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[听觉神经病患者的耳声发射、听觉诱发电位、纯音听阈及言语清晰度]

[Otoacoustic emissions, auditory evoked potentials, pure tone thresholds and speech intelligibility in cases of auditory neuropathy].

作者信息

Ptok M

机构信息

Klinik und Poliklinik für Phoniatrie und Pädaudiologie (Direktor: Prof. Dr. M. Ptok), Medizinische Hochschule Hannover.

出版信息

HNO. 2000 Jan;48(1):28-32. doi: 10.1007/s001060050005.

Abstract

The combined findings of "normal evoked otoacoustic emissions (EOAE) and absent or markedly disturbed auditory evoked potentials from the brainstem and/or cortex" has been named auditory neuropathy in the English literature. The pure tone thresholds in these patients range from mild to severe loss. The loss of speech comprehension is out of proportion in comparison to the pure tone threshold elevation. This combination of findings suggests that cochlear function and in particular outer hair cell function, is normal in these patients but also suggests that the inner hair cell / VIII nerve functional unit is abnormal. Disruption in neural synchrony has previously been postulated as a reasonable explanation for the absent auditory brainstem response while otoacoustic emissions are preserved. Because the long-latency auditory evoked potentials, not having the stringent synchrony requirements of the ABR, may also be missing, the term synchrony - disruption may be somewhat misleading. The literature about auditory neuropathy is reviewed here: We now know that a set of salient features distinguishes these patients from the majority of patients with sensorineural hearing loss or other described syndromes. The symptoms defining auditory neuropathy are mild, moderate or severe elevation of auditory thresholds to pure tone stimuli by air and bone conduction, absent to severely abnormal ABRs to high level stimuli, present otoacoustic emissions (that do not suppress with contralateral noise), word recognition ability poorer than expected from the pure tone hearing loss configuration (in cases with mild to moderate hearing threshold elevation) and absent acoustic reflexes to both ipsilateral and contralateral tones. The entire set of findings, consistently seen in these patients, supports the importance of the crosscheck principle in diagnostic evaluation especially in children with delayed and/or impaired language acquisition. It is of ponderous importance that this disorder is not being confused with sensory hearing loss.

摘要

英文文献中已将“正常的诱发耳声发射(EOAE)以及脑干和/或皮层听觉诱发电位缺失或明显异常”这一综合表现命名为听神经病。这些患者的纯音听阈范围从轻度到重度听力损失。与纯音听阈升高相比,言语理解能力的丧失程度不成比例。这一综合表现表明,这些患者的耳蜗功能,尤其是外毛细胞功能正常,但也表明内毛细胞/第八神经功能单元异常。此前曾推测神经同步性中断是听觉脑干反应缺失而耳声发射保留的合理原因。由于长潜伏期听觉诱发电位不像听性脑干反应那样有严格的同步性要求,也可能缺失,因此“同步性中断”这一术语可能会有些误导性。本文对有关听神经病的文献进行了综述:我们现在知道,有一系列显著特征可将这些患者与大多数感音神经性听力损失患者或其他已描述的综合征患者区分开来。定义听神经病的症状包括:气导和骨导对纯音刺激的听阈轻度、中度或重度升高,对高强度刺激的听性脑干反应缺失至严重异常,存在耳声发射(不被对侧噪声抑制),单词识别能力比纯音听力损失情况预期的要差(在听阈轻度至中度升高的病例中),以及对同侧和对侧纯音均无听觉反射。在这些患者中一致观察到的所有这些表现,支持了交叉核对原则在诊断评估中的重要性,尤其是在语言发育迟缓或受损的儿童中。极为重要的是,这种疾病不能与感音性听力损失相混淆。

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