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Trends in mortality risk of patients with congenital heart disease during the COVID-19 pandemic.
Yang, Yanxu; Kuo, Kristina; Claxton, J'Neka S; Knight, Jessica H; Huang, Yijian; Oster, Matthew E; Kochilas, Lazaros K.
Afiliación
  • Yang Y; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Kuo K; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Claxton JS; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
  • Knight JH; Department of Epidemiology and Biostatistics, University of Georgia College of Public Health, Athens, GA.
  • Huang Y; Department of Biostatistics and Bioinformatics, Rollins School of Public Health of Emory University, Atlanta, GA.
  • Oster ME; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA; Children's Healthcare of Atlanta Cardiology, Atlanta, GA.
  • Kochilas LK; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA; Children's Healthcare of Atlanta Cardiology, Atlanta, GA. Electronic address: Lazaros.Kochilas@emory.edu.
Am Heart J ; 268: 9-17, 2024 Feb.
Article en En | MEDLINE | ID: mdl-37967642
BACKGROUND: Cardiovascular conditions are considered risk factors for poor outcomes associated with COVID-19. However, the effect of the COVID-19 pandemic on the mortality of patients with congenital heart disease (CHD) is unclear. Our study aims to examine the trends in mortality risk of CHD patients during the COVID-19 pandemic. METHODS: This is a retrospective cohort study from the Pediatric Cardiac Care Consortium, a US-based registry of interventions for CHD. We included patients having US residence and direct identifiers; death events were captured by matching with the National Death Index. The observation window (2017-2022) was divided into pre-COVID-19 and COVID-19 era defined around the national onset of COVID-19 disease in 2020. Stratified Cox model was used to assess all-cause mortality between the pre- and the COVID-19 era. RESULTS: Among 45,130 patients with CHD (median age in 2017: 23.3 years, IQR: 19.0-28.4), 503 deaths occurred during the pandemic with 44 deaths (8.7%) attributed to COVID-19 (COVID-19 mortality rate of 0.09%). The overall risk of death for patients with all types of CHD during the pandemic was significantly higher compared to the pre-COVID-19 era (aHR 1.28, 95%CI: 1.08-1.53), with a differential trend towards increased risk in patients with two-ventricle (aHR 1.44, 95% CI: 1.19-1.76) vs unchanged risk for those with single ventricle CHD (aHR = 0.83, 95% CI: 0.57-1.21). Adjusted subgroup analysis revealed a higher risk of death during the pandemic for CHD patients with male and chromosomal abnormalities. The excess deaths during the pandemic were attributed to COVID-19 itself rather than CHD or cardiovascular conditions. CONCLUSION: In this large CHD cohort study, there was a higher risk of death among CHD patients with male and chromosomal abnormalities. A differential trend towards higher risk for those with two vs. unchanged risk for single ventricle CHD was presented. The excess mortality was attributed to the COVID-19 itself and not to conditions potentially related to deferral of care. These results justify targeted protective measures towards the CHD population and may provide guidance for public health and medical care response in future epidemics.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / COVID-19 / Cardiopatías Congénitas Límite: Adult / Child / Humans / Male Idioma: En Revista: Am Heart J Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / COVID-19 / Cardiopatías Congénitas Límite: Adult / Child / Humans / Male Idioma: En Revista: Am Heart J Año: 2024 Tipo del documento: Article