CC BY 4.0 · Int Arch Otorhinolaryngol
DOI: 10.1055/s-0043-1776728
Original Research

Assessment of Peripheral and Central Auditory Processing after Treatment for Idiopathic Sudden Sensorineural Hearing Loss

Soheila Khakzand
1   Audiology Department, School of Rehabilitation, Iran University of Medical Sciences, Tehran, Iran
,
1   Audiology Department, School of Rehabilitation, Iran University of Medical Sciences, Tehran, Iran
,
1   Audiology Department, School of Rehabilitation, Iran University of Medical Sciences, Tehran, Iran
,
2   Ear, Nose and Throat Department, Amir-Alam Hospital, Tehran University of Medical Sciences, Tehran, Iran
› Author Affiliations
Funding The authors declare that they have received no funding from any source for the conduction of the present study.

Abstract

Introduction When cases of idiopathic sudden sensorineural hearing loss (SSNHL) are treated successfully, most clinicians assume the normality and symmetry of the auditory processing. This assumption is based on the recovery of the detection ability on the part of the patients, but the auditory processing involves much more than detection alone. Since certain studies have suggested a possible involvement of the central auditory system during the acute phase of sudden hearing loss, the present study hypothesized that auditory processing would be asymmetric in people who have experienced sudden hearing loss.

Objective To assess the physiologic and electrophysiological conditions of the cochlea and central auditory system, as well as behavioral discrimination, of three primary aspects of sound (intensity, frequency, and time) in subjects with normal ears and ears treated successfully for SSNHL.

Methods The study included 19 SSNHL patients whose normal and treated ears were assessed for otoacoustic emissions, speech auditory brainstem response, intensity and pitch discrimination, and temporal resolution in a within-subject design.

Results The otoacoustic emissions were poorer in the treated ears compared to the normal ears. Ear- and sex-dependent differences were observed regarding otoacoustic emissions and pitch discrimination.

Conclusion The asymmetrical processing observed in the present study was not consistent with the hearing threshold values, which might suggest that the central auditory system would be affected regardless of the status of the peripheral hearing. Further experiments with larger samples, different recovery scenarios after treatment, and other assessments are required.



Publication History

Received: 14 February 2023

Accepted: 09 September 2023

Article published online:
15 March 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil

 
  • References

  • 1 Chen J, Hu B, Qin P. et al. Altered Brain Activity and Functional Connectivity in Unilateral Sudden Sensorineural Hearing Loss. Neural Plast 2020; 2020: 9460364
  • 2 Cheng Y-F, Chu Y-C, Tu T-Y, Shiao A-S, Wu S-L, Liao W-H. Modified Siegel's criteria for sudden sensorineural hearing loss: Reporting recovery outcomes with matched pretreatment hearing grades. J Chin Med Assoc 2018; 81 (11) 1008-1012
  • 3 Cho CS, Choi YJ. Prognostic factors in sudden sensorineural hearing loss: a retrospective study using interaction effects. Rev Bras Otorrinolaringol (Engl Ed) 2013; 79 (04) 466-470
  • 4 Sara SA, Teh BM, Friedland P. Bilateral sudden sensorineural hearing loss: review. Review J Laryngol Otol 2014; 128 (Suppl. 01) S8-S15
  • 5 Micarelli A, Chiaravalloti A, Viziano A, Danieli R, Schillaci O, Alessandrini M. Early cortical metabolic rearrangement related to clinical data in idiopathic sudden sensorineural hearing loss. Hear Res 2017; 350: 91-99
  • 6 Xu H, Fan W, Zhao X. et al. Disrupted functional brain connectome in unilateral sudden sensorineural hearing loss. Hear Res 2016; 335: 138-148
  • 7 Kuhn M, Heman-Ackah SE, Shaikh JA, Roehm PC. Sudden sensorineural hearing loss: a review of diagnosis, treatment, and prognosis. Trends Amplif 2011; 15 (03) 91-105
  • 8 Ciorba A, Bianchini C, Crema L. et al. White matter lesions and sudden sensorineural hearing loss. J Clin Neurosci 2019; 65: 6-10
  • 9 Jan TA, Kozin ED, Kanumuri VV, Sethi RK, Jung DH. Improvement in word recognition following treatment failure for sudden sensorineural hearing loss. World J Otorhinolaryngol Head Neck Surg 2016; 2 (03) 168-174
  • 10 Chen WT, Lee JW, Yuan CH, Chen RF. Oral steroid treatment for idiopathic sudden sensorineural hearing loss. Saudi Med J 2015; 36 (03) 291-296
  • 11 Härkönen K, Kivekäs I, Rautiainen M, Kotti V, Vasama JP. Quality of Life and Hearing Eight Years After Sudden Sensorineural Hearing Loss. Laryngoscope 2017; 127 (04) 927-931
  • 12 Chao TK, Chen TH. Distortion product otoacoustic emissions as a prognostic factor for idiopathic sudden sensorineural hearing loss. Audiol Neurotol 2006; 11 (05) 331-338
  • 13 Hoth S. On a possible prognostic value of otoacoustic emissions: a study on patients with sudden hearing loss. Eur Arch Otorhinolaryngol 2005; 262 (03) 217-224
  • 14 Nemati S, Naghavi S, Kazemnejad S, Banan R. Otoacoustic Emissions in Sudden Sensorineural Hearing Loss. : Changes of Measures with Treatment. Iranian Journal of Otorhinolaryngology 2011; 23 (62) 37-44
  • 15 Pecorari G, Riva G, Naqe N, Bruno G, Nardo M, Albera R. Long-term Audiometric Outcomes in Unilateral Sudden Sensorineural Hearing Loss without Recurrence. J Int Adv Otol 2019; 15 (01) 56-61
  • 16 Ganesan P, Kothandaraman PP, Swapna S, Manchaiah V. A Retrospective Study of the Clinical Characteristics and Post-treatment Hearing Outcome in Idiopathic Sudden Sensorineural Hearing Loss. Audiology Res 2017; 7 (01) 168-172
  • 17 Lee HS, Lee YJ, Kang BS, Lee BD, Lee JS. A clinical analysis of sudden sensorineural hearing loss cases. Korean J Audiol 2014; 18 (02) 69-75
  • 18 Haro S, Smalt CJ, Ciccarelli GA, Quatieri TF. Deep Neural Network Model of Hearing-Impaired Speech-in-Noise Perception. Front Neurosci 2020; 14: 588448
  • 19 Noguchi Y, Takahashi M, Ito T, Fujikawa T, Kawashima Y, Kitamura K. Delayed restoration of maximum speech discrimination scores in patients with idiopathic sudden sensorineural hearing loss. Auris Nasus Larynx 2016; 43 (05) 495-500
  • 20 Kitoh R, Nishio SY, Usami SI. Speech perception in noise in patients with idiopathic sudden hearing loss. Acta Otolaryngol 2022; 142 (3-4): 302-307
  • 21 Okada M, Parthasarathy A, Welling DB, Liberman MC, Maison SF. Idiopathic Sudden Sensorineural Hearing Loss: Speech Intelligibility Deficits Following Threshold Recovery. Ear Hear 2021; 42 (04) 782-792
  • 22 Diao T, Duan M, Ma X. et al. The impairment of speech perception in noise following pure tone hearing recovery in patients with sudden sensorineural hearing loss. Sci Rep 2022; 12 (01) 866
  • 23 Koravand A, Jutras B, Lassonde M. Auditory event related potentials in children with peripheral hearing loss. Clin Neurophysiol 2013; 124 (07) 1439-1447
  • 24 Ciorba A, Corazzi V, Bianchini C. et al. Sudden sensorineural hearing loss: Is there a connection with inner ear electrolytic disorders? A literature review. Int J Immunopathol Pharmacol 2016; 29 (04) 595-602
  • 25 Koravand A, Al Osman R, Rivest V, Poulin C. Speech-evoked auditory brainstem responses in children with hearing loss. Int J Pediatr Otorhinolaryngol 2017; 99: 24-29
  • 26 Liang M, Wu H, Chen J. et al. Vestibular evoked myogenic potential may predict the hearing recovery in patients with unilateral idiopathic sudden sensorineural hearing loss. Front Neurol 2022; 13: 1017608
  • 27 Kitoh R, Takumi Y, Nishio SY, Usami SI. Sound localization in patients with idiopathic sudden hearing loss. Acta Otolaryngol 2023; 143 (01) 43-48
  • 28 Gelfand SA. Essentials of Audiology:. Thieme; 2016
  • 29 Peixe BP, Silva DDD, Biaggio EPV, Bruno RS, Sanguebuche TR, Garcia MV. Applicability of Evoked Auditory Brainstem Responses with Complex Stimuli in Adults with Hearing Loss. Int Arch Otorhinolaryngol 2018; 22 (03) 239-244
  • 30 Nakamura M, Yamasoba T, Kaga K. Changes in otoacoustic emissions in patients with idiopathic sudden deafness. Audiology 1997; 36 (03) 121-135
  • 31 Tadros SF, Frisina ST, Mapes F, Kim S, Frisina DR, Frisina RD. Loss of peripheral right-ear advantage in age-related hearing loss. Audiol Neurotol 2005; 10 (01) 44-52
  • 32 McFadden D, Pasanen EG, Maloney MM, Leshikar EM, Pho MH. Correlations between otoacoustic emissions and performance in common psychoacoustical tasks. J Acoust Soc Am 2018; 143 (04) 2355
  • 33 Ren T, Avinash GB, Nuttall AL, Miller JM, Laurikainen EA, Quirk WS. Dynamic response of cochlear blood flow to occlusion of anterior inferior cerebellar artery in guinea pigs. J Appl Physiol 1994; 76 (01) 212-217
  • 34 Musiek FE, Chermak GD. Handbook of Central Auditory Processing Disorder. Plural Publishing; 2013
  • 35 Sininger YS, Cone-Wesson B. Asymmetric cochlear processing mimics hemispheric specialization. Science 2004; 305 (5690) 1581
  • 36 Tabuchi K, Tsuji S, Fujihira K, Oikawa K, Hara A, Kusakari J. Outer hair cells functionally and structurally deteriorate during reperfusion. Hear Res 2002; 173 (1-2): 153-163
  • 37 Morizane I, Hakuba N, Shimizu Y. et al. Transient cochlear ischemia and its effects on the stria vascularis. Neuroreport 2005; 16 (08) 799-802
  • 38 Kim JS, Lee H. Inner ear dysfunction due to vertebrobasilar ischemic stroke. Semin Neurol 2009; 29 (05) 534-540
  • 39 Jiang XJ, Ito H. [Auditory brainstem response in the anterior inferior cerebellar artery insufficiency]. Nippon Jibiinkoka Gakkai Kaiho 1991; 94 (12) 1811-1815
  • 40 Jeong KH, Choi JW, Shin JE, Kim CH. Abnormal Magnetic Resonance Imaging Findings in Patients With Sudden Sensorineural Hearing Loss: Vestibular Schwannoma as the Most Common Cause of MRI Abnormality. Medicine (Baltimore) 2016; 95 (17) e3557
  • 41 Wioland N, Rudolf G, Metz-Lutz MN, Mutschler V, Marescaux C. Cerebral correlates of hemispheric lateralization during a pitch discrimination task: an ERP study in dichotic situation. Clin Neurophysiol 1999; 110 (03) 516-523
  • 42 Gaab N, Keenan JP, Schlaug G. The effects of gender on the neural substrates of pitch memory. J Cogn Neurosci 2003; 15 (06) 810-820
  • 43 Samelli AG, Schochat E. The gaps-in-noise test: gap detection thresholds in normal-hearing young adults. Int J Audiol 2008; 47 (05) 238-245