Sensorineural hearing loss

感音神经性听力损失
  • 文章类型: Journal Article
    为了评估选择性5-羟色胺再摄取抑制剂(SSRIs)和三环抗抑郁药(TCA)在减少眩晕中的作用,耳鸣,梅尼埃病(MD)患者的听力损失。
    本范围审查中使用了以下数据库:OvidMedline,PubMed-NCBI,CINAHL,科克伦图书馆,WebofScience,和临床试验。
    通过以下搜索短语确定了研究:“5-羟色胺特异性再摄取抑制剂”或“三环抗抑郁药”和“梅尼埃病”。“对纳入手稿的参考文献进行了检查,以可能纳入其他研究。
    文献检索产生了23个结果,由三名独立审稿人筛选。排除17项研究和3项重复。对纳入研究的参考文献的检查产生了另外两个出版物。最终纳入了在147名MD患者中评估SSRIs和TCA的4项已发表的研究。四项研究描述了与治疗前基线相比,接受SSRIs或TCA治疗的患者的眩晕发作频率显着降低。三项研究评估了药物对听力的影响,其中在接受SSRIs或TCA治疗的患者中没有发现显着差异。一项研究发现,与治疗前基线相比,TCA或SSRI治疗后患者报告的耳鸣显着减少。
    在MD患者中探索SSRIs和TCA的数据表明,这些药物可以降低耳鸣和眩晕的频率,尽管结果报告存在显著异质性.仍然需要更大规模的前瞻性研究,强调客观数据来评估其减轻常见MD症状的有效性。
    UNASSIGNED: To assess the effect of selective serotonin reuptake inhibitors (SSRIs) and tricyclic antidepressants (TCAs) in reducing vertigo, tinnitus, and hearing loss among patients with Meniere\'s disease (MD).
    UNASSIGNED: The following databases were utilized in this scoping review: Ovid Medline, PubMed-NCBI, CINAHL, Cochrane Library, Web of Science, and Clinicaltrials.gov.
    UNASSIGNED: Studies were identified through the following search phrases: \"serotonin specific reuptake inhibitors\" OR \"tricyclic antidepressants\" AND \"Meniere\'s disease.\" References from included manuscripts were examined for possible inclusion of additional studies.
    UNASSIGNED: The literature search yielded 23 results, which were screened by three independent reviewers. Seventeen studies and three duplicates were excluded. An examination of references from the included studies yielded two additional publications. A total of four published studies assessing SSRIs and TCAs among 147 patients with MD were ultimately included. Four studies described significant reductions in vertigo attack frequency among patients treated with either SSRIs or TCAs compared to their pretreatment baseline. Three studies assessed the drugs\' effects on hearing, of which none found a significant difference among patients treated with SSRIs or TCAs. One study found a significant decrease in patient-reported tinnitus following treatment with TCAs or SSRIs compared to their pretreatment baseline.
    UNASSIGNED: Data exploring SSRIs and TCAs among patients with MD suggests that these medications may reduce the frequency of tinnitus and vertigo, although there was significant heterogeneity in outcome reporting. There remains a need for larger-scale prospective studies that emphasize objective data to evaluate their effectiveness in reducing common MD symptoms.
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  • 文章类型: Journal Article
    目的:已经报道了在给予单克隆抗体teprotumumab后听力损失。这项研究的目的是回顾有关teprotumumab相关耳毒性模式的现有证据。
    方法:PubMed,EMBASE,科克伦图书馆
    方法:使用标准化方法进行系统评价。如果研究包括处方teprotumumab的受试者,则包括这些研究。排除标准包括非英语文章,摘要,信件/评论,病例报告,和评论。没有治疗前和治疗后测听数据的受试者也被排除。使用混合方法评估工具评估偏差。
    结果:从76篇文章的初始搜索中,纳入了109例独特患者的7项研究报告。四项研究是4级证据,1项研究是3级证据,2项研究为2级证据。平均年龄为55±14岁,女性占主导地位(64%)。最常见的症状是听力损失(22%),其次是饱满度(18%)和耳鸣(14%)。总的来说,41%有可用数据的患者符合耳毒性标准,都表现出中频或更高的变化。15例(14%)患者接受了超高频测听测试,8例(53%,8/15)仅在此范围内显示出变化。
    结论:耳毒性可能发生在用teprotumumab治疗的患者中。听力损失主要发生在较高的频率,和常规听力筛查与超高频测试可能是必要的。使用teprotumumab的耳毒性的真实发生率仍然未知,和更多的数据需要阐明潜在的机制和制定战略,以尽量减少风险。
    OBJECTIVE: Hearing loss has been reported after administration of the monoclonal antibody teprotumumab. The purpose of this study was to review available evidence regarding the patterns of teprotumumab-related ototoxicity.
    METHODS: PubMed, EMBASE, and Cochrane Library.
    METHODS: A systematic review was performed using standardized methodology. Studies were included if they included subjects who were prescribed teprotumumab. Exclusion criteria included non-English articles, abstracts, letters/commentaries, case reports, and reviews. Subjects without both pre- and posttreatment audiometric data were also excluded. Bias was assessed using the Mixed Methods Appraisal Tool.
    RESULTS: From an initial search of 76 articles, 7 studies reporting on 109 unique patients were included. Four studies were level 4 evidence, 1 study was level 3 evidence, and 2 studies were level 2 evidence. Mean age was 55 ± 14 years with a female predominance (64%). The most commonly reported symptoms were hearing loss (22%), followed by fullness (18%) and tinnitus (14%). In total, 41% of patients with available data met criteria for ototoxicity, all exhibiting shifts in the middle frequencies or higher. Fifteen (14%) patients underwent ultrahigh frequency audiometric testing and 8 (53%, 8/15) demonstrated shifts exclusively in this range.
    CONCLUSIONS: Ototoxicity may occur in patients treated with teprotumumab. Hearing loss occurs primarily in higher frequencies, and routine hearing screening with ultrahigh frequency testing may be warranted. The true incidence of ototoxicity with teprotumumab remains unknown, and more data is needed to elucidate underlying mechanisms and develop strategies to minimize risks.
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  • 文章类型: Journal Article
    几十年来,系统性红斑狼疮患者的听觉前庭功能障碍一直被低估。系统性红斑狼疮可同时影响听觉和前庭系统。已经提出了系统性红斑狼疮相关的听觉前庭功能障碍背后的几种潜在的病理生理机制。包括抗体介导的免疫反应,细胞介导的细胞毒性,免疫复合物在微血管中的沉积,中枢参与听觉前庭通路,以及系统性红斑狼疮治疗药物的耳毒性。目前可用的评估系统性红斑狼疮患者听觉前庭功能的测试既不特异也不敏感。然而,对于此类患者的前庭听觉功能障碍的治疗效果尚无共识.在这次系统审查中,我们电子搜索了PubMed,Embase,ClinicalKey,WebofScience,和ScienceDirect平台寻找合格的文章。首次检查日期为2023年12月29日,最终更新搜索日期为2024年6月11日。Further,我们用纽卡斯尔-渥太华量表对收录文章的质量进行了评价。根据上述系统审查过程,我们总结了目前可用的关于这些特征的证据,病理生理学,考试,与系统性红斑狼疮相关的听觉前庭功能障碍的治疗。此外,我们提出了一种特定的类固醇治疗方案来管理与系统性红斑狼疮相关的听觉前庭功能障碍.与系统性红斑狼疮相关的听觉前庭功能障碍可能对适当的治疗有反应,如果及时识别和管理疾病,则可能允许可逆性。因此,为临床医生提供临床相关证据,我们组织了这篇文献综述文章,以总结有关特征的可用证据,病理生理学,考试,系统性红斑狼疮患者的听力前庭功能障碍的治疗。最后,根据我们改良的类固醇治疗方案,我们希望为临床医生提供一种新的治疗策略,以治疗系统性红斑狼疮相关的听前庭功能障碍.
    Audiovestibular dysfunction in patients with systemic lupus erythematosus has been underestimated for decades. Systemic lupus erythematosus can affect both the auditory and vestibular systems simultaneously. Several potential pathophysiological mechanisms behind systemic lupus erythematosus-related audiovestibular dysfunction have been proposed, including antibody-mediated immune responses, cell-mediated cytotoxicity, immune complex deposition in microvessels, central involvement in the audiovestibular pathway, and ototoxicity from medications used in systemic lupus erythematosus treatment. Currently available tests to evaluate audiovestibular function in systemic lupus erythematosus patients are neither specific nor sensitive. Nevertheless, there is no consensus regarding the efficacy of treatments for audiovestibular dysfunction in such patients. In this systematic review, we electronically searched the PubMed, Embase, ClinicalKey, Web of Science, and ScienceDirect platforms to find eligible articles. The first inspection date was on 29 December 2023 and the final update search date was on 11 June 2024. Further, we rated the quality of the included articles with Newcastle-Ottawa Scale. Based upon the aforementioned systematic review process, we have summarized the currently available evidence on the characteristics, pathophysiology, examination, and treatment of audiovestibular dysfunction related to systemic lupus erythematosus. Furthermore, we have proposed a specific steroid treatment protocol to manage audiovestibular dysfunction related to systemic lupus erythematosus. Audiovestibular dysfunction related to systemic lupus erythematosus may be responsive to adequate treatments, potentially allowing for reversibility if the disease is recognized and managed in a timely manner. Therefore, to provide clinically relevant evidence to clinicians, we have organized this literature review article to summarize the available evidence on the characteristics, pathophysiology, examination, and treatment of audiovestibular dysfunction in patients with systemic lupus erythematosus. Finally, based on our modified steroid treatment protocol, we would like to provide a new treatment strategy to clinicians to manage systemic lupus erythematosus-related audiovestibular dysfunction.
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  • 文章类型: Systematic Review
    背景:DNA甲基化可能在单基因感音神经性听力损失和复合体中起调节作用,听力损失的多基因表型形式,包括年龄相关的听力障碍或梅尼埃病。本系统评价的目的是批判性地评估支持DNA甲基化在与听力损失相关的表型中的功能作用的证据。
    结果:搜索策略共产生661篇文章。经过质量评估,选择了25条记录(12项人类DNA甲基化研究,5个实验动物研究和8个报告DNMT1基因突变的研究)。尽管一些甲基化研究报道了与复杂听力损失表型相关的不同基因启动子中CpG甲基化的显着差异(ARHI,耳硬化症,MD),只有一项研究包括一个复制队列,该队列支持在ARHI中TCF25和POLE基因中CpG甲基化的调节作用.相反,几项研究独立证实了DNMT1基因外显子21内的致病性突变,其编码DNA(胞嘧啶-5)-甲基转移酶1酶。这种甲基化酶与一种由常染色体显性遗传的小脑共济失调定义的罕见疾病密切相关。耳聋和嗜睡症(ADCA-DN)。值得注意的是,DNMT1和DNMT3A基因的罕见变异也被报道在噪声诱导的听力损失中。
    结论:支持DNA甲基化在听力损失中的功能作用的证据仅限于ARHI等复杂疾病中的少数基因。DNMT1基因突变与ADCA-DN,表明听力损失基因中的CpG甲基化值得在听力研究中进一步关注。
    BACKGROUND: DNA methylation may have a regulatory role in monogenic sensorineural hearing loss and complex, polygenic phenotypic forms of hearing loss, including age-related hearing impairment or Meniere disease. The purpose of this systematic review is to critically assess the evidence supporting a functional role of DNA methylation in phenotypes associated with hearing loss.
    RESULTS: The search strategy yielded a total of 661 articles. After quality assessment, 25 records were selected (12 human DNA methylation studies, 5 experimental animal studies and 8 studies reporting mutations in the DNMT1 gene). Although some methylation studies reported significant differences in CpG methylation in diverse gene promoters associated with complex hearing loss phenotypes (ARHI, otosclerosis, MD), only one study included a replication cohort that supported a regulatory role for CpG methylation in the genes TCF25 and POLE in ARHI. Conversely, several studies have independently confirmed pathogenic mutations within exon 21 of the DNMT1 gene, which encodes the DNA (cytosine-5)-methyltransferase 1 enzyme. This methylation enzyme is strongly associated with a rare disease defined by autosomal dominant cerebellar ataxia, deafness and narcolepsy (ADCA-DN). Of note, rare variants in DNMT1 and DNMT3A genes have also been reported in noise-induced hearing loss.
    CONCLUSIONS: Evidence supporting a functional role for DNA methylation in hearing loss is limited to few genes in complex disorders such as ARHI. Mutations in the DNMT1 gene are associated with ADCA-DN, suggesting the CpG methylation in hearing loss genes deserves further attention in hearing research.
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  • 文章类型: Journal Article
    描述患有与Noonan综合征(NS)相关的病理性PTPN11变异的患者双侧人工耳蜗植入(CI)后的结果。此外,根据我们的结果和以前的报告,评估CI在这一特定人群中的效用。
    使用系统评价和荟萃分析指南的首选报告项目进行文献综述的回顾性病例报告。
    一个有各种多器官异常的小男孩,言语和语言延迟,和2岁时发现PTPN11基因杂合突变的持续性听力损失。
    双侧鼓膜置管,诊断成像,最终上演双边CI。
    客观听力测试和发展里程碑成就。
    BilateralCI在2个月内成功完成。患者在客观听力学测量方面表现出显着改善。然而,他继续签署作为他的主要形式的沟通没有显著的言语进展。
    NS/NSML患者的早期诊断和治疗干预有助于改善长期听力学和言语发育。鉴于NS/NSML的异质性,需要采用多学科方法才能取得最佳成果。
    UNASSIGNED: To describe outcomes after bilateral cochlear implantation (CI) in a patient with a pathologic PTPN11 variant associated with Noonan syndrome (NS) and Noonan syndrome with multiple lentigines (NSML). Additionally, to assess the utility of CI in this specific population based on our outcome and previous reports.
    UNASSIGNED: Retrospective case report with literature review using Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
    UNASSIGNED: A young boy with various multiorgan abnormalities, speech and language delay, and persistent hearing loss who was found to have a heterozygous PTPN11 gene mutation at age 2.
    UNASSIGNED: Bilateral tympanostomy tube placement, diagnostic imaging, and eventual staged bilateral CI.
    UNASSIGNED: Objective audiometric testing and developmental milestone attainment.
    UNASSIGNED: Bilateral CI was successfully completed over a 2-month period. The patient illustrated significant improvement in objective audiologic measurement. However, he continues to sign as his main form of communication without significant speech progression.
    UNASSIGNED: Early diagnostic and therapeutic intervention in patients with NS/NSML can help improve long-term audiologic and speech development. Given the heterogeneity of NS/NSML, a multidisciplinary approach is needed for optimal outcomes.
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  • 文章类型: Journal Article
    我们介绍了一名患有颞骨骨折(TBF)的患者,该患者包括骨迷宫。确认了感觉神经性听力损失,预后不良。十三年后,有听力损失的消退。
    We present a patient who suffered a temporal bone fracture (TBF) encompassing the bony labyrinth. Sensorineural hearing loss was confirmed with an unfavorable prognosis for recovery. Thirteen years later, there is regression of the hearing loss.
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  • 文章类型: Journal Article
    似乎食物因素和营养类型对听觉系统的功能有影响。听觉是社会交往和高级认知行为的重要感官之一。感觉神经性听力损失在受影响患者的个人和社会生活的各个方面都会产生不利和永久性的后果。因此,这项叙述性综述研究旨在确定感觉神经性听力损失与饮食类型之间的关系。根据纳入标准,2005年至2023年发表的62篇文章全文摘自Scopus,Medline[PubMed],WebofScience,和谷歌学者网站,构成了本研究的来源。研究结果表明,通过限制富含胆固醇的食物的消费,糖,碳水化合物,和蛋白质,听力受到保护,免受引起感音神经性听力损失的因素的影响。此外,增加蔬菜的消费,水果,omega-3,维生素A形式的抗氧化剂,C,E由于噪声暴露而降低了听力敏感性,长老会,耳毒剂,等。健康的饮食包括以平衡的方式摄入身体所需的所有营养。健康的生活方式因素,包括持续的体力活动,睡眠质量好,戒烟,远离压力因素或放松,避免暴露在环境噪声中。通过遵循健康的饮食和生活方式,听证的条件,提供身心健康。
    It seems that food factors and the type of nutrition have an effect on the function of the auditory system. Hearing is one of the most important senses for social communication and high cognitive behaviors. Sensorineural hearing loss leaves adverse and permanent consequences in all aspects of personal and social life of affected patients. Hence, this narrative review study was designed to determine the relationship between sensorineural hearing loss and type of diet. Based on the inclusion criteria, the full text of 62 articles published between 2005 and 2023 were extracted from Scopus, Medline [PubMed], Web of Science, and Google Scholar websites and constituted the sources of this research. The results of the studies showed that by limiting the consumption of foods rich in cholesterol, sugar, carbohydrates, and protein, hearing is protected against the factors that cause sensorineural hearing loss. Also, increasing the consumption of vegetables, fruits, omega-3, antioxidants in the form of vitamins A, C, E reduce hearing susceptibility due to noise exposure, presbycusis, ototoxic agents, and etc. Healthy diet includes eating all the nutrients the body needs in a balanced way. Healthy lifestyle factors including continuous physical activity, good sleep quality, quitting smoking, stay away from stressful factors or relaxation, and avoiding exposure to environmental noise. By following healthy eating and lifestyle patterns, the conditions for hearing, physical and mental health are provided.
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  • 文章类型: Systematic Review
    目的:本系统综述旨在评估感音神经性听力损失(SNHL)对各种频率跟随反应(FFR)参数的影响。
    方法:遵循PRISMA指南,使用PubMed进行了系统审查,WebofScience,和截至2023年1月的Scopus数据库。包括评估SNHL患者和正常听力对照的FFRs的研究。
    结果:纳入了16项病例对照研究,揭示采集参数的可变性。在时域中,SNHL患者潜伏期延长.延长的特定波在研究中有所不同。关于时域中的波幅没有共识。在频域中,专注于激发170毫秒或更长刺激的FFRs的研究,SNHL患者的基本频率(F0)明显较小.关于时间精细结构(TFS)变化的结果不一致。
    结论:SNHL患者可能需要更多的时间来处理(语音)刺激,反映在长时间的延迟中。然而,这种延迟的确切时间仍不清楚。此外,当呈现更长的刺激(≥170ms)时,SNHL患者难以追踪(言语)刺激的F0。对于时域中的波幅和频域中的TFS的变化,无法得出明确的结论。患者特征,采集参数,FFR结果参数在各研究中差异很大。未来的研究应该在更大和仔细匹配的受试者组中进行,两组使用以相同强度以dBHL表示的较长刺激,或在仔细确定的最大舒适响度水平。
    OBJECTIVE: This systematic review aims to assess the impact of sensorineural hearing loss (SNHL) on various frequency-following response (FFR) parameters.
    METHODS: Following PRISMA guidelines, a systematic review was conducted using PubMed, Web of Science, and Scopus databases up to January 2023. Studies evaluating FFRs in patients with SNHL and normal hearing controls were included.
    RESULTS: Sixteen case-control studies were included, revealing variability in acquisition parameters. In the time domain, patients with SNHL exhibited prolonged latencies. The specific waves that were prolonged differed across studies. There was no consensus regarding wave amplitude in the time domain. In the frequency domain, focusing on studies that elicited FFRs with stimuli of 170 ms or longer, participants with SNHL displayed a significantly smaller fundamental frequency (F0). Results regarding changes in the temporal fine structure (TFS) were inconsistent.
    CONCLUSIONS: Patients with SNHL may require more time for processing (speech) stimuli, reflected in prolonged latencies. However, the exact timing of this delay remains unclear. Additionally, when presenting longer stimuli (≥ 170 ms), patients with SNHL show difficulties tracking the F0 of (speech) stimuli. No definite conclusions could be drawn on changes in wave amplitude in the time domain and the TFS in the frequency domain. Patient characteristics, acquisition parameters, and FFR outcome parameters differed greatly across studies. Future studies should be performed in larger and carefully matched subject groups, using longer stimuli presented at the same intensity in dB HL for both groups, or at a carefully determined maximum comfortable loudness level.
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  • 文章类型: Systematic Review
    背景:本系统综述探讨了成人发病HL的危险因素的多面性。目的是综合最新的流行病学证据,以产生已识别的危险因素的合并比例发生率。
    方法:我们对电子数据库进行了广泛的搜索(MEDLINE,EMBASE,和psychINFO)用于提供与听力损失相关的危险因素的流行病学证据的研究。首先使用潜在狄利克雷分配(LDA)进行主题建模,以确定论文中有多少风险因素主题。通过使用比例荟萃分析计算合并比例发生率来分析数据。
    结果:从回顾的72项研究中,通过LDA主题建模,出现了六个关键风险因素主题。审查确定了耳毒性,主要由癌症治疗和抗生素引起,传染病,如COVID-19,职业噪声暴露,生活方式因素,健康状况,生物反应,和年龄进展是HL的重要危险因素。与癌症相关的耳毒性比例最高,为55.4%(95CI:39.0-70.7)。其次是感染性疾病的耳毒性,占50.0%(95CI:28.5-71.5)。这种高比例的发病率表明需要探索破坏性较小的疗法,并在治疗期间积极监测听力功能。
    结论:本综述的结果,结合流行病学证据的综合,增强我们对听力损失(HL)发病机制的理解,并突出潜在的干预领域,从而为更有效地预防和管理全球老龄化人口中的成人听力损失铺平了道路。
    BACKGROUND: This systematic review explores the multifaceted nature of risk factors contributing to adult-onset HL. The objective was to synthesise the most recent epidemiological evidence to generate pooled proportional incidences for the identified risk factors.
    METHODS: We conducted an extensive search of electronic databases (MEDLINE, EMBASE, and psychINFO) for studies providing epidemiological evidence of risk factors associated with hearing loss. Topic modelling using Latent Dirichlet Allocation (LDA) was first conducted to determine how many risk factor themes were available from the papers. Data were analysed by calculating the pooled proportional incidence using a meta-analysis of proportions.
    RESULTS: From the 72 studies reviewed, six key risk factor themes emerged through LDA topic modelling. The review identified ototoxicity, primarily caused by cancer treatments and antibiotics, infectious diseases like COVID-19, occupational noise exposure, lifestyle factors, health conditions, biological responses, and age progression as significant risk factors for HL. The highest proportional incidence was found with cancer-related ototoxicity at 55.4% (95%CI: 39.0-70.7), followed closely by ototoxicity from infectious diseases at 50.0% (95%CI: 28.5-71.5). This high proportional incidence suggests the need to explore less destructive therapies and proactively monitor hearing function during treatments.
    CONCLUSIONS: The findings of this review, combined with the synthesis of epidemiological evidence, enhance our understanding of hearing loss (HL) pathogenesis and highlight potential areas for intervention, thereby paving the way for more effective prevention and management of adult-onset hearing loss in our ageing global population.
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  • 文章类型: Journal Article
    突发性感觉神经性听力损失(SSNHL)是听觉功能的快速下降,需要紧急医疗管理。虽然病因因素,包括病毒感染,自身免疫性疾病,和血管问题,有助于理解SSNHL,在大多数情况下,病情尚不清楚。全身性类固醇通常被用作一线治疗,因为它们可以减少内耳炎症;然而,关于替代疗法的有效性仍有许多讨论。预测听力恢复在患者咨询中至关重要,包括延迟治疗,眩晕,和其他健康状况,这表明预后不良。在这里,我们回顾了关于SSNHL治疗方法和结局预测的当代研究,为医师评估和治疗SSNHL患者建立重要的指南.
    Sudden sensorineural hearing loss (SSNHL) is a rapid decline in auditory function that needs urgent medical management. Although etiologic factors, including viral infections, autoimmune diseases, and vascular issues, contribute to the understanding of SSNHL, the condition remains unclear in most cases. Systemic steroids are often used as the first-line treatment because they reduce inner ear inflammation; however, there remains numerous discussions about the effectiveness of alternative treatments. To predict hearing recovery is crucial in patients\' counseling with factors, including delayed treatment, vertigo, and other health conditions, which indicate poor prognosis. Herein, we review contemporary research on the treatment approaches and outcome predictions of SSNHL to establish important guidelines for physicians in evaluating and treating patients with SSNHL.
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