Evidence map›Paper›PMID 40742435›Full record

ArticlePediatric cardiology2026

Reported Impacts of Congenital Heart Disease on Functional Outcomes in Adults with Down Syndrome.

Stephanie S Gaydos, Andreana Benitez, Paul J Nietert, Kimberly E McHugh, Andrew Atz

Abstract read
In one paragraph

Article in Pediatric cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Stephanie S GaydosDivision of Pediatric Cardiology, Department of Pediatrics, MUSC Shawn Jenkins Children's Hospital, Medical University of South Carolina, 10 McClennan Banks Dr. (MSC915), Charleston, SC, 29425, USA. gaydoss@musc.edu.ORCID http://orcid.org/0000-0002-8536-9899
Andreana BenitezDepartment of Neurology, Medical University of South Carolina, Charleston, SC, 29425, USA.
Paul J NietertDepartment of Public Health Services, Medical University of South Carolina, Charleston, SC, 29425, USA.
Kimberly E McHughDivision of Pediatric Cardiology, Department of Pediatrics, MUSC Shawn Jenkins Children's Hospital, Medical University of South Carolina, 10 McClennan Banks Dr. (MSC915), Charleston, SC, 29425, USA.
Andrew AtzDivision of Pediatric Cardiology, Department of Pediatrics, MUSC Shawn Jenkins Children's Hospital, Medical University of South Carolina, 10 McClennan Banks Dr. (MSC915), Charleston, SC, 29425, USA.

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
MIS-C Program: Data Coordinating Center for the Pediatric Heart Network MIS-C ProgramU24HL135691 · NHLBI · NEW ENGLAND RESEARCH INSTITUTES, INC. · PI MILLER, JULIE ELAINE, TRACHTENBERG, FELICIA LYNN · 2017 to 2024
$37.9M
NCATS NIH HHS UL1 TR001450NHLBI NIH HHS U24 HL135691
6 · The paper itself

Abstract

To evaluate whether having congenital heart disease (CHD) mediates community engagement, neuropsychiatric conditions, and quality of life (QOL) in adults with Down syndrome (DS). Cross-sectional survey of adults ages 18-45 years with DS and their caregiver, identified from NIH DS Registry, regional DS groups, and Cardiology clinics. The study survey consisted of adapted instruments (validated or prior use in this cohort) assessing medical history, employment/volunteer experience, QOL, mental health, and caregiver burden. Primary outcome was employment. Outcomes were compared between DS groups with and without CHD via Chi-squared test, t tests, and two proportion Z tests as appropriate. 287 subjects completed the study. Adults with DS and CHD (n = 104, 36%) reported similar employment rates as those without CHD: 61% and 60%, respectively (p = 0.87). Current volunteerism was significantly higher in DS + CHD subjects (32%) compared to DS alone (19%); p = 0.01. There were higher rates of stroke and seizure in DS + CHD (p < 0.01 for both), although no significant difference in psychological comorbidities (p = 0.67). 69% of all DS adults reported mental health problems. Proxy-reported mean QOL scores were similar between DS groups (p = 0.52). Mild-moderate caregiver burden was reported in both groups, with significantly greater burden reported in guardians of DS + CHD (p = 0.03). CHD is not associated with reduced employment or community engagement in adults with DS, despite significantly greater neurologic comorbidities. Similar QOL and mental health issues were reported in adults with DS regardless of having CHD. Findings may convey optimism to families of children born with both health issues.

Indexed as

Down SyndromeHeart Defects, CongenitalQuality of LifeAdolescentAdultCaregiversCross-Sectional StudiesEmploymentFemaleHumansMaleMental HealthMiddle AgedSurveys and QuestionnairesYoung AdultCongenital heart diseaseDown syndromeOutcomes

Identifiers

PMID40742435
PMCPMC13144255

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.