Parent and healthcare professional experiences of critical congenital heart disease in New Zealand to advance health equity
According to the experiences of parents and healthcare professionals, persisting inequities in CCHD healthcare quality occur by ethnic group, with the New Zealand healthcare system privileging European families. The concepts from this study could be translated by healthcare leaders, policymakers, and professionals into evidence-based healthcare system improvements to enhance experiences for non-European families more broadly.
Authors
- Elza Cloete (ORCID: https://orcid.org/0000-0003-2190-0959)
- Kim Ward (ORCID: https://orcid.org/0000-0002-4436-8267)
- Lynn Sadler (ORCID: https://orcid.org/0000-0003-0681-6652)
- Ruth Gorinski
- Teuila Percival (ORCID: https://orcid.org/0000-0002-3361-8304)
- Thomas L. Gentles (ORCID: https://orcid.org/0000-0001-6149-2596)
- Sue Crengle (ORCID: https://orcid.org/0000-0001-9367-1492)
- Rachel Brown
- Frank H. Bloomfield (ORCID: https://orcid.org/0000-0001-6424-6577)
- S Watkins (ORCID: https://orcid.org/0000-0003-3211-403X)
- Monique WM de Laat
Institutions
- University of Auckland (NZ)
- Auckland City Hospital (NZ)
- Christchurch Hospital (NZ)
- National Heart Foundation of New Zealand (NZ)
- University of Otago (NZ)
Publication Details
- Journal
- BMC Health Services Research
- Published
- 2024-08-26
- DOI
- https://doi.org/10.1186/s12913-024-11410-4
- Citations
- 2
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.77
Funders
- Health Research Council of New Zealand