Shehata-Dieler W, Völter C, Hildmann A, Hildmann H, Helms J
Universitätsklinikum Würzburg, Klinik und Poliklinik für Hals-, Nasen- und Ohrenkranke, Würzburg.
Laryngorhinootologie. 2007 Jan;86(1):15-21. doi: 10.1055/s-2006-925369.
Auditory neuropathy is a disorder characterised by preservation of outer hair cells function with normal otoacoustic emissions (OAEs), but with absent auditory brainstem responses (ABR). Perisynaptic synchronisation disorder is one of the possible pathogenesis underlying auditory neuropathy. In this paper we describe the clinical presentation and audiological findings in pediatric auditory neuropathy and its management.
9 children with auditory neuropathy could be included in the study. An audiological evaluation was performed in all children including behavioural audiometry, measurement of the OAEs as well as electrocochleography (ECoG) and ABR recordings. Children who failed to get any benefit from conventional amplification received a cochlear implant. Prior to implantation the responses to electrical stimuli were examined with the promontory test and with the electrically evoked ABR.
One child showed auditory neuropathy only on one side with normal hearing thresholds on the contralateral ear. Another child had normal hearing thresholds after the follow up period. Four children received a hearing aid. But variable hearing reactions were observed. Thus in three cases a CI is planned. In three children cochlea implantation was done. Following implantation a remarkable improvement in hearing/speech capabilities with the CI compared to conventional hearing aids were observed in all three cases. Beside, these three children developed open set speech discrimination and are using now oral language for communication.
Auditory neuropathy is a disorder which presents with different clinical and audiological findings. Thus the management of this disorder must be an individual one. In light of our findings we support the use of cochlear implants as an option for children with auditory neuropathy in cases where conventional amplification does not work sufficiently.
听觉神经病是一种以外毛细胞功能保留、耳声发射(OAE)正常,但听觉脑干反应(ABR)缺失为特征的疾病。突触周围同步障碍是听觉神经病潜在的发病机制之一。本文描述了儿童听觉神经病的临床表现、听力学检查结果及其治疗方法。
9名患有听觉神经病的儿童纳入本研究。对所有儿童进行了听力学评估,包括行为测听、耳声发射测量以及耳蜗电图(ECoG)和听觉脑干反应记录。对传统放大治疗无效的儿童接受了人工耳蜗植入。植入前,通过岬部测试和电诱发听觉脑干反应检查对电刺激的反应。
1名儿童仅一侧表现为听觉神经病,对侧耳听力阈值正常。另1名儿童在随访期后听力阈值正常。4名儿童佩戴了助听器,但观察到不同的听力反应。因此,计划对3例患儿进行人工耳蜗植入。3名儿童接受了人工耳蜗植入。植入后,与传统助听器相比,这3例患儿的听力/言语能力均有显著改善。此外,这3名儿童能够进行开放式言语辨别,并开始使用口语进行交流。
听觉神经病是一种具有不同临床和听力学表现的疾病。因此,对该疾病的治疗必须因人而异。根据我们的研究结果,我们支持在传统放大治疗效果不佳的情况下,将人工耳蜗植入作为患有听觉神经病儿童的一种治疗选择。