“I don’t think service changed, I think people changed”: Palliative care delivery in Aotearoa/New Zealand after COVID-19
Palliative care services needed to adapt rapidly and creatively to the threats posed by COVID-19. The threats posed were a motivator to shift thinking about palliative care delivery regarding services, relationships, and empowerment. This shift in thinking led to changes in ways of working, revising, and establishing new policies and practices. The driving force underpinning the changes and innovations is the desire to provide patient-centred care. Indeed, the findings build a case for patient-centred, sustainable, and effective innovation. From the perspective of health professionals, the findings may inform strategies to sustain new practices in delivering quality palliative care. Additionally, they may also provide insights into possible methods to grow individual and community capacity to face future pandemics.
Authors
- Merryn Gott (ORCID: https://orcid.org/0000-0003-4399-962X)
- Tess Moeke‐Maxwell (ORCID: https://orcid.org/0000-0002-3980-3228)
- Jenny Thurston
- Deborah Raphael (ORCID: https://orcid.org/0000-0002-7556-392X)
- Jackie Robinson (ORCID: https://orcid.org/0000-0002-9678-2005)
- Rosemary Frey (ORCID: https://orcid.org/0000-0002-8758-5675)
- Lisa A. Williams (ORCID: https://orcid.org/0000-0002-0021-5613)
- Erica Munro
Institutions
- University of Auckland (NZ)
- Mercy Hospital (NZ)
Publication Details
- Journal
- Palliative Care and Social Practice
- Published
- 2025-06-24
- DOI
- https://doi.org/10.1177/26323524251343095
- Primary Topic
- Palliative Care and End-of-Life Issues
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Cancer Research Trust New Zealand