Exploring palliative care debates: Equitable access and the role of social workers
DOI:
https://doi.org/10.11157/anzswj-vol36iss4id1170Keywords:
older adults, equity, palliative care, social work, literature reviewAbstract
INTRODUCTION: Equity of access to palliative care for older adults and the role of social work are interwoven as older adults are the largest population group requiring end-of-life care and hospice social workers predominantly work alongside older adults. This article explores the intersections of palliative care policy and practice, older adults’ inequitable outcomes, Te Tiriti o Waitangi (1840), and challenges faced by social workers seeking to be effective advocates for older adults.
APPROACH: Undertaking post-graduate study in palliative care allowed for an exploration of the literature and older adults’ experiences of inequity observed in practice through a social work lens. Literature reviews completed during post-graduate study foreground the literature search informing this article. The literature search was completed using University of Canterbury Library and CINAHL Health sciences databases focused on palliative and end-of-life care, older adults and caregivers. Keywords used included literature reviews, palliative or end-of-life, older adults or elderly, caregivers or family, psychosocial, New Zealand, caregiver distress, and ageism. Abstracts of articles were reviewed; literature was chosen based on relevance to the topic. Additional literature was sourced through Google Scholar, Google searches of current proposals/reports, and international databases.
CONCLUSIONS: The current Aotearoa New Zealand Ministry of Health (MoH) (2001) Palliative Care Strategy does not effectively respond to older adults’ end-of-life care needs or acknowledge the roles and contributions of social workers within palliative care. Improving older adults’ equity of access to palliative care requires interlinking and prioritising older adults’ end-of-life care and empowering the contributions of social workers.
References
Agnew, A., Manktelow, R., Haynes, T., & Jones, L. (2011). Bereavement assessment practice in hospice settings: Challenges for palliative care social workers. British Journal of Social Work, 41(1), 111130. https://doi.org/10.1093/bjsw/bcq055
Allied Health Workgroup. (2022). Hidden in plain sight; Recognising and growing the palliative care skills of allied health professionals. Christchurch: Te Whatu Ora – Health New Zealand Te Waipounamu Regional Programme Office.
Altilio, T. & Otis-Green, S. (Eds.). (2011). The Oxford textbook of palliative social work. Oxford University Press.
Aotearoa New Zealand Association of Social Workers. (2018). Health social work scope of practice. https://anzasw.nz/wp-content/uploads/NZ-Health-SW-Scope-of-Practice-Final-24-April-2018.pdf
Aotearoa New Zealand Association of Social Workers. (2019). Code of ethics. Blueprint Publishing.
Bates, M. J., Namisango, E., Tomeny, E., Muula, A., Squire, S. B., & Niessen, L. (2019). Palliative care within universal health coverage: The Malawi Patient-and-Carer Cancer Cost Survey. BMJ Supportive & Palliative Care. 14 (e1), p.e353-e356
Belasco, A., Barbosa, D., Bettencourt, A. R., Diccini, S., & Sesso, R. (2006). Quality of life of family caregivers of elderly patients on haemodialysis and peritoneal dialysis. American Journal of Kidney Diseases, 48(6), 955–963. https://doi.org/10.1053/j.ajkd.2006.08.017
Bevin, N., Eggleton, K., & Herbert, S. (2023). Envisioning a Tiriti-responsive New Zealand Health Plan: lessons from district health boards’ annual plans. The New Zealand Medical Journal (Online), 136(1580), 40–47.
Blacker, S., Head, B. A., Jones, B. L., Remke, S. S., & Supiano, K. (2016). Advancing hospice and palliative care social work leadership in interprofessional education and practice. Journal of Social Work in End-of-Life & Palliative Care, 12(4), 316–330.
Boyd, M., Broad, J. B., Kerse, N., Foster, S., von Randow, M., Lay‐Yee, R., . . . Connolly, M. J. (2011). Twenty‐year trends in dependency in residential aged care in Auckland, New Zealand: A descriptive study. Journal of the American Medical Directors Association,12(7), 535–540. http://www.ncbi.nlm.nih.gov/pubmed/21450250
Boulton, A., Levy, M., & Cvitanovic, L. (2020). Beyond Pūao-te-Āta-tū: Realising the promise of a new day (Te Arotahi Paper Series, December 2020, No. 06). Ngā Pae o te Māramatanga, New Zealand’s Māori Centre of Research Excellence. https://www.maramatanga.ac.nz/ news-events/news/te-arotahi-paper-series-december- 2020-no-06
Brandsen, C. K. (2005). Social work and end-of-life care: Reviewing the past and moving forward. Journal of Social Work in End-of-Life & Palliative Care, 1(2), 45–70.
Cadell, S., Johnston, M., Bosma, H., & Wainright, W. (2010). An overview of contemporary social work practice in palliative care. Progress in Palliative Care, 18(4), 205–211.
Cardona-Morrell, M., Kim, J., Turner, R., Anstey, M., Mitchell, I., & Hillman, K. (2016). Non-beneficial treatments in hospital at the end of life: A systematic review on extent of the problem. International Journal for Quality in Health Care, 28(4), 456–469. https://doi.org/10.1093/intqhc/mzw060
Carroll, T., & Quill, T. (2015). Use of generalist and specialist palliative care for older people. In L. Van Den Block (Ed.), Palliative care for older people: A public health perspective (pp. 181—192). Oxford University Press. https://doi.org/10.1093/acprof:oso/9780198717614.001.0001
Castelli Dransart, D.A., Lapierre, S., Erlangsen, A., Canetto, S.S., Heisel, M., Draper, B., Lindner, R., Richard-Devantoy, S., Cheung, G., Scocco, P., Gusmão, R., De Leo, D., Inoue, K., De Techterman, V., Fiske, A., Hong, J.P., Landry, M., Lepage, A., Marcoux, I., Na, P.J., Neufeld, E., Ummel, D., Winslov, J., Wong, C., Wu, J., Wyart, M., Department of Sociology and Work Science, Göteborgs universitet, Gothenburg University, Samhällsvetenskapliga fakulteten, Institutionen för sociologioch arbetsvetenskap & Faculty of Social Sciences. (2021). A systematic review of older adults' request for or attitude toward euthanasia or assisted suicide. Aging & Mental Health, 25(3), 420–430.
Chambers, D. A., Glasgow, R. E., & Stange, K. C. (2013). The dynamic sustainability framework: Addressing the paradox of sustainment amid ongoing change. Implementation Science, 8(1), 1–11.
Cheyne, C., O’Brien., & Belgrave, M. (2011). Social policy in Aotearoa New Zealand (4th ed.). Oxford University Press.
Clark, D. (2019). Controversies in palliative care: A matter of definition. http://endoflifestudies.academicblogs.co.uk/controversies-in-palliative- care-a-matter-of-definition/
Connolly, M. J., Broad, J. B., Boyd, M., Kerse, N., & Gott, M. (2014). Residential aged care: the de facto hospice for New Zealand's older people. Australasian Journal on Ageing, 33(2), 114–120. https://doi.org/10.1111/ajag.12010
Connolly, M., & Harms, L. (2015). Social work: From theory to practice (2nd ed.). Cambridge University Press. https://doi.org/10.1017/9781316104644
Coyle, N., & Sculco, L. (2004). Expressed desire for hastened death in seven patients living with advanced cancer: A phenomenologic inquiry. Oncology Nursing Forum, 31(4), 699–706.
Coym, A., Oechsle, K., Kanitz, A., Puls, N., Blum, D., Bokemeyer, C., & Ullrich, A. (2020). Impact, challenges and limits of inpatient palliative care consultations: Perspectives of requesting and conducting physicians. BMC Health Services Research, 20(1), 86–86. https://doi.org/10.1186/s12913-020-4936-x
Devik, S. A., Hellzen, O., & Enmarker, I. (2015). “Picking up the pieces”—Meanings of receiving home nursing care when being old and living with advanced cancer in a rural area. International Journal of Qualitative Studies on Health and Well-being, 10(1), 28382.
Dunbrack, J. (2005). The information needs of informal caregivers involved in providing support to a critically ill loved one. Health Canada.
Durie, M. (2011). Ngā tini Whetū: Navigating Māori futures. Huia.
Egan, R., & Maidment, J. (2016). Practice skills in social work and welfare: More than just common sense (3rd ed.). Allen & Unwin.
Enguidanos, S., Housen, P., Penido, M., Mejia, B., & Miller, J. A. (2014). Family members’ perceptions of inpatient palliative care consult services: A qualitative study. Palliative Medicine, 28(1), 42–48.
Erlenwein, J., Geyer, A., Schlink, J., Petzke, F., Nauck, F., & Alt-Epping, B. (2014). Characteristics of a palliative care consultation service with a focus on pain in a German university hospital. BMC Palliative Care, 13(1), 1345. https://doi.org/10.1186/1472-684X-13-45
Etkind, S. N., Bone, A. E., Gomes, B., Lovell, N., Evans, C. J., Higginson, I. J., & Murtagh, F. E. M. (2017). How many people will need palliative care in 2040? Past trends, future projections and implications for services. BMC Medicine, 15(1), 102–112. https://doi.org/10.1186/s12916-017-0860-2
Firn, J., Preston, N., & Walshe, C. (2016). What are the views of hospital-based generalist palliative care professionals on what facilitates or hinders collaboration with in-patient specialist palliative care teams? A systematically constructed narrative synthesis. Palliative Medicine, 30(3), 240–256.
Frey, R., Robinson, J., Old, A., Raphael, D., & Gott, M. (2020). Factors associated with overall satisfaction with care at the end‐of‐life: Caregiver voices in New Zealand. Health & Social Care in the Community, 28(6), 2320–2330. https://doi.org/10.1111/hsc.13053
Gaertner, J., Wolf, J., Frechen, S., Klein, U., Scheicht, D., Hellmich, M., Toepelt, K., Glossmann, J., Ostgathe, C., Hallek, M., & Voltz, R. (2012). Recommending early integration of palliative care—does it work? Supportive Care in Cancer, 20(3), 507–513. https://doi.org/10.1007/s00520-011-1111-2
Gamondi, C., Larkin, P., & Payne, S. (2013a). Core competencies for palliative care social work in Europe: An EAPC paper. (Part 1). European Journal of Palliative Care, 20(2), 86–96.
Gamondi, C., Larkin, P., & Payne, S. (2013b). Core competencies for palliative care social work in Europe: an EAPC White Paper (Part 2). European Journal of Palliative Care, 20(3), 140–145.
Giles, R. (2016). Social workers’ perceptions of multi-disciplinary team work: A case study of health social workers at a major regional hospital in New Zealand. Aotearoa New Zealand Social Work, 28(1), 25–33. https://doi.org/10.11157/anzswj-vol28iss1id113
Gilissen, J., Pivodic, L., Unroe, K. T., & Van den Block, L. (2020). International COVID-19 palliative care guidance for nursing homes leaves key themes unaddressed. Journal of Pain and Symptom Management, 60(2), e56–e69. https://doi.org/10.1016/j. jpainsymman.2020.04.151
Gjerberg, E., Lillemoen, L., Førde, R., & Pedersen, R. (2015). End-of-life care communications and shared decision-making in Norwegian nursing homes-experiences and perspectives of patients and relatives. BMC Geriatrics, 15, 1–13.
Golden, A. (2019). Supporting families and lay caregivers on the palliative care journey. Adult Palliative Care for Nursing, Health and Social Care, 134–151. https://doi. org/10.4135/9781526465580
Gott, M., Allen, R., Moeke-Maxwell, T., Gardiner, C., & Robinson, J. (2015). “No matter what the cost”: A qualitative study of the financial costs faced by family and family, whānau caregivers within a palliative care context. Palliative Medicine, 29(6), 518–528. https://doi.org/10.1177/0269216315569337
Gott, M., Frey, R., Wiles, J., Rolleston, A., Teh, R., Moeke- Maxwell, T., & Kerse, N. (2017). End of life care preferences among people of advanced age: LiLACS NZ. BMC Palliative Care, 16(1), 76–76. https://doi. org/10.1186/s12904-017-0258-0
Gott, M., Ibrahim, A. M., & Binstock, R. H. (2011). The disadvantaged dying: Ageing, ageism, and palliative care provision for older people in the UK. In M. Gott & C. Ingleton (Eds.), Living with ageing and dying: Palliative and end of life care for older people (pp. 52–62). Oxford University Press.
Gott, M., & Ingleton, C. (2011). How can we improve palliative care provision for older people? Global perspectives. BMJ Supportive & Palliative Care, 1(2), 115-116.
Hess, S., Stiel, S., Hofmann, S., Klein, C., Lindena, G., & Ostgathe, C. (2014). Trends in specialized palliative care for non-cancer patients in Germany—Data from the national hospice and palliative care evaluation (HOPE). European Journal of Internal Medicine, 25(2), 187–192. https://doi.org/10.1016/j.ejim.2013.11.012
Hogan, S. (2021). Hidden in plain sight: Optimising the allied health professions for better, more sustainable integrated care. New Zealand Institute of Economic Research. https://www.alliedhealth.org.nz/uploads/8/8/9/4/88944696/hidden_in_plain_sight_final_23_06_2021.pdf
Honinx, E., Van Dop, N., Smets, T., Deliens, L., Van Den Noortgate, N., Froggatt, K., Gambassi, G., Kylänen, M., Onwuteaka-Philipsen, B., Szczerbin ́ska, K., & Van den Block, L. (2019). Dying in long-term care facilities in Europe: The PACE epidemiological study of deceased residents in six countries. BMC Public Health, 19(1), 1–12. https://doi.org/10.1186/s12889-019-7532-4
Hunt, S., Lowe, S., Smith, K., Kuruvila, A., & Webber-Dreadon, E. (2016). Transition to professional social work practice: The initial year. Advances in Social Work and Welfare Education, 18(1), 55–71. https://doi/10.3316/informit.061710845032755
International Federation of Social Workers. (2024). Global definition of social work. https://www.ifsw.org/what-is-social-work/global-definition-of-social-work/
Jackson, N., & Healthwatch, A. (2019). Submission to the Office for Seniors on the draft strategy: Better later life–He Oranga Kauma ̄ tua 2019 to 2034. https://officeforseniors.govt.nz/better-later-life-strategy/
Kellehear, A. (2015). Compassionate communities: Caring for older people towards end of life. In L. Van Den Block (Ed.), Palliative care for older people: A public health perspective (pp. 195–199). Oxford University Press.
https://doi.org/10.1093/acprof:oso/9780198717614.001.0001
Kelly, B., Burnett, P., Pelusi, D., Badger, S., Varghese, F., & Robertson, M. (2002). Terminally ill cancer patients’ wish to hasten death. Palliative Medicine, 16(4), 339–345.
Kidd, J., Came, H., Doole, C., & Rae, N. (2021). A critical analysis of te Tiriti o Waitangi application in primary health organisations in Aotearoa New Zealand: Findings from a nationwide survey. Health & Social Care in the Community, 30(1), e105–e112. https://doi.org/10.1111/ hsc.13417
Lewis, E. T., Harrison, R., Hanly, L., Psirides, A., Zammit, A., McFarland, K., Dawson, A., Hillman, K., Barr, M., & Cardona, M. (2019). End‐of‐life priorities of older adults with terminal illness and caregivers: A qualitative consultation. Health Expectations, 22(3), 405–414.
Lilley, D., & Reid, K. (2023). Utilising literature and systems theory to explore the intersections between policy, practice and equity of access to palliative care for older adults in Aotearoa New Zealand. Aotearoa New Zealand Social Work, 35(1), 48-59.
Luckett, T., Phillips, J., Agar, M., Virdun, C., Green, A., & Davidson, P. M. (2014). Elements of effective palliative care models: A rapid review. BMC Health Services Research, 14(1), 136–136. https://doi.org/10.1186/1472-6963-14-136
Maidment, J., & Beddoe, L. (2016). Social policy, social work and social change. In J. Maidment & L. Beddoe (Eds.), Social policy for social work and human services in Aotearoa New Zealand (pp. 21-33) Canterbury University Press.
Marmo, S., & Berkman, C. (2020). Hospice social workers’ perception of being valued by the interdisciplinary team and the association with job satisfaction. Social Work in Health Care, 59(4), 219–235.
Mason, K., Toohey, F., Gott, M., & Moeke-Maxwell, T. (2019). Māori: Living and dying with cardiovascular disease in Aotearoa New Zealand. Current Opinion in Supportive and Palliative Care, 13(1), 3–8.
McLeod, H., & Atkinson, J. (2019). Policy brief on trajectories of care at the end-of-life in New Zealand. Ministry of Health.
Ministry of Health. (2001). The New Zealand palliative care strategy.
https://www.health.govt.nz/system/files/documents/publications/palliativecarestrategy.pdf
Ministry of Health. (2012). Resource and capability framework for integrated adult palliative Care Services in New Zealand. http://www.health.govt.nz/publication/ resource‐and‐capability‐framework‐integrated‐adult‐palliative‐care‐services‐new‐zealand
Ministry of Health. (2015). New Zealand palliative care glossary. http://www.health.govt.nz/publication/new‐zealand‐palliative‐care‐glossary
Ministry of Health. (2017). Review of adult palliative care services in New Zealand. https://www.health.govt.nz/publication/review-adult-palliative-care-services-new-zealand
Morgan, T., Wiles, J., Williams, L., & Gott, M. (2021). COVID-19 and the portrayal of older people in New Zealand news media. Journal of the Royal Society of New Zealand, 51(Suppl. 1), S127–S142. https://doi.org/10.1080/03036758.2021.1884098
Motamedi, M., Brandenburg, C., Bakhit, M., Michaleff, Z. A., Albarqouni, L., Clark, J., ... & Cardona, M. (2021). Concerns and potential improvements in end-of-life care from the perspectives of older patients and informal caregivers: A scoping review. BMC Geriatrics, 21, 1–12.
Motamedi, M., Brandenburg, C., Bakhit, M., Michaleff, Z. A., Albarqouni, L., Clark, J., Ooi, M., Bahudin, D., Chróinín, D. N., & Cardona, M. (2021). Concerns and potential improvements in end-of-life care from the perspectives of older patients and informal caregivers: A scoping review. BMC Geriatrics, 21(1), 729–729. https://doi.org/10.1186/s12877-021-02680-2
Murray, S. A., Kendall, M., Mitchell, G., Moine, S., Amblas-Novellas, J., & Boyd, K. (2017). Palliative care from diagnosis to death. BMJ, 356. https://doi.org/10.1136/bmj.j878
Nicholson, C., & Richardson, H. (2018). Age-attuned hospice care: An opportunity to better end of life care for older people. https://www.stchristophers.org.uk/wp-content/ uploads/2018/10/Age-attuned-Hospice-care-document.pdf
Payne, M. (2004). Social work practice identities: An agency study of a hospice. Practice 16(1), 5–15.
Payne, M. (2014). Modern social work theory (4th ed.). Palgrave Macmillan.
Phillips, J. L., & Currow, D. C. (2017). Would reframing aged care facilities as a “hospice” instead of a “home” enable older people to get the care they need? Collegian, 24(1), 1–2.
Pihama, L., Smith, L. T., Cameron, N., Te Nana, R., Kohu Morgan, H. R., Skipper, H., & Mataki, T. (2020). He oranga ngā kau: Māori approaches to trauma informed care. Te Kotahi Research Institute.
Pihama, L., Smith, L. T., Evans-Campbell, T., Kohu-Morgan, H., Cameron, N., Mataki, T., Te Nana, R., Skipper, H., & Southey, K. (2017). Investigating Māori approaches to trauma-informed care. Journal of Indigenous Well-being, 2(3), 18–31.
Pivodic, L., Smets, T., Van den Noortgate, N., Onwuteaka- Philipsen, B. D., Engels, Y., Szczerbińska, K., Finne-Soveri, H., Froggatt, K., Gambassi, G., Deliens, L. & Van den Block, L. (2018). Quality of dying and quality of end-of-life care of nursing home residents in six countries: An epidemiological study. Palliative Medicine, 32(10), 1584–1595.
Randall, F., & Downie, R. S. (2006). The philosophy of palliative care: Critique and reconstruction. Oxford University Press.
Reese, D. (2013). Hospice social work. Columbia University Press.
Reese, D. J., & Sontag, M. A. (2001). Successful interprofessional collaboration on the hospice team. Health & Social Work, 26(3), 167–175.
Roberts, S. (2016). Assessment with Māori. In R. Egan & J. Maidment (Eds.), Practice skills in social work and welfare: More than just common sense (3rd ed., pp. 207–225). Allen & Unwin.
Rodríguez-Prat, A., Balaguer, A., Booth, A., & Monforte-Royo, C. (2017). Understanding patients’ experiences of the wish to hasten death: An updated and expanded systematic review and meta-ethnography. BMJ Open, 7(9), e016659.
Rosa, W. E., Bhadelia, A., Knaul, F. M., Travers, J. L., Metheny, N., & Fulmer, T. (2022). A longevity society requires integrated palliative care models for historically excluded older people. The Lancet Healthy Longevity, 3(4), e227–e228.
Sasahara, T., Miyashita, M., Umeda, M., Higuchi, H., Shinoda, J., Kawa, M., & Kazuma, K. (2010). Multiple evaluation of a hospital-based palliative care consultation team in a university hospital: Activities, patient outcome, and referring staff's view. Palliative &Supportive Care, 8(1), 49–57. https://doi.org/10.1017/S1478951509990708
Schoenmakers, B., Buntinx, F., & Delepeleire, J. (2010). Factors determining the impact of caregiving on caregivers of elderly patients with dementia: A systematic literature review. Maturitas, 66(2), 191–200.
Smith, J., Borchelt, M., Maier, H., & Jopp, D. (2002). Health and well–being in the young old and oldest old. Journal of Social Issues, 58(4), 715–732.
Social Workers Registration Board. (2024). Core competence standards. https://swrb.govt.nz/for-social-workers/core-competence-standards/
Taels, B., Hermans, K., Van Audenhove, C., Boesten, N., Cohen, J., Hermans, K., & Declercq, A. (2021). How can social workers be meaningfully involved in palliative care? A scoping review on the prerequisites and how they can be realised in practice. Palliative Care and Social Practice, 15, doi: 10.1177/26323524211058895
Tarter, R., Demiris, G., Pike, K., Washington, K., & Parker Oliver, D. (2016). Pain in hospice patients with dementia: The informal caregiver experience. American Journal of Alzheimer's Disease & Other Dementias, 31(6), 524–529.
Te Tiriti o Waitangi. (1840). https://nzhistory.govt.nz/politics/treaty/read-the-treaty/maori-text
Thompson, N. (2016). Anti-discriminatory practice: Equality, diversity, and social justice. Macmillan International Higher Education.
Van Den Block, L. (2015). Palliative care for older people: A public health perspective. Oxford University Press.
https://doi.org/10.1093/acprof:oso/9780198717614.001.0001
Volicer, L., Binte Ali, N., & Simard, J. (2015). Palliative care for older people with dementia. In L. Van Den Block (Ed.), Palliative care for older people: A public health perspective (pp. 200–212). Oxford University Press. https://doi.org/10.1093/acprof:oso/9780198717614.001.0001
Wang, L., & Wang, Z. (2020). Research on the quality hospice care of elderly cancer patients in China under social work intervention. Environmental Health and Preventive Medicine, 25(1), 36–36. https://doi. org/10.1186/s12199-020-00867-4
World Health Organisation. (2022). Definition of palliative care. https://www.who.int/cancer/palliative/definition/en/
Wong, E. L. Y., Lau, J. Y. C., Chau, P. Y. K., Chung, R. Y. N., Wong, S. Y. S., Woo, J., & Yeoh, E. K. (2022). Caregivers’ experience of end-of-life stage elderly patients: Longitudinal qualitative interview. International Journal of Environmental Research and Public Health, 19(4), 2101.
Yang, G. M., Kwee, A. K., & Krishna, L. (2012). Should patients and family be involved in “Do not resuscitate” decisions? Views of oncology and palliative care doctors and nurses. Indian Journal of Palliative Care, 18(1), 52.
Zambas, S. I., & Wright, J. (2016). Impact of colonialism on Māori and aboriginal healthcare access: A discussion paper. Contemporary Nurse, 52(4), 398–409. https://www.tandfonline.com/doi/full/10.1080/10376178.2016.1195238
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Aotearoa New Zealand Association of Social Workers
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
By completing the online submission process, you confirm you accept this agreement. The following is the entire agreement between you and the Aotearoa New Zealand Association of Social Workers (ANZASW) and it may be modified only in writing.
You and any co-authors
If you are completing this agreement on behalf of co-authors, you confirm that you are acting on their behalf with their knowledge.
First publication
By submitting the work you are:
- granting the ANZASW the right of first publication of this work;
- confirming that the work is original; and
- confirming that the work has not been published in any other form.
Once published, you are free to use the final, accepted version in any way, as outlined below under Copyright.
Copyright
You assign copyright in the final, accepted version of your article to the ANZASW. You and any co-authors of the article retain the right to be identified as authors of the work.
The ANZASW will publish the final, accepted manuscript under a Creative Commons Attribution licence (CC BY 4.0). This licence allows anyone – including you – to share, copy, distribute, transmit, adapt and make commercial use of the work without needing additional permission, provided appropriate attribution is made to the original author or source.
A human-readable summary of the licence is available from http://creativecommons.org/licenses/by/4.0, which includes a link to the full licence text.
Under this licence you can use the final, published version of the article freely – such as depositing a copy in your institutional research repository, uploading a copy to your profile on an academic networking site or including it in a different publication, such as a collection of articles on a topic or in conference proceedings – provided that original publication in Aotearoa New Zealand Social Work is acknowledged.
This agreement has no effect on any pre-publication versions or elements, which remain entirely yours, and to which we claim no right.
Reviewers hold copyright in their own comments and should not be further copied in any way without their permission.
The copyright of others
If your article includes the copyright material of others (e.g. graphs, diagrams etc.), you confirm that your use either:
- falls within the limits of fair dealing for the purposes of criticism and review or fair use; OR
- that you have gained permission from the rights holder for publication in an open access journal.