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J Audiol Otol > Volume 24(3); 2020 > Article
Yücel and Özbuğday: Comparison of Steroid Treatment with and without Hyperbaric Oxygen Therapy for Idiopathic Sudden Sensorineural Hearing Loss

Abstract

Background and Objectives

In this study, we compared the outcomes of patients with idiopathic sudden sensorineural hearing loss who underwent steroid treatment with or without hyperbaric oxygen (HBO) therapy and were followed-up in our clinic.

Subjects and Methods

Patients were divided into two groups according to their treatment regimen. Steroid group received intravenous 1 mg/kg methylprednisolone which was due to be completed in 2-3 weeks with decreasing doses, and five doses of 0.5 mL intratympanic dexamethasone. Steroid+HBO group received the same steroid treatment with the addition of HBO therapy. The audiologic results of both treatment groups were compared after considering the patients’ risk factors.

Results

There was no significant difference between the steroid and Steroid+HBO groups in terms of hearing gain and degree of recovery, both at all degrees of hearing loss, and in severe and profound hearing loss. Hearing gain was similar when evaluated by audiogram type and admission time in both treatment groups.

Conclusions

We found that the addition of HBO therapy to systemic plus intratympanic steroid treatment did not affect hearing gain at all degrees of hearing loss in this study. Furthermore, audiogram type and admission time did not affect hearing gain between the two groups.

Introduction

Idiopathic sudden sensorineural hearing loss (ISSNHL) is defined as sensorineural hearing loss that develops in 3 days or less, at 3 consecutive frequencies based on pure tone audiometry (PTA) [1]. Despite its clear definition, there is no consensus on its etiology and treatment. A specific cause is identified in only 10% of cases [2]. Viral infections, circulatory disorders, labyrinth membrane rupture, autoimmune reactions, metabolic dysfunction, and the production of toxic substances are among the leading etiologies [3,4]. The treatment modalities are also very varied due to such different etiologies. Vasodilators, systemic and topical steroids, antiviral agents, vitamins, anticoagulants, hemodilution, prostacyclin, ganglion blockade, and hyperbaric oxygen (HBO) therapy have been the most recently used agents for the treatment of ISSNHL [5,6]. In clinical practice, steroids are the most commonly used treatment [7].
In our clinical practice, intravenous (IV) and intratympanic (IT) steroids are used as the first choice for the treatment of ISSNHL. In addition, since our center has a HBO therapy unit, patients also benefit from HBO therapy frequently. We attempted to evaluate the contribution of HBO therapy to systemic and IT steroid treatment by considering patients prognosis and risk factors. In this study, we compared the outcomes of ISSNHL patients who underwent treatment with or without HBO therapy who were followed up in our clinic.

Subjects and Methods

Patients

The files of patients aged 10 years and over who were diagnosed and treated for ISSHL in our clinic between 2016 and 2018 were reviewed retrospectively. Patients with unilateral sudden onset of 30 decibel (dB) or more sensorineural type hearing loss, an unknown cause of hearing loss, less than 30 days between the onset of hearing loss and the onset of treatment, and patients without fluctuating hearing loss were included in this study.
Patients with a history of otological surgery and ototoxic drug use, acoustic trauma and barotrauma, genetic sensorineural hearing loss, and patients with evidence of retrocochlear disease on magnetic resonance imaging were excluded from the study. Information on patient characteristics such as age, sex, PTA tests after the admission and treatment (1-3 months), degree of hearing loss, type of audiometry (descending, ascending, flat, and bowl), and duration of treatment (0-3, 4-10, >10 days) were recorded.

Treatment protocols

Patients were divided into two groups according to the treatment regimen. The first group (Steroid group) received IV 1 mg/kg methylprednisolone (Precort-Liyo 40 mg, KoçakFarma, İstanbul, Turkey) which was due to be completed in 2-3 weeks with decreasing doses, and five doses of 0.5 mL IT dexamethasone (İnfladox 8 mg/2 mL, My Farma Drug Industry, İstanbul, Turkey).The second group (Steroid+HBO group) received the same steroid treatment in addition to HBO therapy. Each HBO therapy session was performed at 2 atmospheres absolut (ATA) for 1 hour, with a total of 20 sessions daily, excluding weekends. IT and IV steroid treatment was started simultaneously in both patient groups.

Assessment of hearing gain

All patients were evaluated by a PTA test at frequencies of 250-6,000 Hertz (Hz) before and after treatment. PTA was evaluated by calculating the average of the hearing thresholds at 500, 1,000, 2,000, 4,000 Hz during each audiometry test. Audiometry tests performed between 1 and 3 months after treatment were considered. Improvement in hearing was evaluated by two methods. First, hearing gain was calculated by subtracting the pretreatment PTA value from posttreatment PTA value. In the second method, Clinical Practice Guideline: Sudden Hearing Loss, American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS Criteria) [8] was taken into consideration. Complete recovery was considered if the follow-up PTA (dB HL) or speech recognition threshold (SRT) (dB HL) improved to within 10 dB of the pre-sudden hearing loss hearing level. Partial recovery was considered if the follow-up PTA (dB HL) or SRT (dB HL) improved to within 50% of the pre-sudden hearing loss hearing level. No recovery was considered if the follow-up PTA (dB HL) or SRT (dB HL) was less than 50% of the pre-sudden hearing loss hearing level.

Compliance with ethical standards

Approval was obtained from the Ethics Committee of the local University for this study (No: 2019/1730).

Statistical analysis

Descriptive statistics were used to compare the general characteristics of all participants. Test of Normality, including Kolmogorov-Smirnov and Shapiro-Wilk tests, were used to determine the distribution of data. Data with normal distribution are presented as mean±standard deviation. Categorical variables are shown as a number (n). The comparison of the numerical data between groups and categorical variables was performed with the appropriate test such as the independent samples t-test, Mann-Whitney, chi-squared test, and Fisher’sexact test. Statistical Package for Social Sciences Windows software (ver. 22; IBM Corp., Armonk, NY, USA) was used for all statistical analyses. A p value less than 0.05 was considered statistically significant.

Results

A total of 272 patients who were diagnosed with ISSNHL, were followed-up at our clinic, and whose files were fully accessible were included in this study. There were 194 patients in the Steroid+HBO group and 78 patients in the Steroid group. The mean age of the Steroid+HBO and Steroid groups were 48 and 46 years, respectively. The female/male ratio was 83/111 in the Steroid+HBO group and 31/47 in the Steroid group. There was no statistically significant difference between the two groups in terms of mean age and gender (p<0.05). The pre- and post-treatment PTA levels were 65 and 43 dB, respectively in both the Steroid+HBO and Steroid groups. There was no statistically significant difference between groups in terms of pre-treatment PTA values and hearing gains (p>0.05) (Table 1). When the patients were evaluated according to the degree of recovery (AAO-HNS Criteria), there was no significant difference between the two groups in terms of all degrees of recovery (p>0.05) (Table 2). Table 2 shows the word reconstruction score (WRS), presence of vertigo, tinnitus, cigarette usage, and additional diseases of both groups. There was no statistically significant difference between the two groups in terms of these indicated parameters (p>0.05).
When patients with severe and severe hearing loss (>60 dB) were evaluated separately, there were 104 patients in the Steroid+HBO group and 40 patients in the Steroid group. The pre-treatment PTA value was 82 dB in the Steroid+HBO group and the 88 dB in the Steroid group. The post-treatment PTA value was 54 dB in the Steroid+HBO group and 64 dB in the Steroid group. There was no statistically significant difference between groups in terms of the pre-treatment PTA values and hearing gains (p>0.05) (Table 3).
When both treatment groups were grouped according to audiogram type, bowl type audiograms were not included in the evaluation due to the low number of patients. There was no statistically significant difference in hearing gain between the two groups in the descending, ascending, and flat type audiograms (p>0.05) (Table 4). When considering the duration from the onset of ISSHL to the beginning of treatment, there was no significant difference in hearing gain in patients admitting between 1-3, 4-10, and after 10 days in both treatment groups (p>0.05) (Table 5).

Discussion

Most ISSHL cases are idiopathic at presentation [9]. The treatment of ISSHL is highly controversial as the cause of the disease is unclear in many cases. Many theories have been proposed on the cause of ISSHL, some of which include vascular disorders, viral infections, immune disorders, labyrinth membrane rupture, metabolic dysfunction, and production of toxic substances [3,10,11]. Due to its multifactorial etiology, many agents are used for the treatment of ISSHL. Vasodilators, anticoagulants, corticosteroids, plasma expanders, antiviral therapies, vitamins, stellate ganglion blockers, and HBO therapy are among the most preferred treatment strategies [12,13]. Although several treatment regimens have been proposed, steroid therapy is the most commonly used and most effective pharmacological agent for ISSHL. It was also reported that over half of the patients received high-dose steroids during hospitalization [6,7]. HBO therapy was first reported to improve acute noise-induced hearing loss, sudden deafness, and peripheral vestibular disorders in the late 1960s [14]. HBO aims to improve microcirculation by increasing partial oxygen pressure and oxygen concentration in the inner ear for the treatment of ISSHL [15,16].
There are many reports that HBO therapy has beneficial effects for the treatment of ISSHL [6,10,12,17]. Recent studies have also shown that addition of HBO to corticosteroid treatment may be beneficial in both acute acoustic trauma and ISSHL, especially when initiated early [18]. It was reported that HBO therapy was found to cause a significant improvement in PTA thresholds in ISSHL cases where primary corticosteroid therapy failed and were within 4 weeks of onset of hearing loss [17]. HBO therapy has beneficial effects when administered concomitantly with steroids in the early stages of the disease, and should be considered especially in patients with total or profound hearing loss [6,10]. In our study, 34.5% of patients in the Steroid+HBO group received HBO therapy within the first 3 days after the onset of hearing loss, and 87.6% of patients received treatment in the first 10 days. In general, most of our patients started HBO therapy during the early disease stage. Therefore, the lack of a significant difference in hearing gain between the two groups cannot be attributed to delayed HBO therapy in this study.
Although many prognostic factors have been identified for ISSHL, the consensus on this is incomplete. Profound hearing loss, advanced age, delay in treatment, presence of comorbidities, and audiogram type are some of the prognostic factors of ISSHL. A descending type audiogram negatively affects the prognosis, whereas patients with an ascending audiogram have been reported to be associated with a better prognosis [19]. In this study, we did not examine the difference between audiogram types in terms of hearing gain. However, when we separated the patients according to audiogram types, we examined whether there was a difference between the two treatment methods. Consequently, there was no significant difference in the descending, ascending, and flat audiogram types between the two groups in terms of recovery. Similarly, we divided patients into three groups based on the duration between the onset of hearing loss and treatment. There was no significant difference between the groups in terms of hearing gain during all three time periods. At this point, it is unclear whether there is a difference between the two treatment methods according to the time of admission and audiometry type, or whether a decision on the choice of treatment can be made in the light of these parameters. We were only able to evaluate the two groups based on the gain in hearing. When we divided patients into subgroups, we could not make a comparison according to the recovery rate due to the low number of patients in the steroid subgroups. Therefore, this is alimitation of this study, and we believe that further studies need to be conductedon this subject.
In a study, considering the degree of hearing loss, they found that the rate of improvement in hearing was significantly higher in the Steroid+HBO group compared to the Steroid group in patients with an initial hearing level of 80 dB and above; therefore, HBO should be used in such patients [12]. However, although many studies have reported that adding HBO to steroid treatment provides additional benefits, there have also been some reports claiming the opposite. In a study comparing three different treatment modalities in ISSHL, it was indicated that although the response rate to oral steroid and oral Steroid+HBO treatment was 50.8% and 61.5%, respectively, there was no significant difference between these two groups in terms of response to treatment [20]. In a recent study, comparing oral+IT steroid and oral+IT steroid+HBO therapies in ISSHL patients with severe and profound hearing loss (>70 dB), the addition of HBO to steroid combination therapy did not improve the mean PTA values. However, in the same study, they reported that the addition of HBO was beneficial for improving low-frequency hearing and word discrimination scores [21]. In our study, when the patients with severe and profound hearing loss (>60 dB) were evaluated separately, there was no significant difference between the two treatment groups in terms of both hearing gain and recovery rate. We speculate that this may be due to the fact that steroid treatment was used in combination and not alone, which could be considered as an intensive steroid treatment. This could explain the lack of a significant difference between the two groups. However, considering the average hearing gain of 24 dB in the steroid group and 28 dB in the HBO group in patients with severe and profound hearing loss, we did not consider this improvement to be significant in both groups. Therefore, although we found no difference between the two groups, we believe that HBO should be considered as a treatment strategy in this patient group, especially for severe and profound hearing loss. In a review conducted in 2018, it was reported that adding HBO to steroid treatment may be beneficial in cases of severe and profound hearing impairment [22]. The guideline for clinical practice for ISSHL, which was updated this year, states that HBO can be administered as the initial therapy in combination with steroids within the first two weeks of onset, or as salvage therapy within the first month [23].
In conclusion, in this study, there was no significant difference in terms of hearing gain and degree of recovery between the steroid and Steroid+HBO groups in ISSHL patients. Furthermore, there was no significant difference between the two groups in the patients with severe and profound hearing loss. Hearing gain was similar when evaluated by audiogram type and admission time in both treatment groups. In conclusion, we found that the addition of HBO therapy to systemic and IT steroid treatment did not affect hearing gain at all degrees of hearing loss at this study.

Acknowledgments

None.

Notes

Conflicts of interest

The authors have no financial conflicts of interest.

Author Contributions

Conceptualization: all authors. Data Curation: all authors. Formal Analysis: Abitter Yücel. Funding Acquisition: all authors. Investigation: all authors. Methodology: all authors. Project Administration: all authors. Resources: all authors. Software: all authors. Supervısıon: all authors. Validation: all authors. Visualization: all authors. Writing—original draft: all authors. Writing—review & editing: all authors. Approval of final manuscript: all authors.

Table 1.
Pre- and post-treatment PTA values and hearing gains of the groups at the beginning and end of treatment
Treatment groups Pre-treatment PTA Post-treatment PTA p value Hearing gain p value
Mean±SD (dB) Mean±SD (dB) Mean±SD (dB)
Steroid (n=78) 64.53±3.07 43.20±3.43 <0.001* 21.33±2.08
Steroid+HBO (n=194) 64.58±1.65 43.13±1.87 <0.001* 21.11±1.58 0.742

* Wilcoxon signed ranks test,

Mann-Whitney U test.

PTA: pure tone average, HBO: hyperbaric oxygen

Table 2.
Distribution of recovery and demographic parameters of groups (AAO-HNS Criteria, 2012)
Parameters Steroid group (n=78) Steroid+HBO group (n=194) p value
AAO-HNS Criterion, n (%) 0.219
 Complete recovery 34 (43.6) 63 (32.5)
 Partial recovery 23 (29.5) 71 (36.6)
 No recovery 21 (26.9) 60 (30.9)
WRS 59 (67)* 58 (61)* 0.884
Vertigo, n (%) 0.857
 Yes 25 (32.1) 60 (30.9)
 No 53 (67.9) 134 (69.1)
Tinnitus, n (%) 0.967
 Yes 42 (53.8) 105 (54.1)
 No 36 (46.2) 89 (45.9)
Cigarette, n (%) 0.700
 Yes 26 (33.3) 60 (69.1)
 No 52 (66.7) 134 (30.9)
Additional disease, n (%) 0.905
 No 53 (67.9) 128 (66)
 HT 9 (11.5) 25 (12.9)
 HL 4 (5.1) 14 (7.2)
 DM 12 (15.4) 27(13.9)

* median (interquartile range),

chi-square test.

AAO-HNS: American Academy of Otolaryngology-Head and Neck Surgery, HBO: hyperbaric oxygen, WRS: word recognation score, HT: hypertension, HL: hyperlipidemia, DM: diabetes mellitus

Table 3.
PTA values before and after the treatment, hearing gains and recovery rates (AAO-HNS Criteria) of the two groups at patients with severe and profound hearing loss
Treatment groups Pre-treatment PTA Post-treatment PTA p value Hearing gain p value AAO-HNS Criteria
p value
Mean±SD (dB) Mean±SD (dB) Mean±SD (dB) Complete recovery (%) Partial recovery (%) No recovery (%)
Steroid (>60 dB) (n=40) 88.45±2.07 64.50±4.36 <0.001* 23.95±3.74 0.374 6 (15) 18 (45) 16 (40) 0.300
Steroid+HBO (>60 dB) (n=104) 82.45±1.47 54.37±2.75 <0.001* 28.07±2.46 28 (26.9) 43 (41.3) 33 (31.7)

* Wilcoxon signed ranks test,

Mann-Whitney U test,

chi-square test.

PTA: pure tone average, AAO-HNS: American Academy of Otolaryngology-Head and Neck Surgery, HBO: hyperbaric oxygen

Table 4.
Hearing gain levels in both treatment modalities according to audiogram type
Treatment group/type of audiogram Median hearing gain (dB) p value
Steroid/descending (n=17) 16.88±2.59 0.908
Steroid+HBO/descending (n=32) 15.06±2.93
Steroid/ascending (n=14) 20.42±1.92 0.254
Steroid+HBO/ascending (n=37) 17.75±2.75
Steroid/flat (n=44) 23.21±3.27 0.993
Steroid+HBO/flat (n=114) 23.53±2.31

Mann-Whitney U test. HBO: hyperbaric oxygen

Table 5.
Hearing gain levels in both treatment modalities by time of application
Treatment group/application time Median hearing gain (dB) p value
Steroid/1-3 days (n=32) 28.93±3.70 0.544
Steroid+HBO/1-3 days (n=67) 27.11±3.13
Steroid/4-10 days (n=34) 16.08±2.59 0.356
Steroid+HBO/4-10 days (n=103) 19.66±1.89
Steroid/>10 days (n=12) 15.91±3.76 0.344
Steroid+HBO/>10 days (n=24) 10.62±3.64

Mann-Whitney U test. HBO: hyperbaric oxygen

REFERENCES

1. Byl FM Jr. Sudden hearing loss: eight years’ experience and suggested prognostic table. Laryngoscope 1984;94(5 Pt 1):647–61.
crossref pmid
2. Haberkamp TJ, Tanyeri HM. Management of idiopathic sudden sensorineural hearing loss. Am J Otol 1999;20:587–92. discussion 593-5.
pmid
3. Eisenman D, Arts HA. Effectiveness of treatment for sudden sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 2000;126:1161–4.
crossref pmid
4. Quaranta N, Ramunni A, De Luca C, Brescia P, Dambra P, De Tullio G, et al. Endothelial progenitor cells in sudden sensorineural hearing loss. Acta Otolaryngol 2011;131:347–50.
crossref pmid
5. Toroslu T, Erdoğan H, Çağlar Ö, Güçlü O, Dereköy FS. Comparison of different treatment methods for idiopathic sudden sensorineural hearing loss. Turk Arch Otorhinolaryngol 2018;56:226–32.
crossref
6. Körpinar S, Alkan Z, Yiğit O, Gör AP, Toklu AS, Cakir B, et al. Factors influencing the outcome of idiopathic sudden sensorineural hearing loss treated with hyperbaric oxygen therapy. Eur Arch Otorhinolaryngol 2011;268:41–7.
crossref pmid pdf
7. Labus J, Breil J, Stützer H, Michel O. Meta-analysis for the effect of medical therapy vs. placebo on recovery of idiopathic sudden hearing loss. Laryngoscope 2010;120:1863–71.
crossref pmid
8. Stachler RJ, Chandrasekhar SS, Archer SM, Rosenfeld RM, Schwartz SR, Barrs DM, et al. Clinical practice guideline: sudden hearing loss. Otolaryngol Head Neck Surg 2012;146(3 Suppl):S1–35.
crossref pmid
9. Rauch SD. Clinical practice. Idiopathic sudden sensorineural hearing loss. N Engl J Med 2008;359:833–40.
crossref pmid
10. Topuz E, Yigit O, Cinar U, Seven H. Should hyperbaric oxygen be added to treatment in idiopathic sudden sensorineural hearing loss? Eur Arch Otorhinolaryngol 2004;261:393–6.
crossref pmid pdf
11. Stokroos RJ, Albers FW. The etiology of idiopathic sudden sensorineural hearing loss. A review of the literature. Acta Otorhinolaryngol Belg 1996;50:69–76.
pmid
12. Fujimura T, Suzuki H, Shiomori T, Udaka T, Mori T. Hyperbaric oxygen and steroid therapy for idiopathic sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol 2007;264:861–6.
crossref pmid pdf
13. Suzuki H, Hashida K, Nguyen KH, Hohchi N, Katoh A, Koizumi H, et al. Efficacy of intratympanic steroid administration on idiopathic sudden sensorineural hearing loss in comparison with hyperbaric oxygen therapy. Laryngoscope 2012;122:1154–7.
crossref pmid
14. Appaix A, Demard F. [Hyperbaric oxygenotherapy and sudden perceptive deafness]. Rev Laryngol Otol Rhinol (Bord) 1970;91:951–72.
pmid
15. Lamm K, Lamm H, Arnold W. Effect of hyperbaric oxygen therapy in comparison to conventional or placebo therapy or no treatment in idiopathic sudden hearing loss, acoustic trauma, noise-induced hearing loss and tinnitus. A literature survey. Adv Otorhinolaryngol 1998;54:86–99.
crossref pmid
16. Goto F, Fujita T, Kitani Y, Kanno M, Kamei T, Ishii H. Hyperbaric oxygen and stellate ganglion blocks for idiopathic sudden hearing loss. Acta Otolaryngol 1979;88:335–42.
crossref pmid
17. Pezzoli M, Magnano M, Maffi L, Pezzoli L, Marcato P, Orione M, et al. Hyperbaric oxygen therapy as salvage treatment for sudden sensorineural hearing loss: a prospective controlled study. Eur Arch Otorhinolaryngol 2015;272:1659–66.
crossref pmid pdf
18. Bayoumy AB, de Ru JA. The use of hyperbaric oxygen therapy in acute hearing loss: a narrative review. Eur Arch Otorhinolaryngol 2019;276:1859–80.
crossref pmid pmc pdf
19. Edizer DT, Çelebi Ö, Hamit B, Baki A, Yiğit Ö. Recovery of idiopathic sudden sensorineural hearing loss. J Int Adv Otol 2015;11:122–6.
crossref
20. Ergun Taşdöven G, Derin AT, Yaprak N, Özçağlar HÜ. The place of hyperbaric oxygen therapy and ozone therapy in sudden hearing loss. Braz J Otorhinolaryngol 2017;83:457–63.
crossref pmid
21. Cho I, Lee HM, Choi SW, Kong SK, Lee IW, Goh EK, et al. Comparison of two different treatment protocols using systemic and intratympanic steroids with and without hyperbaric oxygen therapy in patients with severe to profound idiopathic sudden sensorineural hearing loss: a randomized controlled trial. Audiol Neurootol 2018;23:199–207.
crossref pmid
22. Eryigit B, Ziylan F, Yaz F, Thomeer HGXM. The effectiveness of hyperbaric oxygen in patients with idiopathic sudden sensorineural hearing loss: a systematic review. Eur Arch Otorhinolaryngol 2018;275:2893–904.
crossref pmid pmc pdf
23. Chandrasekhar SS, Tsai Do BS, Schwartz SR, Bontempo LJ, Faucett EA, Finestone SA, et al. Clinical Practice Guideline: Sudden Hearing Loss (Update). Otolaryngol Head Neck Surg 2019;161(1_ suppl):S1–45.
crossref pmid


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