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Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service
BACKGROUND: In November 2021, assisted dying (AD) became lawful in Aotearoa New Zealand. A terminally ill person may now request, and receive, pharmacological assistance (self-administered or provided by a medical practitioner/nurse practitioner) to end their life, subject to specific legal criteria...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362551/ https://www.ncbi.nlm.nih.gov/pubmed/37480024 http://dx.doi.org/10.1186/s12904-023-01222-4 |
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author | Snelling, Jeanne Young, Jessica Beaumont, Sophie Diesfeld, Kate White, Ben Willmott, Lindy Robinson, Jacqualine Moeke-Maxwell, Tess |
author_facet | Snelling, Jeanne Young, Jessica Beaumont, Sophie Diesfeld, Kate White, Ben Willmott, Lindy Robinson, Jacqualine Moeke-Maxwell, Tess |
author_sort | Snelling, Jeanne |
collection | PubMed |
description | BACKGROUND: In November 2021, assisted dying (AD) became lawful in Aotearoa New Zealand. A terminally ill person may now request, and receive, pharmacological assistance (self-administered or provided by a medical practitioner/nurse practitioner) to end their life, subject to specific legal criteria and processes. Exploring the experiences of health providers in the initial stage of the implementation of the End of Life Choice Act 2019 is vital to inform the ongoing development of safe and effective AD practice, policy and law. AIM: To explore the early experiences of health care providers (HCPs) who do and do not provide AD services seven months after legalisation of AD to provide the first empirical account of how the AD service is operating in New Zealand’s distinctive healthcare environment and cultural context. DESIGN: Qualitative exploratory design using semi-structured individual and focus group interviewing with a range of HCPs. RESULTS: Twenty-six HCPs participated in the study. Through a process of thematic analysis four key themes were identified: (1) Difference in organisational response to AD; (2) challenges in applying the law; (3) experiences at the coal face; and (4) functionality of the AD system. CONCLUSION: A range of barriers and enablers to successful implementation of AD were described. Adoption of open and transparent organisational policies, ongoing education of the workforce, and measures to reduce stigma associated with AD are necessary to facilitate high quality AD service provision. Future research into the factors that influence responses to, and experience of AD; the impact of institutional objection; and the extent to which HCP perspectives evolve over time would be beneficial. In addition, further research into the integration of AD within Māori health organisations is required. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12904-023-01222-4. |
format | Online Article Text |
id | pubmed-10362551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103625512023-07-23 Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service Snelling, Jeanne Young, Jessica Beaumont, Sophie Diesfeld, Kate White, Ben Willmott, Lindy Robinson, Jacqualine Moeke-Maxwell, Tess BMC Palliat Care Research BACKGROUND: In November 2021, assisted dying (AD) became lawful in Aotearoa New Zealand. A terminally ill person may now request, and receive, pharmacological assistance (self-administered or provided by a medical practitioner/nurse practitioner) to end their life, subject to specific legal criteria and processes. Exploring the experiences of health providers in the initial stage of the implementation of the End of Life Choice Act 2019 is vital to inform the ongoing development of safe and effective AD practice, policy and law. AIM: To explore the early experiences of health care providers (HCPs) who do and do not provide AD services seven months after legalisation of AD to provide the first empirical account of how the AD service is operating in New Zealand’s distinctive healthcare environment and cultural context. DESIGN: Qualitative exploratory design using semi-structured individual and focus group interviewing with a range of HCPs. RESULTS: Twenty-six HCPs participated in the study. Through a process of thematic analysis four key themes were identified: (1) Difference in organisational response to AD; (2) challenges in applying the law; (3) experiences at the coal face; and (4) functionality of the AD system. CONCLUSION: A range of barriers and enablers to successful implementation of AD were described. Adoption of open and transparent organisational policies, ongoing education of the workforce, and measures to reduce stigma associated with AD are necessary to facilitate high quality AD service provision. Future research into the factors that influence responses to, and experience of AD; the impact of institutional objection; and the extent to which HCP perspectives evolve over time would be beneficial. In addition, further research into the integration of AD within Māori health organisations is required. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12904-023-01222-4. BioMed Central 2023-07-22 /pmc/articles/PMC10362551/ /pubmed/37480024 http://dx.doi.org/10.1186/s12904-023-01222-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Snelling, Jeanne Young, Jessica Beaumont, Sophie Diesfeld, Kate White, Ben Willmott, Lindy Robinson, Jacqualine Moeke-Maxwell, Tess Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title | Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title_full | Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title_fullStr | Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title_full_unstemmed | Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title_short | Health care providers’ early experiences of assisted dying in Aotearoa New Zealand: an evolving clinical service |
title_sort | health care providers’ early experiences of assisted dying in aotearoa new zealand: an evolving clinical service |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362551/ https://www.ncbi.nlm.nih.gov/pubmed/37480024 http://dx.doi.org/10.1186/s12904-023-01222-4 |
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