Data that matter: what outcomes matter to patients with congenital heart disease and their carers and which should be routinely measured? A qualitative asynchronous online discussion forum
- DOI
- 10.1136/bmjopen-2025-111466
- Published
- 2026-09
- Container
- BMJ Open
- Publisher
- BMJ
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1136/bmjopen-2025-111466,
title = {Data that matter: what outcomes matter to patients with congenital heart disease and their carers and which should be routinely measured? A qualitative asynchronous online discussion forum},
author = {Jo Wray and Katherine L Brown and Fiona Kennedy and Christina Pagel and Sonya Crowe},
year = {2026},
journal = {BMJ Open},
doi = {10.1136/bmjopen-2025-111466},
url = {https://doi.org/10.1136/bmjopen-2025-111466}
}RIS
TY - JOUR TI - Data that matter: what outcomes matter to patients with congenital heart disease and their carers and which should be routinely measured? A qualitative asynchronous online discussion forum AU - Jo Wray AU - Katherine L Brown AU - Fiona Kennedy AU - Christina Pagel AU - Sonya Crowe PY - 2026 JO - BMJ Open DO - 10.1136/bmjopen-2025-111466 UR - https://doi.org/10.1136/bmjopen-2025-111466 ER -
APA
Wray, J., Brown, K. L., Kennedy, F., Pagel, C., & Crowe, S. (2026). Data that matter: what outcomes matter to patients with congenital heart disease and their carers and which should be routinely measured? A qualitative asynchronous online discussion forum. BMJ Open. https://doi.org/10.1136/bmjopen-2025-111466
Source records
- crossref · retrieved 2026-09-26T07:53:25.169Z