Evidence map›Paper›PMID 42463189›Full record

ArticleBMJ open2026

BRIGHT pathways: recommendations to improve the developmental follow-up of children with CHD in Canada - protocol for a nominal group study.

Marie-Eve Bolduc, Brahmdeep S Saini, Andrea M Patey, Eric Sadiku, Steven P Miller, Marie-Noelle Simard, Marie Brossard-Racine, Annette Majnemer, Linh G Ly, Renee Sananes and 1 more

Abstract read
In one paragraph

Article in BMJ open, 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

11 authors.

Marie-Eve BolducSchool of Physical and Occupational Therapy, McGill University, Montreal, Quebec, Canada marie-eve.bolduc@mcgill.ca.ORCID http://orcid.org/0000-0002-2208-620X
Brahmdeep S SainiDivision of Cardiology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Andrea M PateyDepartment of Medicine, Quality and Safety, IWK Health Centre, Halifax, Nova Scotia, Canada.
Eric SadikuTranslational Medicine Program, SickKids Research Institute, Toronto, Ontario, Canada.
Steven P MillerPediatrics, BC Children's Hospital and University of British Columbia, Vancouver, British Columbia, Canada.
Marie-Noelle SimardAzrieli Research Centre of the CHU Sainte-Justine, Université de Montréal, Montreal, Quebec, Canada.
Marie Brossard-RacineSchool of Physical and Occupational Therapy, McGill University, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0003-0641-0054
Annette MajnemerSchool of Physical and Occupational Therapy, McGill University, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0001-7712-3509
Linh G LyNeonatology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Renee SananesDepartment of Psychology, Division of Cardiology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Mike SeedDivision of Cardiology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSystematic developmental follow-up for children with congenital heart disease (CHD) is essential for the timely detection of developmental delays and disorders and to put in place the supports and resources necessary to maximise function and support family well-being. Best practice guidelines recommend follow-up for children with CHD at high risk of developmental delays. However, many countries, including Canada, have faced barriers such as limitations in financial and human resources which have limited their ability to implement these important neurodevelopmental follow-up programmes. The aim of this project is to develop recommendations for evidence-based care pathways for the developmental follow-up of children and adolescents with CHD that are adapted to the Canadian health care context.

methodsThis study includes two steps: (1) a narrative review of current literature on the developmental follow-up of children with CHD and (2) a nominal group process involving patients, families, healthcare workers, researchers, policy-makers and government representatives that will be used to achieve consensus on practice recommendations. Purposive sampling will be used to select eligible participants so that all interested parties are well represented and reflective of a variety of experiences and opinions. Two to three groups of approximately 10 participants will be held via videoconferencing. The nominal groups will consist of a five-step process that will be repeated for each topic: (1) question; (2) idea generation; (3) discussion; (4) ranking; and (5) consensus. ANALYSIS: Data from the different groups will be merged. Ideas for which a consensus was reached (>80% agreement) during the meetings will be summarised. ETHICS AND DISSEMINATION: Ethical approval was obtained from The Hospital for Sick Children, Toronto, Canada (#1000081399) and McGill University, Montreal, Canada (#25-09-006). The findings of this study will be disseminated in peer-reviewed journals and conferences, presented at local, national and international conferences and disseminated to local, provincial and national governments to inform policy.

Indexed as

Developmental DisabilitiesHeart Defects, CongenitalAdolescentCanadaChildConsensusHumansPractice Guidelines as TopicResearch DesignCongenital heart diseaseHealth ServicesImplementation SciencePAEDIATRICS

Identifiers

PMID42463189
PMCPMC13374422

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.