Revisiting Oto-acoustic Emissions
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REVIEW Revisiting Oto-acoustic Emissions Leonard Jie Min Soh, MBBS, MRCS, Yew Meng Chan, MBBS, FRCS, FAMS Department of Otorhinolaryngology, Singapore General Hospital, Singapore ABSTRACT Oto-acoustic emissions (OAEs) are an audiometric diagnostic test that allows quick objective measure of hair cell function in the inner ear. It is a reflection of hearing function at the interface of conductive and sensorineural components in the human ear. Unfortunately, it is not commonly used due to the unique expertise and niche equipment required to successfully carry it out. This article is to further shed light about the use of such tests to junior doctors so that such resources can be better utilised. It also reviews the current and possible future applications of OAEs at the frontiers in otology today. Keywords: Oto-acoustic emissions, TEOAE, DPOAE INTRODUCTION battery. It is a means of non-invasively acquiring The Singapore General Hospital ENT hearing centre information about disorders of an essential element has an armamentarium of audiological resources to of sound processing and hence allows assessment help establish hearing thresholds accurately and to of loss of sensitivity, compression, and frequency- determine the presence of impairment; site, type selectivity of the hearing organ. They are a fast and (conductive, sensorineural or mixed) and severity easy-to-handle method for objectively examining of the hearing loss. Tests are mainly divided into cochlear function. behavioural (pure tone and speech) and objective (tympanometry, auditory evoked potentials, Present OAEs in an ear indicate many things about otoacoustic emissions etc.) the auditory system. First, they tell us that the conductive mechanism of the ear is functioning By and far, the workhorse audiological properly. This includes proper forward and reverse investigations of choice are mainly behavioural transmission, no blockage of the external auditory pure tone and speech audiometry testing which canal, normal tympanic membrane movement, requires the cooperation of the patient. However, and a functioning impedance matching system. objective tests such as the acoustic reflexes and Present OAEs also indicate that outer hair cell oto-acoustic emissions (OAEs) are not commonly (OHC) function is normal, which, in most cases, used due to the unique expertise and niche correlates with normal hearing sensitivity. equipment required to successfully carry it out. Subjective tests such as pure tone audiometry, are only able to assess disorders of sound processing Oto-acoustic emission measurements are a as a whole. Tympanometry, OAEs, and auditory standard part of the audiological diagnostic test brainstem responses (ABRs), in combination, allow 86 Proceedings of Singapore Healthcare Volume 24 Number 2 2015
Revisiting OAEs for a differentiation between sound-conductive, provide a means of conveying vibrational energy cochlear, and neural hearing loss. Minute changes back to the middle ear in a reversal of the process in hearing capability are detectable by OAEs. They that normally delivers auditory stimulation to the are therefore a suitable means for detecting early hair cells. Theses sounds can be picked up and impairment, for example, caused by noise exposure recorded by a sensitive microphone fitted in the ear or ototoxic drugs, as well as for monitoring hearing canal. Most patients with cochlear sensorineural recovery after a sudden hearing loss. They are also hearing impairment have a loss of this amplification the first choice investigations for newborn hearing mechanism. screening programs around the world. They are easy to obtain, non-invasive, and provide reliable Oto-acoustic emissions are generated only when information regarding cochlear status in a relatively the organ of corti and the middle ear are in near short time. With all its benefits, OAE testing does normal conditions; Being able to reach as loud as have some limitations; It does not evaluate the 30dB SPL. They measure specifically cochlear hair inner hair cells (IHC), 8th cranial nerve function, function in the peripheral auditory system. ascending central auditory pathway, or auditory processing function. Thus, they are not always used HISTORY OF OAEs in isolation. Oto-acoustic emissions were discovered in July 1977 by Professor David Kemp, a physicist working THE SCIENCE BEHIND OAEs at the Royal National Ear, Nose and Throat Hospital Oto-acoustic emissions are air pressure fluctuations at that time1. Kemp was conducting psychoacoustic in the ear canal caused by vibration of the experiments on his own ears measuring changes eardrum driven by the cochlea. It is a common in hearing thresholds and loudness perception misconception to think of OAE as sounds “emitted” associated with small changes in frequency. He by the cochlea itself, but technically sound pressure was motivated by his observations that hearing is not produced in any measurable quantity until thresholds exhibited periodic patterns of peaks and the eardrum, driven by the cochlea, vibrates against valleys, as did loudness estimates, when measured the adjacent air in the ear canal. The physical in small increments of frequency. Interestingly, construction of the middle ear positively helps us the valleys in hearing thresholds (frequencies to observe OAEs. The efficient coupling that the where hearing appeared to be most sensitive) middle ear provides between the low impedance approximately aligned with peaks in loudness of the thin light eardrum and the high impedance estimates (frequencies where sounds seemed of the closed fluid-filled capsule, that is the inner disproportionately louder). These observations ear, operates equally well in both directions. It reminded Kemp of a prediction made by the British matches cochlea to eardrum just as well as eardrum astrophysicist Thomas Gold. Upon observing the to cochlea. expansive dynamic range of hearing, Gold had postulated that the ear must contain a nonlinear How does the cochlea vibrate the eardrum to amplifier – an amplifier that provided gain for low create sound, i.e., an OAE? Simply put, moving the inputs to make them audible but became passive eardrum from within the sealed fluid-filled cochlea to make high inputs tolerable. This is known today requires an imbalance of vibrational fluid pressure as the cochlea amplifier; Kemp connected his on the oval and round windows. This requires the observation of the peaks and valleys in behavioural diversion of vibrational energy away from the data and Gold’s predictions and hypothesised primary hearing process and the transmission of that the valleys in hearing sensitivity and peaks that energy back to the base of the cochlea in a way in loudness estimates could be due to these that can physically create this pressure difference sounds produced by the ear. That is, the presence and cause middle ear motion. The initial source of an internal sound source at a given frequency of vibrational energy needed to generate OAEs is would add to any external tone played leading to generally considered to be the electromotility of hypersensitivity in threshold measures as well as the three outer rows of the cochlea’s sensory hair a heightened perception of loudness. With this cells, the outer hair cells (OHCs)1,2. Motility of OHCs notion, he salvaged a miniature microphone from a as they respond to auditory stimulation provides hearing aid and sealed it with silicone putty to keep the engine of the “cochlear amplifier.” A reverse the sound in over his ear, and attached the output travelling wave along the basilar membrane would to an analyser to see if sounds could be picked up. Proceedings of Singapore Healthcare Volume 24 Number 2 2015 87
Review Temporal bone Pinna Malleus Waveform 1 Attenuator Semicircular Waveform 2 Attenuator canals Sound source 1 Cochlear nerve (VIII) Sound source 2 Microphone Cochlea Analyser Amplifier Incus External Stapes in Eustachian tube auditory oval Earpiece sealed canal window into ear canal Cochlear emission Fig. 1. Oto-acoustic emission system. Indeed they did and today we know them as oto- from patients who are comatose. The recording acoustic emissions (OAEs) and use them routinely time for OAEs is quick. Quiet and cooperative for a multitude of clinical purposes. patients usually require less than a few minutes per ear to get an accurate reading but for METHOD uncooperative or noisy patients, recordings may Oto-acoustic emissions are measured by presenting take significantly longer or may be impossible to a series of sounds or “clicks” to the ear through a obtain on a given visit. Each individual has his/ probe that is snugly inserted into the ear canal her own characteristic repeatable OAEs and hence probe (Fig. 1). It contains: repeatability or reproducibility of OAEs can help to verify the response. 1. A loudspeaker that generates the sounds Although testing does not require patient 2. A sensitive microphone that measures the cooperation, a seal probe, which helps to block resulting OAEs that are produced in the out external noise, ear canal patency with an cochlea and are transmitted through the unobstructed outer ear canal and absence of middle ear into the outer ear canal significant middle ear pathology and background room noise should be below 40dB due to the 3. A signal separating processor that can sensitivity of OAEs to noise. All OAEs are analysed discriminate the sound of the OAE from the relative to the noise floor; therefore, reduction of stimulus sound and other noise. physiologic and acoustic ambient noise is critical for good recordings. Depending on the intended A probe with a soft flexible tip is inserted in the ear portion of the cochlea that is of concern (frequency canal to obtain a seal. Different probes are used specific response), the acoustic stimulus can be for neonates and adults and are calibrated varied from no stimulus, to click stimuli (wide-band differently because of the significant difference in noise), or tones (narrow band noise). ear canal volume. Oto-acoustic emissions are the only audiological Oto-acoustic emissions are appropriate for use in test to selectively assess cochlear dysfunction. difficult to test patients: newborn infants, young Along with tympanometry and auditory uncooperative children and individuals with brain stem responses, OAEs can aid in the developmental delays. Because no behavioural differentiation between middle-ear, cochlear, and response is required, OAEs can be obtained even neural disorders. 88 Proceedings of Singapore Healthcare Volume 24 Number 2 2015
Revisiting OAEs Table 1. Types of OAEs. Sounds emitted without an acoustic stimulus (i.e., spontaneously) Spontaneous OAEs in humans usually consist of a stable tone with a bandwidth (frequency stability) within the 1-2 kHz region; amplitudes are between -5 and 14 dB SPL. They are generally not found Spontaneous OAEs (SOAEs) in individuals with hearing thresholds worse than 30 dB HL. Therefore, the presence of SOAEs are usually considered a sign of cochlear health, but the absence of SOAEs are not necessarily a sign of abnormality. Occur during or after a stimulus and can be further classified into: Transient evoked OAEs (TEOAEs) Sounds emitted in response to an acoustic stimulus of very short duration; usually clicks but can be tone-bursts. Produces complex frequency-dispersed oscillation consisting mainly of the frequencies present in the stimulus. Because OAEs are evoked by transient signals that have a wide frequency response, a broad region of the cochlea responds, providing information on the frequency range from 1 to 4 kHz, and only if hearing thresholds are 20 dB HL or better. Stimulus frequency OAEs (SFOAEs) Stimulus frequency OAEs are responses recorded by stimulation Evoked OAEs (EOAEs) of a continuous pure tone. Because the stimulus and the emission overlap in the ear canal, the recording microphone detects both. Therefore, interpretation depends on reading complicated series of ripples in the recording. At present, SFOAEs are not used clinically. Distortion product OAEs (DPOAEs) Occur as a response to two simultaneous pure tones (typically 55 & 65 dB SPL) at two different frequencies. It allows greater frequency specificity and can be used to record at higher frequencies than TOAEs. The use of different frequency combinations allows a larger portion of the basilar membrane to be stimulated and its response analysed (between 1–8 kHz frequency range). TYPES OF OAEs that patient can still be monitored (so long as Oto-acoustic emissions can be broadly classified their hearing loss is not too great) for possible into two groups (Table 1). Two main types of evoked progression. Lastly, using DPOAEs can provide OAE are used in clinical practice: TEOAEs & DPOAEs. some indication of degree and configuration Both are complementary, as the former is best of the hearing loss given its ability to estimate detecting threshold elevation below 4kHz, giving (albeit not accurately) thresholds as well as its an overview of cochlear activity; the latter above spectrum of frequency detection. it, giving specific quantitative information about sound processing at distinct cochlear places. In CLINICAL APPLICATIONS short, the TEOAE response “sees” almost the whole There are four main OAE applications in clinical cochlea, whereas the DPOAE response reflects only diagnostics: newborn hearing screening, a limited region of the cochlea but gives some Topological diagnostics, quantitative evaluation indication of the extent of loss. of hearing loss and recruitment, and monitoring cochlear function. The advantages of DPOAE as compared to TEOAE are summarised as below: Newborn Hearing Screening Otoacoustic emissions (TEOAE and DPOAE) are • First, DPOAEs are able to test higher frequencies widely regarded as being suitable for screening in than TEOAEs, making them more sensitive newborns and infants3–5, since they are not present to the high frequencies affected first in in the case of OHC dysfunction6,7. The premise certain conditions e.g. ototoxicity and noise for this approach is that inner-ear hearing loss induced damage. always includes OHC damage or malfunction. Its use is widely incorporated into universal newborn • Secondly, DPOAEs can be recorded in the hearing screening programs and in pediatric clinics presence of mild to moderate hearing loss as where the patients are too young to be cooperative compared to TEOAEs, which give a more binary in conventional hearing tests8. The OAE technology response. Therefore, if hearing loss already exists, can have a sensitivity of 95% and specificity of 90%9 Proceedings of Singapore Healthcare Volume 24 Number 2 2015 89
Review whilst the referral rate is 5–20% when screening is evaluation before the age of 3 months. With performed within the first 24 hours of life10. successful implementation of an extensive UNHS coupled with early and effective intervention, This is usually combined with ABR methods for this maximises the chances of affected children to screening protocols due to the disadvantage of better integrate into mainstream society. OAEs giving false positive results ranging from 11 to 35%7,11 in paediatric patients with significant Topological Diagnostics conductive losses12; more often than not due to The management for a hearing disorder can be Eustachian tube dysfunction or residual amniotic developed only after knowing which stage of the fluid in the tympanic cavity which attenuates auditory pathway is impaired. Psychoacoustic the OAE signal. To avoid high referral rates, some tests are able to differentiate between conductive, hearing screening protocols add on ABR screening sensorineural or mixed hearing loss by evaluating before referral for diagnostic assessment13. the difference between air and bone-conductive pure-tone thresholds. However, the differentiation It is widely accepted that children with untreated between a sensory (cochlear) and a neural disorder loss generally perform poorly academically as with subjective testing is unreliable. In addition, in compared to their peers. Hearing loss affects uncooperative patients or infants, psychoacoustic both reading and writing skills, resulting in tests cannot be performed. In such cases, only poor communication and language skills. The objective tests help in achieving the goal of literature supports the trend that the longer the determining end-organ integrity. delay in intervention, the poorer the academic outcomes tended to be14. In Yoshinaga-Itano’s The use of OAEs to assist in the diagnosis of retro- 10-year longitudinal study15 on the effect of early cochlear pathologies have become standard in identification on the development of deaf and clinical practice. OAEs arise from the peripheral hard-of-hearing infants and toddlers, the language auditory system; therefore, a logical conclusion is abilities of hearing-impaired children identified that they will be present in cases of retro-cochlear before 6 months were pitted against those pathology. One of the most common applications identified after 6 months. The results were not would be in the diagnosis of auditory neuropathy; surprising, whereby those detected early before 6 In such a condition, the patient displays auditory months had a significantly better average language characteristics consistent with normal OHC and quotient as compared to those after 6 months, abnormal neural function at the level of the VIIIth across all degrees of hearing loss. In addition, if nerve; where these characteristics are observed such a disability is untreated, it can also lead to on clinical audiologic tests as normal oto-acoustic emotional and psychosocial handicaps16. Delayed emissions (OAEs) in an absent or severely abnormal identification and management can impede a auditory brainstem response (ABR), result in child’s ability to adapt to the hearing world, and poor word recognition and variable audiogram if remedied early facilitates full advantage of the findings18,19. These patients are distinguished plasticity of the developing sensory systems, so as from patients with space-occupying lesions, such to allow normal social development and improved as VIIIth nerve tumours, or multiple sclerosis, in future prospects. that radiological evaluation yields normal results and even the most peripheral responses from the In Singapore, the Universal National Hearing VIIIth nerve are absent. The role of OAEs is evident Screening programme was set up in 2002, and in ruling out OHC dysfunction, and together first implemented in KK Women’s and Children’s with a normal tympanometry points to a retro- Hospital (KKWCH) which accounts for a third cochlear lesion. of deliveries; and subsequently adopted by all public and private hospitals in the country which A combination of present OAEs with altered boasts obstetrics services. The programme17 aims ABRs must also bring into mind other differential to screen all neonates before they are discharged diagnosis. These cases belong to clinical profiles from the hospital. Newborns who failed the involving vestibular schwanommas and other screening had a repeat screening within 4 to 6 central auditory system disorders. In the setting of a weeks; failing both screening tests would result tumour in the internal auditory canal, interestingly in referral for audiological diagnosis and medical OAEs (TEOAES or DPOAEs) can be affected or 90 Proceedings of Singapore Healthcare Volume 24 Number 2 2015
Revisiting OAEs unaffected by the presence of space occupying frequencies first, with hearing loss systematically lesion such as a vestibular schwanomma. An progressing to the lower frequencies26,27. explanation for such data can be derived from information of how the growth of the tumor affects The biggest limitation to OAEs is that they are the vascular supply of the cochlea; especially if it very sensitive to middle ear dysfunction, which is impinges on the internal auditory artery or how common in children and in those who are immuno- the growth of the tumors induces mechanical compromised. Although OAEs are being employed pressure alterations on the vascular supply and the for ototoxicity monitoring, they are rarely used in cochlea itself20. OAE-based measures can provide isolation. A change in OAEs from one test session to information on the sensory component of any the next is a strong indicator for the need for more hearing disorder, thus they can provide precise conventional and HFA testing. This allows cost indices of evaluating sensori-neural hearing effective testing whereby further testing is avoided impairment cases. In addition, in patients with unless OAEs suggest otherwise. Early detection suspected labrynthine schwanommas, the OAE of ototoxicity is an important signal for alternate can be of some assistance in the differentiation management options such as substitution of of cochlea and vestibular types of schwannomas medications, change of dosages, and mode serving as an adjunct to imaging investigations21. of administration. Quantitative Evaluation of Hearing Response Much like the use of OAEs in ototoxicity and Recruitment monitoring, OAEs can be used to provide objective The concept behind this lies in the ability of OAEs confirmation of cochlea dysfunction in patients to identify regions of the cochlea with damage, with normal audiograms. In noise induced hearing which can assist in programming a hearing aid. loss, threshold elevations are proven to be in the Simply explained, when OAEs are absent, we mid to high frequencies28; OAE protocols can thus assume hearing loss of greater than about 25 dB HL be used very efficiently to monitor small elevations at the frequency where the emission is absent and in threshold progress29. Oto-acoustic emissions this gives us some idea of hearing levels. Bear in can provide an early and reliable warning sign of mind however, amplification protocols for different cochlea dysfunction due to noise/music exposure patient groups are much more complex, usually before any problem is evident on the audiogram30. requiring a battery of tools such as ABR before we Some studies even go as far as to say that OAEs can use this data to program amplification for these can be a diagnostic predictor for noise-induced- patients. Oto-acoustic emissions are one of the hearing-loss-risk31. many tools that help influence the programming. Intra-operatively, its use can be seen in its live Monitoring Cochlea Function monitoring of changes in cochlea status over Oto-acoustic-emission measures are stable time during surgery, where morbidity is high through time in any particular individual and and utmost care is taken to minimise damage hence are capable of monitoring recovery from to cochlea nerve function32. For example in the OHC impairment22,23. Three main approaches have context of vestibular schwanomma surgery, OAEs been used for monitoring the effects of ototoxic are taken during pre- as well as intraoperative medications: basic audiologic assessment, high monitoring to prognosticate post-operative frequency audiometry (HFA; 10–18 kHz), and cochlea function33,34. OAEs24. Ototoxic drugs exert their effect on OHC function (although not solely on OHCs), and Future Applications OAEs are OHC dependent. With ototoxicity, OAEs Our persistent uncertainties about OAEs are a have been shown to decrease simultaneously testament to their complex nature. Not only are we with changes in HFA thresholds and before still debating about their generation mechanisms, changes appear in the conventional audiometric different ideas about how they transmit out of frequencies24. Part of this group are therapeutic the cochlea still exist. One thing is clear, the uses drugs such as antibiotic (e.g., aminoglycosides) of OAE measurements as diagnostic tools have and antitumor chemotherapeutic (e.g., cisplatin) obvious advantages (especially in their objectivity agents25, are reported to induce an irreversible and restriction to the cochlea) that they have been hearing loss, which typically affects the highest rapidly incorporated as clinical tools. Proceedings of Singapore Healthcare Volume 24 Number 2 2015 91
Review Arch Otorhinolaryngol 1979;224(1–2):37–45 doi: The holy grail is to be able to use OAEs to 10.1007/BF00455222. definitively determine hearing thresholds; 3. American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 position statement: currently it cannot be used in isolation for such a Principles and guidelines for early hearing detection and purpose. In many cases, it is probably better off intervention programs. Pediatrics 2007;120(4):898–921 to stick with behavioural threshold estimation, doi: 10.1542/peds.2007-2333. 4. Berninger E, Westling B. Outcome of a universal newborn but one can certainly see the benefit of having an hearing-screening programme based on multiple objective non-invasive tool for gathering threshold transient-evoked otoacoustic emissions and clinical information in certain populations and situations. brainstem response audiometry. Acta Otolaryngol 2011;131(7):728–39 doi: 10.3109/00016489.2011.554440. So far, attempts to predict hearing thresholds from 5. Akinpelu OV, Peleva E, Funnell WR, Daniel SJ. Otoacoustic DPOAE and TEOAE levels measured in response emissions in newborn hearing screening: A systematic to fixed-level stimuli varied in frequency were not review of the effects of different protocols on test conclusive35,36. However, there have been efforts at outcomes. Int J Pediatr Otorhinolaryngol 2014;78(5):711– 7 doi: 10.1016/j.ijporl.2014.01.021. predicting hearing thresholds using DPOAE input/ 6. Kemp DT, Ryan S. Otoacoustic emission tests in output functions37 which may open the door to neonatal screening programmes. Acta Otolaryngol such an avenue in future. 1991;111(s482):73–84 doi: 10.3109/00016489109128029. 7. Norton SJ, Gorga MP, Widen JE, Folsom RC, Sininger Y, Cone-Wesson B, et al. Identification of neonatal hearing Age related hearing loss is one of the most impairment: Evaluation of transient evoked otoacoustic ubiquitous pathology that is commonly seen emission, distortion product otoacoustic emission, and auditory brain stem response test performance. Ear Hear in clinics. It is well known that signs of aging are 2000;21(5):508–28 doi: 10.1097/00003446-200010000- evident at higher frequencies. However, new 00013. findings have demonstrated that signs of aging 8. Berg AL, Prieve BA, Serpanos YC, Wheaton MA. Hearing screening in a well-infant nursery: Profile of automated are visible in DPOAE levels at frequencies as low as abr-fail/oae-pass. Pediatrics 2011;127(2):269–75 doi: 1000 Hz for individuals as young as 20 years old38. 10.1542/peds.2010-0676. This forces us to change our perception about 9. Taylor CL, Brooks RP. Screening for hearing loss and middle-ear disorders in children using teoaes. Am J Audiol auditory aging and when might be the right time 2000;9(1):50–5 doi: 10.1044/1059-0889(2000/001). to start awareness campaigns to protect our ears. 10. Erenberg A, Lemons J, Sia C, Trunkel D, Ziring P. Newborn and infant hearing loss: Detection and intervention. American academy of pediatrics. Task force on With innovative applications of OAEs emerging newborn and infant hearing, 1998–1999. Pediatrics everyday, there is no lack of controversy over its 1999;103(2):527–30 doi: 10.1542/peds.103.2.527. reliability in uses such as for tinnitus monitoring, 11. Barker SE, Lesperance MM, Kileny PR. Outcome of newborn hearing screening by ABR compared with four Meniere’s disease and even acoustic fingerprinting. different DPOAE pass criteria. Am J Audiol 2000;9(2):142– Further research has to be put into its validation for 8 doi: 10.1044/1059-0889(2000/017). such purposes. No doubt, OAEs have been able to 12. Doyle KJ, Rodgers P, Fujikawa S, Newman E. External effectively segregate good and bad ears over the and middle ear effects on infant hearing screening test results. Otolaryngol Head Neck Surg 2000;122(4):477–81 past decade, with newborn hearing screening as doi: 10.1067/mhn.2000.102573. the main driving force. The techniques for making 13. Arslan S, Isik AU, Imamoglu M, Topbas M, Aslan Y, Ural such decisions are still being refined today39. A. Universal newborn hearing screening; automated transient evoked otoacoustic emissions. B-ENT 2012;9(2):122–31. Its main strength is in its non-invasive, frequency 14. Yoshinaga-Itano C, Apuzzo ML. The development of deaf specific, objective measurement of cochlea and hard of hearing children identified early through the high-risk registry. Am Ann Deaf 1998;143(5):416–24 doi: audiological function, which charges it with 10.1353/aad.2012.0118. invaluable roles. It is safe to say that OAEs will 15. Yoshinaga-Itano C, Sedey AL, Coulter DK, Mehl AL. continue to play an important role in routine Language of early- and later-identified children with hearing loss. Pediatrics 1998;102(5):1161–71. audiological assessments as well as its less known 16. Filipo R, Bosco E, Barchetta C, Mancini P. Cochlear uses. Its promise in further developments can only implantation in deaf children and adolescents: Effects on open up exciting possibilities in the years to come. family schooling and personal well-being. Int J Pediatr Otorhinolaryngol 1999;49(1 Suppl):S183–7 doi: 10.1016/ S0165-5876(99)00212-8. REFERENCES 17. Low WK, Pang KY, Ho LY, Lim SB, Joseph R. Universal 1. Kemp DT. Stimulated acoustic emissions from newborn hearing screening in Singapore: The need, within the human auditory system. J Acoust Soc Am implementation and challenges. Ann Acad Med 1978;64(5):1386–91 doi: 10.1121/1.382104. Singapore 2005;34(4):301–6. 2. Kemp DT. Evidence of mechanical nonlinearity and 18. Narne VK, Prabhu PP, Chatni S. Time-frequency analysis frequency selective wave amplification in the cochlea. of transient evoked-otoacoustic emissions in individuals 92 Proceedings of Singapore Healthcare Volume 24 Number 2 2015
Revisiting OAEs with auditory neuropathy spectrum disorder. Hear Res 30. Baradarnfar MH, Karamifar K, Mehrparvar AH, 2014;313:1–8 doi: 10.1016/j.heares.2014.04.005. Mollasadeghi A, Gharavi M, Karimi G, et al. Amplitude 19. Norrix LW, Velenovsky DS. Auditory neuropathy spectrum changes in otoacoustic emissions after exposure to disorder (ANSD): A review. J Speech Lang Hear Res industrial noise. Noise Health 2012;14(56):28–31 doi: 2014;57(4):1564–76 doi: 10.1044/2014_JSLHR-H-13-0213. 10.4103/1463-1741.93329. 20. Telischi FF, Roth J, Stagner BB, Lonsbury-Martin BL, Balkany 31. Lapsley Miller JA, Marshall L, Heller LM, Hughes LM. Low- TJ. Patterns of evoked otoacoustic emissions associated level otoacoustic emissions may predict susceptibility with acoustic neuromas. Laryngoscope 1995;105(7 Pt to noise-induced hearing loss. J Acoust Soc Am 1):675–82 doi: 10.1288/00005537-199507000-00002. 2006;120(1):280–96 doi: 10.1121/1.2204437. 21. Kagoya R, Shinogami M, Kohno M, Yamasoba T. 32. Cueva RA. Preoperative, intraoperative, and postoperative Distortion-product otoacoustic emission tests evaluate auditory evaluation of patients with acoustic neuroma. cochlear function and differentiate cochlear and Otolaryngol Clin North Am 2012;45(2):285–90 doi: vestibular schwannoma. Otolaryngol Head Neck Surg 10.1016/j.otc.2011.12.002. 2013;148(2):267–71 doi: 10.1177/0194599812469502. 33. Morawski K, Namyslowski G, Lisowska G, Bazowski P, 22. McMillan GP, Reavis KM, Konrad-Martin D, Dille MF. The Kwiek S, Telischi FF. Intraoperative monitoring of cochlear statistical basis for serial monitoring in audiology. Ear Hear function using distortion product otoacoustic emissions 2013;34(5):610–8 doi: 10.1097/AUD.0b013e31828a21b3. (dpoaes) in patients with cerebellopontine angle tumors. 23. Reavis KM, Phillips DS, Fausti SA, Gordon JS, Helt WJ, Otol Neurotol 2004;25(5):818–25 doi: 10.1097/00129492- Wilmington D, et al. Factors affecting sensitivity of 200409000-00028. distortion-product otoacoustic emissions to ototoxic 34. Kim AH, Edwards BM, Telian SA, Kileny PR, Arts HA. hearing loss. Ear Hear 2008;29(6):875–93 doi: 10.1097/ Transient evoked otoacoustic emissions pattern as a AUD.0b013e318181ad99. prognostic indicator for hearing preservation in acoustic 24. American academy of audiology clinical practice neuroma surgery. Otol Neurotol 2006;27(3):372–9 doi: guidelines on ototoxicity monitoring oct 2009; 10.1097/00129492-200604000-00014. 25. Reavis KM, McMillan G, Austin D, Gallun F, Fausti SA, 35. Mertes IB, Goodman SS. Short-latency transient-evoked Gordon JS, et al. Distortion-product otoacoustic emission otoacoustic emissions as predictors of hearing status and test performance for ototoxicity monitoring. Ear Hear thresholds. J Acoust Soc Am 2013;134(3):2127–35 doi: 2011;32(1):61–74 doi: 10.1097/AUD.0b013e3181e8b6a7. 10.1121/1.4817831. 26. Kopelman J, Budnick AS, Sessions RB, Kramer MB, 36. Shaffer LA, Dhar S. DPOAE component estimates and Wong GY. Ototoxicity of high-dose cisplatin by bolus their relationship to hearing thresholds. J Am Acad administration in patients with advanced cancers and Audiol 2006;17(4):279–92 doi: 10.3766/jaaa.17.4.6. normal hearing. Laryngoscope 1988;98(8 Pt 1):858–64 37. Neely ST, Johnson TA, Kopun J, Dierking DM, Gorga MP. doi: 10.1288/00005537-198808000-00014. Distortion-product otoacoustic emission input/output 27. Stavroulaki P, Apostolopoulos N, Segas J, Tsakanikos characteristics in normal-hearing and hearing-impaired M, Adamopoulos G. Evoked otoacoustic emissions--an human ears. J Acoust Soc Am 2009;126(2):728–38 doi: approach for monitoring cisplatin induced ototoxicity in 10.1121/1.3158859. children. Int J Pediatr Otorhinolaryngol 2001;59(1):47–57 38. Poling GL, Siegel JH, Lee J, Lee J, Dhar S. Characteristics doi: 10.1016/S0165-5876(01)00455-4. of the 2f1-f2 distortion product otoacoustic emission 28. Attias J, Horovitz G, El-Hatib N, Nageris B. Detection in a normal hearing population. J Acoust Soc Am and clinical diagnosis of noise-induced hearing loss by 2014;135(1):287–99 doi: 10.1121/1.4845415. otoacoustic emissions. Noise Health 2001;3(12):19–31. 39. Reuven ML, Neely ST, Kopun JG, Rasetshwane DM, Allen 29. Sisto R, Chelotti S, Moriconi L, Pellegrini S, Citroni A, JB, Tan H, et al. Effect of calibration method on distortion- Monechi V, et al. Otoacoustic emission sensitivity to low product otoacoustic emission measurements at and levels of noise-induced hearing loss. J Acoust Soc Am around 4 kHz. Ear Hear 2013;34(6):779–88 doi: 10.1097/ 2007;122(1):387–401 doi: 10.1121/1.2737668. AUD.0b013e3182994f15. Proceedings of Singapore Healthcare Volume 24 Number 2 2015 93
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