Abstract
Health disparities in palliative care are preventable consequences of structural discrimination and marginalization. The first step in addressing a problem is recognizing there is one and devotion to fully understanding its multifaceted nature. Palliative care clinicians, educators and researchers must prioritize investigating and mitigating the effects of racial, social, and intersectional injustice.
Explore related subjects
Find the latest articles, discoveries, and news in related topics.Main text
Health disparities are the preventable consequences of structural discrimination and marginalization that, if left unaddressed, lead to and perpetuate substantial preventable morbidity and mortality [1]. When it comes to the delivery of high-quality palliative care, there is now increasing evidence of systematic and structural health disparities that stymie the possibility of achieving what people refer to as a "good death" [2,3,4] and contribute to prolonged or complicated grief among caregivers [5]. There are notable disparities in accessing palliative care among minority groups as well as across global settings [6].
Health equity is recognized by the World Health Organisation as a vital component of social justice and is described as the absence of unfair or avoidable differences [6]. The Worldwide Hospice Palliative Care Alliance has recently called out palliative care as "one of the most inequitable areas of healthcare" and emphasized the need to improve equitable access to palliative care [7]. Equity is recognized to be a key component of palliative care and is achieved when all can reach their fullest health potential through timely, appropriate, and high-quality care [8]. Diversity considers what makes each person unique in their illness narrative in terms of heritage, sociodemographic characteristics, and identity expression including a thorough reflection of intersectional identities [9]. Palliative care services that relieve suffering and improve quality of life must be provided to all people irrespective of who they are, where they live, or their life experiences.
While this is not a new phenomenon, recent global movements have emphasized societal fissures that demand attention [10]. Among many other sociopolitical and environmental issues, international movements like Black Lives Matter [11], national scandals like the residential schools scandal in Canada and the “Windrush” scandal in the UK [12], the disproportionate impact of the COVID-19 pandemic on those living on the margins of society, who already experienced multiple disadvantages [13], global discrimination of those who are 2SLGBTQIA + [14, 15], have underscored societal fissures and inequities that demand attention. It is also important to recognize that future environmental and political events, such as climate change, war and disasters, may compound inequalities in accessing palliative care. All have particular emphasis on end-of-life care; inequities in life are mirrored in the experience of dying.
Enhancing equity and diversity in palliative care practice will require a person-centred approach with community support that advocates for change on multiple levels: individual (patient and caregiver), interpersonal (health care team), organizational, and policy (Fig. 1). Equitable access is required across the entire continuum of palliative care services that begins with early interventions, continuing with symptom-focused treatment, hospice, and end-of-life care, as well as bereavement and grief support. Reducing disparities in palliative care must be concerned with the clinical practice of palliative care, as well as diversity, inclusion and access in education, training, and research. In education and training, the discipline of palliative care must take an active role in recruiting and teaching diverse clinicians, nationally and internationally. In terms of equity in palliative care research, there is a need to develop diverse research teams, partner with community groups and patients with lived experience, and enable the democratic expression of ideas in research teams who are involved in the production and review of new knowledge.
The first step in addressing a problem is recognizing there is one and devotion to fully understanding its multifaceted nature. Palliative care clinicians, educators and researchers must prioritize investigating and mitigating the effects of racial, social, and intersectional injustice. This collection on 'Equity and diversity in palliative care" (https://www.biomedcentral.com/collections/EDPC) therefore welcomes contributions from clinical research as well as original theoretical reflections relating to philosophical, ethical, and policy issues specific to this theme to mitigate the effects of racial, social and intersectional injustice. We actively encourage critical self-reflection and acknowledgement of conscious and implicit bias that has shaped the research questions we ask, how we address them, the way we report study findings, and the composition of research teams.
Availability of data and materials
Not applicable.
Abbreviations
- 2SLGBTQIA +:
-
Two-Spirit, Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, Asexual, and ( +) any gender identities or sexual orientations not included in this acronym
References
Dye BA, et al. The importance of evaluating health disparities research. Am J Public Health. 2019;109(S1):S34–40.
Davies JM, et al. Socioeconomic position and use of healthcare in the last year of life: a systematic review and meta-analysis. PLoS Med. 2019;16(4): e1002782.
Stajduhar KI. Provocations on privilege in palliative care: Are we meeting our core mandate? Progress in Palliative Care. 2020;28(2):89–93.
Hussain JA, Koffman J, Bajwah S. Invited editorials: racism and palliative care Palliat Med. 2021;35(5):810–3.
Roulston A, et al. Bereavement outcomes: a quantitative survey identifying risk factors in informal carers bereaved through cancer. Palliat Med. 2016;31(2):162–70.
World Health Organization, Closing the gap in a generation: Health equity through action on the social determinants of health. Commission on social determinants of health final report. 2008, World Health Organisation: Geneva. p. 40.
Worldwide Hospice Palliative Care Alliance 2021. Equity in Access to Palliative Care Report 2021. https://www.thewhpca.org/resources-2021/item/equity-in-access-to-palliative-care-report-2021.
Richards N. The equity turn in palliative and end of life care research: Lessons from the poverty literature. Sociol Compass. 2022;16(5):e12969. https://doi.org/10.1111/soc4.12969.
Koffman J, et al. Researching minoritised communities in palliative care: An agenda for change. Palliat Med. 2023;37(4):530–42. https://doi.org/10.1177/02692163221132091.
Ishkanian A. Social movements and social policy: new research horizons. J Soc Policy. 2022;51(3):582–95.
Barber S. Death by racism. Lancet Infect Dis. 2020;20(8):903.
Horton R. Offline: a caribbean consciousness. The Lancet. 2018;391(10132):1757.
Marmot, M., et al., The pandemic, socioeconomic and health inequalities in England. Institute of Health Equity, 2020.
Wakefield D, et al. Why does palliative care need to consider access and care for LGBTQ people? Palliat Med. 2021;35(10):1730–2. https://doi.org/10.1177/02692163211055011.
Bristowe K, Hodson M, Wee B, Almack K, Johnson K, Daveson BA, Koffman J, McEnhill L, Harding R. Recommendations to reduce inequalities for LGBT people facing advanced illness: ACCESSCare national qualitative interview study. Palliat Med. 2018;32(1):23–35. https://doi.org/10.1177/0269216317705102.
Acknowledgements
We would like to acknowledge Brendan Lyver who contributed to developing Fig. 1.
Funding
GKS reports funding from the Canadian Institutes of Health Research (#WHR-185783). CSQ reports funding from Young Leaders and Cancer Experience Program at the Princess Margaret Cancer Centre and funding from the Academic Scholars Award, Department of Psychiatry, University of Toronto. Funders had no role in the conceptualization, design, and writing of this manuscript.
Author information
Authors and Affiliations
Contributions
JK, GKS and CSQ conceived and drafted the Editorial. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
JK, GKS and CSQ are Guest Editors of the Collection' Equity and diversity in palliative care'. JK and CSQ are editorial board members of BMC Palliative Care. GKS is a research consultant for the World Health Organization. CSQ receives royalties from Springer International.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
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/. The Creative Commons Public Domain Dedication waiver (http://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.
About this article
Cite this article
Koffman, J., Shapiro, G.K. & Schulz-Quach, C. Enhancing equity and diversity in palliative care clinical practice, research and education. BMC Palliat Care 22, 64 (2023). https://doi.org/10.1186/s12904-023-01185-6
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12904-023-01185-6