Evidence map›Paper›PMID 38108249›Full record

ArticleJournal of the American Heart Association2023

Timing of Cardiac Surgical Interventions and Postoperative Mortality in Children With Severe Congenital Heart Defects Across Europe: Data From the EUROlinkCAT Study.

Mads Damkjær, Ester Garne, Maria Loane, Stine K Urhoj, Elisa Ballardini, Clara Cavero-Carbonell, Alessio Coi, Laura García-Villodre, Joanne Given, Mika Gissler and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Thrombus formation in neonates and early infants undergoing congenital heart surgery.International journal of cardiology. Congenital heart disease · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Discovery and functional investigation ofAmerican journal of translational research · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 10 institutions in 6 countries.

Mads DamkjærDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital University Hospital of Southern Denmark Kolding Denmark.ORCID 0000-0001-7410-8573
Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital University Hospital of Southern Denmark Kolding Denmark.ORCID 0000-0003-0430-2594
Maria LoaneFaculty of Life & Health Sciences Ulster University Northern Ireland UK.ORCID 0000-0002-1206-3637
Stine K UrhojSection of Epidemiology, Department of Public Health University of Copenhagen Copenhagen Denmark.ORCID 0000-0002-2069-9723
Elisa BallardiniNeonatal Intensive Care Unit, Paediatric Section, IMER Registry, Department of Medical Sciences University of Ferrara Ferrara Italy.ORCID 0000-0002-8813-1835
Clara Cavero-CarbonellRare Diseases Research Unit Foundation for the Promotion of Health and Biomedical Research in the Valencian Region Valencia Spain.ORCID 0000-0002-4858-6456
Alessio CoiUnit of Epidemiology of Rare Diseases and Congenital Anomalies Institute of Clinical Physiology, National Research Council Pisa Italy.ORCID 0000-0002-9816-3144
Laura García-VillodreRare Diseases Research Unit Foundation for the Promotion of Health and Biomedical Research in the Valencian Region Valencia Spain.ORCID 0000-0001-9094-7107
Joanne GivenFaculty of Life & Health Sciences Ulster University Northern Ireland UK.ORCID 0000-0003-4921-1944
Mika GisslerDepartment of Knowledge Brokers THL Finnish Institute for Health and Welfare Helsinki Finland.ORCID 0000-0001-8254-7525
Anna HeinoDepartment of Knowledge Brokers THL Finnish Institute for Health and Welfare Helsinki Finland.
Sue JordanFaculty of Medicine, Health and Life Science Swansea University Swansea UK.ORCID 0000-0002-5691-2987
Elizabeth LimbPopulation Health Research Institute, St George's University of London London UK.ORCID 0000-0003-0830-7376
Amanda J NevilleRegistro IMER - IMER Registry (Emila Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research University of Ferrara Azienda Ospedaliero-Universitaria di Ferrara Ferrara Italy.
Anna PieriniUnit of Epidemiology of Rare Diseases and Congenital Anomalies Institute of Clinical Physiology, National Research Council Pisa Italy.ORCID 0000-0003-3321-9343
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt Medical Faculty Otto-von-Guericke-University Magdeburg Magdeburg Germany.ORCID 0000-0002-9437-2790
Joachim TanPopulation Health Research Institute, St George's University of London London UK.
Ieuan ScanlonFaculty of Medicine, Health and Life Science Swansea University Swansea UK.
Joan K MorrisPopulation Health Research Institute, St George's University of London London UK.ORCID 0000-0002-7164-612X
St George's, University of London · GBFinnish Institute for Health and Welfare · FIFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESIstituto di Fisiologia Clinica · ITSwansea University · GBUniversity of Ferrara · ITUniversity of Southern Denmark · DKUniversity of Ulster · GBOtto-von-Guericke-Universität Magdeburg · DEUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of this study was to evaluate the timing of the first cardiac surgery, the number of cardiac surgeries performed, and 30-day postoperative mortality rate for children with severe congenital heart defects (sCHDs) in their first 5 years of life. METHODS AND

resultsThis was a population-based data linkage cohort study linking information from 9 European congenital anomaly registries to vital statistics and hospital databases. Data were extracted for 5693 children with sCHDs born from 1995 to 2004. Subgroup analyses were performed for specific types of sCHD. Children with sCHDs underwent their first surgical intervention at a median age of 3.6 (95% CI, 2.6-4.5) weeks. The timing of the first surgery for most subtypes of sCHD was consistent across Europe. In the first 5 years of life, children with hypoplastic left heart underwent the most cardiac surgeries, with a median of 4.4 (95% CI, 3.1-5.6). The 30-day postoperative mortality rate in children aged <1 year ranged from 1.1% (95% CI, 0.5%-2.1%) for tetralogy of Fallot to 23% (95% CI, 12%-37%) for Ebstein anomaly. The 30-day postoperative mortality rate was highest for children undergoing surgery in the first month of life. Overall 5-year survival for sCHD was <90% for all sCHDs, except transposition of the great arteries, tetralogy of Fallot, and coarctation of the aorta.

conclusionsThere were no major differences among the 9 regions in the timing, 30-day postoperative mortality rate, and number of operations performed for sCHD. Despite an overall good prognosis for most congenital heart defects, some lesions were still associated with substantial postoperative death.

Indexed as

Cardiac Surgical ProceduresHeart Defects, CongenitalTetralogy of FallotTransposition of Great VesselsChildCohort StudiesEuropeHumansInfant, Newborncardiac surgerycongenital heart defectspediatric cardiology

Identifiers

PMID38108249
PMCPMC10863769
OpenAlexW4389894352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.