Evidence map›Paper›PMID 39104126›Full record

ArticleActa obstetricia et gynecologica Scandinavica2024

Down syndrome and associated atrioventricular septal defects in a nationwide Norwegian cohort: Prevalence, time trends, and outcomes.

Cecilie Bryn Nordklev, Ola Gjesdal, Nina Gunnes, Henrik Holmstrøm, Nils-Halvdan Morken, Siri Vangen, Vasilis Sitras

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

7 authors.

Cecilie Bryn NordklevDepartment of Fetal Medicine, Oslo University Hospital, Oslo, Norway.ORCID 0009-0003-2832-4226
Ola GjesdalDepartment of Cardiology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0003-1913-6445
Nina GunnesNorwegian Research Center for Women's Health, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-2606-0648
Henrik HolmstrømFaculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0003-4745-5267
Nils-Halvdan MorkenDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Siri VangenFaculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0003-4681-4774
Vasilis SitrasDepartment of Fetal Medicine, Oslo University Hospital, Oslo, Norway.ORCID 0000-0003-3264-3302

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe prevalence of Down syndrome (DS) is approximately 1 per 1000 births and is influenced by increasing maternal age over the last few decades. DS is strongly associated with congenital heart defects (CHDs), especially atrioventricular septal defect (AVSD). Our objectives were to investigate the prevalence of live-born infants with DS having a severe CHD in the Norwegian population over the last 20 years and compare outcomes in infants with AVSD with and without DS. MATERIAL AND

methodsInformation on all births from January 1, 2000 to December 31, 2019 was obtained from the Medical Birth Registry of Norway. We also obtained data on all infants with severe CHDs in Norway registered in Oslo University Hospital's Clinical Registry for Congenital Heart Defects during 2000-2019 and accessed individual-level patient data from the electronic hospital records of selected cases. Infants with AVSD and DS were compared to infants with AVSD without chromosomal defects. Crude and adjusted odds ratios (ORs) of infant mortality and need for surgery during the first year of life, with associated 95% confidence intervals (CIs), were estimated by logistic regression.

resultsA total of 1 177 926 infants were live-born in Norway during the study period. Among these, 1456 (0.1%) had DS. The prevalence of infants with DS having a severe CHDs was relatively stable, with a mean of 17 cases per year. The most common CHD associated with DS was AVSD (44.4%). Infants with AVSD and DS were more likely to have cardiac intervention during their first year of life compared to infants with AVSD without chromosomal defects (adjusted OR [aOR]: 2.52; 95% CI 1.27, 4.98). However, we observed no difference in infant mortality during first year of life between the two groups (aOR: 1.08; 95% CI 0.43, 2.70).

conclusionsThe prevalence of live-born infants with severe CHDs and DS has been stable in Norway across 20 years. Infants with AVSD and DS did not have higher risk of mortality during their first year of life compared to infants with AVSD without chromosomal defects, despite a higher risk of operative intervention.

Indexed as

Down SyndromeHeart Septal DefectsRegistriesAdultCohort StudiesFemaleHumansInfantInfant MortalityInfant, NewbornMaleNorwayPrevalenceatrioventricular septal defectcardiac interventioncongenital heart defectsDown syndromeepidemiologyinfant mortalitytime trendstrisomy 21

Identifiers

PMID39104126
PMCPMC11426216

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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.