Evidence map›Paper›PMID 38969815›Full record

ArticlePediatric research2025

Cardiovascular disease risk factors in congenital heart disease survivors are associated with heart failure.

Andrew P Landstrom, Tracy Spears, Alfred D'Ottavio, Karen Chiswell, Kristin Sommerhalter, Aida Soim, Sherry L Farr, Tessa Crume, Wendy M Book, Kevin Whitehead and 3 more

Abstract read
In one paragraph

Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Andrew P LandstromDuke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA. andrew.landstrom@duke.edu.ORCID 0000-0002-1878-9631
Tracy SpearsDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Alfred D'OttavioDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Karen ChiswellDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Kristin SommerhalterBureau of Environmental and Occupational Epidemiology, New York State Department of Health, Albany, NY, USA.
Aida SoimBureau of Environmental and Occupational Epidemiology, New York State Department of Health, Albany, NY, USA.
Sherry L FarrNational Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Tessa CrumeDepartment of Epidemiology, Colorado School of Public Health, University of Colorado, Aurora, CO, USA.
Wendy M BookDepartment of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Kevin WhiteheadDepartment of Pediatrics, University of Utah, Salt Lake City, UT, USA.
Lorenzo D BottoDepartment of Pediatrics, University of Utah, Salt Lake City, UT, USA.
Jennifer S LiDuke Department of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, NC, USA.
Daphne T HsuPediatric Heart Center, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.

Funding

Exploring the role of ATP1A3 mutations in sudden unexplained death in epilepsyR01HL160654 · NHLBI · DUKE UNIVERSITY · PI Andrew P. Landstrom · 2022 to 2026
$3.4M
Determining the genetic and social determinants of heart failure and mortality in patients with congenital heart disease (DEFINE)R01HL166217 · NHLBI · DUKE UNIVERSITY · PI Andrew P. Landstrom · 2023 to 2026
$2.8M
Intramural CDC HHS CC999999NHLBI NIH HHS R01 HL160654NHLBI NIH HHS R01 HL166217
6 · The paper itself

Abstract

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

objectiveTo 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.

methodsFive 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.

resultsA 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.

conclusionsWithin 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.

Indexed as

Cardiovascular DiseasesHeart Defects, CongenitalHeart FailureAdolescentAdultChildComorbidityFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedPrevalenceRisk FactorsSurvivorsUnited States

Identifiers

PMID38969815
PMCPMC11700225

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.