Your browser doesn't support javascript.
loading
Updated EUROCAT guidelines for classification of cases with congenital anomalies.
Bergman, Jorieke E H; Perraud, Annie; Barisic, Ingeborg; Kinsner-Ovaskainen, Agnieszka; Morris, Joan K; Tucker, David; Wellesley, Diana; Garne, Ester.
Afiliação
  • Bergman JEH; University of Groningen, University Medical Center Groningen, department of Genetics, Groningen, The Netherlands.
  • Perraud A; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Morris JK; Population Health Research Institute, St George's University of London, London, UK.
  • Tucker D; Congenital Anomaly Register and Information Service for Wales (CARIS), Public Health Wales, Swansea, UK.
  • Wellesley D; University Hospitals Southampton, Southampton, UK.
  • Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Birth Defects Res ; 116(2): e2314, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38361485
ABSTRACT

BACKGROUND:

Precise and correct classification of congenital anomalies is important in epidemiological studies, not only to classify according to etiology but also to group similar congenital anomalies together, to create homogeneous subgroups for surveillance and research. This paper presents the updated EUROCAT (European surveillance of congenital anomalies) subgroups of congenital anomalies and the updated multiple congenital anomaly (MCA) algorithm and provides the underlying arguments for the revisions.

METHODS:

The EUROCAT methodology is described. In addition, we show how we validated the revised EUROCAT subgroups and MCA algorithm, which are both based on the International Classification of Diseases (ICD10/ICD9) codes.

RESULTS:

The updated EUROCAT subgroups and the updated MCA algorithm are described in detail and the updated version is compared to the previous versions.

CONCLUSION:

The EUROCAT subgroups and MCA algorithm provide a standardized and clear methodology for congenital anomaly research and epidemiological surveillance of congenital anomalies in order to facilitate the identification of teratogenic exposures and to assess the impact of primary prevention and prenatal screening policies. The EUROCAT subgroups and MCA algorithm are made freely available for other researchers via the EUROCAT Database Management Software.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Teratogênese Tipo de estudo: Guideline Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Teratogênese Tipo de estudo: Guideline Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda