Current situation and new steps in newborn screening in Spain

María L. Couce , María Cernada , Hector Boix , María Dolores Sánchez-Redondo , María Gracia Espinosa Fernández , Noelia González-Pacheco , Ana Martín , Alejandro Pérez-Muñuzuri , en representación del Comité de Estándares Sociedad Española de Neonatología
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Abstract

After more than 50 years of experience, newborn screening (NBS) programs represent one of the most significant advancements in public health, particularly in pediatric and neonatal care, benefiting almost 350 000 children annually in Spain. Following the inclusion of congenital hearing loss screening in 2003 and screening for seven congenital diseases by newborn blood spot test in 2014 as part of the population-wide neonatal screening program of the National Health System (NHS), significant advances have been achieved in recent years. This progress is evident in the implementation of screening for critical congenital heart diseases, approved in January 2024 by the National Public Health Commission of the Interterritorial Council of the NHS, as well as screening for congenital diseases through the newborn blood spot test, with the incorporation of new conditions enabled by advances in second-tier testing and emerging scientific evidence. Neonatologists and pediatricians must keep abreast of these developments and where the field is heading, as even more rapid progress may take place with the advent of genomic newborn screening.
西班牙新生儿筛查的现状和新措施。
经过50多年的经验,新生儿筛查(NBS)项目是公共卫生领域,特别是儿科和新生儿护理领域最重大的进步之一,每年使西班牙近35万名儿童受益。继2003年将先天性听力损失筛查和2014年将新生儿血斑试验筛查7种先天性疾病纳入国家卫生系统(NHS)全民新生儿筛查方案之后,近年来取得了重大进展。这一进展在以下方面得到了明显体现:2024年1月,国民保健制度跨地区理事会国家公共卫生委员会批准了对严重先天性心脏病的筛查,以及通过新生儿血液斑点检测筛查先天性疾病,并结合了二级检测的进步和新出现的科学证据所带来的新条件。新生儿学家和儿科医生必须跟上这些发展和该领域的发展方向,因为随着新生儿基因组筛查的出现,可能会取得更快的进展。
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