Current situation and new steps in newborn screening in Spain

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.

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Publication Details

Journal
Anales de Pediatría (English Edition)
Published
2025-03-01
DOI
https://doi.org/10.1016/j.anpede.2025.503775
Citations
1
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
1.32
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article

Current situation and new steps in newborn screening in Spain

Noelia González‐Pacheco, Héctor Boix, Alejandro Pérez‐Muñuzuri, María Cernada et al.
1 citations
Anales de Pediatría (English Edition)
Metabolism and Genetic Disorders
1.32
article

Current situation and new steps in newborn screening in Spain

Noelia González‐Pacheco, Héctor Boix, Alejandro Pérez‐Muñuzuri, María Cernada, María Dolores Sánchez-Redondo, María Luz Couce, María Gracia Espinosa Fernández, Ana Garrido Martín
article en
1 citations

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.

Anales de Pediatría (English Edition)Vol. 102(3)
Hospital Sant Joan de Déu Barcelona (ES), Hospital General Universitario Gregorio Marañón (ES), Hospital Universitario Dexeus (ES), Complejo Hospitalario Universitario de Santiago (ES), Hospital Regional Universitario de Málaga (ES), Hospital Virgen de la Salud (ES), USP Institut Universitari Dexeus (ES), Hospital Universitari de Vic (ES), Instituto de Investigación Sanitaria de Santiago (ES), Instituto de Investigación Sanitaria La Fe (ES)
Openalex Percentile: Top 22%
Metabolism and Genetic Disorders
1.32
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