Evidence map›Paper›PMID 40170988›Full record

ArticleCJC pediatric and congenital heart disease2025

Growing Up With Congenital Heart Disease: A Qualitative Research Study of Parents' and Clinicians' Experiences and Perspectives.

F Dylan Nemes, Erica V Bennett, Kevin C Harris, Nicholas Wall, Christine Voss

Abstract read
In one paragraph

Article in CJC pediatric and congenital heart disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Living with congenital heart disease: a qualitative study to explore psychosocial impacts in adulthood.International journal of cardiology. Congenital heart disease · 2025
    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.

F Dylan NemesSouthern Medical Program, the University of British Columbia, Kelowna, British Columbia, Canada.
Erica V BennettSchool of Kinesiology, the University of British Columbia, Vancouver, British Columbia, Canada.
Kevin C HarrisDivision of Cardiology, BC Children's Hospital, Vancouver, British Columbia, Canada.
Nicholas WallCentre for Chronic Disease Prevention and Management, the University of British Columbia, Kelowna, British Columbia, Canada.
Christine VossDepartment of Pediatrics, the University of British Columbia, Vancouver, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Families of children with congenital heart disease (CHD) may experience a range of challenges, such as interactions with the medical system, parental stress, and the child's physical activity (PA) participation. The aim of this study is to explore how those with CHD and their families experience childhood based on parents' and clinicians' experiences and perspectives. The ultimate goal is to identify lacking supports (if any) and when children and their parents may be most amendable to receive them. Methods: We recruited parents/guardians of children with CHD and clinicians involved in care provision for children with CHD. Participants completed life story interviews, with key events from parent/guardian interviews mapped to a timeline. Data were analysed using reflexive thematic analysis. Results: Twelve parents of 11 children with CHD, with diagnoses spanning from mild to complex, and 12 clinicians (42% paediatric cardiologists, 33% nurses, and 25% other) were interviewed. Three themes were identified: (1) overwhelmed-the relationship between parents and the health care system, (2) trauma and resilience-the emotional side to raising a child with CHD, and (3) PA … more than just fun. Subthemes explored challenges of education, communication, and living away from the hospital, traumatic experiences, the need for parental support, different approaches to PA counselling, providing role models, barriers to successful PA promotion, and tools for improvement. Conclusions: This study highlights the need for changes to how and when information is communicated to families of children with CHD and an increase in the number and types of support mechanisms available.

Identifiers

PMID40170988
PMCPMC11955727

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.