Timing of Cardiac Surgical Interventions and Postoperative Mortality in Children With Severe Congenital Heart Defects Across Europe: Data From the EUROlinkCAT Study

Author:

Damkjær Mads12ORCID,Garne Ester12ORCID,Loane Maria3ORCID,Urhoj Stine K.4ORCID,Ballardini Elisa5ORCID,Cavero‐Carbonell Clara6ORCID,Coi Alessio7ORCID,García‐Villodre Laura6ORCID,Given Joanne3ORCID,Gissler Mika8ORCID,Heino Anna8,Jordan Sue9ORCID,Limb Elizabeth10ORCID,Neville Amanda J11,Pierini Anna7ORCID,Rissmann Anke12ORCID,Tan Joachim10,Scanlon Ieuan9,Morris Joan K10ORCID

Affiliation:

1. Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital University Hospital of Southern Denmark Kolding Denmark

2. Department of Regional Health Research University of Southern Denmark Odense Denmark

3. Faculty of Life & Health Sciences Ulster University Northern Ireland UK

4. Section of Epidemiology, Department of Public Health University of Copenhagen Copenhagen Denmark

5. Neonatal Intensive Care Unit, Paediatric Section, IMER Registry, Department of Medical Sciences University of Ferrara Ferrara Italy

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

7. Unit of Epidemiology of Rare Diseases and Congenital Anomalies Institute of Clinical Physiology, National Research Council Pisa Italy

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

9. Faculty of Medicine, Health and Life Science Swansea University Swansea UK

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

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

12. Malformation Monitoring Centre Saxony‐Anhalt Medical Faculty Otto‐von‐Guericke‐University Magdeburg Magdeburg Germany

Abstract

Background The purpose of this study was to evaluate the timing of the first cardiac surgery, the number of cardiac surgeries performed, and 30‐day postoperative mortality rate for children with severe congenital heart defects (sCHDs) in their first 5 years of life. Methods and Results This was a population‐based data linkage cohort study linking information from 9 European congenital anomaly registries to vital statistics and hospital databases. Data were extracted for 5693 children with sCHDs born from 1995 to 2004. Subgroup analyses were performed for specific types of sCHD. Children with sCHDs underwent their first surgical intervention at a median age of 3.6 (95% CI, 2.6–4.5) weeks. The timing of the first surgery for most subtypes of sCHD was consistent across Europe. In the first 5 years of life, children with hypoplastic left heart underwent the most cardiac surgeries, with a median of 4.4 (95% CI, 3.1–5.6). The 30‐day postoperative mortality rate in children aged <1 year ranged from 1.1% (95% CI, 0.5%–2.1%) for tetralogy of Fallot to 23% (95% CI, 12%–37%) for Ebstein anomaly. The 30‐day postoperative mortality rate was highest for children undergoing surgery in the first month of life. Overall 5‐year survival for sCHD was <90% for all sCHDs, except transposition of the great arteries, tetralogy of Fallot, and coarctation of the aorta. Conclusions There were no major differences among the 9 regions in the timing, 30‐day postoperative mortality rate, and number of operations performed for sCHD. Despite an overall good prognosis for most congenital heart defects, some lesions were still associated with substantial postoperative death.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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