second group, indicating an order effect. Conclusions: Either method might be useful in universal newborn hearing screening. However, the lower referal rate obtained by a-ABR and its potential to recognize infants at risk for auditory neuropathy and central pathology should be considered. en
heal.publisher INT SCIENTIFIC LITERATURE, INC en
heal.journalName MEDICAL SCIENCE MONITOR en
dc.identifier.isi ISI:000238542000009 en
dc.identifier.volume 12 en
dc.identifier.issue 6 en
dc.identifier.spage CR260 en
dc.identifier.epage CR263 en


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