首页> 外文期刊>The Lancet >Controlled trial of universal neonatal screening for early identification of permanent childhood hearing impairment. Wessex Universal Neonatal Hearing Screening Trial Group (see comments)
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Controlled trial of universal neonatal screening for early identification of permanent childhood hearing impairment. Wessex Universal Neonatal Hearing Screening Trial Group (see comments)

机译:早期新生儿永久性听力障碍的通用新生儿筛查的对照试验。威塞克斯通用新生儿听力筛查试验组(请参阅评论)

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BACKGROUND: Congenital permanent childhood hearing impairment (PCHI) impairs communication skills and, possibly, mental health and employment prospects. Management within 1 year of birth can alleviate most of its adverse effects. Neonatal screening for this disorder is feasible but its benefit for all babies is disputed. We investigated whether neonatal screening of all babies born in hospital, in addition to the standard health visitor distraction test, would increase the rates of early referral, confirmation, and management. METHODS: Between 1993 and 1996, two teams of four part-time testers and equipment moved between two pairs of hospitals to achieve four periods with neonatal screening and four without neonatal screening, each of 4-6 months' duration. Babies did or did not undergo neonatal screening dependent on during which periods they were born. We used a transient evoked otoacoustic emissions test and, in babies who failed this test, an automated auditory brainstem response test on the same day. We referred babies with positive results for audiological assessment. FINDINGS: 53,781 babies were included in the trial, and 25,609 were born during periods with neonatal screening. Neonatal screening achieved 87% coverage of births, with a false-alarm rate of 1.5%, and an overall yield of 90 cases of bilateral PCHI of 40 dB or more relative to hearing threshold level per 100,000 target population, equivalent to 80% of the expected prevalence of the disorder in the population. 71 more babies with moderate or severe PCHI per 100,000 target population were referred before age 6 months during periods with neonatal screening than during periods without. Early confirmation and management of PCHI were significantly increased. The rate of false-negative results from neonatal screening was significantly lower than that for the distraction test (4 vs 27% p=0.041). INTERPRETATION: Neonatal screening is effective in identification of congenital PCHI early and may be particularly useful for babies with moderate and severe PCHI for whom early management may have the most benefit.
机译:背景:先天性儿童永久性永久性听力障碍(PCHI)损害了沟通技巧,并可能损害心理健康和就业前景。出生后1年内进行管理可以减轻大多数不良影响。新生儿筛查这种疾病是可行的,但其对所有婴儿的益处尚存争议。我们调查了对医院出生的所有婴儿进行的新生儿筛查,除了标准的健康访客分心测试之外,还可以提高早期转诊,确诊和管理的比率。方法:从1993年到1996年,两支由四名兼职测试人员和设备组成的团队在两对医院之间移动,以实现四个阶段的新生儿筛查和四个不进行新生儿筛查,每个阶段为4-6个月。婴儿是否出生取决于新生儿出生的时间。我们使用了瞬态诱发的耳声发射测试,对于未通过测试的婴儿,在同一天进行了自动听觉脑干反应测试。我们将婴儿转入阳性结果以进行听力学评估。结果:试验中有53,781例婴儿,新生儿筛查期间有25,609例出生。新生儿筛查覆盖了87%的婴儿,误报率为1.5%,相对于每10万目标人群的听力阈值水平,90例双侧PCHI的总收率为40 dB或更高,相当于80%的目标人群。人群中疾病的预期患病率。在进行新生儿筛查的6个月龄之前,每10万目标人群中有71例中度或重度PCHI婴儿被转诊,而未进行检查的婴儿则多于71个。对PCHI的早期确认和管理显着增加。新生儿筛查的假阴性结果发生率显着低于分散测试的发生率(4比27%,p = 0.041)。解释:新生儿筛查可早期有效地识别先天性PCHI,对于中,重度PCHI的婴儿,早期治疗可能最有利,这可能特别有用。

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