Abstract
Background: New Zealand’s End of Life Choice Act 2019 was enacted in 2021, allowing terminally ill people experiencing unbearable suffering to request assisted dying if they are expected to die within six months. Healthcare professionals not directly involved in assisted dying provision may have unique perspectives on implementation, yet this remains under-explored. Methods: This qualitative study was conducted between June and November 2022. We used purposive and snowball sampling to recruit potential participants through various sources, including the Ministry of Health’s assisted dying training and communication email list. A multidisciplinary research team developed a semi-structured interview guide. The individual interviews were recorded, transcribed, and thematically analysed to identify core themes. Results: Ten healthcare professionals with palliative and primary care backgrounds participated. Five main themes were generated: diverse views on assisted dying; views on the End of Life Choice Act; the interface between palliative care and assisted dying services; education on palliative care and assisted dying; and self-care coping and support. Participants expressed varied attitudes and ethical concerns, with most emphasising the need for reforms in eligibility criteria and improved public understanding. These healthcare professionals provided valuable insights into the broader impact of assisted dying on the healthcare system and the complexities of integrating it with palliative care. Conclusions: Integration between palliative care and assisted dying services is crucial for delivering patient-centred care and addressing stigma surrounding end-of-life choices in New Zealand. Adapting international policies around eligibility criteria and safeguards can help streamline the process.
RAS ID
82691
Document Type
Journal Article
Date of Publication
12-1-2025
Volume
24
Issue
1
Funding Information
Auckland Medical Research Foundation
PubMed ID
40629332
School
School of Nursing and Midwifery
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Publisher
Springer
Identifier
Melissa Carey: https://orcid.org/0000-0002-2392-173X
Recommended Citation
Arshad, W., Dehkhoda, A., Carey, M., Menkes, D. B., Hoeh, N., Sundram, F., Frey, R., & Cheung, G. (2025). The first year of assisted dying in New Zealand through the lens of healthcare professionals not directly involved in the process. Retrieved from https://ro.ecu.edu.au/ecuworks2022-2026/6687
Comments
Arshad, W., Dehkhoda, A., Carey, M., Menkes, D. B., Hoeh, N., Sundram, F., Frey, R., & Cheung, G. (2025). The first year of assisted dying in New Zealand through the lens of healthcare professionals not directly involved in the process. BMC Palliative Care, 24. https://doi.org/10.1186/s12904-025-01838-8