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患有听神经病的婴幼儿的耳蜗微音电位特征

Characteristics of cochlear microphonics in infants and young children with auditory neuropathy.

作者信息

Shi Wei, Ji Fei, Lan Lan, Liang Si-Chao, Ding Hai-Na, Wang Hui, Li Na, Li Qian, Li Xing-Qi, Wang Qiu-Ju

机构信息

Department of Otolaryngology/Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, China.

出版信息

Acta Otolaryngol. 2012 Feb;132(2):188-96. doi: 10.3109/00016489.2011.630016. Epub 2011 Nov 21.

Abstract

CONCLUSIONS

Cochlear microphonics (CMs) play an important role in the diagnosis of auditory neuropathy (AN). It is necessary and helpful to diagnose the sites-of-lesion in infants and children with AN by analyzing the patterns of CM amplitudes and I/O functions together.

OBJECTIVES

To investigate the characteristics and clinical significance of CMs in the diagnosis of AN among infants and children.

METHODS

A total of 36 infants and children (16 males and 20 females) were divided into two groups. Group A included 15 children (30 ears) with auditory brainstem response (ABR) absent and distortion product otoacoustic emissions (DPOAEs) present and group B included 21 children (30 ears) with ABR absent and DPOAEs absent. Fifteen normal-hearing infants (30 ears) made up the control group. Click eliciting CMs were recorded at stimulus levels of 100, 90, 80, and 70 dB nHL for each ear using a button electrode placed at the top of the forehead. A tube-clamping method was used to distinguish CMs from artifacts, and an averaging algorithm was used to obtain a clear CM waveform. The time delay and amplitude of CMs were measured in both children with AN and normal-hearing infants on (C-R)/2 waveforms, and an I/O function curve for each group was plotted with the stimulating level as input and the CM amplitude as output.

RESULTS

The largest identifiable CMs were generally found between 0.5 and 0.8 ms after stimulation with mean delay of 0.63 ± 0.04 ms in both group A and the control group, and 0.63 ± 0.07 ms in group B. There was no significant difference between the AN group and the control group in CM time delay. There was no significant difference (p > 0.05) between group A (AN with OAEs present, 0.47 ± 0.15 μV) and the control group (0.45 ± 0.13 μV) in CM amplitude, while CM amplitudes in children with AN with DPOAEs absent (0.24 ± 0.08 μV) were significantly lower than those in either the control group or group A (p < 0.01). The amplitude of CMs reduced with stimulus intensity in all the subjects. There was obvious nonlinearity in group A and the control group, while there was a more linear tendency in amplitude increasing on the I/O function curve in group B.

摘要

结论

耳蜗微音电位(CMs)在听神经病(AN)的诊断中起重要作用。通过综合分析CMs振幅和输入/输出(I/O)功能模式来诊断婴幼儿AN的病变部位是必要且有帮助的。

目的

探讨CMs在婴幼儿AN诊断中的特征及临床意义。

方法

选取36例婴幼儿(男16例,女20例),分为两组。A组15例患儿(30耳),听性脑干反应(ABR)消失但畸变产物耳声发射(DPOAE)存在;B组21例患儿(30耳),ABR消失且DPOAE消失。15例听力正常的婴幼儿(30耳)作为对照组。使用置于前额顶部的纽扣电极,在100、90、80和70 dB nHL的刺激强度下记录每只耳朵的短声诱发CMs。采用夹管法区分CMs与伪迹,并使用平均算法获得清晰的CM波形。在AN患儿和听力正常的婴幼儿中,在(C-R)/2波形上测量CMs的时间延迟和振幅,并以刺激强度为输入、CM振幅为输出绘制每组的I/O功能曲线。

结果

在A组和对照组中,刺激后最大可识别的CMs通常出现在0.5至0.8 ms之间,平均延迟为0.63±0.04 ms,B组为0.63±0.07 ms。AN组和对照组在CM时间延迟方面无显著差异。A组(存在耳声发射的AN,0.47±0.15 μV)与对照组(0.45±0.13 μV)在CM振幅方面无显著差异(p>0.05),而DPOAE消失的AN患儿的CM振幅(0.24±0.08 μV)显著低于对照组或A组(p<0.01)。所有受试者的CM振幅均随刺激强度降低。A组和对照组存在明显的非线性,而B组在I/O功能曲线上振幅增加的趋势更呈线性。

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