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Idiopathic sudden sensorineural hearing loss and acute low-tone sensorineural hearing loss: a comparison of the results of a nationwide epidemiological survey in Japan

机译:特发性突然感觉神经性听力减退和急性低音感觉神经性听力减退:日本全国流行病学调查结果的比较

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摘要

Objectives: The aim of this study was to investigate the differences between idiopathic sudden sensorineural hearing loss (SSNHL), and acute low-tone sensorineural hearing loss (ALHL) using the results of a nationwide survey database in Japan and to analyze the variables associated with their clinical features and the severity of hearing impairment, treatment, and prognosis.Methods: Participants were patients registered between April 2014 and March 2016 in a multicenter epidemiological survey database involving 30 university hospitals and medical centers across Japan. Statistical analysis was performed to clarify the factors associated with their clinical characteristics and the severity of hearing impairment, treatment, and prognosis.Results: Idiopathic SSNHL and ALHL differed significantly in terms of male-to-female ratio, age distribution, and time from onset to start of treatment. The treatment methods and hearing prognosis also differed markedly between the two diseases. A majority (92%) of idiopathic SSNHL patients were administered some type of corticosteroid, while half of the ALHL patients received corticosteroids and a diuretic agent.Conclusion: The results suggested that idiopathic SSNHL and ALHL belonged to different categories of inner ear disease.
机译:目的:本研究旨在利用日本全国调查数据库的结果,调查特发性突然感觉神经性听力损失(SSNHL)和急性低音感觉神经性听力损失(ALHL)之间的差异,并分析与方法:研究对象为2014年4月至2016年3月在日本全国30所大学医院和医疗中心的多中心流行病学调查数据库中登记的患者。进行统计分析以明确其临床特征,听力障碍严重程度,治疗和预后的相关因素。结果:特发性SSNHL和ALHL在男女比例,年龄分布和发病时间方面存在显着差异开始治疗。两种疾病之间的治疗方法和听觉预后也明显不同。大多数(92%)特发性SSNHL患者服用某种类型的皮质类固醇激素,而一半的ALHL患者接受了皮质类固醇激素和利尿剂。

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