Evidence map›Paper›PMID 42647254›Full record

ArticleInternational journal of neonatal screening2026

The Spanish Uniform Newborn Screening Panel (SUSP): A National Consensus Framework for Harmonized Newborn Screening.

Judit García-Villoria, Rosa María López-Galera, Carmen Delgado-Pecellín, Dolores Rausell Félix, Cristóbal Colón, Hugo Rocha, Belén Pérez, Antonia Ribes, María Luz Couce, Domingo González-Lamuño and 1 more

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Judit García-VilloriaDivision of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics, Biomedical Diagnostic Center, Hospital Clinic of Barcelona, 08028 Barcelona, Spain.
Rosa María López-GaleraDivision of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics, Biomedical Diagnostic Center, Hospital Clinic of Barcelona, 08028 Barcelona, Spain.
Carmen Delgado-PecellínDivision of Metabolic Disorders Unit, Department of Biochemistry, Hospital Universitario Virgen del Rocio, IBIS, 41013 Sevilla, Spain.
Dolores Rausell FélixLaboratory of Metabolic Disorders, Department of Clinical Analysis, Hospital Universitari i Politècnic La Fe, 46026 Valencia, Spain.ORCID 0000-0001-5784-7526
Cristóbal ColónLaboratory of Metabolic Disorders, Unit for the Diagnosis and Treatment of Congenital Metabolic Diseases, Spanish (CSUR) and European (MetabERN) Reference Center, Clinical University Hospital of Santiago de Compostela, 15706 Santiago de Compostela, Spain.ORCID 0000-0002-9711-2812
Hugo RochaNewborn Screening, Metabolism and Genetics Unit, Human Genetics Department of the National Institute of Heath Doutor Ricardo Jorge, 4000-055 Porto, Portugal.ORCID 0000-0001-5447-615X
Belén PérezCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, 28029 Madrid, Spain.ORCID 0000-0002-3190-1958
Antonia RibesDivision of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics, Biomedical Diagnostic Center, Hospital Clinic of Barcelona, 08028 Barcelona, Spain.ORCID 0000-0002-2249-246X
María Luz CouceCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, 28029 Madrid, Spain.ORCID 0000-0003-4861-9905
Domingo González-LamuñoDivision of Pediatrics, University Hospital Marqués de Valdecilla, University of Cantabria and Research Insitiute Valdecilla (IDIVAL), 39008 Santander, Spain.ORCID 0000-0002-7578-241X
Neonatal Screening Working Group of AECOM

Funding

AECOM
6 · The paper itself

Abstract

Newborn screening (NBS) is a cornerstone of preventive medicine, enabling early diagnosis and treatment of severe congenital disorders. In Spain, despite the existence of a Basic Common Portfolio, the absence of a harmonized national panel has led to significant inter-regional variability, affecting equity in access to early diagnosis. The Spanish Uniform Screening Panel (SUSP) was developed through a structured nationwide consensus process involving all NBS centers in Spain, with additional input from Portugal. The process included a comprehensive survey of current practices, expert workshops, multiple consensus rounds, and predefined inclusion criteria. Disease nomenclature was standardized using OMIM and ORPHAcode identifiers. Conditions were classified as primary screening targets or secondary findings, and consensus was reached on confirmatory biochemical and genetic testing pathways. The operational dataset comprised 48 biomarker-based screening entries. Because some conditions can be detected through multiple primary markers, duplicate analytical routes were retained but counted once, resulting in a total 189 unique clinical conditions, including 87 primary and 102 secondary conditions. The SUSP represents the first nationwide harmonized framework for newborn screening in Spain and constitutes a major step toward equitable and standardized implementation. It provides a scalable model that may inform other countries facing similar disparities.

Indexed as

genomic newborn screeninghealth equityinborn errors of metabolismnational consensusnewborn screeningprimary and secondary conditionspublic health policySpain

Identifiers

PMID42647254
PMCPMC13510814

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.