Skip to main content
The Journal of International Medical Research logoLink to The Journal of International Medical Research
. 2020 Jan 15;48(1):0300060519889426. doi: 10.1177/0300060519889426

Research progress in refractory sudden hearing loss: steroid therapy

Ya Liu 1, Qiongqiong Chen 1, Yaping Xu 1,
PMCID: PMC7254608  PMID: 31939327

Short abstract

Sudden sensorineural hearing loss (SSNHL) is a common condition with a rapid onset, and its worldwide frequency is increasing each year. Importantly, a significant number of patients with SSNHL do not respond to initial treatment, which is termed refractory sudden hearing loss (RSHL), and further treatment is not standardized in terms of type, duration, administration route, and concentration of topical steroid therapy. Dexamethasone and methylprednisolone are effective in treating RSHL, and salvage treatment typically consists of 2 weeks of steroid therapy followed by 3–6 months of follow-up. Near-continual steroid perfusion appears to be more effective than intermittent steroid injection. Furthermore, several novel therapeutic regimens have shown promising results in small-scale studies. However, the optimum treatment needs to be confirmed in larger randomized controlled trials.

Keywords: Refractory sudden sensorineural hearing loss, salvage treatment, research progress, steroid therapy, pure-tone average, intratympanic

Introduction

Sudden sensorineural hearing loss (SSNHL) is defined as a reduction in hearing of greater than 30 dB over at least three consecutive frequencies, occurring over a period of 72 hours or less.1 In the United States (US), SSNHL affects 5–30 in 100,000 individuals per year,2 with about 4000 new cases per year. In Japan and Germany, there are 60.9 3 and 160 4 new cases, respectively, of SSNHL per 100,000 individuals per annum. Furthermore, based on epidemiological investigations in Japan 57 and Germany,8 the morbidity of SSNHL is expected to increase globally.

The spontaneous recovery rate of SSNHL ranges from 32% to 65%.9,10 However, approximately 30%–50% of patients do not experience an acceptable therapeutic effect following treatment with oral or intravenous steroids.11 Therefore, patients who do not respond, or who respond insufficiently, to systemic steroids are typically considered to have refractory sudden hearing loss (RSHL).12 However, the standard definition of RSHL remains highly controversial. In previous trials, some researchers have defined RSHL as an improvement in the pure-tone average (PTA) of less than 10 dB,1215 less than 15 dB,1618 or less than 20 dB 19,20 after initial treatment, while others have defined RSHL as less than 50% recovery.21 Regarding an international consensus, panelists at the International Federation of ORL Societies (IFOS) 2017 ENT World Congress suggested that any PTA change exceeding 10 dB could be considered as significant.22 We can therefore consider patients with a PTA increase less than 10 dB after initial treatment to have RSHL.

Multiple prognostic factors affecting sudden deafness have been reported, including patient age, absence of vertigo and tinnitus, degree of hearing loss, shape of the audiogram, and time between the onset and treatment of SSNHL.2327 In China, there is presumably a large population of individuals with RSHL, although the incidence of this condition in China has not yet been reported. Although steroid therapy is generally believed to be effective in RSHL,1214,28 few studies have examined the correlation between prognosis and type, duration, and administration route of steroid treatment. Therefore, an investigation of the efficacy of steroid treatment in RSHL is highly relevant. The aim of the present review was to evaluate recent studies to investigate the relationship between the prognosis and duration of steroid treatment in patients with RSHL, including the type, durations, administration route, and concentration of topical steroids. A MEDLINE literature search was performed using a combination of low-specificity keywords including “hearing loss,” “steroid,” and “refractory,” supported by searches of PubMed, to yield all potentially relevant results. However, most of the identified studies did not meet current criteria for high-quality evidence, such as that provided by randomized controlled trials, meta-analyses, systematic reviews, and evidence reports, so the current report represents a non-systematic review. To facilitate a clear comparison of the therapeutic effects and administration routes of various types of steroids, information on the identified RSHL studies is summarized in Table 1.

Table 1.

Summary of studies of trans-tympanic steroid use for the treatment of refractory sudden hearing loss

Study/No. Inclusion criteria Salvage therapy method / dose / duration of injection Outcome measures Outcomes
Wu et al.19 2011, n = 55 Improvement in PTA <20 dB IT§, dexamethasone 4 mg/mL, 0.5 mL 4 times within a 2-week period (n = 27)vs. IT, normal saline 0.5 mL, four times within a 2-week period (n = 28) Improvement in PTA >10 dB Study group: 44.4% (12/27)Control group: 10.7% (3/28)
Lee et al.13 2011, n = 46 Improvement in PTA <10 dB IT, dexamethasone 5 mg/mL; 0.3–0.4 mL (n = 21) four times within a 2-week periodvs. no further steroid treatment (n = 25) Improvement in PTA >10 dB Study group: 47.6% (10/21)Control group: 16% (4/25)
Erdur et al.20 2014, n = 51 Improvement in PTA <20 dB within 14 days Insert dexamethasone through a ventilation tube, five drops four times per day for 2 weeks (n = 21)vs. no further treatment (n = 30) Improvement in PTA >20 dB Study group: 47.6% (10/21)Control group: 10% (3/30)
Hunchaisri et al.12 2010, n = 21 Improvement in PTA <10 dB or <15% in SDS IT, dexamethasone 4 mg/mL, 0.3–0.4 mL once per week for a maximum of three sessions (n = 14)vs. no further treatment (n = 7) Improvement in PTA >10 dB or SDS >15% Study group: 43% (6/14)Control group: 0% (0/7)
Ahn et al.16 2008, n = 99 Improvement in PTA <15 dB IT, dexamethasone 5 mg/mL, 0.3–0.4 mL twice weekly for 2 consecutive weeks (n = 49)vs. no further treatment (n = 50) Improvement in PTA >15 dB Study group: 30.6% (15/49)Control group: 16.0% (8/50)
Choung et al.14 2006, n = 66 Improvement in PTA <10 dB IT, dexamethasone 5 mg/mL, 0.3–0.4 mL twice per week for 2 consecutive weeks (n = 33)vs. no further treatment (n = 33) Improvement in PTA >10 dB or SDS >15% Study group: 38.2% (13/34)Control group: 6.1% (2/33)
Moon et al.15 2011, n = 151 Improvement in PTA <10 dB IT, dexamethasone 5 mg/mL, 0.4–0.5 mL every other day for five treatments (n = 66)vs. systemic reapplication group (n = 26)vs. control group, no further treatment (n = 59) Improvement in PTA >15 dB IT group: 48.5% (32/66)Systemic reapplication group: 15.4% (4/26)Control group: 16.9% (10/59)
Ferri et al.21 2012, n = 55 Improvement in PTA <50% IT, methylprednisolone 40 mg/mL, 0.4–0.5 mL once every 2–3 days for seven treatments Improvement in PTA >15 dB 52.7% (29/55)
She et al.17 2010, n = 49 Improvement in PTA <15 dB Methylprednisolone through a microcatheter 40 mg/mL, 0.5 mL/d for 10 days (n = 26)vs. placebo (n = 23) Improvement in PTA >15 dB Study group: 50% (13/26)Control group: 21.7% (5/23)
Berjis et al.18 2016, n = 50 Improvement in PTA <15 dB IT, methylprednisolone 40 mg/mL, 0.5 mL three times, once every 3 days (n = 25)vs. dexamethasone 4 mg/mL, 0.5 mL, three times, once every 3 days (n = 25) Improvement in PTA >15 dB Methylprednisolone group: 84% (21/25)Dexamethasone group: 64% (16/25)

IT: intratympanic therapy; PTA: pure-tone average; SDS: speech discrimination score

Types of steroids

Steroids can be classified as short-acting, medium-acting, and long-acting according to the duration of drug effect. Short-acting steroids include cortisone (360.444) and hydrocortisone (362.47); medium-acting steroids include prednisone (400.47), prednisolone (402.4807), and methylprednisolone (372.4547); while long-acting steroids include dexamethasone (392.5) and betamethasone (392.4641). The steroids most commonly used in the treatment of RSHL are methylprednisolone and dexamethasone,1216,18,19,2831 both of which have been shown to be effective in clinical use.

Based on extensive research into the treatment of RSHL,1216,19,29 the cure rate of RSHL following intratympanic low-dose dexamethasone therapy ranges from 30.6%16 to 48.5%.15 Approximately 0%12,32 to 16.9%15 of patients who do not receive further treatment can expect a further hearing improvement of 10 dB or 15 dB 2–3 months after the initial steroid treatment. Furthermore, Wu et al.19 conducted a double-blind controlled trial of the effect of intratympanic dexamethasone (ITD) in patients with RSHL. The study group consisted of 27 people who received 4 injections of 0.5 mL of dexamethasone (4 mg/mL) within a 2-week period and a control group included 28 people who received the same volume of normal saline. After treatment, 44.4% and 10.7% of subjects improved by 10 dB or more in the study group and the control group, respectively.

To investigate the effect of intratympanic methylprednisolone therapy on RSHL, Xenellis et al.32 carried out a study in 37 patients with RSHL, of which 19 patients received approximately 0.5 mL of methylprednisolone (40 mg/mL) while the other 18 patients received no further treatment. The cure rate was 47.3% in the methylprednisolone treatment group while no patient in the no further treatment group had an increase in PTA greater than 10 dB.

From these previous studies, we cannot infer whether methylprednisolone is superior to dexamethasone for the treatment of RSHL. Following tympanic injection with methylprednisolone, some of the drug can flow into the mouth through the eustachian tube.33 Therefore, Berjis et al.18 compared the effects of intratympanic dexamethasone and methylprednisolone injections in patients with RSHL and found that prednisolone (84%; 21/25) was significantly more effective than dexamethasone (64%; 16/25). This outcome may be related to the fact that methylprednisolone is active for longer and at higher concentrations than dexamethasone.34 Furthermore, methylprednisolone has been shown to regulate sodium transport and/or reabsorption in the cochlea.35 However, further studies in larger populations are needed to determine the optimal steroid therapy for patients with RSHL.

Duration of steroid therapy

According to US guidelines, early treatment within 2 weeks to 3 months (i.e., from the onset of symptoms to the start of treatment) is more beneficial than later treatment.1 The maximum spontaneous improvement or treatment-related improvement in hearing frequently occurs during the first 2 weeks, with little benefit typically seen after 4–6 weeks.36,37 Where hearing loss persists over 2 to 3 months, it may develop into permanent deafness.38 However, Wang et al.39 found that there was a therapeutic value in administering steroids to patients with an SSNHL duration of onset greater than 3 months, especially in those with mild or moderate hearing loss. Similarly, a recent study 40 showed a hearing improvement in patients with SSNHL after 3 months from symptom onset. Additionally, after a 10-day course of systemic steroid therapy and a long-term follow-up of more than 3 months, Yeo et al.41 found that 35.54%, 8.26%, and 1.65% of patients with SSNHL recovered within 1 month, 1–3 months, and >3 months, respectively, while a previous case report described a complete spontaneous recovery of hearing at approximately 9 months after the onset of SSNHL.42 Plontke et al.43 found that hearing gain and final hearing thresholds appeared to be independent of the start of secondary therapy. Therefore, further studies are needed to determine of the duration of time after which the initiation of treatment for SSNHL is ineffective.

Although there is no consensus on the duration of steroid treatment as salvage therapy, most salvage treatment comprises 2 weeks of treatment and 3–6 months of follow-up. As shown in Table 1, the number of intratympanic steroid treatments ranges from three 18 to seven,21 although in most studies steroids are applied twice per week for 2 consecutive weeks.14,16,19,32 However, if patients receive steroids via a ventilation tube, they may receive steroid treatment once per day for 10 days 17 or four times per day for 2 weeks.20 Because the t1/2 of a steroid is directly related to its frequency of use, it is necessary to consider the t1/2 of commonly used steroids such as prednisone, methylprednisolone, and dexamethasone. The serum t1/2 for prednisone is 2 hours, and tissue t1/2 is 12–36 hours; serum t1/2 of methylprednisolone is 2.3 hours, and tissue t1/2 is 12–36 hours; and serum t1/2 of dexamethasone is 3.5 hours, and tissue t1/2 is 36–54 hours.44 To date, no randomized controlled trial has examined the duration of steroid therapy. Further research is therefore needed to determine how often steroids should be administered in this patient population.

Steroid administration routes

Although evidence supporting the efficacy of steroid treatment in SSNHL may be considered insufficient, steroid is therapy is used as standard for first-line treatment of SSNHL, including as primary therapy and salvage therapy.1 Systemic steroid administration can be considered the current standard of primary therapy of SSNHL.22 Research has shown that high doses of steroids are required to achieve an adequate perilymphatic concentration.45 Because an initial dose of 1 mg/kg is generally needed for systemic steroids,45 many physicians are hesitant to initiate a second round of treatment in patients who fail to respond to initial treatment.16 New methods of steroid administration for RSHL, such as topical application, are therefore of increasing clinical interest. Steroids used to treat RSHL can be applied topically using methods such as a transtympanic needle, tympanostomy tube, microcatheter, postauricular steroid injection, and round window niche drilling combined with intratympanic steroids.20,28,31,34,46,47

Erdur et al.20 reported a 47.6% improvement in PTA in subjects who received dexamethasone through a ventilation tube. Similar studies by Ferri et al.21 and She et al.17 showed that 52.7% and 50% of RSHL patients, respectively, achieved an improvement in PTA of more than 15 dB.

Although postauricular steroid injection is widely used as an initial treatment in China,30,48 there are relatively few reports on its use in RSHL. Jing et al. has suggested that postauricular methylprednisolone injection is an effective therapy for RSHL, especially in patients with low-frequency involvement.49

To explore the effects of different delivery methods, Li et al.33 performed a prospective randomized clinical study in patients with RSHL and found that the effective rate in a perfusion group treated via round window microcatheter with an electronic pump was 40.6%, which was significantly higher than that achieved using ITD at the same dosage or no further treatment (20.6% and 7.7%, respectively). Similarly, Chou et al.50 showed the superiority of applying near-continual transtympanic steroid perfusion compared with intermittent intratympanic steroid injection (53.3% vs 43.3%). However, in these studies, patients in the perfusion group reported events such as a fibrous plug covering the round window, bleeding incisions, microcatheter extrusion from the middle ear, and mild otalgia; while patients in the injection group reported vertigo and perforation of the tympanic membrane.33,50

Si et al.34 reported that round window niche drilling combined with daily intratympanic methylprednisolone was a safe and effective therapy in patients with RSHL, with up to 90% efficacy observed (9/10). In this study, the width of the round window membrane ranged from 1.97 to 2.50 mm, which may have increased the contact area and time of methylprednisolone. However, drilling of the round window niche was associated with complications of total hearing loss.

Recently, several novel routes of administration have been used for the topical application of steroids to treat SSNHL.51,52 Lundy et al.51 reported that the application of intratympanic dexamethasone using saturated Gelfoam prolonged the contact time of steroids with the round window membrane, thus improving the hearing of patients with severe SSNHL. Furthermore, Shimoji et al.52 found that the magnetic injection of prednisolone into the rat cochlea is a safe and effective strategy for the treatment of SSNHL. However, further trials are needed to determine whether these treatments are also effective in RSHL.

Concentration of topical steroids

The concentration of steroids used for treatment is one of the most important factors affecting recovery in patients with RSHL. A 40.7% improvement was reported in a study in which patients with RSHL received high-dose (24 mg/mL) ITD as salvage therapy.53 However, multiple trials have shown that the use of low-dose (4 mg/mL) ITD as salvage therapy might be more effective in this patient group.12,14,19 However, there are insufficient data at present from randomized controlled trials to evaluate the correlation between prognosis and steroid concentration.

Conclusions

Previous studies have shown that both dexamethasone and methylprednisolone are effective for the treatment of RSHL, and that methylprednisolone is more effect than dexamethasone for this indication. Salvage treatment generally consists of 2 weeks of treatment and 3–6 months of follow-up. Furthermore, research has demonstrated that near-continual steroid perfusion is more effective than intermittent steroid injection, although a number of innovative treatment approaches are under development. However, these novel strategies have to date been shown to be effective in limited numbers of study subjects; therefore, randomized controlled trials are needed to confirm their efficacy.

Declaration of conflicting interest

The authors declare that there is no conflict of interest.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

ORCID iD

Ya Liu https://orcid.org/0000-0001-7386-4641

References

  • 1.Stachler RJ, Chandrasekhar SS, Archer SMet al. Clinical practice guideline: sudden hearing loss. Otolaryngol Head Neck Surg 2012; 146: S1–S35. [DOI] [PubMed] [Google Scholar]
  • 2.Schreiber BE, Agrup C, Haskard DOet al. Sudden sensorineural hearing loss. Lancet 2010; 375: 1203–1211. [DOI] [PubMed] [Google Scholar]
  • 3.Nakashima T, Sato H, Gyo Ket al. Idiopathic sudden sensorineural hearing loss in Japan. Acta Otolaryngol 2014; 134: 1158–1163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Klemm E, Deutscher A, Mösges R. A present investigation of the epidemiology in idiopathic sudden sensorineural hearing loss. Laryngorhinootologie 2009; 88: 524–527. [DOI] [PubMed] [Google Scholar]
  • 5.Nakashima T, Yanagita N, Ohno Yet al. Comparative study on sudden deafness by two nationwide epidemiological surveys in Japan. Acta Otolaryngol Suppl 1994; 514: 14–16. [DOI] [PubMed] [Google Scholar]
  • 6.Nakashima T, Itoh A, Misawa Het al. Clinicoepidemiologic features of sudden deafness diagnosed and treated at university hospitals in Japan. Otolaryngol Head Neck Surg 2000; 123: 593–597. [DOI] [PubMed] [Google Scholar]
  • 7.Teranishi M, Katayama N, Uchida Yet al. Thirty-year trends in sudden deafness from four nationwide epidemiological surveys in Japan. Acta Otolaryngol 2007; 127: 1259–1265. [DOI] [PubMed] [Google Scholar]
  • 8.Michel O. The revised version of the German guidelines “sudden idiopathic sensorineural hearing loss”. Laryngorhinootologie 2011; 90: 290–293. [DOI] [PubMed] [Google Scholar]
  • 9.Mattox DE, Simmons FB. Natural history of sudden sensorineural hearing loss. Ann Otol Rhinol Laryngol 1977; 86: 463–480. [DOI] [PubMed] [Google Scholar]
  • 10.Conlin AE, Parnes LS. Treatment of sudden sensorineural hearing loss, II: a meta-analysis. Arch Otolaryngol Head Neck Surg 2007; 133: 582–586. [DOI] [PubMed] [Google Scholar]
  • 11.Mort DJ, Bronstein AM. Sudden deafness. Curr Opin Neurol 2006; 19: 11–13. [DOI] [PubMed] [Google Scholar]
  • 12.Hunchaisri N, Chantapant S, Srinangyam N. Intratympanic dexamethasone for refractory sudden sensorineural hearing loss. J Med Assoc Thai 2010; 93: 1406–1414. [PubMed] [Google Scholar]
  • 13.Lee JB, Choi SJ, Park Ket al. The efficiency of intratympanic dexamethasone injection as a sequential treatment after initial systemic steroid therapy for sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol 2011; 268: 833–839. [DOI] [PubMed] [Google Scholar]
  • 14.Choung YH, Park K, Shin YRet al. Intratympanic dexamethasone injection for refractory sudden sensorineural hearing loss. Laryngoscope 2006; 116: 747–752. [DOI] [PubMed] [Google Scholar]
  • 15.Moon IS, Lee JD, Kim Jet al. Intratympanic dexamethasone is an effective method as a salvage treatment in refractory sudden hearing loss. Otol Neurotol 2011; 32: 1432–1436. [DOI] [PubMed] [Google Scholar]
  • 16.Ahn JH, Han MW, Kim JHet al. Therapeutic effectiveness over time of intratympanic dexamethasone as salvage treatment of sudden deafness. Acta Otolaryngol 2008; 128: 128–131. [DOI] [PubMed] [Google Scholar]
  • 17.She W, Dai Y, Du Xet al. Hearing evaluation of intratympanic methylprednisolone perfusion for refractory sudden sensorineural hearing loss. Otolaryngol Head Neck Surg 2010; 142: 266–271. [DOI] [PubMed] [Google Scholar]
  • 18.Berjis N, Soheilipour S, Musavi Aet al. Intratympanic dexamethasone injection vs methylprednisolone for the treatment of refractory sudden sensorineural hearing loss. Adv Biomed Res 2016; 5: 1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Wu HP, Chou YF, Yu SHet al. Intratympanic steroid injections as a salvage treatment for sudden sensorineural hearing loss: a randomized, double-blind, placebo-controlled study. Otol Neurotol 2011; 32: 774–779. [DOI] [PubMed] [Google Scholar]
  • 20.Erdur O, Kayhan FT, Cirik AA. Effectiveness of intratympanic dexamethasone for refractory sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol 2014; 271: 1431–1436. [DOI] [PubMed] [Google Scholar]
  • 21.Ferri E, Frisina A, Fasson ACet al. Intratympanic steroid treatment for idiopathic sudden sensorineural hearing loss after failure of intravenous therapy. ISRN Otolaryngol, 2012; 2012: 1–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Marx M, Younes E, Chandrasekhar SSet al. International consensus (ICON) on treatment of sudden sensorineural hearing loss. Eur Ann Otorhinolaryngol Head Neck Dis 2018; 135: S23–S28. [DOI] [PubMed] [Google Scholar]
  • 23.Lionello M, Staffieri C, Breda Set al. Uni- and multivariate models for investigating potential prognostic factors in idiopathic sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol 2015; 272: 1899–1906. [DOI] [PubMed] [Google Scholar]
  • 24.Enache R, Sarafoleanu C. Prognostic factors in sudden hearing loss. J Med Life 2008; 1: 343–347. [PMC free article] [PubMed] [Google Scholar]
  • 25.Hosokawa S, Sugiyama K, Takahashi Get al. Prognostic factors for idiopathic sudden sensorineural hearing loss treated with hyperbaric oxygen therapy and intravenous steroids. J Laryngol Otol 2017; 131: 77–82. [DOI] [PubMed] [Google Scholar]
  • 26.Bulgurcu S, Sahin B, Akgul Get al. The effects of prognostic factors in idiopathic sudden hearing loss. Int Arch Otorhinolaryngol 2018; 22: 33–37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Cheng YF, Chu YC, Tu TYet al. Modified Siegel's criteria for sudden sensorineural hearing loss: reporting recovery outcomes with matched pretreatment hearing grades. J Chin Med Assoc 2018; 81: 1008–1012. [DOI] [PubMed] [Google Scholar]
  • 28.Zanetti D, Di BF, Nassif Net al. Intratympanic steroid delivery by an indwelling catheter in refractory severe sudden sensorineural hearing loss. Auris Nasus Larynx 2018; 45: 227–233. [DOI] [PubMed] [Google Scholar]
  • 29.Lee HS, Kim JM, Kim YJet al. Results of intratympanic dexamethasone injection as salvage treatment in idiopathic sudden hearing loss. J Otolaryngol Head Neck Surg 2008; 37: 263–268. [PubMed] [Google Scholar]
  • 30.Zhang T, Shang X, Xie Yet al. The effects of postauricular injection of methylprednisolone on medium-high frequency sudden hearing loss. Journal of Clinical Otorhinolaryngology Head & Neck Surgery 2018; 32: 537–540. [DOI] [PubMed] [Google Scholar]
  • 31.Li H, Feng G, Wang Het al. Intratympanic steroid therapy as a salvage treatment for sudden sensorineural hearing loss after failure of conventional therapy: a meta-analysis of randomized, controlled trials. Clin Ther 2015; 37: 178–187. [DOI] [PubMed] [Google Scholar]
  • 32.Xenellis J, Papadimitriou N, Nikolopoulos Tet al. Intratympanic steroid treatment in idiopathic sudden sensorineural hearing loss: a control study. Otolaryngol Head Neck Surg 2006; 134: 940–945. [DOI] [PubMed] [Google Scholar]
  • 33.Li L, Ren J, Yin Tet al. Intratympanic dexamethasone perfusion versus injection for treatment of refractory sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol 2013; 270: 861–867. [DOI] [PubMed] [Google Scholar]
  • 34.Si Y, Jiang HL, Chen YBet al. Round window niche drilling with intratympanic steroid is a salvage therapy of sudden hearing loss. Audiol Neurootol 2019; 23: 309–315. [DOI] [PubMed] [Google Scholar]
  • 35.Liebau A, Pogorzelski O, Salt ANet al. Hearing changes after intratympanically applied steroids for primary therapy of sudden hearing loss: a meta-analysis using mathematical simulations of drug delivery protocols. Otol Neurotol 2017; 38: 19–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Cvorović L, Deric D, Probst Ret al. Prognostic model for predicting hearing recovery in idiopathic sudden sensorineural hearing loss. Otol Neurotol 2008; 29: 464–469. [DOI] [PubMed] [Google Scholar]
  • 37.Rauch SD. Clinical practice. Idiopathic sudden sensorineural hearing loss. N Engl J Med 2008; 359: 833–840. [DOI] [PubMed] [Google Scholar]
  • 38.Moon IS, Kim J, Lee SYet al. How long should the sudden hearing loss patients be followed after early steroid combination therapy?. Eur Arch Otorhinolaryngol 2009; 266: 1391–1395. [DOI] [PubMed] [Google Scholar]
  • 39.Wang M, Han Y, Fan Zet al. Therapeutic effect on idiopathic sudden sensorineural hearing loss with duration of onset more than 3 months. Indian J Otolaryngol Head Neck Surg 2013; 65: 61–65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Anyah A, Mistry D, Kevern Eet al. Idiopathic sudden sensorineural hearing loss: average time elapsed before presentation to the otolaryngologist and effectiveness of oral and/or intratympanic steroids in late presentations. Cureus 2017; 9: 1945–1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Yeo SW, Lee DH, Jun BCet al. Hearing outcome of sudden sensorineural hearing loss: long-term follow-up. Otolaryngol Head Neck Surg 2007; 136: 221–224. [DOI] [PubMed] [Google Scholar]
  • 42.Ortmann AJ, Neely JG. Sudden sensorineural hearing loss and delayed complete sudden spontaneous recovery. J Am Acad Audiol 2012; 23: 249–255. [DOI] [PubMed] [Google Scholar]
  • 43.Plontke SK. Diagnostics and therapy of idiopathic sudden sensorineural hearing loss. Laryngorhinootologie 2017; 96: S103–S122. [DOI] [PubMed] [Google Scholar]
  • 44.Nocentini G, Ronchetti S, Bruscoli Set al. The clinical pharmacology of past, present, and future glucocorticoids In: R Cimaz. (ed) Systemic corticosteroids for inflammatory disorders in pediatrics. Cham: Adis, 2015, pp.43–58. [Google Scholar]
  • 45.Niedermeyer HP, Zahneisen G, Luppa Pet al. Cortisol levels in the human perilymph after intravenous administration of prednisolone. Audiol Neurootol 2003; 8: 316–321. [DOI] [PubMed] [Google Scholar]
  • 46.Herr BD, Marzo SJ. Intratympanic steroid perfusion for refractory sudden sensorineural hearing loss. Otolaryngol Head Neck Surg 2005; 132: 527–531. [DOI] [PubMed] [Google Scholar]
  • 47.Rauch SD, Halpin CF, Antonelli PJet al. Oral vs intratympanic corticosteroid therapy for idiopathic sudden sensorineural hearing loss: a randomized trial. JAMA 2011; 305: 2071–2079. [DOI] [PubMed] [Google Scholar]
  • 48.Yan G, Wang C, Yan Zet al. Clinical curative effect analysis of postauricular topical injection combining with oral hormone in the treatment of the flat type of sudden hearing loss. Journal of Clinical Otorhinolaryngology Head & Neck Surgery 2017; 31: 1639–1641. [DOI] [PubMed] [Google Scholar]
  • 49.Jing YY, YU LS, Ma Xet al. Efficacy of postauricular methylprednisolone injection for refractory sudden hearing loss[Chinese]. Chinese Journal of Otology 2014; 12: 452–452. [Google Scholar]
  • 50.Chou YF, Chen PR, Kuo IJet al. Comparison of intermittent intratympanic steroid injection and near-continual transtympanic steroid perfusion as salvage treatments for sudden sensorineural hearing loss. Laryngoscope 2013; 123: 2264–2269. [DOI] [PubMed] [Google Scholar]
  • 51.Lundy L, Karatayli OS, Kleindienst S. Intratympanic dexamethasone via saturated gelfoam for idiopathic sudden sensorineural hearing loss. Otolaryngol Head Neck Surg 2018; 160: 361–363. [DOI] [PubMed] [Google Scholar]
  • 52.Shimoji M, Ramaswamy B, Shukoor MIet al. Toxicology study for magnetic injection of prednisolone into the rat cochlea. Eur J Pharm Sci 2019; 126: 33–48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Kordis S, Battelino S. The role of high dose intratympanic dexamethasone as salvage therapy for idiopathic sudden sensorineural hearing loss. J Int Adv Otol 2017; 13: 318–321. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of International Medical Research are provided here courtesy of SAGE Publications

RESOURCES