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新生儿听力普遍筛查。

Universal newborn hearing screening.

作者信息

Wrightson A Stevens

机构信息

Department of Family and Community Medicine, University of Kentucky, Lexington, Kentucky 40536, USA.

出版信息

Am Fam Physician. 2007 May 1;75(9):1349-52.

Abstract

Congenital hearing loss is estimated to affect one in every 1,000 newborns. Causes of hearing loss can be conductive, sensorineural, mixed, or central. Known risk factors for congenital hearing loss include cytomegalovirus infection and premature birth necessitating a stay in the neonatal intensive care unit. However, up to 42 percent of profoundly hearing-impaired children will be missed using only risk-based screening. Universal newborn hearing screening is a way to identify hearing-impaired newborns with or without risk factors. Newborns with positive screening tests should be referred for definitive testing and intervention services. Whether early intervention in hearing-impaired children identified with universal screening improves language and communication skills has not been established by good-quality studies. However, universal screening has been endorsed by most national children's health organizations because of the ease of administering the screening tests and the ability to identify children who may need early intervention.

摘要

据估计,每1000名新生儿中就有1人患有先天性听力损失。听力损失的原因可以是传导性、感音神经性、混合性或中枢性的。已知的先天性听力损失风险因素包括巨细胞病毒感染和需要入住新生儿重症监护病房的早产。然而,仅采用基于风险的筛查,高达42%的重度听力受损儿童将会被漏诊。新生儿听力普遍筛查是一种识别有无风险因素的听力受损新生儿的方法。筛查试验呈阳性的新生儿应被转诊接受确诊检测和干预服务。高质量研究尚未证实,对通过普遍筛查确定的听力受损儿童进行早期干预是否能提高语言和沟通能力。然而,由于筛查试验易于实施,且能够识别可能需要早期干预的儿童,普遍筛查已得到大多数国家儿童健康组织的认可。

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