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Prescription of cardiovascular medication in children with congenital heart defects across six European Regions from 2000 to 2014: data from the EUROlinkCAT population-based cohort study.
Damkjaer, Mads; Urhoj, Stine Kjaer; Tan, Joachim; Briggs, Gillian; Loane, Maria; Given, Joanne Emma; Barrachina-Bonet, Laia; Cavero-Carbonell, Clara; Coi, Alessio; Neville, Amanda J; Heino, Anna; Kiuru-Kuhlefelt, Sonja; Jordan, Susan; Scanlon, Ieuan; Pierini, Anna; Puccini, Aurora; Garne, Ester; Morris, Joan K.
Afiliação
  • Damkjaer M; Department of Paediatrics, Sygehus Lillebalt Kolding Sygehus, Kolding, Denmark mads.damkjaer2@rsyd.dk.
  • Urhoj SK; Department of Regional Health Research, University of Southern Denmark, Kolding, Denmark.
  • Tan J; Department of Paediatrics, Sygehus Lillebalt Kolding Sygehus, Kolding, Denmark.
  • Briggs G; Section of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark.
  • Loane M; Population Health Research Institute, St George's University of London, London, UK.
  • Given JE; Population Health Research Institute, St George's University of London, London, UK.
  • Barrachina-Bonet L; Institute of Nursing and Health Research, University of Ulster, Coleraine, UK.
  • Cavero-Carbonell C; Ulster University Faculty of Life and Health Sciences, Coleraine, UK.
  • Coi A; Rare Diseases Research Unit, Foundation for the Promotion of the Research in Healthcare and Biomedicine, Valencia, Spain.
  • Neville AJ; Rare Diseases Research Unit, Foundation for the Promotion of the Research in Healthcare and Biomedicine, Valencia, Spain.
  • Heino A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Kiuru-Kuhlefelt S; Registro IMER, University of Ferrara, Ferrara, Emilia-Romagna, Italy.
  • Jordan S; Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Scanlon I; Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Pierini A; Faculty of Medicine, Health & Life Sciences, Swansea University, Swansea, Wales.
  • Puccini A; Faculty of Medicine, Health & Life Sciences, Swansea University, Swansea, Wales.
  • Garne E; Institute of Clinical Physiology National Research Council, Pisa, Italy.
  • Morris JK; Drug and Medical Device Area, Emilia Romagna Health Department, Emilia-Romagna Regional Healthcare Services, Bologna, Emilia-Romagna, Italy.
BMJ Open ; 12(4): e057400, 2022 04 21.
Article em En | MEDLINE | ID: mdl-35450908
ABSTRACT

OBJECTIVES:

Advances in surgical management strategies have substantially reduced fatality from congenital heart defects (CHD). Decreased infant mortality might be expected, consequentially to result in greater morbidity in older children due to complications later in childhood and adolescence. This study aims to evaluate the use of cardiovascular medication (CVM) as an indicator of disease burden in children born with CHD in the first 10 years of life.

DESIGN:

Population-based cohort study.

SETTING:

Six population-based registries from the European Surveillance of Congenital Anomalies (EUROCAT) network participated. Data from live born children with major congenital anomalies (CA) born from 2000 to 2014 were linked to prescription databases. Four groups of children were analysed CA, CHD, severe CHD (sCHD) and ventricular septal defect (VSD) without sCHD. Live born children without CA were included as reference group.

PARTICIPANTS:

We obtained data on 61 038 children born with a CA, including 19 678 with CHD, 3392 with sCHD, 12 728 children with VSD without sCHD, and 1 725 496 reference children.

RESULTS:

Children born with sCHD were the most likely to receive a CVM prescription (42.9%, 95% CI, 26.3 to 58.5) in the first year of life compared with 13.3% (6.7 to 22.0) of children with any CHD, 5.9% (3.7 to 8.7) of children with any CA and 0.1% (0.0 to 0.1) of reference children. Medication was less likely to be prescribed after the first year of life for sCHD; 18.8% (14.8 to 23.1) for children 1-4 years and 15.8% (12.0 to 20.1) 5-9 years. Children with sCHD were most likely to receive a diuretic (36.4%, 18.6 to 54.5), an antihypertensive (6.9%, 3.7 to 11.3) or a beta-blocker (5.5%, 2.9 to9.2).

CONCLUSION:

Almost half of all children with sCHD were prescribed CVM in their first year of life. For all four groups of children with anomalies, the proportion of children with a CVM prescription decreased with age.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fármacos Cardiovasculares / Cardiopatias Congênitas / Comunicação Interventricular Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Infant / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fármacos Cardiovasculares / Cardiopatias Congênitas / Comunicação Interventricular Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Infant / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article