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Universal newborn hearing screening.

机译:通用新生儿听力筛查。

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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.
机译:据估计,先天性听力损失影响每千名新生儿中的一名。听力损失的原因可能是传导性的,感觉神经性的,混合性的或中心性的。先天性听力损失的已知危险因素包括巨细胞病毒感染和早产,因此必须留在新生儿重症监护病房。但是,仅基于风险的筛查会漏掉多达42%的严重听力障碍儿童。新生儿通用听力筛查是一种识别有或没有危险因素的听力受损新生儿的方法。筛查试验阳性的新生儿应转诊接受最终检查和干预服务。高质量的研究尚未确定对通过普适筛查确定的听力障碍儿童进行早期干预是否可以提高语言和沟通技巧。但是,由于易于执行筛查测试以及能够识别可能需要早期干预的儿童的能力,大多数国家的儿童健康组织都认可进行普查。

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