Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based study.


Journal

European journal of public health
ISSN: 1464-360X
Titre abrégé: Eur J Public Health
Pays: England
ID NLM: 9204966

Informations de publication

Date de publication:
09 Dec 2023
Historique:
pubmed: 18 8 2023
medline: 18 8 2023
entrez: 18 8 2023
Statut: ppublish

Résumé

Children with major congenital anomalies may be at risk of poor educational outcomes. We aimed to evaluate the educational achievement of children born with major congenital anomalies compared with children without major congenital anomalies in relation to sociodemographic factors. We performed a registry-based study including 401 544 children in Finland, graduates of the compulsory school who applied to secondary education. We used health data from the Finnish Register of Congenital Malformations for children born from 1995 to 2002 linked with education data from the Finnish Ministry of Education and Culture. We used generalized linear regression to compare the mean grade differences of children with specific major congenital anomalies and 'All anomalies' subgroup (major congenital anomalies, chromosomal syndromes, and multiple anomalies) with reference children. Children with major congenital anomalies were less likely to apply for further education than reference children (88.0% vs. 96.8%; odds ratio = 4.13; 95% confidence interval, 3.92-4.36). For most non-chromosomal congenital anomalies, children born with congenital anomalies had similar educational achievement to the reference children. For the 'All anomalies' subgroup, children with congenital anomalies had lower educational achievement than reference children. Among children with congenital anomalies, male sex, lower maternal educational levels and younger maternal age were associated with lower educational achievement. For children applying to further education, most non-chromosomal congenital anomalies were not associated with lower educational achievement. Nevertheless, efforts are needed to improve educational achievement in children with major congenital anomalies associated with maternal sociodemographic background.

Sections du résumé

BACKGROUND BACKGROUND
Children with major congenital anomalies may be at risk of poor educational outcomes. We aimed to evaluate the educational achievement of children born with major congenital anomalies compared with children without major congenital anomalies in relation to sociodemographic factors.
METHODS METHODS
We performed a registry-based study including 401 544 children in Finland, graduates of the compulsory school who applied to secondary education. We used health data from the Finnish Register of Congenital Malformations for children born from 1995 to 2002 linked with education data from the Finnish Ministry of Education and Culture. We used generalized linear regression to compare the mean grade differences of children with specific major congenital anomalies and 'All anomalies' subgroup (major congenital anomalies, chromosomal syndromes, and multiple anomalies) with reference children.
RESULTS RESULTS
Children with major congenital anomalies were less likely to apply for further education than reference children (88.0% vs. 96.8%; odds ratio = 4.13; 95% confidence interval, 3.92-4.36). For most non-chromosomal congenital anomalies, children born with congenital anomalies had similar educational achievement to the reference children. For the 'All anomalies' subgroup, children with congenital anomalies had lower educational achievement than reference children. Among children with congenital anomalies, male sex, lower maternal educational levels and younger maternal age were associated with lower educational achievement.
CONCLUSIONS CONCLUSIONS
For children applying to further education, most non-chromosomal congenital anomalies were not associated with lower educational achievement. Nevertheless, efforts are needed to improve educational achievement in children with major congenital anomalies associated with maternal sociodemographic background.

Identifiants

pubmed: 37594898
pii: 7245878
doi: 10.1093/eurpub/ckad149
pmc: PMC10710322
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1027-1034

Subventions

Organisme : European Union's Horizon 2020 research and innovation programme
ID : 733001
Organisme : Helsinki University Library
Organisme : European Cohort of Children
Organisme : European Union's Horizon 2020
ID : 733001

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the European Public Health Association.

Références

Eur J Public Health. 2017 Oct 1;27(5):850-855
pubmed: 28957474
PLoS Med. 2020 Sep 28;17(9):e1003356
pubmed: 32986711
Nat Hum Behav. 2018 Feb;2(2):117-125
pubmed: 30406209
Arch Pediatr Adolesc Med. 2002 Nov;156(11):1143-8
pubmed: 12413345
BMJ Open. 2021 Jun 28;11(6):e047859
pubmed: 34183346
J Pediatr. 2008 Jul;153(1):55-60
pubmed: 18571536
Dev Med Child Neurol. 2018 Dec;60(12):1209-1224
pubmed: 30028505
Cleft Palate Craniofac J. 2017 Jul;54(4):371-380
pubmed: 27043652
Birth Defects Res. 2017 Jul 17;109(13):1048-1056
pubmed: 28569399
J Pediatr Psychol. 1991 Aug;16(4):423-8
pubmed: 1941424
Pediatrics. 2022 Mar 1;149(3):
pubmed: 35146505
Birth Defects Res. 2021 Dec 1;113(20):1431-1462
pubmed: 34672115
Cardiol Young. 2006 Feb;16 Suppl 1:92-104
pubmed: 16401370
Paediatr Perinat Epidemiol. 2022 Nov;36(6):792-803
pubmed: 35675091
Hum Reprod Update. 2011 Sep-Oct;17(5):589-604
pubmed: 21747128
Cardiol Young. 2015 Apr;25(4):655-62
pubmed: 24784451
Front Pediatr. 2021 Nov 29;9:654883
pubmed: 34912754
Clin Pediatr (Phila). 2003 Jun;42(5):401-9
pubmed: 12862342
Lancet. 2011 Oct 8;378(9799):1325-38
pubmed: 21944375
BMJ. 2023 Jan 18;380:e072779
pubmed: 36653028
J Thorac Cardiovasc Surg. 2014 Nov;148(5):1790-1
pubmed: 25444179
J Pediatr. 2016 Nov;178:47-54.e1
pubmed: 27453376
Rev Saude Publica. 2005 Aug;39(4):606-11
pubmed: 16113911
Circ Cardiovasc Qual Outcomes. 2017 Feb;10(2):
pubmed: 28228450
Circulation. 2012 Aug 28;126(9):1143-72
pubmed: 22851541
AANA J. 2019 Jun;87(3):231-242
pubmed: 31584401
Arch Dis Child. 2021 Feb;106(2):154-159
pubmed: 32816695
J Rehabil Med. 2021 Sep 9;53(9):jrm00225
pubmed: 34448489
Pediatrics. 2020 Jul;146(1):
pubmed: 32503936
Dev Sci. 2006 Jul;9(4):368-78
pubmed: 16764610
Science. 2015 Dec 4;350(6265):1262-6
pubmed: 26785492
Dev Disabil Res Rev. 2010;16(1):31-9
pubmed: 20419769

Auteurs

Zahra Roustaei (Z)

Department of Health Sciences, University of Helsinki, Helsinki, Finland.

Anna Heino (A)

Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.

Sonja Kiuru-Kuhlefelt (S)

Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.

Joan K Morris (JK)

Population Health Research Institute, St George's, University of London, London, UK.

Svetlana V Glinianaia (SV)

Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.

Ester Garne (E)

Paediatric Department, Hospital Lillebælt, Kolding, Denmark.

Maria Loane (M)

Faculty of Life and Health Sciences, Ulster University, Belfast, UK.

Judith Rankin (J)

Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.

Mika Gissler (M)

Department of Knowledge Brokers, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
Academic Primary Health Care Centre, Region Stockholm, Stockholm, Sweden.
Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.

Classifications MeSH