Extratympanic electrocochleography in the diagnosis of auditory neuropathy/auditory dyssynchrony

Abstracts

O potencial evocado auditivo de tronco encefálico (PEATE) vem sendo amplamente utilizado como método para avaliação da função coclear em indivíduos com diagnóstico de neuropatia/dessincronia auditiva (NA/DA). Na ausência das emissões otoacústicas, muitos casos de NA/DA foram diagnosticados pela presença do microfonismo coclear (MC) identificado no PEATE. OBJETIVO: Demonstrar a aplicabilidade clínica da eletrococleografia extratimpânica (Ecog-ET) no diagnóstico diferencial da NA/DA quando comparada ao PEATE. MATERIAL E MÉTODO: Uma criança com 4 anos de idade, com diagnóstico de NA/DA atendida no Centro de Pesquisas Audiológicas realizou a Ecog-ET com tone burst de 2000Hz nas polaridades de rarefação e condensação. RESULTADOS: Ilustrou-se o registro da Ecog-ET. Com a utilização de protocolo apropriado, o MC pode ser evidenciado e confirmado na Ecog, com qualidade de registro superior ao obtido no PEATE. CONCLUSÃO: A Ecog-ET permitiu uma análise mais detalhada do MC quando comparada ao PEATE tendo, portanto aplicabilidade clínica na investigação da função coclear na NA/DA.

audiometria de resposta evocada; criança; perda auditiva; potenciais microfônicos cocleares

REVIEW ARTICLE

Extratympanic electrocochleography in the diagnosis of auditory neuropathy/auditory dyssynchrony

Adriana Ribeiro Tavares Anastasio^I; Kátia de Freitas Alvarenga^II; Orozimbo Alves Costa Filho^III

^IDoctor, Speech Therapist, Adjunct Professor, Speech Therapy Course, FMRP-USP

^IISpeech Therapist, Habilitation Degree (Livre-Docente) Associate Professor, Speech Therapy Course, FOB-USP

^IIIPhysician, Otologist, Full Professor, USP Bauru Campus

^{Address for correspondence}

SUMMARY

The brainstem auditory evoked potential (BAEP) is being extensively used as a method for the evaluation of cochlear function in individuals with diagnosis of auditory neuropathy/auditory dyssynchrony (AN/AD). In the absence of otoacoustic emissions, many cases of AN/AD have been diagnosed by the presence of CM identified in the BAEP.

AIM: to demonstrate the clinical applicability of extratympanic electrocochleography (ET-Ecochg) in the differential diagnosis of AN/AD compared to the BAEP.

METHOD: a 4-year-old child with a diagnosis of AN/AD seen at the Audiological Research Center was submitted to ET-Ecochg with a 2000 Hz tone burst in rarefaction and condensation polarities.

RESULTS: the ET-Ecochg exam was illustrated. Using an appropriate protocol, it was possible to demonstrate CM and to confirm it in the Ecochg, with a recording quality superior to that obtained in the BAEP.

CONCLUSION: ET-Ecochg permitted a more detailed analysis of CM compared to the BAEP, thus showing clinical applicability for the investigation of cochlear function in AN/AD.

Keywords: audiometry evoked response, child, hearing loss, cochlear microphonic potentials.

INTRODUCTION

In the past 20 years, scientists have described patients with similar clinical findings, but with a wide variety of terms to name those symptoms, such as brainstem processing syndrome, central auditory dysfunction, neural synchrony disorder, auditory neuropathy, and recently auditory dyssynchrony.^1,2

The term auditory neuropathy was first used in a paper published in 1996³ that attempted to classify patients that had a variety of auditory symptoms, a normal-functioning cochlea, and altered cochlear nerve function.

In 2001, some authors1 suggested the term auditory dyssynchrony instead of auditory neuropathy, as the cochlear nerve was not always injured, and therefore the old term would be semantically incorrect. Even with this recommendation, however, both terms are still used in papers that describe these patients. As a result, auditory neuropathy/dyssynchrony (AN/AD) has emerged as a third term.^3-10

AN/AD patients are subjects that may have normal tone thresholds or profound hearing loss. The condition is usually bilateral, but there are reports of unilateral cases in the literature. The disorder may be diagnosed at any age. Otoacoustic emissions (OAEs) and/or cochlear microphonics (CMs) are present regardless of the degree of hearing loss. Auditory brainstem evoked potentials (ABEPs), middle ear muscle reflexes and olivocochlear reflexes are absent. Audiograms, when they can be applied, may be flat or show an upward or downward-sloping curve or be completely irregular; findings usually do not match speech understanding difficulties.^1,11-15

It may be difficult to locate the injury site in AN/AD, although the presence of OAEs and/or CMs suggests that outer hair cells (OHC) are intact. The ABEP wave I, however, which is generated by the myelin-sheathed peripheral portion of the cochlear nerve, is absent in this auditory condition. Symptoms suggest a disorder involving inner hair cells (IHC), the synapses between IHC and the auditory nerve, and peripheral portions of the cochlear nerve.^16-18

Although the risk factors for AN/AD are unclear, some of the children with this disorder have a history of neonatal events such as premature birth, low birth weight, anoxia and hyperbilirubinemia.¹⁹

The presence of OAEs associated with absent ABEPs is pathognomonic of AN/AD, although in some cases OAE recordings may be absent. Consequently, depending on when the initial diagnosis is made, OAEs and absent ABEPs will not provide a final definition and diagnosis of AN/AD. In such cases, the presence of CMs becomes the determinant finding in the differential diagnosis of this condition.^1,20,21 Some authors have proposed that AN/AD be defined as a condition with absent or abnormal ABEPs including wave I, associated with present OAEs and/or CMs.²⁰

In the past 10 years, many papers on auditory neuropathy have underlined the role of CMs, which are now analyzed with greater care in AN/AD patients. Reports in the literature have shown that CMs in these patients are more prominent, having an abnormally increased amplitude,^23-26 and persist for up to 4 to 6 milliseconds after click stimulation,²² contrary to what is found in normal subjects.

Electrocochleography (ECoG), which had a significant clinical impact in the diagnosis and monitoring of Ménière’s disease,^27-29 and which objectively assesses cochlear potentials, is the indicated clinical procedure to analyze CMs.^30,31 The recent development of various non-invasive electrodes have reawakened interest in the clinical use of ECoG.^27,32 Although transtympanic electrocochleography (TT-ECoG) yields recordings with higher amplitudes and lower test-retest variability, it has the disadvantage of being an invasive procedure. Extratympanic electrocochleography (ET-ECoG), therefore, is clinically more useful in this context, supporting an audiological diagnosis and increasing knowledge about cochlear function in AN/AD.

Even though ECoG is the most appropriate procedure for assessing cochlear function, and therefore helping identify CMs and diagnosing AN/AD, there is little information in the literature on its use in this disorder.^4,5,33

ABEP testing has also been widely used in identifying CMs, the rationale being that insertion phones avoid the extensive magnetic field caused by supra-aural phones, which obscure cochlear potentials and, at times, the nerve action potential. Furthermore, CMs may be identified by recording auditory evoked potentials using negative and positive polarity acoustic stimuli in which results may be compared, given that CMs are affected by the stimulus polarity, contrary to ABEPs.^1,20,25,34

To confirm the presence of CMs, some researchers block the insertion phone plastic tube to guarantee that recordings are auditory neurophysiological responses that truly reflect acoustic stimulation, rather than electrical artifacts.^3,20,24

Although the literature has suggested that cochlear function is normal in AN/AD,^3,13,34 it is important to analyze CMs in these cases; a number of findings about this specific cochlear potential in AN/AD patients appear to show that the cochlea may be dysfunctional.^23-26

The use of ABEP testing of CMs seems inadequate, as CMs cannot be carefully analyzed by this method. A better analysis of CM amplitude and morphology would be obtained with tone bursts, rather than the clicks usually used in ABEP testing.^28,35,36

Based on this assumption, the aim of this paper was to demonstrate the clinical applicability of ET-ECoG in the differential diagnosis of AN/AD, compared to ABEP testing.

MATERIAL AND METHOD

A case description is made of a four-year-old child diagnosed with AN/AD. Following a term birth and the presentation of apnea and cyanosis three days later, the child was admitted into hospital and given gentamycin for 14 days. Hyperbilirubinemia ensued, requiring blood transfusion. Free-field audiological testing found a decreased auditory threshold that suggested a downward-sloping configuration moderate to severe hearing loss. Responses to intense speech were inconsistent. Immitance testing showed normal tympanometric curves and absent contralateral and ipsilateral acoustic reflexes. Transient and distortion product OAEs were present in both ears.

ABEP testing and ET-ECoG were done to aid in the differential diagnosis of AN/AD. The test protocol is described in Table 1. Both ABEP testing and ET-ECoG were done in an acoustically and electromagnetically treated room, using a Bio-logic Systems Corp.® Navigator Pro device, version 4.2.0. The skin was cleaned with abrasive paste; a small amount of electrolytic paste was placed on disposable electrodes. After electrode placement, the cables were connected. An Ear Tone 3A earphone was used. The following electrode arrangement was used for ABEP testing: active-frontal; reference-mastoid, and ground on the contralateral mastoid to the stimulated side. The active and ground ET-ECoG electrodes were placed frontally, and the reference electrode (TIPtrode model) was introduced into the acoustic canal.

Etymotic Research laboratories, based on insertion phone structure, developed the TIPtrode. It contains a plastic tube that conveys sound and that connects to the insertion phone tube. It is coated by a thin gold layer that conducts the auditory evoked potential electrical activity to the preamplifier.³⁷ The TIPtrode not only initiates acoustic stimuli, but is also the receptor for electrical activity. Following the registration protocol, the procedure for both ABEP testing and ET-ECoG was repeated in rarefaction polarity by blocking the insertion phone plastic tube with appropriate forceps that had two rubber olives on its extremity to avoid damage to the plastic tube and to stop the acoustic stimulus from reaching the auditory canal. In these circumstances, the cochlear potential disappears, and only any signal electrical artifacts remain.^20,24,38 This sequence aimed to assure the reliability of recordings and to confirm the biological response.

RESULTS

Figure 1 shows ABEP recordings in both ears in a four-year-old child diagnosed with AN/AD. CMs may be seen in the two upper recordings (R-rarefaction, and C-condensation) as well as absence of neural components. Cochlear CMs were not completely cancelled in the intermediate recording (A-alternated). The lower recording (Bloq-blocked) shows the absence of a biological response.

Figure 2 shows ET-ECoG recordings in both ears in a four-year-old child diagnosed with AN/AD. CMs may be seen in the two upper recordings (R-rarefaction, and C-condensation) as well as absence of neural components. Cochlear CMs were not completely cancelled in the intermediate recording (A-alternated). The lower recording (Bloq-blocked) shows the absence of a biological response. CMs are seen with better quality in these recordings, making it possible to analyze CM morphology, amplitude and duration more precisely.

Figure 3 shows inversion of CM tracings at 180° on the upper ET-ECoG recording when using rarefaction (R) e condensation (C) polarities. CM authenticity is shown on the lower recording, where the cochlear potential disappears when blocking the insertion phone tube (Bloq-blocked).

DISCUSSION

Auditory neuropathy/dyssynchrony (AN/AD) is a relatively new condition in audiology that has been investigated in many recent papers. OAEs and ABEP testings are the methods used in diagnosing this disorder. When OAEs are absent in these patients, however, the differential diagnosis depends on CM recordings.^1-18,20,21

It seems inappropriate to analyze CMs by using ABEP testing for the following reasons: the stimulus (click) that is used to initiate neural potentials limits the conditions for recording CMs;^1,20,25,34 and secondly, many clinicians perform ABEP testing with supra-aural phones, in which blocking the plastic tube to confirm a biological response is not possible.

ET-ECoG is a non-invasive technique that may be used in young children, without sedation; the diagnosis of AN/AD, therefore, may be expedited. The recording amplitude is increased, compared to ABEP testing, by locating the electrodes closer to the site of origin of cochlear potentials, which is extremely relevant in AN/AD, as published papers have shown that CMs are ampler in such testing conditions.^22-26 Higher quality recordings make it possible to evaluate not only the amplitude but also the duration of CMs; the literature suggests that CMs are more prolonged in AN/AD, compared to normal subjects.

A further points is that ET-ECoG also evaluates cochlear function, thereby providing an audiological assessment if OAEs are absent.

It is important to note that even when using ET-ECoG to evaluate CMs in AN/AD patients, an appropriate protocol using strategies to assure recording reliability should be applied. Tone burst stimulation should be used, and rarefaction and condensation polarities should be used to confirm inversion of recordings, and therefore, confirmation of CMs. We also recommend using insertion phones to provide confirmation of a biological response, where the plastic tube may be blocked to discard possible signal electrical artifacts.

CONCLUSION

Our findings show that ET-ECoG may be applied clinically in the differential diagnosis of AN/AD, making it possible to analyze cochlear function in greater detail compared to ABEP testing, particularly in identifying CMs.

We aimed to provide additional data in support of a more effective diagnosis of AN/AD, especially in small children in whom electrophysiological methods frequently are the only available tools for evaluating auditory function.

REFERENCES

Paper submitted to the ABORL-CCF SGP (Management Publications System) on June 15th, 2006 and accepted for publication on November 2nd, 2006. cod. 2132

• ¹
  Berlin CI, Hood LJ, Rose K. On renaming auditory neuropathy as auditory dys-syncrony: implications for a clearer understanding mechanisms and management options. Audiol Today 2001;13(6):15-7.
• ²
  Kraus N. Auditory neuropathy: an historical and current perspective. In: Sininger, YS, Starr A, editores. Auditory neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 1-14.
• ³
  Starr A, Picton TW, Sininger YS, Hood LJ, Berlin CI. Auditory neuropathy. Brain 1996;119:741-53.
• ⁴
  Kaga M, Kon K, Uno A, Horiguchi T, Yoneyama H, Inagaki M. Auditory perception in auditory neuropathy: clinical similarity with auditory verbal agnosia. Brain 2002;24:197-202.
• ⁵
  Santarelli R, Arslan E. Electrocochleography in auditory neuropathy. Hear Res 2002;170:32-47.
• ⁶
  Berlin CI, Morlet T, Hood LJ. Auditory neuropathy/dyssinchrony. Its diagnosis and management. Pediatr Clin N Am 2003;50:331-40.
• ⁷
  Rapin I, Gravel J. "Auditory neuropathy": physiologic and pathologic evidence calls for more diagnostic specificity. Int J Pediatric Otorhinolaryngol. 2003;67:707-28.
• ⁸
  Tang TPY, McPherson B, Yuen KCP, Wong LLN, Lee JSM. Auditory neuropathy/auditory dys-synchrony in school children with hearing loss; frequency of occurrence. Int J Ped Otorhinolaryngol 2004;68:175-83.
• ⁹
  Loundon N, Marcolla A, Roux I, Rouillon I, Denoyelle F, Feldmann D, Marlin S, Garabedian EN. Auditory neuropathy or endocochlear hearing loss? Otol Neurotol 2005;26 (4):748-54.
• ¹⁰
  Ngo RYS, Tan HKK, Balakrishnan A, Lim SB, Lazaroo DT. Auditory neuropathy/auditory dys-synchrony detected by universal newborn hearing screening. Int J Ped Otorhinolaryngol (In press); 2006.
• ¹¹
  Zeng F, Oba S, Garde S, Sininger YS, StarrA. Temporal and speech processing deficits in auditory neuropathy. Neuro Report 1999;10:3429-35.
• ¹²
  Hood LJ, Berlin CI. Auditory neuropathy (auditory dys-syncrony) disables efferent suppression of otoacoustic emissions. In: Sininger, YS, Starr A, editores. Auditory neuropathy:a new perspective on hearing disorders. San Diego: Singular; 2001. p. 183-202.
• ¹³
  Sininger YS, Oba S. Patients with auditory neuropathy: who are they and what can they hear? In: Sininger YS, Starr A, editores. Auditory Neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 15-35.
• ¹⁴
  Zeng F, Oba S, Garde S, Sininger YS, Starr A. Psychoacoustics and speech perception in auditory neuropathy. In: Sininger YS, Starr A, editores. Auditory Neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 141-64.
• ¹⁵
  Sininger YS, Trautwein PG. Electrical stimulation of the auditory nerve via cochlear implants in patients with auditory neuropathy. Ann Otol Rhinol Laryngol 2002;111:29-31.
• ¹⁶
  Nadol Jr JB. Primary cochlear neuronal degeneration. In: Sininger, YS, Starr A, editores. Auditory neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 99-140.
• ¹⁷
  Starr A. The neurology of auditory neuropathy. In: Sininger YS, Starr A, editores. Auditory Neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 37-50.
• ¹⁸
  Starr A, Picton T, Kim R. Pathophysiology of auditory neuropathy. In: Sininger YS, Starr A, editores. Auditory Neuropathy: a new perspective on hearing disorders. San Diego: Singular; 2001. p. 67-82.
• ¹⁹
  Madden C, Rutter M, Hilbert L, Greinwald JH, Choo DI. Clinical and audiological features in auditory neuropathy. Arch Otolaryngol Head Neck Surg 2002;128:1026-30.
• ²⁰
  Deltenre P, Mansbach AL, Bozet C, Barthelemy P, Paulissen D, Renglet T. Auditory neuropathy with preserved cochlear microphonics and secondary loss of otoacoustic emissions. Audiology 1999;38:187-95.
• ²¹
  Withnell RH. Brief report: the cochlear microphonic as an indication of outer hair cell function. Ear Hear 2001;22:75-7.
• ²²
  Berlin C.I, Hood LJ, Goforth-Barter L, Bordelon J. Clinical Application of Auditory Efferent Studies. In: Berlin CI, editor. The Efferent Auditory System. Basic Science and Clinical Applications. San Diego: Singular; 1999. p.105-25.
• ²³
  Starr A, McPherson D, Patterson J, Don M, Luxford W, Shannon R, Sininger YS, Tonakawa L, Waring M. Absence of both auditory evoked potentials an auditory percepts dependent on timing cues. Brain 1991;114:1157-80.
• ²⁴
  Deltenre P, Mansbach AL, Bozet C, Clercx A, Hecox KE. Auditory neuropathy: a report on three cases with early onsets and major neonatal illnesses. Electroencephalogr Clin Neurophysiol. 1997;104:17-22.
• ²⁵
  Berlin CI, Bordelon J, St John P, Wilensky D, Hurley A, Kluka E, Hood LJ. Reversing click polarity may uncover auditory neuropathy in infants. Ear Hear 1998;19:37-47.
• ²⁶
  Starr A, Sininger YS;Nguyen T, Michalewski HJ, Oba S, Abdala C. Cochlear receptor (microphonic and summating potentials, otoacoustic emissions) and auditory pathway (auditory brain stem potentials) activity in auditory neuropathy. Ear Hear 2001;22:91-9.
• ²⁷
  Ferraro JA, Krishnan G. Cochlear potentials in clinical audiology. Audiol Neurootol 1997;2:241-56.
• ²⁸
  Margolis RH. Electrocochleography. Seminars in hearing 1999;20(1):46-61.
• ²⁹
  Pappas Jr DG, Pappas DG, Carmichael L, Hyatt DP, Toohey LM. Extratympanic electrocochleography: diagnostic and predictive value. Am J Otol 2000;21(1):81-7.
• ³⁰
  Hall JW. Handbook of auditory evoked response. Needham Heights: Allyn and Bacon; 1992.
• ³¹
  Noguchi Y, Nishida H, Komatsuzaki A. A comparison of extratympanic versus transtympanic recordings in electrocochleography. Audiology 1999;38 (3):135-40.
• ³²
  Sheykholeslami K, Kaga K, Murofushi T, Hughes DW. Vestibular function in auditory neuropathy. Acta Otolaryngol 2000;120:849-54.
• ³³
  Hood LJ. Auditory neuropathy: what is it and what can we do about it? Hear J 1998;51(8):10-8.
• ³⁴
  Elberling C, Salomon G. Cochlear microphonics recorded from the ear canal in man. Acta Otolaryng 1973;75:489-95.
• ³⁵
  Winzenburg SM, Margolis RH, Levine SC, Haines SJ, Fournier EM. Tympanic and transtympanic electrocochleography in acoustic neuroma and vestibular nerve section surgery. Am J Otol 1993;14(1):63-9.
• ³⁶
  Roland PS, Yellin MW, Meyerhoff WL, Frank T. Simultaneous comparison between transtympanic and extratympanic electrocochleography. Am J Otol 1995;16(4):444-50.
• ³⁷
  Rance G, Beer DE, Cone-Wesson B, Shepherd RK, Dowell RC, King AM, Rickards FW, Clark GM. Clinical findings for a group of infants and young children with auditory neuropathy. Ear Hear 1999;20:238-52.

Address for correspondence:

Adriana Ribeiro Tavares Anastasio

Travessa dois número 70 Jardim Recreio

Ribeirao Preto SP 14040-160

Publication Dates

• Publication in this collection
  31 Mar 2008
• Date of issue
  Feb 2008

History

• Accepted
  02 Nov 2006
• Received
  15 June 2006