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The need for integrating palliative care in ageing and dementia policies
Open accessAbstract
Ageing and dementia is high on policy agendas around the world as is evidenced by recent activities of the European Commission, Council of Europe, World Health Organization (WHO), Organization for Economic Co-operation and Development (OECD), United Nations, the G8 Dementia Summit (11 December 2013) and the European Union (EU) summit on chronic diseases (3–4 April 2014) organized by the European Commission. Motivated by the huge expected increase of the number of people over 80—expected to double by 2050 increasing from 3ċ9 of the population to 9ċ1% in 2050 across OECD countries and from 4ċ7 to 11ċ3% across 27 EU members1—and of older people with reduced physical and mental abilities, these initiatives focus extensively on promoting ‘Active and Healthy Ageing’ (one of five European Innovation Partnerships in the Europe 2020 Initiatives), protecting the human rights of older persons, preventing and delaying neurodegenerative diseases such as dementia and other chronic diseases and improving quality of life and long-term care for people affected by chronic diseases while ensuring sustainable and affordable health care for everybody. Studying these different policy initiatives, it is highly remarkable how little they focus on the importance and added value of palliative care for older people with chronic and life-threatening diseases, and how small the involvement is of palliative care associations in this existing policy work. This Commentary arguments the need for and potential added value of integrating palliative care in policies on ageing and dementia and highlights the need and timeliness to take action. While the aims of prevention and cure or disease modification are undoubtedly necessary in future research and policy, older people are at high risk of dying with complex and multiple conditions and experiencing significant care needs.1,2 Current health policies have focused extensively on preventing illness, but death is inevitable for everyone and is often preceded by a relatively long period of gradual decline and potential complex symptoms and problems. Epidemiological research has shown that older people clearly have special needs that are different and often more complex than those of younger people, including multiple medical problems of varying severity, several long-term conditions with an increased risk of adverse drug reactions and iatrogenic illness, minor problems that have great cumulative psychological or social impact and acute illnesses that lead to physical or mental impairment, economic hardship and social isolation.3 Currently, dementia still is an incurable and life-limiting illness, and recent research has shown the high level of clinical complications and burdensome symptoms among people dying with dementia.4–6 Although healthy ageing and palliative care seem to refer to different challenges at first glance, healthy ageing includes dealing with the specific needs of older people with functional limitation, frailty and co-morbid diseases and providing a care context ensuring that older people can determine how to live the final years of their lives.2 Although traditionally palliative care was almost exclusively focused on cancer and the end of life, it is since 2002 defined by the WHO as an approach that improves the quality of life of all patients with life-threatening illnesses and their families, focusing on physical, psychosocial and spiritual problems. It is applicable early in the course of illness, in conjunction with other therapies that are intended to prolong life.3 The idea that palliative care is relevant only in the last few weeks of life and concerns a stage that can and should be clearly different from a previous life-prolonging or curative phase, has been replaced with the concept that the palliative care approach should be offered increasingly and gradually alongside curative treatment, to support people with chronic progressive illnesses over many years.3,7 This was also recently reaffirmed by the Worldwide Palliative Care Alliance in the Global Atlas on Palliative Care and the WHO resolution on palliative care.8 Hence, palliative care is not only about dying but also about living well with life-limiting chronic illnesses. Important to recognize is that this approach does not imply that all older people should be treated as ‘palliative’ in terms of dying or in a terminal phase of life, but that they would need to be supported in a way that corresponds to the principles important in a palliative care approach. The core values of such a palliative care approach concern person-centredness, quality of life and dignity, patient autonomy, the provision of needs-based (as opposed to diagnosis-based) compassionate care and coordination and continuity of care, which are all values of great importance for frail older people and people with dementia regardless of whether they are at the very end of their life. Current research in palliative care has also shown the potential b
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“For example, while palliative care can support quality of life and prevent unnecessary transitions, older adults with MLTCiD were rarely referred to these services early in their dementia journey due to a lack of awareness of the benefits for patients with dementia (CMOC10) [59, 64, 85, 86].”
From Do hospital-to-home transitions work for older adults with multiple long-term conditions including dementia? A realist review (2025) · cites this paper as [85]
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“When dementia was diagnosed, limited knowledge often prevented HCPs from effectively planning care or addressing the impact of dementia symptoms on condition management (CMOC9) [46, 51, 54, 73, 74, 77, 83–85].”
From Do hospital-to-home transitions work for older adults with multiple long-term conditions including dementia? A realist review (2025) · cites this paper as [85]
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Cites
Early Palliative Care for Patients with Metastatic Non–Small-Cell Lung Cancer
Temel, J. S., Greer, J. A., Muzikansky, A., Gallagher, E. R., Admane, S., Jackson, V. A., Dahlin, C. M., Blinderman, C. D., Jacobsen, J., Pirl, W. F., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1000678 · Cited by 7,482
Palliative Care Consultation Teams Cut Hospital Costs For Medicaid Beneficiaries
Morrison, R. S., Dietrich, J., Ladwig, S., Quill, T. E., Sacco, J., Tangeman, J. C., & Meier, D. E. (2011) · Health Affairs · doi:10.1377/hlthaff.2010.0929 · Cited by 469
Living Well at the End of Life: Adapting Health Care to Serious Chronic Illness in Old Age
Lynn, J., & Adamson, D. M. (2003) · RAND Corporation eBooks · doi:10.7249/wp137 · Cited by 451
Palliative Care for Older People: Better Practices
Who Regional Office for Europe (2011) · World Health Organization, Regional Office for Europe eBooks · Cited by 220
Interventions for improving palliative care for older people living in nursing care homes
HALL, S. L., Kolliakou, A., Petkova, H., Froggatt, K. A., & Higginson, I. J. (2011) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007132.pub2 · Cited by 160
Vandervoort, A., den Block, L. V., van der Steen, J. T., Volicer, L., Stichele, R. V., Houttekier, D., & Deliëns, L. (2013) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2013.01.016 · Cited by 113
Vandervoort, A., den Block, L. V., van der Steen, J. T., Volicer, L., Stichele, R. V., Houttekier, D., & Deliëns, L. (2012) · VUBIR (Vrije Universiteit Brussel) · Cited by 84
Living Well at the End of Life
Lynn, J., & Adamson, D. M. (2003) · Cited by 53
Older people dying with dementia: a nationwide study
Meeussen, K., den Block, L. V., Echteld, M. A., Boffin, N., Bilsen, J. J. R., Casteren, V. V., & Deliëns, L. (2012) · International Psychogeriatrics · doi:10.1017/s1041610212000865 · Cited by 38
Quality of dying of nursing home residents with dementia as judged by relatives
van Uden, N., den Block, L. V., van der Steen, J. T., Onwuteaka-Philipsen, B. D., Vandervoort, A., Stichele, R. V., & Deliëns, L. (2013) · International Psychogeriatrics · doi:10.1017/s1041610213000756 · Cited by 25
Research works printed but not linked: 1
- 2011, Cochrane database of systematic reviews (Online), 16, CD007132
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Lawson, L., Cooper, M., Tolley, C., Hand, A., & Nazar, H. (2025) · BMC Geriatrics · doi:10.1186/s12877-025-06123-0 · Cited by 10
“When dementia was diagnosed, limited knowledge often prevented HCPs from effectively planning care or addressing the impact of dementia symptoms on condition management (CMOC9) [46, 51, 54, 73, 74, 77, 83–85].”
Metadata
- Authors
- Van den Block, L.
- Venue
- The European Journal of Public Health
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-07-04
- Volume
- 24
- Issue
- 5
- Pages
- 705-706
- ISSN
- 1101-1262 (ISSN-L)
- 1464-360X
- OpenAlex
- W2045538105
- Cited by
- 12
- References
- 10
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 1 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 4
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Journal of Public Health (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Vlaamse regering
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
- Social Sciences › Life-span and Life-course Studies › Aging, Elder Care, and Social Issues
- Keywords
- palliative care, dementia, aging, health policy, active and healthy ageing, older adults, end-of-life care, long-term care, chronic disease, policy integration, quality of life, symptom burden, Europe 2020 strategy, human rights of older persons, iatrogenic disease, social isolation
- MeSH terms
- Aged, 80 and over, Aging, Dementia, European Union, Health Policy, Health Services for the Aged, Health Services Needs and Demand, Humans, Palliative Care
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