Evidence map›Paper›PMID 33072975›Full record

ReviewInternational journal of neonatal screening2019

Newborn Screening for Sickle Cell Disease in Europe.

Yvonne Daniel, Jacques Elion, Bichr Allaf, Catherine Badens, Marelle J Bouva, Ian Brincat, Elena Cela, Cathy Coppinger, Mariane de Montalembert, Béatrice Gulbis and 6 more

Abstract readReview
In one paragraph

Review in International journal of neonatal screening, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Optimizing the "right" patient selection for treatment for sickle cell disease.Hematology. American Society of Hematology. Education Program · 2025
    Article
  6. Molecular Characterization of Three Novel Large Deletions Causing αInternational journal of molecular sciences · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Sickle Cell Disease.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

16 authors.

Yvonne DanielPublic Health England, NHS Sickle Cell and Thalassemia Screening Programme, London SE16LH, UK.
Jacques ElionLaboratoire d'Excellence GR-Ex, UMR_S1134, Inserm, Université Paris Diderot, Sorbonne Paris Cité, Institut National de la Transfusion Sanguine, 75015 Paris, France.ORCID https://orcid.org/0000-0002-8407-1783
Bichr AllafNBS Laboratory for Haemoglobinopathies, Hôpital Universitaire Robert-Debré, 75019 Paris, France.
Catherine BadensDépartement de génétique médicale, Aix-Marseille Université, Hôpital de la Timone, 13385 Marseille, France.
Marelle J BouvaNational Institute for Public Health and the Environment, Centre for Health Protection, 3720 Bilthoven, The Netherlands.
Ian BrincatPediatric Medicine Laboratory, Department of Pathology, Mater Dei Hospital, Triq Tal-Qroqq, MSD2090 Msida, Malta.
Elena CelaDepartment of Pediatric Oncology/Hematology, Hospital Universitario General Gregorio Marañón, Facultad de Medicina, Universidad Complutense Madrid, 28007 Madrid, Spain.ORCID https://orcid.org/0000-0001-5264-8544
Cathy CoppingerPublic Health England, NHS Sickle Cell and Thalassemia Screening Programme, London SE16LH, UK.
Mariane de MontalembertDepartment of Pediatrics, Reference Center for Sickle Cell Disease, AP-HP Hôpital Universitaire Necker-Enfants Malades, 75743 Paris, France.
Béatrice GulbisDepartment of Clinical Chemistry, Cliniques Universitaires de Bruxelles, Hôpital Erasme-ULB, 1070 Bruxelles, Belgium.
Joan HenthornPublic Health England, NHS Sickle Cell and Thalassemia Screening Programme, London SE16LH, UK.
Olivier KetelslegersLaboratoire-Biologie Clinique, Centre Hospitalier Régional de la Citadelle, 4000 Liège, Belgium.
Corrina McMahonOur Lady's Children's Hospital, Crumlin, D12V004 Dublin, Ireland.
Allison StreetlySchool of Population Health and Environmental Sciences, Faculty of Life Sciences & Medicine, King's College London, London WC2R2LS, UK.
Raffaella ColombattiDepartment of Child and Maternal Health, Clinic of Pediatric Hematology/Oncology, Azienda Ospedaliera-Università di Padova, 35129 Padova, Italy.
Stephan LobitzDepartment of Pediatric Oncology/Hematology, Kinderkrankenhaus Amsterdamer Straße, 50735 Cologne, Germany.ORCID https://orcid.org/0000-0001-5398-0610

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The history of newborn screening (NBS) for sickle cell disease (SCD) in Europe goes back almost 40 years. However, most European countries have not established it to date. The European screening map is surprisingly heterogenous. The first countries to introduce sickle cell screening on a national scale were France and England. The French West Indies started to screen their newborns for SCD as early as 1983/84. To this day, all countries of the United Kingdom of Great Britain and Northern Ireland have added SCD as a target disease to their NBS programs. The Netherlands, Spain and Malta also have national programs. Belgium screens regionally in the Brussels and Liège regions, Ireland has been running a pilot for many years that has become quasi-official. However, the Belgian and Irish programs are not publicly funded. Italy and Germany have completed several pilot studies but are still in the preparatory phase of national NBS programs for SCD, although both countries have well-established concepts for metabolic and endocrine disorders. This article will give a brief overview of the situation in Europe and put a focus on the programs of the two pioneers of the continent, England and France.

Indexed as

newbornscreeningsickle cell disease

Identifiers

PMID33072975
PMCPMC7510219

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.