Evidence map›Paper›PMID 40908890›Full record

ArticleChild: care, health and development2025

Support Needs of Parents of Children With Congenital Anomalies Across Europe: A EUROlinkCAT Survey.

Elena Marcus, Anna Latos-Bielenska, Anna Jamry-Dziurla, Ingeborg Barišić, Clara Cavero-Carbonell, Elly Den Hond, Ester Garne, Lucas Genard, Ana João Santos, L Renée Lutke and 10 more

Abstract read
In one paragraph

Article in Child: care, health and development, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

20 authors.

Elena MarcusPopulation Health Research Institute, St George's, University of London, London, UK.ORCID https://orcid.org/0000-0003-0900-8976
Anna Latos-BielenskaChair and Department of Medical Genetics, Poznan University of Medical Sciences, Collegium Maius, Poznań, Poland.
Anna Jamry-DziurlaChair and Department of Medical Genetics, Poznan University of Medical Sciences, Collegium Maius, Poznań, Poland.
Ingeborg BarišićChildren's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Elly Den HondProvincial Institute for Hygiene (PIH), Antwerpen, Belgium.
Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.ORCID https://orcid.org/0000-0003-0430-2594
Lucas GenardProvincial Institute for Hygiene (PIH), Antwerpen, Belgium.
Ana João SantosEpidemiology Department, National Institute of Health Doctor Ricardo Jorge, Lisbon, Portugal.ORCID https://orcid.org/0000-0003-0556-5513
L Renée LutkeDepartment of Genetics, University Medical Center, University of Groningen, Groningen, the Netherlands.
Carlos Matias DiasEpidemiology Department, National Institute of Health Doctor Ricardo Jorge, Lisbon, Portugal.
Lucía Páramo-RodríguezRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Christina Neergaard PedersenDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Amanda J NevilleIMER Registry (Emilia Romagna Registry of Birth Defects), University of Ferrara and Azienda Ospedaliero Universitaria di Ferrara, Ferrara, Italy.
Annika NiemannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Ljubica OdakChildren's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
Anna PieriniUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Judith RankinPopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Joan K MorrisPopulation Health Research Institute, St George's, University of London, London, UK.

Funding

European Union 733001
6 · The paper itself

Abstract

backgroundParents and carers of children with congenital anomalies can experience stress when managing their child's healthcare needs. It is important that they are well supported. This study explored the support needs of parents/carers of children with a congenital anomaly across Europe.

methodsWe developed a cross-sectional online survey to measure parents' experiences of support at diagnosis and in subsequent years. We recruited parents/carers of children (0-10 years) with cleft lip, congenital heart defect requiring surgery, Down syndrome and/or spina bifida, online via relevant organisations in 10 European countries (March-July 2021).

resultsA total of 1109 parents/carers were recruited in Poland (n = 476), the United Kingdom (n = 120), Germany (n = 97), Belgium/Netherlands (n = 74), Croatia (n = 68), Italy (n = 59), other European countries (n = 92) and unspecified/non-European countries (n = 84). At diagnosis, only 27% (262/984) of parents/carers reported feeling well supported by HCPs, and 49% (468/959) reported that they would have liked professional psychological support but did not receive it. After diagnosis, satisfaction with support from HCPs differed significantly across countries, whereas satisfaction with support from participants' personal networks was more consistent.

conclusionOur findings suggest that parents require greater support from HCPs at diagnosis, particularly psychological support. Further research in a European context is needed to understand what the barriers to support might be and how it may be integrated more effectively into existing healthcare systems.

Indexed as

CaregiversCongenital AbnormalitiesParentsSocial SupportAdultChildChild, PreschoolCross-Sectional StudiesEuropeFemaleHealth Services Needs and DemandHumansInfantInfant, NewbornMaleMiddle Agedcongenital anomalypaediatricparentssupport needssurvey

Identifiers

PMID40908890
PMCPMC12411889

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.