Evidence map›Paper›PMID 37789312›Full record

ArticleBMC musculoskeletal disorders2023

Trends in congenital clubfoot prevalence and co-occurring anomalies during 1994-2021 in Denmark: a nationwide register-based study.

Paula L Hedley, Ulrik Lausten-Thomsen, Kristin M Conway, Klaus Hindsø, Paul A Romitti, Michael Christiansen

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. 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

6 authors at 3 institutions in 2 countries.

Paula L HedleyDepartment for Congenital Disorders, Statens Serum Institut, 5 Artillerivej DK2300S, Copenhagen, Denmark. phy@ssi.dk.ORCID http://orcid.org/0000-0001-5801-960X
Ulrik Lausten-ThomsenDepartment of Neonatology, University Hospital Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-1136-4347
Kristin M ConwayDepartment of Epidemiology, College of Public Health, The University of Iowa, Iowa City, IA, USA.ORCID http://orcid.org/0000-0001-8633-966X
Klaus HindsøPediatric Section, Department of Orthopedic Surgery, University Hospital Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5209-3024
Paul A RomittiDepartment for Congenital Disorders, Statens Serum Institut, 5 Artillerivej DK2300S, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5393-9984
Michael ChristiansenDepartment for Congenital Disorders, Statens Serum Institut, 5 Artillerivej DK2300S, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-4713-755X
Statens Serum Institut · DKRigshospitalet · DKUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital talipes equinovarus (clubfoot) is a common musculoskeletal anomaly, with a suspected multifactorial etiopathogenesis. Herein, we used publicly available data to ascertain liveborn infants with clubfoot delivered in Denmark during 1994-2021, and to classify co-occurring congenital anomalies, estimate annual prevalence, and compare clubfoot occurrence with maternal smoking rates, a commonly reported risk factor. Characterizing this nationwide, liveborn cohort provides a population-based resource for etiopathogenic investigations and life course surveillance.

methodsThis case-cohort study used data from the Danish National Patient Register and Danish Civil Registration System, accessed through the publicly available Danish Biobank Register, to identify 1,315,282 liveborn infants delivered during 1994-2021 in Denmark to Danish parents. Among these, 2,358 infants (65.1% male) were ascertained with clubfoot and classified as syndromic (co-occurring chromosomal, genetic, or teratogenic syndromes) and nonsyndromic (isolated or co-occurring multiple congenital anomalies [MCA]). Annual prevalence estimates and corresponding 95% confidence intervals (CIs) for children with nonsyndromic clubfoot were estimated using Poisson regression and compared with population-based, maternal annual smoking rates obtained from publicly available resources.

resultsInfants most often presented with nonsyndromic clubfoot (isolated = 88.6%; MCA = 11.4%); limb and heart anomalies were the most frequently identified MCAs. Prevalence (per 1,000 liveborn infants) was 1.52 (CI 1.45-1.58) for isolated and 0.19 (CI 0.17-0.22) for MCA clubfoot. Prevalence estimates for both isolated and MCA clubfoot remained relatively stable during the study period, despite marked decreases in population-based maternal smoking rates.

conclusionsFrom 1994 to 2021, prevalence of nonsyndromic clubfoot in Denmark was relatively stable. Reduction in population-level maternal smoking rates did not seem to impact prevalence estimates, providing some support for the suspected multifactorial etiopathogenesis of this anomaly. This nationwide, liveborn cohort, ascertained and clinically characterized using publicly available data from the Danish Biobank Register, provides a population-based clinical and biological resource for future etiopathogenic investigations and life course surveillance.

Indexed as

ClubfootChildCohort StudiesDenmarkFemaleHumansInfantMalePrevalenceRisk FactorsClubfootCongenital abnormalitiesEpidemiological monitoringFoot deformities, congenitalNeonatal biobankingTalipes equinovarus

Identifiers

PMID37789312
PMCPMC10548612
OpenAlexW4387307261

What OpenQuestion holds

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LicenceCC BY
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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.