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Screening of hearing impairment in the newborn using the auditory response cradle.

机译:使用听觉响应支架筛查新生儿的听力障碍。

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摘要

The Auditory Response Cradle (ARC) is a fully automated microprocessor controlled machine that was designed for the hearing screening of full term neonates. In order to evaluate the ARC, 6000 babies were screened at a district maternity hospital over a period of three years. Every infant subsequently entered a three year follow up programme. One hundred and two babies (1.7%) failed the ARC screen (that is, they failed two ARC tests) and 20 of these were found to have some hearing impairment: in 10 it was severe (80-90 dBHL), in seven moderate (45-60 dBHL), and in three it was mild to moderate (less than 45 dBHL). In addition, of the 20 babies who failed a first test and were discharged before a second could be performed, two were confirmed to have a severe hearing loss; 79 infants failing the screen were cleared on further testing, giving the ARC a false positive rate of 1.3%. On following up all 6000 infants for three years, seven children who passed the neonatal screen were subsequently found to have a hearing loss. For two babies the aetiology was unknown but for five the hearing impairment was either due to a hereditary progressive loss or definite postnatal factors. Progressive and acquired hearing losses cannot be detected at a neonatal screen and this emphasises the need for follow up screens at other stages in the child's life. In this long term study the ARC has been found to have a high detection rate for severe hearing loss and confirms the practical possibility of using a behavioural technique for the universal screening of hearing in neonates.
机译:听觉响应摇篮(ARC)是一款全自动的微处理器控制的机器,专为足月新生儿的听力筛查而设计。为了评估ARC,在为期三年的地区妇产医院对6000例婴儿进行了筛查。随后,每个婴儿都进入了三年的随访计划。 102个婴儿(1.7%)未通过ARC筛查(即,他们两次未通过ARC测试),其中20个被发现有听力障碍:10个严重(80-90 dBHL),7个中度(45-60 dBHL),三分之二为轻度至中度(小于45 dBHL)。另外,在第一次测试中未通过并在第二次测试之前就出院的20名婴儿中,有2名被确认患有严重的听力损失。 79例筛查不合格的婴儿在进一步检查中被清除,ARC的假阳性率为1.3%。在对所有6000名婴儿进行为期三年的随访之后,随后发现有7名通过新生儿筛查的儿童听力受损。对于两个婴儿,其病因不明,但是对于五个婴儿,听力障碍是由于遗传性进行性丧失或确定的产后因素所致。在新生儿筛查中无法检测到进行性和后天性听力损失,这强调了在孩子生命的其他阶段需要进行后续筛查的必要性。在这项长期研究中,发现ARC对严重的听力损失具有很高的检出率,并且证实了使用行为技术对新生儿的听力进行普遍筛查的实际可能性。

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