Idiopathic Sudden Sensorineural Hearing Loss: Should Otoacoustic Emissions Be Added to the Monitoring Protocol? A Systematic Review
Abstract
:1. Introduction
2. Materials and Methods
2.1. Inclusion Time Period
2.2. Search Strategy
- (otoacoustic emissions) AND (sudden hearing loss)
- (OAE) AND (sudden hearing loss)
- (otoacoustic emissions) AND (sudden deafness)
2.3. Selection Criteria
2.4. Level of Evidence and Quality Assessment
2.5. Data Synthesis
3. Results
3.1. Physiologic Measures
3.1.1. Distortion Product Otoacoustic Emissions
3.1.2. Transient Evoked Otoacoustic Emissions
3.1.3. Spontaneous Evoked Otoacoustic Emissions
3.2. Behavioral Measures
Pure Tone Audiometry
4. Discussion
4.1. Aggregate Analysis
4.2. Limitations
4.3. Developing an OAE Monitoring Protocol for ISSNHL
5. Conclusions
- Twelve out of fourteen studies in this systematic review support the use of OAEs as a prognostic indicator for hearing improvement in cases of ISSNHL.
- OAEs are an important component of a diagnostic and monitoring auditory test battery to help determine site of lesion, make proper diagnostic referrals (e.g., for imaging), and predict benefit from aural rehabilitation.
- No unifying OAE protocol was identified in this systematic review. The choice to use TEOAE, DPOAE, or both measures should be based on available equipment, patient age, and pre-existing hearing loss (which, in unilateral cases, may be inferred from the unaffected ear).
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
Acronyms
References
- Rauch, S. Idiopathic Sudden Sensorineural Hearing Loss. N. Engl. J. Med. 2008, 359, 833–840. [Google Scholar] [CrossRef] [PubMed]
- Watanabe, T.; Suzuki, M. Analysis of the audiogram shape in patients with idiopathic sudden sensorineural hearing loss using a cluster analysis. ENT-Ear Nose Throat J. 2018, 97, e36–e40. [Google Scholar] [CrossRef] [PubMed]
- NIDCD. U.S. Department of Health and Human Serices—National Institute of Health, March 2018. Available online: www.nidcd.nih.gov/health/sudden-deafness (accessed on 1 March 2018).
- Mori, T.; Suzuke, H.; Hiraki, N.; Hashida, K.; Ohbuchi, T.; Katho, A.; Udaka, T. Prediction of hearing outcomes by distortion product otoacoustic emissions in patients with idiopathic sudden sensorineural hearing loss. Auris Nasus Larynx 2011, 38, 564–569. [Google Scholar] [CrossRef] [PubMed]
- Massachusetts Eye and Ear Infirmary. 2019. Available online: http://www.masseyeandear.org/for-patients/patient-guide/patient-education/diseases-and-conditions/sudden-deafness (accessed on 1 May 2019).
- Kemp, D. Otoacoustic emissions, their origin in cochlear function, and use. Br. Med Bull. 2002, 63, 223–241. [Google Scholar] [CrossRef] [PubMed]
- Seixas, N.; Kujawa, S.; Norton, S.; Sheppard, L.; Neitzel, R.; Slee, A. Predictors of hearing threshold levels and distortion product otoacoustic emissions among noise exposed young adults. Occup. Environ. Med. 2004, 61, 899–907. [Google Scholar] [CrossRef] [Green Version]
- Konrad-Martin, D.; Poling, G.; Dreisbach, L.; Reavis, K.; McMillan, G.; Lapsley Miller, J.; Marshall, L. Serial monitoring of otoacoustic emissions in clinical trials. Otol. Neurotol. 2016, 37, e286–e294. [Google Scholar] [CrossRef]
- Zhao, F.; Wada, H.; Koike, T.; Stephens, D. The influence of middle ear disorders on otoacoustic emissions. Clin. Otolaryngol. Allied Sci. 2000, 25, 3–8. [Google Scholar] [CrossRef]
- Ryan, A. The Anatomic, physioogic, and Molecular Basis of Cochlear Function. In Otoacoustic Emissions Clinical Application, 3rd ed.; Robinette, M., Glattke, T., Eds.; Thieme Medical Group: New York, NY, USA, 2007; pp. 43–68. [Google Scholar]
- Gorga, M.; Neely, S.; Bergman, B.; Beauchaine, K.; Kaminski, J.; Peters, J.; Jesteadt, W. Otoacoustic emissions from normal-hearing and hearing-impaired subjects: Distortion product responses. J. Acoust. Soc. Am. 1993, 93, 2050–2060. [Google Scholar] [CrossRef]
- Sisto, R.; Chelotti, S.; Moriconi, L.; Pellegrini, S.; Citroni, A.; Monechi, V.; Gaeta, R.; Pinto, I.; Stacchini, N.; Moleti, A. Otoacoustic emission sensitivity to low levels of noise-induced hearing loss. J. Acoust. Soc. Am. 2007, 122, 387–401. [Google Scholar] [CrossRef]
- Prieve, B.; Gorga, M.; Schmidt, A.N.S.; Peters, J.; Schultes, L.; Jesteadt, W. Analysis of transient-evoked otoacoustic emissions in normal-hearing and hearing-impaired ears. J. Acoust. Soc. Am. 1993, 93, 3308–3319. [Google Scholar] [CrossRef]
- Shera, C. Mammalian spontaneous otoacoustic emissions are amplitude-stabilized cochlear standing waves. J. Acoust. Soc. Am. 2003, 114, 244–262. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Shera, C.; Guinan, J. Evoked otoacoustic emissions arise by two fundamentally different mechanisms: A taxonomy for mammalian OAEs. J. Acoust. Soc. Am. 1999, 105, 782–798. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Braun, M. High-multiple spontaneous otoacoustic emissions confirm theory of local tuned oscillators. SpringerPlus 2013, 2, 135. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Snihur, A.; Hampson, E. Sex and ear differences in spontaneous and click-evoked otoacoustic emissions in young adults. Brain Cogn. 2011, 77, 40–47. [Google Scholar] [CrossRef]
- Otodynamics Ltd. User Manual for ILO88; Otodynamics Ltd.: London, UK, 1992. [Google Scholar]
- Grason-Stadler. Grason-Stadler GSI-60 DPOAE-Distortion Product Otoacoustic Emissions System User Manual; GSI GrasonStadler: Milford, NH, USA, 1996. [Google Scholar]
- Otometrics. Madsen Capella and the OTOsuite Otoacoustic Emissions Module. User Guide; GN Otometrics: Schaumberg, IL, USA, 2013. [Google Scholar]
- Moher, D.; Liberati, A.; Tetzlaff, J.; Atlman, D.; The PRISMA GROUP. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. PLoS Med. 2009, 6, e1000097. [Google Scholar] [CrossRef] [Green Version]
- Phillips, B.; Ball, C.; Sackett, D.; Badenoch, D.S.S.; Haynes, M.; Dawes, M. Level of Evidence Table; Oxford Center for Evidence Basdic Medicine: Oxford, UK, 1998. [Google Scholar]
- ASHA. Evidence-Based Practice, Step 3: Assess the Evidence. Available online: http:www.asha.org/Research/EBP/Assess-the-Evidence (accessed on 1 May 2019).
- Bashiruddin, J.; Risdawati Bramantyo, B.; Bardosono, S. Relationship between distortion product otoacoustic emission signal-to-noise ratio and hearing threshold change during methylprednisone therapy for sudden deafness. In Proceedings of the 2nd Physics and Technologies in Medicine and Dentistry Symposium, Depok, Indonesia, 18 July 2018. [Google Scholar]
- Canale, T.; Lacilla, M. The prognostic value of the otoacoustic emission test in low frequency sudden hearing loss. Eur. Arch. Otorhinolaryngol. 2005, 262, 208–212. [Google Scholar] [CrossRef]
- Chao, T.; Chen, T. Distortion product otoacoustic emissions as a prognostic factor for idiopathic sudden sensorineural heairng loss. Audiol. Neurotol. 2006, 11, 331–338. [Google Scholar] [CrossRef]
- Chao, T.; Chen, T. Predictive model for improvement of idiopathic sudden sensorineural hearing loss. Audiol. Neurotol. 2010, 31, 385–393. [Google Scholar] [CrossRef]
- Hoth, S. On a possible prognostic value of otoacoustic emissions: A study on patients with sudden hearing loss. Eur. Arch. Otorhinolaryngol. 2005, 262, 217–224. [Google Scholar] [CrossRef]
- Ishida, T.; Sugiura, M.; Katayma, N.; Nahashima, T. Otoacoustic emissions, ear fullness and tinnitus in recovery course of sudden deafness. Auris Nasus Larynx 2008, 35, 41–46. [Google Scholar] [CrossRef]
- Lalaki, P.; Markou, K.; Tsalighopoulos, M.; Danilidis, I. Transiently evoked otoacoustic emissions as a prognostic indicator in idiopathic sudden hearing loss. Scand. Audiol. 2001, 30, 41–145. [Google Scholar] [CrossRef] [PubMed]
- Nakamura, M.; Yamasoba, T.; Kaga, K. Changes in otoacoustic emissions in patients with idiopathic sudden deafness. Audiology 1997, 36, 121–135. [Google Scholar] [CrossRef] [PubMed]
- Nemati, S.; Naghavi, S.; Kazemnejad, E.; Banan, R. Otoacoustic emissions in sudden sensorineural hearing loss: Changes of measures with treatment. Iran. J. Otolaryngol. 2011, 23, 37–44. [Google Scholar]
- Park, H.; Lee, Y.; Park, M.; Kim, J.; Na, B.; Shin, J. Short-term changes of hearing and distortion-product otoacoustic emissions in sudden sensorineural hearing loss. Otol. Neurotol. 2010, 31, 862–866. [Google Scholar] [CrossRef] [PubMed]
- Schweinfurth, J.; Cacace, T.; Parnes, S. Clinical application of otoacoustic emissions in sudden hearing loss. Laryngoscope 1997, 107, 1457–1463. [Google Scholar] [CrossRef]
- Shupak, A.; Zeidan, R.; Shemesh, R. Otoacoustic emissions in th eprediction of sudden sensorineural hearing loss outcome. Otol. Neurotol. 2014, 30, 1691–1697. [Google Scholar] [CrossRef]
- Truy, E.; Veuillet, E.; Collet, L.; Morgon, A. Characteristics of transient otoacoustic emissios in patients with sudden idiopathic hearing loss. Br. J. Audiol. 1993, 27, 379–385. [Google Scholar] [CrossRef]
- Abdala, C.; Ortmann, A.; Shera, C. Reflection- and distortion-source otoacoustic emissions: Evidence for increased irregularlity in the human cochlea during aging. JARO 2018, 19, 493–510. [Google Scholar] [CrossRef]
- Gorga, M.; Neely, S.; Ohlrich, S.; Hoover, B.; Redner, J.; Peters, J. From Laboratory to Clinic: A Large Scale Study of Distortion Product Otoacoustic Emissions in Ears with Normal Hearing and Ears with Hearing Loss. Ear Hear. 1997, 18, 440–455. [Google Scholar] [CrossRef]
- Siegel, J. Calibrating Otoacoustic Emission Probes. In Otoacoustic Emissions Clinical Applications, 3rd ed.; Robinette, M., Glattke, T., Eds.; Thieme Medical Publishers, Ltd.: New York, NY, USA, 2007; pp. 403–428. [Google Scholar]
- Charaziak, K.; Shera, C. Compensating for ear-canal acoustics when measuring otoacoustic emissions. J. Acoust. Soc. Am. 2017, 141, 515. [Google Scholar] [CrossRef] [Green Version]
- Souza, N.; Dhar, S.; Neely, S.; Siegel, J. Comparison of nine methods to estimate ear-canal stimulus levels. J. Acoust. Soc. Am. 2014, 136, 1768–1787. [Google Scholar] [CrossRef] [PubMed]
- Dreisbach, L.; Long, L.; Lees, S. Repeatability of high-freqeuncy distortion-product otoacoustic emissions in normal-hearing adults. Ear Hear. 2006, 27, 466–479. [Google Scholar] [CrossRef]
- Reavis, K.M.; Garnett, M.; Donald, A.; Frederick, G.; Stephen, A.F.; Jane, S.G.; Wendy, J.H.; Dawn, K.-M. Distortion-product otoacoustic emission test performance for ototoxicity monitoring. Ear Hear. 2011, 31, 61–74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Cheatham, M.; Goodyear, R.; Homma, K.; Legan, P.; Korchagina, J.; Naskar, S.; Siegel, J.; Dallos, P.; Zheng, J.; Richardson, G. Loss of tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions. J. Neurosci. 2014, 34, 10325–10338. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Variable | Inclusion | Exclusion |
---|---|---|
Population | 10–86 years (mean 47.2) | |
Language | English | All other languages |
Publication Date | 1991–2018 | |
Diagnostic Methods | Evoked otoacoustic emissions Pure tone audiometry | Did not include evoked otoacoustic emissions and pure tone audiometry |
Report Type | Published in peer-reviewed sources, meta-analyses, randomized controlled trials, cohort studies, case control, cross-sectional studies, retrospective studies, and prospective studies | Theoretical papers, opinion-based editorials, reviews, qualitative studies, case studies, records with no statistical data reported, theses, and dissertations |
Diagnosis | Idiopathic sudden sensorineural hearing loss (ISSNHL) | Sudden sensorineural hearing loss (SSNHL) with a known cause |
Physiologic Measurements | Otoacoustic emissions (DPOAEs, TEOAEs, and SOAEs), Auditory Brainstem Response (ABR(, and Vestibular Evoked Myogenic Potential (VEMP( | |
Behavioral Measurements | Pure tone audiometry thresholds; pure tone average (PTA) |
Authors | N | Age in Years (Mean) | Gender M/F |
---|---|---|---|
Bashiruddin et al. (2018) [23] | 22 | ≥18 (NR *) | 13/9 |
Canale & Lacilla (2005) [24] | 20 | 19–77 (44) | 9/11 |
Chao & Chen (2006) [25] | 108 | 10–86 (45) | 48/60 |
Chao & Chen (2010) [26] | 200 | 10–86 (46) | 98/102 |
Hoth (2005) [27] | 25 | 20–73 (41) | 15/10 |
Ishida et al. (2008) [28] | 16 | Group A: 18–58 (39.6) Group B: 35–57 (48) | 10/6 |
Lalaki et al. (2001) [29] | 30 | NR | NR |
Mori et al. (2011) [30] | 78 | 16–80 (62.9) | 42/36 W |
Nakamura, et al. (1997) [4] | 15 | 19–71 (50.8) | 8/7 |
Nemati et al. (2011) [31] | 26 | 25.3–55.8 (40.5) | 16/10 |
Park et al. (2010) [32] | 33 | 16–66 (38) | 17/16 |
Schweinfurth et al. (1997) [33] | 10 | 21–86 (51) | NR |
Shupak et al. (2014) [34] | 15 | 41.4–73.8 (57.6) | 11/4 |
Truy et al. (1993) [35] | 24 | 15–67 (41.25) | 10/14 |
Article | Monitoring Measurements | Monitoring Schedule |
---|---|---|
Bashiruddin et al. (2018) [36] | DPOAEs 500–12,000 Hz PTA | Before treatment and 15th day of treatment |
Canale & Lacilla (2005) [24] | DPOAEs 1000–3000 Hz TEOAEs 500–5000 Hz SOAEs (present/absent) PTA | Before/after treatment |
Chao & Chen (2006) [25] | DPOAEs 1093–5500 Hz PTA ABR VEMP | Every day for maximum of 7 days during hospital admission; every other week or monthly following discharge |
Chao & Chen (2010) [26] | DPOAEs 1093–5500 Hz PTA ABR VEMP | Every day for maximum of 7 days during hospital admission; every other week or monthly following discharge |
Hoth (2005) [27] | DPOAEs 1000–4000 Hz TEOAEs 1000–4000 Hz PTA | 3–9 examinations (average) performed following symptom onset in intervals between 3 and 505 days (average of 53 days) |
Ishida et al. (2008) [28] | DPOAEs 1000–6000 Hz PTA Tinnitus/Ear Fullness | Day of hospital admission and on a weekly basis until hearing stabilized |
Lalaki, et al. (2001) [29] | TEOAEs 500–5600 Hz PTA | On admission, at least 2× during admission, 8–10 days after admission |
Mori et al. (2011) [30] | DPOAEs 593–6031 Hz PTA | First hospital visit & one month post treatment |
Nakamura, et al. (1997) [4] | DPOAEs 708–6299 Hz TEOAEs 1000–1500 Hz SOAEs 1000–6000 Hz PTA | Every 2–7 days during course of treatment |
Article | Conclusions | Support/Reject |
---|---|---|
Bashiruddin et al. (2018) [44] | Significant changes in DPOAE SNR at 1500, 2000, and 8000 Hz; Significant associations between SNR change and hearing threshold at 8000 and 10,000 Hz; Relationship between treatment-induced change in hearing threshold and DPOAE SNR may help predict outcome at certain frequencies | Support |
Canale & Lacilla (2005) [24] | The relationship between pre-treatment presence/absence of SOAEs, DPOAEs, and TEOAEs and thresholds was not significant; The study supports that OAEs can be an indicator of inner ear functional state, but they cannot be used as a prognostic test in cases of LFSNHL | Reject |
Chao & Chen (2006) [25] | Results showed that a greater DPOAE amplitude was a significant prognostic indicator; Established a model that revealed prognostic value of DPOAEs for ISSNHL patients; The model can be used for comparison of different treatment protocols | Support |
Chao & Chen (2010) [26] | Results showed that a greater DPOAE amplitude was a significant prognostic indicator; Established a model that revealed prognostic value of DPOAEs for ISSNHL patients; The model can be used for comparison of different treatment protocols | Support |
Hoth (2005) [27] | Greater OAE levels following the drop in hearing thresholds were correlated with better outcome; Monitoring TEOAEs and DPOAEs in patients with ISSNHL during/after treatment gives insight into the recovery process of OHC function parallel to subjective hearing improvement, but also reveals paradoxical cases where OAEs are unexpectedly large compared with thresholds | Support |
Ishida et al. (2008) [28] | ISSNHL patients with significant hearing improvement tended to have OAE responses; Greater recovery was seen in the low-mid vs. high frequencies; When hearing recovery was not full, OAEs did not reappear | Support |
Lalaki et al. (2001) [29] | Presence of TEOAEs in early stages of ISSNHL in those with hearing thresholds >40 dB HL indicates a positive prognosis; No significant correlation between TEOAE peak amplitude and pure tone improvement; TEOAEs may serve as a clinical tool for prediction of recovery in ISSNHL cases | Support |
Mori et al. (2011) [30] | DPOAE amplitude in patients with hearing improvement rate of >50% was significantly larger compared with those with hearing improvement rate of 50% at frequencies of 3031 and 4812 Hz; Significant correlation between DPOAEs before treatment and hearing recovery indicates they are a potentially useful means for predicting prognosis | Support |
Nakamura et al. (1997) [4] | Amplitudes of TEOAEs and DPOAEs increased concurrently with recovery of hearing threshold; In 27% of cases, SOAEs were detected when hearing recovered; Results suggest that the function of OHCs deteriorated when thresholds were elevated and recovered as hearing improved to nearly normal levels in ISSNHL cases with a good outcome | Support |
Nemati et al. (2011) [31] | No significant change in DPOAE SNR or amplitude when comparing findings before/after treatment for patients with significant hearing recovery; Significant and positive change in TEOAE SNR and reproducibility when comparing findings for patients with significant hearing recovery; TEOAEs are an objective, rapid, and sensitive tool in the course of ISSNHL | Support TEOAEs; Reject DPOAEs |
Park et al. (2010) [32] | Function of OHCs is spared in ears with initial mild-to-moderate hearing loss and recovery is not related to hearing improvement; Function of OHCs is impaired in ears with initial moderately-severe to profound hearing loss and OHC improvement is important for recovery; Although presence of initial DPOAE responses indicated good prognosis, absence did not always indicate poor prognosis | Support |
Shupak et al. (2014) [33] | Three patients with intact DPOAEs at presentation had an average improvement of 33 dB in the PTA at 500–2000 Hz in conjunction with steroid therapy, whereas five of seven patients with absent DPOAEs had no improvement in hearing despite therapy. The presence of DPOAEs may be a useful prognostic indicator that positively correlates with recovery from ISSNHL | Support |
Schweinfurth et al. (1997) [35] | Function of OHCs is relatively spared in ears with initial mild-to-moderate hearing loss and recovery is not related to hearing improvement; Function of OHCs is impaired in ears with initial moderately-severe to profound hearing loss and functional improvement of OHCs is important for recovery; Although the presence of initial DPOAE responses indicated good prognosis, absence did not always indicate poor prognosis | Support |
Truy et al. (1993) [34] | The TEOAE amplitude at initial follow-up was correlated with improvement in thresholds at the second follow-up at 2000 Hz. Weak correlations between TEOAE amplitude at 1200 Hz and recovery of hearing. Overall, correlations were too weak to form the basis for a predictive test that could be clinically useful; TEOAE presence is not considered a good prognostic indicator in cases of ISSNHL | Reject |
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Share and Cite
Babich, K.; Dunckley, K.T. Idiopathic Sudden Sensorineural Hearing Loss: Should Otoacoustic Emissions Be Added to the Monitoring Protocol? A Systematic Review. Appl. Sci. 2020, 10, 326. https://doi.org/10.3390/app10010326
Babich K, Dunckley KT. Idiopathic Sudden Sensorineural Hearing Loss: Should Otoacoustic Emissions Be Added to the Monitoring Protocol? A Systematic Review. Applied Sciences. 2020; 10(1):326. https://doi.org/10.3390/app10010326
Chicago/Turabian StyleBabich, Kaley, and Kathleen T. Dunckley. 2020. "Idiopathic Sudden Sensorineural Hearing Loss: Should Otoacoustic Emissions Be Added to the Monitoring Protocol? A Systematic Review" Applied Sciences 10, no. 1: 326. https://doi.org/10.3390/app10010326
APA StyleBabich, K., & Dunckley, K. T. (2020). Idiopathic Sudden Sensorineural Hearing Loss: Should Otoacoustic Emissions Be Added to the Monitoring Protocol? A Systematic Review. Applied Sciences, 10(1), 326. https://doi.org/10.3390/app10010326