Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jun 28;11(6):e047859.
doi: 10.1136/bmjopen-2020-047859.

EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies

Collaborators, Affiliations

EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies

Joan K Morris et al. BMJ Open. .

Abstract

Introduction: Congenital anomalies (CAs) are a major cause of infant mortality, childhood morbidity and long-term disability. Over 130 000 children born in Europe every year will have a CA. This paper describes the EUROlinkCAT study, which is investigating the health and educational outcomes of children with CAs for the first 10 years of their lives.

Methods and analysis: EUROCAT is a European network of population-based registries for the epidemiological surveillance of CAs. EUROlinkCAT is using the EUROCAT infrastructure to support 22 EUROCAT registries in 14 countries to link their data on births with CAs to mortality, hospital discharge, prescription and educational databases. Once linked, each registry transforms their case data into a common data model (CDM) format and they are then supplied with common STATA syntax scripts to analyse their data. The resulting aggregate tables and analysis results are submitted to a central results repository (CRR) and meta-analyses are performed to summarise the results across all registries. The CRR currently contains data on 155 594 children with a CA followed up to age 10 from a population of 6 million births from 1995 to 2014.

Ethics: The CA registries have the required ethics permissions for routine surveillance and transmission of anonymised data to the EUROCAT central database. Each registry is responsible for applying for and obtaining additional ethics and other permissions required for their participation in EUROlinkCAT.

Dissemination: The CDM and associated documentation, including linkage and standardisation procedures, will be available post-EUROlinkCAT thus facilitating future local, national and European-level analyses to improve healthcare. Recommendations to improve the accuracy of routinely collected data will be made.Findings will provide evidence to inform parents, health professionals, public health authorities and national treatment guidelines to optimise diagnosis, prevention and treatment for these children with a view to reducing health inequalities in Europe.

Keywords: epidemiology; paediatrics; statistics & research methods.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Structure of mortality and EUROCAT data used for analysing children’s survival.
Figure 2
Figure 2
Structure of hospital admissions, prescription data and EUROCAT data used for analysing children’s morbidity. ATC code, Anatomical Therapeutic Chemical Classification System code; ICU, intensive care unit.

References

    1. Boyle B, Addor M-C, Arriola L, et al. . Estimating global burden of disease due to congenital anomaly: an analysis of European data. Arch Dis Child Fetal Neonatal Ed 2018;103:F22–8. 10.1136/archdischild-2016-311845 - DOI - PMC - PubMed
    1. Zylbersztejn A, Gilbert R, Hjern A, et al. . Child mortality in England compared with Sweden: a birth cohort study. Lancet 2018;391:2008–18. 10.1016/S0140-6736(18)30670-6 - DOI - PMC - PubMed
    1. Wang H, Liddell CA, Coates MM, et al. . Global, regional, and national levels of neonatal, infant, and under-5 mortality during 1990-2013: a systematic analysis for the global burden of disease study 2013. Lancet 2014;384:957–79. 10.1016/S0140-6736(14)60497-9 - DOI - PMC - PubMed
    1. Copeland GE, Kirby RS. Using birth defects registry data to evaluate infant and childhood mortality associated with birth defects: an alternative to traditional mortality assessment using underlying cause of death statistics. Birth Defects Res A Clin Mol Teratol 2007;79:792–7. 10.1002/bdra.20391 - DOI - PubMed
    1. Wu J, Morris JK. The population prevalence of Down's syndrome in England and Wales in 2011. Eur J Hum Genet 2013;21:1016–9. 10.1038/ejhg.2012.294 - DOI - PMC - PubMed

Publication types