ArticlePediatric cardiology2026
Reported Impacts of Congenital Heart Disease on Functional Outcomes in Adults with Down Syndrome.
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.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Systematic multi-omic deconvolution of the clinical heterogeneity of Down syndrome.Nature communications · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
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.
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Registered trials
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