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Central Annals of Otolaryngology and Rhinology

Short Communication *Corresponding author

Andrea L.O. Hebb, Department of Psychology, Saint Mary’s University, McNally Building South Wing (MS Otoacoustic Emissions: An 323), 923 Robie Street, Halifax, Nova Scotia, B3H 3C3, Canada, Tel: 902-420-5846, Fax: 902-496-8287; Email:

Invaluable Screen of Neonatal Submitted: 13 November 2018 Accepted: 04 December 2018 Published: 05 December 2018 ISSN: 2379-948X 1 1,2 Scott A. Davenport , and Andrea L.O. Hebb * Copyright 1Department of Psychology, Saint Mary’s University, Canada © 2018 Hebb et al. 2Divisions of Neurosurgery, Otolaryngology─Head & Neck Surgery and Department of Radiation Oncology, Dalhousie University, Canada OPEN ACCESS

Keywords Abstract • Otoacoustic emissions Otoacoustic emissions (OAEs) including evoked otoacoustic emissions test (EOAE), • Hearing automated auditory brainstem response (a-ABR), transitory evoked otoacoustic • Hearing loss emissions (TEOAEs) and brainstem auditory evoked potential (BAEP) are invaluable in assessing hearing in the newborn and non-verbal children and young adults. The following article briefly outlines the implementation of OAEs in clinical settings and highlights future research potential.

INTRODUCTION delay, cognitive motor or visual disabilities brainstem auditory evoked potential (BAEP) may be recommended [6]. Comparing Otoacoustic emissions (OAEs) are low-level signals emitted the BAEP, a-ABR, and auditory transitory evoked otoacoustic inside the and recorded in the auditory canal. OAEs were emissions (a-TEOAE); measuring the variables of sensitivity, theorized over 60 years ago by the biophysicist [1]; although his proposal of an active cochlear process was not ratio demonstrated that overall the BAEP was the better test. specificity, positive and negative predictive value and odds recorded and - tentatively - explained by Kemp who used a low- widely accepted until the 1970s. The first human OAEs were to be predictions, and a much lower false positive rate than the EOAE level click as the and recorded the cochlear echoes [2, 3]. andThe a-ABRBAEP had[6]. higher sensitivity and specificity, accuracy in its Since Kemp’s observation and subsequent experiment(s) OAEs have been studied extensively and implemented as a routine OAE use neonatal screening test for hearing loss. In addition, neonatal hyperbilirubinemia, familial auditory neuropathy, end-stage loss occurring in 1-3 infants per 1000 in Canada [9]. Otoacoustic emissionsHearing (OAEs) loss is are a common often used deficit, in combination with severe with to profound detailed the conditions which may precipitate hearing loss in children medical histories to reveal the etiology of hearing loss in infants andrenal in disease, which OAEsand neurofibromatosis have been utilized type[3-7]. II The(NF2) purpose are some of the of ensuing discussion is to demonstrate the effectiveness of OAEs typically normal in familial auditory neuropathy with absence (and the various tests inspired by the mechanism) as a versatile of[7, auditory 10]. For brainstem example, responses otoacoustic [7]. emission The OAE recordings is a normal are component of screening and experimentation. physiologic response generated by the outer hair cells of the Comparison of tests cochlea. A hearing sensitivity of 30 dB HL is indicated by a pass on an OAE test [11]. Hospital based universal neonatal hearing screening programs are at present widely used; the most effective ones Hyperbilirubinemia are evoked otoacoustic emissions test (EOAE), followed by an Hyperbilirubinemia has devastating effects on the auditory automated auditory brainstem response (a-ABR) for all infants system. Even short term increases in bilirubin levels can induce temporary or permanent changes in evoked potentials [4]. for detecting hearing loss in high-risk neonates has not been fully Baradaranfar et al. conducted a study on newborn babies with elucidated.failing the EOAE Examinations [3, 6, 8]. Thehave accuracy often been and hampered efficacy of by these excessive tests environmental electrical “noise”, electro-myogenic interference ABR, 9 with abnormal ABRs, 5 had no ABR waves at all and 4 (from behavioural distress), and cochlear immaturity [6, hadjaundice increased [4]. I-III Thirty-five and III-V infants intervals were and tested, latency 26 in had all normalwaves. 8]. Subsequently, visual reinforcement (VRA) is Twenty-six infants had normal hearing, 4 mild to moderate typically recommended, however, in the case of developmental

Cite this article: Davenport SA, Hebb ALO (2018) Otoacoustic Emissions: An Invaluable Screen of Neonatal Hearing. Ann Otolaryngol Rhinol 5(5): 1222. Hebb et al. (2018) Email: [email protected] Central hearing loss, and 5 suffered from severe to profound hearing loss. screening and experimentalresearch on mechanisms underlying OAE could be recorded in 1 infant with mild to moderate hearing hearing loss. loss and 4 with severe to profound hearing loss. Overall, 26 had normal tests and in 5 infants, abnormal results were localized to REFERENCES the retro-cochlear region indicative of auditory neuropathy [4]. 1. Gold T, Pumphrey RJ. Hearing. I. The cochlea as a frequency analyzer. Proc R Soc Lond B Biol Sci. 1948; 135: 462–491. Kidney Disease 2. Kemp DT. Stimulated acoustic emissions from within the human Abnormalities in auditory systems are frequent in children . JASA. 1978; 64:1386–91. with end-stage renal disease (ESRD); there is not yet any 3. Pigasse G. 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Cite this article Davenport SA, Hebb ALO (2018) Otoacoustic Emissions: An Invaluable Screen of Neonatal Hearing. Ann Otolaryngol Rhinol 5(5): 1222.

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