Evolution and expansion of newborn screening programmes in Singapore

新加坡新生儿筛查项目的演变与扩展

阅读:1

Abstract

In Singapore, the newborn screening programme was started in 1965 in order to reduce the high neonatal mortality and neurological morbidity owing to severe hyperbilirubinaemia caused by erythrocyte glucose-6-phosphate dehydrogenase deficiency. About 25 years later, the national newborn screening for congenital hypothyroidism was established. Subsequently, universal newborn hearing screening and screening for multiple inborn errors of metabolism using tandem mass spectrometry were introduced as national programmes in 2003 and 2006, respectively. All these programmes are widely accepted as standards of care, and practically every newborn is screened despite the absence of any legislation. Two other evidence-based bedside screening tests, namely pulse oximetry screening for critical congenital heart disorders and physical examination of the hips for developmental dysplasia of the hips with selected ultrasonographic screening have been widely performed in hospitals, and they are soon expected to be in the national screening programmes.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。