Prevalence of congenital heart defects in Europe, 2008-2015: A registry-based study.


Journal

Birth defects research
ISSN: 2472-1727
Titre abrégé: Birth Defects Res
Pays: United States
ID NLM: 101701004

Informations de publication

Date de publication:
01 12 2022
Historique:
revised: 28 09 2022
received: 04 07 2022
accepted: 14 10 2022
pubmed: 9 11 2022
medline: 3 12 2022
entrez: 8 11 2022
Statut: ppublish

Résumé

The total prevalence of congenital heart defects (CHDs) varies by populations and over time. Studies that examine trends in the prevalence of CHD in different regions may shed light on our understanding of the occurrence of CHD and the impact of different risk factors. To examine trends in total and live birth prevalence of nonsyndromic CHD in Europe between the years 2008 and 2015 and to investigate if the decreasing trend reported by previous studies is continuing. Cases of CHD delivered between January 1, 2008 and December 31, 2015 notified to 25 population-based EUROCAT (European Surveillance of Congenital Anomalies) registries in 14 countries, formed the population-based case-series. Prevalence (total/live) rates and 95% confidence intervals were calculated as the number of cases per 10,000 births (live and stillbirths). Time trends in prevalence of all nonsyndromic CHDs and for three CHD severity groups (very severe, severe, and less severe) were plotted using a Poisson regression multilevel approach. The total prevalence of nonsyndromic CHD was 57.1 per 10,000 births (live births and stillbirths) for the 8-year period and remained stable across the three CHD severity groups while the live birth prevalence was 60.2 per 10,000 births. There was considerable variation in the reported total CHD prevalence and the direction of trends by registry. A decreasing prevalence of CHD was observed for the Norway and England/Wales registries, whereas the CHD prevalence increased for registries in Italy and Croatia. The total prevalence of CHD in Europe between the years 2008 and 2015 remained stable for all CHD and across the three CHD severity groups. The decreasing trend reported by previous studies has not continued. However, we found significant differences in the total and live birth prevalence by registry.

Sections du résumé

BACKGROUND
The total prevalence of congenital heart defects (CHDs) varies by populations and over time. Studies that examine trends in the prevalence of CHD in different regions may shed light on our understanding of the occurrence of CHD and the impact of different risk factors.
OBJECTIVES
To examine trends in total and live birth prevalence of nonsyndromic CHD in Europe between the years 2008 and 2015 and to investigate if the decreasing trend reported by previous studies is continuing.
METHODS
Cases of CHD delivered between January 1, 2008 and December 31, 2015 notified to 25 population-based EUROCAT (European Surveillance of Congenital Anomalies) registries in 14 countries, formed the population-based case-series. Prevalence (total/live) rates and 95% confidence intervals were calculated as the number of cases per 10,000 births (live and stillbirths). Time trends in prevalence of all nonsyndromic CHDs and for three CHD severity groups (very severe, severe, and less severe) were plotted using a Poisson regression multilevel approach.
RESULTS
The total prevalence of nonsyndromic CHD was 57.1 per 10,000 births (live births and stillbirths) for the 8-year period and remained stable across the three CHD severity groups while the live birth prevalence was 60.2 per 10,000 births. There was considerable variation in the reported total CHD prevalence and the direction of trends by registry. A decreasing prevalence of CHD was observed for the Norway and England/Wales registries, whereas the CHD prevalence increased for registries in Italy and Croatia.
CONCLUSIONS
The total prevalence of CHD in Europe between the years 2008 and 2015 remained stable for all CHD and across the three CHD severity groups. The decreasing trend reported by previous studies has not continued. However, we found significant differences in the total and live birth prevalence by registry.

Identifiants

pubmed: 36345679
doi: 10.1002/bdr2.2117
pmc: PMC10098845
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1404-1416

Subventions

Organisme : Medical Research Council
ID : MR/K02325X/1
Pays : United Kingdom

Informations de copyright

© 2022 The Authors. Birth Defects Research published by Wiley Periodicals LLC.

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Auteurs

Chrysovalanto Mamasoula (C)

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

Marie-Claude Addor (MC)

Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.

Clara Cavero Carbonell (CC)

Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.

Carlos M Dias (CM)

Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.

Luis-Javier Echevarría-González-de-Garibay (LJ)

Directorate for Healthcare Planning, Organisation and Evaluation; Registries and Health Information Unit, Ministry of Health of the Basque Government, Vitoria-Gasteiz, Spain.

Miriam Gatt (M)

Malta Congenital Anomalies Register, Directorate for Health Information and Research, Pietà, Malta.

Babak Khoshnood (B)

INSERM U1153, CRESS, Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), Université de Paris, Paris, France.

Kari Klungsoyr (K)

Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Division for Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.

Kay Randall (K)

National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.

Sylvia Stoianova (S)

South West Congenital Anomaly Register (SWCAR), Bristol Medical School, University of Bristol, Bristol, UK.

Martin Haeusler (M)

Styrian Malformation Registry, Medical University of Graz, Graz, Austria.

Vera Nelen (V)

Provinciaal Instituut voor Hygiene (PIH), Antwerp, Belgium.

Amanda J Neville (AJ)

Registro IMER - IMER Registry (Emilia Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy.

Isabelle Perthus (I)

Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.

Anna Pierini (A)

Tuscany Registry of Congenital Defects (RTDC), Institute of Clinical Physiology - National Research Council/Fondazione Toscana Gabriele Monasterio, Pisa, Italy.

Bénédicte Bertaut-Nativel (B)

Register of Congenital Malformations of Reunion Island, CHU Réunion, St Pierre, France.

Anke Rissmann (A)

Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany.

Florence Rouget (F)

Brittany Registry of Congenital Anomalies, CHU Rennes, University Rennes, Inserm, EHESP, Irset (Institut de Recherche en Santé, Environnement Ettravail), Rennes, France.

Bruno Schaub (B)

French West Indies Registry, Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, France.

David Tucker (D)

CARIS, Public Health Wales, Singleton Hospital, Swansea, UK.

Diana Wellesley (D)

Wessex Clinical Genetics Department, Princess Anne Hospital, Southampton, UK.

Natalya Zymak-Zakutnia (N)

OMNI-Net Ukraine Birth Defects Program, Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.

Ingeborg Barisic (I)

Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.

Hermien E K de Walle (HEK)

Department of Genetics, EUROCAT Northern Netherlands, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Monica Lanzoni (M)

European Commission, Joint Research Centre (JRC), Ispra, Italy.

Carmel Mullaney (C)

Department of Public Health, Health Service Executive (HSE) South East Area, Dublin, Ireland.

Lindsay Pennington (L)

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

Judith Rankin (J)

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

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