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突发性听力损失的诊断与治疗

Diagnostics and therapy of sudden hearing loss.

作者信息

Plontke Stefan K

机构信息

Department of Otorhinolaryngology, Head & Neck Surgery, University Medicine Halle, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.

出版信息

GMS Curr Top Otorhinolaryngol Head Neck Surg. 2018 Feb 19;16:Doc05. doi: 10.3205/cto000144. eCollection 2017.

Abstract

This article reviews recent aspects of diagnostics, differential diagnostics, and evidence in systemic and local therapy of idiopathic sudden sensorineural hearing loss (ISSHL). Since a number of disorders can be accompanied by sudden hearing loss, a meaningful and targeted diagnostic strategy is of utmost importance. An important differential diagnosis of sudden hearing loss are intralabyrinthine schwannomas (ILS). The incidence of ILS is probably significantly underestimated. This may be due to the lack of awareness or lack of explicit search for an intralabyrinthine tumor on MRI or an inappropriate MRI technique for the evaluation of sudden hearing loss ("head MRI" instead of "temporal bone MRI" with too high slice thicknesses). Therefore, the request to the radiologist should specifically include the question for (or exclusion of) an ILS. With special MRI techniques, it is possibly today to visualize an endolymphatic hydrops. The evidence in the therapy of ISSHL is - with respect to the quality and not quantity of studies - unsatisfying. The value of systemically (low dose) or intratympanically applied corticosteroids in the primary treatment of ISSHL is still unclear. In order to investigate the efficacy and safety of high dose corticosteroids as primary therapy for ISSHL, a national, multicenter, three-armed, randomized, triple-blind controlled clinical trial is currently performed in Germany (http://hodokort-studie.hno.org/). After insufficient recovery of the threshold with systemic therapy of ISSHL, intratympanic corticosteroid therapy appears to be associated with a significantly higher chance of an improved hearing threshold than no therapy or placebo. Both, hearing gain and final hearing threshold, however, appear to be independent from the onset of secondary therapy. Based on currently available data from clinical studies, no recommendation can be made with respect to the type of corticosteroid and specifics of the intratympanic application protocol.

摘要

本文综述了特发性突发性感音神经性听力损失(ISSHL)系统及局部治疗中诊断、鉴别诊断和循证医学的最新进展。由于多种疾病都可能伴有突发听力损失,因此有意义且目标明确的诊断策略至关重要。突发听力损失的一个重要鉴别诊断是迷路内神经鞘瘤(ILS)。ILS的发病率可能被严重低估。这可能是由于认识不足,或在MRI上未明确寻找迷路内肿瘤,或用于评估突发听力损失的MRI技术不当(“头部MRI”而非“颞骨MRI”,且切片厚度过大)。因此,向放射科医生提出的要求应特别包括询问(或排除)ILS。借助特殊的MRI技术,如今有可能观察到内淋巴积水。就研究的质量而非数量而言,ISSHL治疗的循证医学情况并不令人满意。全身(低剂量)或鼓室内应用皮质类固醇在ISSHL初始治疗中的价值仍不明确。为了研究高剂量皮质类固醇作为ISSHL初始治疗的疗效和安全性,德国目前正在进行一项全国性、多中心、三臂、随机、三盲对照临床试验(http://hodokort-studie.hno.org/)。在ISSHL全身治疗后阈值恢复不佳时,鼓室内皮质类固醇治疗似乎比不治疗或使用安慰剂更有可能显著提高听力阈值。然而,听力增益和最终听力阈值似乎与二线治疗的开始时间无关。根据目前临床研究可得的数据,无法就皮质类固醇的类型和鼓室内应用方案的具体细节给出推荐。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2e1/5818684/634095e5c0e4/CTO-16-05-t-001.jpg

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