Evidence map›Paper›PMID 41748301›Full record

ArticleArchives of disease in childhood2026

Parent-to-parent recommendations for coping with congenital heart disease: a mixed-methods study.

Katharine Press Callahan, Rebecca Dorner, Magdalena Jaworski, Lauren Capaci, Annie Janvier, Karolane Maltais, Chloe Barsoum, Catherine Martin, Carl H Backes, Thuy Mai Luu

Abstract read
In one paragraph

Article in Archives of disease in childhood, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Katharine Press CallahanThe Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA callahankp@chop.edu.ORCID 0000-0002-2221-6254
Rebecca DornerSharp Mary Birch Hospital for Women and Newborns, San Diego, California, USA.
Magdalena JaworskiCHU Sainte-Justine Département de Pédiatrie, Montreal, Quebec, Canada.
Lauren CapaciNationwide Children's Hospital, Columbus, Ohio, USA.
Annie JanvierDepartment of Pediatrics, Université de Montréal, Montreal, Quebec, Canada.ORCID 0000-0002-5462-9352
Karolane MaltaisDepartment of Pediatrics, Université de Montréal, Montreal, Quebec, Canada.
Chloe BarsoumAzrieli Research Center CHU Sainte-Justine, Montreal, Quebec, Canada.
Catherine MartinParent Representative, CHU Sainte-Justine, Montreal, Quebec, Canada.
Carl H BackesNationwide Children's Hospital, Columbus, Ohio, USA.
Thuy Mai LuuPediatrics and Research Center, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.ORCID 0000-0003-2222-186X

Funding

Managing the Uncertainty of Genetic Information in NeonatesK01HG013114 · NHGRI · CHILDREN'S HOSP OF PHILADELPHIA · PI Katharine Press Callahan · 2023 to 2026
$664k
NHGRI NIH HHS K01 HG013114
6 · The paper itself

Abstract

objectivesTo systematically analyse parent-to-parent guidance for those receiving a diagnosis of congenital heart disease (CHD) to inform clinician counselling and advance development of support programmes.

designWe asked parents of children who had CHD requiring surgery or catheterisation in infancy about their recommendations for parents receiving a new diagnosis. We analysed responses using mixed methods.

settingStand-alone children's hospital. PATIENTS: We interviewed 100 parents of children with CHD with a 96% participation rate.

main outcome measuresQualitative themes for primary recommendations and quantitative analysis of correlation between themes and social/clinical factors.

resultsParents recommended balancing tactics for taking control with strategies for adapting to uncertainty. Parents recognised the importance of acknowledging challenges (noted by 24%) but focused primarily on imperatives to move forward: (1) empower yourself with information and support (50%), (2) take care of yourself (23%), (3) trust your medical team, your child and yourself (31%) and (4) maintain a positive outlook on improvement and believe that normalcy is possible (42%). Recommendations varied little with social or clinical factors.

conclusionsRecommendations from parents provide direct advice for others facing new diagnoses and outline actionable steps for clinicians hoping to support those receiving a CHD diagnosis. Clinicians may acknowledge challenges, help parents reflect on what they can and cannot control and empower parents by providing comprehensible information and connecting them to other parents.

Indexed as

Adaptation, PsychologicalHeart Defects, CongenitalParentsAdultChildChild, PreschoolCounselingFemaleHumansInfantInfant, NewbornMaleProfessional-Family RelationsSocial SupportCardiologyNeonatology

Identifiers

PMID41748301
PMCPMC13051368

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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.