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Epidemiology of Unilateral Sensorineural Hearing Loss With Universal Newborn Hearing Screening

机译:通用新生儿听力筛查的单侧感觉神经性听力损失的流行病学

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Objectives/Hypothesis: Compare the epidemiology of pediatric unilateral sensorineural hearing loss before and after implementation of universal newborn hearing screening in Missouri.Study Design: Inception cohort.Methods: Charts of 134 children born between January 1, 1990 and December 31, 2007, diagnosed with unilateral sensorineural hearing loss at a single institution in Missouri were reviewed to determine the effects of universal newborn hearing screening on age of detection and etiology of hearing loss.Results: Mean age of detection declined from 4.4 (standard deviation [SD] 1.8) to 2.6 (SD 2.6) years of age, whereas the rate of detection by 6 months of age increased from 3% to 42%. The majority (58%) of cases had normal hearing at birth. The most common etiological category was unknown (41%) before screening and congenital (45%) after screening. The use of magnetic resonance imaging has increased by 21% (2-fold), whereas use of computed tomography has declined by 8% since 2002. Yields of connexin, Pendred, electrocardiogram, and syphilis testing were 0/48 and 2/31 before and after screening, respectively.Conclusions: Implementation of universal newborn hearing screening in Missouri is associated with a decrease in age of detection of unilateral sensorineural hearing loss. The majority of cases are either not present or not detectable at birth. The combination of hearing status at birth and imaging findings suggests that the majority of cases are congenital rather than of unknown etiology.
机译:目的/假设:比较密苏里州实施全民新生儿听力筛查前后小儿单侧感觉神经性听力损失的流行病学研究设计:初始队列方法:1990年1月1日至2007年12月31日期间出生的134名儿童的图表对密苏里州一家机构的单侧感觉神经性听力损失进行了回顾,以确定新生儿通用听力筛查对检测年龄和听力损失病因的影响。结果:平均检测年龄从4.4(标准差[SD] 1.8)降低到年龄为2.6(SD 2.6)岁,而6个月大时的检测率从3%增加到42%。大多数病例(58%)出生时听力正常。筛查前最常见的病因学类别是未知的(41%),筛查后是先天性的(45%)。自2002年以来,磁共振成像的使用量增加了21%(2倍),而计算机断层摄影术的使用量却下降了8%。连接蛋白,Pendred,心电图和梅毒检测的产率分别为0/48和2/31。结论:密苏里州实施新生儿通用听力筛查与单侧感觉神经性听力损失检出年龄的降低有关。大多数病例在出生时都不存在或无法检测到。出生时的听力状态和影像学表现的结合表明,大多数病例是先天性的,而不是病因不明。

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