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

Damkjær, M; Garne, E; Loane, M; Urhoj, SK; Ballardini, E; Cavero-Carbonell, C; Coi, A; García-Villodre, L; Given, J; Gissler, M; et al. Damkjær, M; Garne, E; Loane, M; Urhoj, SK; Ballardini, E; Cavero-Carbonell, C; Coi, A; García-Villodre, L; Given, J; Gissler, M; Heino, A; Jordan, S; Limb, E; Neville, AJ; Pierini, A; Rissmann, A; Tan, J; Scanlon, I; Morris, JK (2023) Timing of Cardiac Surgical Interventions and Postoperative Mortality in Children With Severe Congenital Heart Defects Across Europe: Data From the EUROlinkCAT Study. Journal of the American Heart Association, 12 (24). e029871. ISSN 2047-9980 https://doi.org/10.1161/JAHA.122.029871
SGUL Authors: Morris, Joan Katherine

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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.

Item Type: Article
Additional Information: Copyright © 2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
Keywords: 1102 Cardiorespiratory Medicine and Haematology
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Journal of the American Heart Association
ISSN: 2047-9980
Dates:
DateEvent
19 December 2023Published
18 December 2023Published Online
11 October 2023Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
733001Horizon 2020http://dx.doi.org/10.13039/501100007601
URI: https://openaccess.sgul.ac.uk/id/eprint/115797
Publisher's version: https://doi.org/10.1161/JAHA.122.029871

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