Tympanometry screening in developmentally delayed individuals.

The Journal of auditory research Pub Date : 1985-01-01
M K Zoller, D J Ruhe, J R Dunster
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Abstract

Residents of the Huronia Regional Centre for the developmentally disabled (N:900) underwent otoscopic screening (canal "clear" vs "not clear") and tympanometric screening, including tympanometry and physical volume measures (Ss exhibiting Type B tympanograms were classified "hard positive"). Results showed that (1) by otoscopy, 53.2% of all Ss examined had canals "not clear". (2) Overall, degree of retardation was loosely related to prevalence of abnormal otoscopy. (3) The etiologies for mental retardation of "metabolism" and "chromosomal abnormalities" (including all Down's Syndrome cases) were most prone to be in the "not clear" otoscopic category. By tympanometry, 25.8% were classified "hard positive". Overall, conductive disorders as assessed by tympanometry increased significantly with degree of mental retardation. Chromosomal abnormalities yielded a significantly higher proportion of "hard positive" cases (43%) than any other etiology. Identification of sub-populations at risk for conductive disorders, such as those of chromosomal abnormalities and/or more severe developmental delays will enable the employment in the future of more efficient auditory screening techniques.

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发育迟缓个体的鼓室测量筛查。
胡洛尼亚地区发展障碍中心(N:900)的居民接受了耳镜检查(耳道“清晰”与“不清晰”)和鼓室检查,包括鼓室测量和物理容积测量(显示B型鼓室图的患者被归类为“硬阳性”)。结果表明:(1)耳镜检查,53.2%的耳道“不清”。(2)总体而言,听力发育迟缓程度与耳镜检查异常的发生率呈弱相关。(3)“代谢”和“染色体异常”的智力低下病因(包括所有唐氏综合征病例)最容易出现在“不清楚”的耳镜类别中。经鼓室测量,25.8%为硬阳性。总体而言,鼓室测量法评估的传导障碍随着智力迟钝程度的增加而显著增加。染色体异常产生“硬阳性”病例的比例(43%)明显高于其他病因。识别具有传导性障碍风险的亚群体,例如染色体异常和/或更严重的发育迟缓,将使未来能够使用更有效的听觉筛查技术。
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