Suppr超能文献

普遍新生儿听力筛查用于早期识别永久性儿童听力障碍的对照试验。韦塞克斯普遍新生儿听力筛查试验组。

Controlled trial of universal neonatal screening for early identification of permanent childhood hearing impairment. Wessex Universal Neonatal Hearing Screening Trial Group.

出版信息

Lancet. 1998;352(9145):1957-64.

PMID:9872244
Abstract

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.

摘要

背景

先天性永久性儿童听力障碍(PCHI)会损害沟通能力,并可能影响心理健康和就业前景。出生后1年内进行干预可减轻其大部分不良影响。对这种疾病进行新生儿筛查是可行的,但其对所有婴儿的益处存在争议。我们调查了除标准的健康访视员分心测试外,对所有在医院出生的婴儿进行新生儿筛查是否会提高早期转诊、确诊和干预的比例。

方法

1993年至1996年期间,两组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,以实现四个有新生儿筛查的时期和四个没有新生儿筛查的时期,每个时期持续4 - 6个月。婴儿是否接受新生儿筛查取决于他们出生的时期。我们使用了瞬态诱发耳声发射测试,对于该测试未通过的婴儿,在同一天进行自动听性脑干反应测试。我们将检测结果呈阳性的婴儿转诊进行听力评估。

结果

53781名婴儿纳入试验,其中25609名在有新生儿筛查的时期出生。新生儿筛查的覆盖率达到87%,假阳性率为1.5%,每10万目标人群中双侧PCHI且听力阈值水平为40分贝或更高的总体检出率为90例,相当于该疾病在人群中预期患病率的80%。每10万目标人群中,在有新生儿筛查的时期,6个月龄前转诊的中度或重度PCHI婴儿比没有新生儿筛查的时期多71名。PCHI的早期确诊和干预显著增加。新生儿筛查的假阴性率显著低于分心测试(4%对27%,p = 0.041)。

解读

新生儿筛查在早期识别先天性PCHI方面有效,对于中度和重度PCHI婴儿可能特别有用,因为早期干预可能带来最大益处。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验