Survival in Children With Congenital Heart Disease: Have We Reached a Peak at 97%?

• Published in: Journal of the American Heart Association Vol. 9; no. 22; p. e017704
• Main Authors: Mandalenakis, Zacharias, Giang, Kok Wai, Eriksson, Peter, Liden, Hans, Synnergren, Mats, Wåhlander, Håkan, Fedchenko, Maria, Rosengren, Annika, Dellborg, Mikael
• Format: Journal Article
• Language: English
• Published: England John Wiley and Sons Inc 17.11.2020; Wiley
• Subjects: Adolescent; Cardiac and Cardiovascular Systems; Case-Control Studies; Child; Child Mortality; Child, Preschool; congenital heart disease; Female; Heart Defects, Congenital - diagnosis; Heart Defects, Congenital - mortality; Heart Defects, Congenital - therapy; Humans; Infant; Kaplan-Meier Estimate; Kardiologi; Male; nationwide; Original Research; pediatric; Proportional Hazards Models; Registries; registry study; Survival Rate; survivorship; Sweden; Sweden; congenital heart disease; survivorship; nationwide; registry study; pediatric
• ISSN: 2047-9980; 2047-9980
• DOI: 10.1161/JAHA.120.017704

Background Despite advances in pediatric health care over recent decades, it is not clear whether survival in children with congenital heart disease (CHD) is still increasing. Methods and Results We identified all patients with CHD using nationwide Swedish health registries for 1980 to 2017. We examined the survival trends in children with CHD; we investigated the mortality risk in patients with CHD compared with matched controls without CHD from the general population using Cox proportional regression models and Kaplan-Meier survival analysis. Among 64 396 patients with CHD and 639 012 matched controls without CHD, 3845 (6.0%) and 2235 (0.3%) died, respectively. The mean study follow-up (SD) was 11.4 (6.3) years in patients with CHD. The mortality risk was 17.7 (95% CI, 16.8-18.6) times higher in children with CHD compared with controls. The highest mortality risk was found during the first 4 years of life in patients with CHD (hazard ratio [HR], 19.6; 95% CI, 18.5-20.7). When stratified by lesion group, patients with non-conotruncal defects had the highest risk (HR, 97.2; 95% CI, 80.4-117.4). Survival increased substantially according to birth decades, but with no improvement after the turn of the century where survivorship reached 97% in children with CHD born in 2010 to 2017. Conclusions Survival in children with CHD has increased substantially since the 1980s; however, no significant improvement has been observed this century. Currently, >97% of children with CHD can be expected to reach adulthood highlighting the need of life-time management.