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高危新生儿听力筛查

Hearing screening of high risk newborns.

作者信息

Swigonski N, Shallop J, Bull M J, Lemons J A

出版信息

Ear Hear. 1987 Feb;8(1):26-30. doi: 10.1097/00003446-198702000-00005.

Abstract

Prospective screening of an extremely high risk group of 137 infants cared for in the Newborn Intensive Care Unit of the James Whitcomb Riley Hospital for Children was undertaken during 1983. Auditory brain stem responses (ABR) were obtained utilizing a clinical evoked potential system (Madsen 2250). Patients were selected for screening prior to discharge or transfer to the referring hospital on the basis of one or more of the following criteria: birth weight less than 1250 grams; birth weight less than 1500 grams and ventilatory support; significant depression at birth (Apgars less than 3 and 6 at 1 and 5 minutes, respectively); seizures, meningitis, and/or sepsis. Of the original 137 infants tested, 82 passed the initial ABR, 22 conditionally passed, and 34 failed. Eighty-two infants had follow-up behavioral and audiometric testing while 20 infants died and 35 were lost to follow-up. Four infants had severe sensorineural hearing loss, each of whom had failed the initial ABR. None of the infants who initially passed or conditionally passed the ABR had sensorineural hearing loss on follow-up testing. High risk factors for sensorineural hearing loss in the neonatal period included: intraventricular/periventricular hemorrhage, apnea, family history, major malformations of the head and neck, and possibly hyperbilirubinemia and congenital infection. No relationship of sensorineural hearing loss with very low birth weight, hyponatremia, infection, seizures, or medications was found. On the basis of these data, it is suggested that electrophysiologic hearing screening of a high risk population may be delayed until 3 to 6 months of age to improve specificity of testing.

摘要

1983年,对在詹姆斯·惠特科姆·莱利儿童医院新生儿重症监护病房接受护理的137名极高风险婴儿进行了前瞻性筛查。使用临床诱发电位系统(马德森2250)获得听觉脑干反应(ABR)。根据以下一项或多项标准,在出院或转至转诊医院之前选择患者进行筛查:出生体重低于1250克;出生体重低于1500克且需要通气支持;出生时严重抑制(1分钟和5分钟时阿氏评分分别低于3分和6分);癫痫、脑膜炎和/或败血症。在最初测试的137名婴儿中,82名通过了初始ABR,22名有条件通过,34名未通过。82名婴儿接受了后续行为和听力测试,20名婴儿死亡,35名失访。4名婴儿患有严重感音神经性听力损失,他们均未通过初始ABR。最初通过或有条件通过ABR的婴儿在后续测试中均无感音神经性听力损失。新生儿期感音神经性听力损失的高危因素包括:脑室内/脑室周围出血、呼吸暂停、家族史、头颈部严重畸形,可能还有高胆红素血症和先天性感染。未发现感音神经性听力损失与极低出生体重、低钠血症、感染、癫痫或药物之间的关系。根据这些数据,建议对高危人群的电生理听力筛查可推迟至3至6个月龄,以提高检测的特异性。

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