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Cardiovascular disease risk factors in congenital heart disease survivors are associated with heart failure.
Landstrom, Andrew P; Spears, Tracy; D'Ottavio, Alfred; Chiswell, Karen; Sommerhalter, Kristin; Soim, Aida; Farr, Sherry L; Crume, Tessa; Book, Wendy M; Whitehead, Kevin; Botto, Lorenzo D; Li, Jennifer S; Hsu, Daphne T.
Afiliación
  • Landstrom AP; Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA. andrew.landstrom@duke.edu.
  • Spears T; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
  • D'Ottavio A; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
  • Chiswell K; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
  • Sommerhalter K; Bureau of Environmental and Occupational Epidemiology, New York State Department of Health, Albany, NY, USA.
  • Soim A; Bureau of Environmental and Occupational Epidemiology, New York State Department of Health, Albany, NY, USA.
  • Farr SL; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Crume T; Department of Epidemiology, Colorado School of Public Health, University of Colorado, Aurora, CO, USA.
  • Book WM; Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
  • Whitehead K; Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • Botto LD; Department of Medicine, University of Utah, Salt Lake City, UT, USA.
  • Li JS; Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • Hsu DT; Duke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.
Pediatr Res ; 2024 Jul 05.
Article en En | MEDLINE | ID: mdl-38969815
ABSTRACT

BACKGROUND:

Despite advances in treatment and survival, individuals with congenital heart defects (CHD) have a higher risk of heart failure (HF) compared to the general population.

OBJECTIVE:

To evaluate comorbidities associated with HF in patients with CHD with a goal of identifying potentially modifiable risk factors that may reduce HF-associated morbidity and mortality.

METHODS:

Five surveillance sites in the United States linked population-based healthcare data and vital records. Individuals with an ICD-9-CM code for CHD aged 11-64 years were included and were stratified by presence of HF diagnosis code. Prevalence of death and cardiovascular risk factors based on diagnosis codes were compared by HF status using log-linear regression.

RESULTS:

A total of 25,343 individuals met inclusion/exclusion criteria. HF was documented for 2.2% of adolescents and 12.9% of adults with CHD. Adolescents and adults with HF had a higher mortality than those without HF. In both age groups, HF was positively associated with coronary artery disease, hypertension, obesity, diabetes, and increased healthcare utilization compared to those without HF.

CONCLUSIONS:

Within this population-based cohort, over 1 in 50 adolescents and 1 in 8 adults with CHD had HF, which was associated with increased mortality. Modifiable cardiovascular comorbidities were associated with HF. IMPACT Five sites in the United States linked population-based healthcare data and vital records to establish surveillance network for identifying the factors which influence congenital heart disease (CHD) outcomes. Survivors of CHD frequently develop heart failure across the lifespan. Over 1 in 50 adolescent and 1 in 8 adult survivors of CHD have heart failure which is associated with increased mortality compared to CHD survivors without heart failure. Heart failure development is associated with potentially modifiable cardiovascular risk factors such as hypertension, coronary artery disease, and diabetes. Controlling modifiable cardiovascular risk factors may serve to lower the risk of heart failure and mortality in survivors of congenital heart disease of all ages.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pediatr Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pediatr Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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