View source for Palliative care

{{Short description|Area of healthcare that focuses on relieving and preventing suffering}}
{{cs1 config|name-list-style=vanc|display-authors=6}}
{{Use dmy dates|date=August 2022}}
{{Infobox Occupation
| name = Palliative medicine physician
| image =
| caption =
| official_names =
| type = [[Specialty (medicine)|Specialty]]
| activity_sector = [[Medicine]]
| competencies =
| formation =
* [[Doctor of Medicine]] (M.D.)
* [[Bachelor of Medicine, Bachelor of Surgery]] (e.g. MBBS or MBChB)
* UK: Certificate of Completion of Specialist Training (4 years full-time)
* (US only) [[Doctor of Osteopathic medicine]] (D.O.)
| employment_field = [[Hospital]]s, [[clinic]]s
| related_occupation =
}}
{{wikt | palliative}}

'''Palliative care''' (from Latin root {{Lang|la|[[wikt:palliare|palliare]]}} "to cloak") is an interdisciplinary medical care-giving approach aimed at optimizing [[quality of life]] and mitigating or reducing suffering among people with serious, complex, and often [[Terminal illness|terminal]] illnesses.<ref name="Zhukovsky_2019">{{cite book |title =Primer of Palliative Care | vauthors = Zhukovsky D |publisher =American Association of Hospice and Palliative Medicine|year =2019|isbn =978-1-889296-08-1}}</ref> Many definitions of palliative care exist. 

The [[World Health Organization]] (WHO) describes palliative care as:
<blockquote>[A]n approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial, and spiritual.<ref>{{cite web|url =https://www.who.int/cancer/palliative/definition/en/|archive-url =https://web.archive.org/web/20031004221126/http://www.who.int/cancer/palliative/definition/en/|archive-date =4 October 2003|title =WHO Definition of Palliative Care|website =WHO|access-date =4 December 2019 | quote = Palliative care is an approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual.}}</ref></blockquote> Since the 1990s, many palliative care programs involved a disease-specific approach. However, as the field developed throughout the 2000s, the WHO began to take a broader patient-centered approach that suggests that the principles of palliative care should be applied as early as possible to any chronic and ultimately fatal illness.<ref>{{cite journal | vauthors = Sepúlveda C, Marlin A, Yoshida T, Ullrich A | title = Palliative Care: the World Health Organization's global perspective | journal = Journal of Pain and Symptom Management | volume = 24 | issue = 2 | pages = 91–96 | date = August 2002 | pmid = 12231124 | doi = 10.1016/S0885-3924(02)00440-2 | doi-access = free }}</ref> This shift was important because if a disease-oriented approach is followed, the needs and preferences of the patient are not fully met and aspects of care, such as pain, quality of life, and social support, as well as spiritual and emotional needs, fail to be addressed.<ref>{{Cite journal |last1=Rosa |first1=William E. |last2=Meghan |first2=McDarby |last3=Haley |first3=Buller |last4=Ferrell |first4=Betty R. |date=12 August 2023 |title=Palliative Care Clinician Perspectives on Person-Centered End-of-Life Communication for Racially and Culturally Minoritized Persons with Cancer |journal=Cancers |language=en |volume=15 |issue=16 |page=4076 |doi=10.3390/cancers15164076 |pmid=37627105 |pmc=10452546 |doi-access=free |issn=2072-6694 }}</ref> Rather, a patient-centered model prioritizes relief of suffering and tailors care to increase the quality of life for terminally ill patients.<ref name="Khosla_2012a">{{cite journal |vauthors=Khosla D, Patel FD, Sharma SC |date=September 2012 |title=Palliative care in India: current progress and future needs |journal=Indian Journal of Palliative Care |volume=18 |issue=3 |pages=149–154 |doi=10.4103/0973-1075.105683 |pmc=3573467 |pmid=23439559 |quote="Palliative care improves health care quality in three domains: the relief of physical and emotional suffering; improvement and strengthening of the process of patient–physician communication and decision-making; and assurance of coordinated continuity of care across multiple healthcare settings—hospital, home, hospice, and long-term care." |doi-access=free}}</ref>

Palliative care is appropriate for individuals with serious/chronic illnesses across the age spectrum and can be provided as the main goal of care or in tandem with [[curative treatment]]. It is ideally provided by interdisciplinary [[team]]s which can include physicians, nurses, occupational and physical therapists, psychologists, social workers, chaplains, and dietitians. Palliative care can be provided in a variety of contexts, including but not limited to: hospitals, outpatient clinics, and home settings. Although an important part of [[end-of-life care]], palliative care is not limited to individuals nearing end of life and can be helpful at any stage of a complex or chronic illness.<ref name="Zhukovsky_2019"/><ref>{{Cite web |title=What is Palliative Care? {{!}} Definition of Palliative Care {{!}} Get Palliative Care |url=https://getpalliativecare.org/whatis/ |url-status=live |archive-url=https://web.archive.org/web/20200705054043/https://getpalliativecare.org/whatis/ |archive-date=5 July 2020 |access-date=12 May 2020 |language=en}}</ref>

==Scope==

Palliative care is able to improve healthcare quality in three sectors: Physical and emotional relief, strengthening of patient-physician communication and decision-making, and coordinated continuity of care across various healthcare settings, including hospital, home, and hospice.<ref name="Khosla_2012a"/> The overall goal of palliative care is to improve quality of life of individuals with serious illness, any life-threatening condition which either reduces an individual's daily function <u>or</u> quality of life or increases caregiver burden, through pain and symptom management, identification and support of caregiver needs, and care coordination. Palliative care can be delivered at any stage of illness alongside other treatments with curative or life-prolonging intent and is not restricted to people receiving [[end-of-life care]].<ref name="National Consensus Project for Quality Palliative Care 2018">{{cite web|url=https://www.nationalcoalitionhpc.org/ncp|title=Clinical Practice Guidelines for Quality Palliative Care, 4th edition|last=National Consensus Project for Quality Palliative Care|date=2018|access-date=18 December 2019|archive-date=23 December 2019|archive-url=https://web.archive.org/web/20191223002910/https://www.nationalcoalitionhpc.org/ncp/|url-status=live}}</ref><ref name="Ahluwalia_2018">{{cite journal | vauthors = Ahluwalia SC, Chen C, Raaen L, Motala A, Walling AM, Chamberlin M, O'Hanlon C, Larkin J, Lorenz K, Akinniranye O, Hempel S | title = A Systematic Review in Support of the National Consensus Project Clinical Practice Guidelines for Quality Palliative Care, Fourth Edition | journal = Journal of Pain and Symptom Management | volume = 56 | issue = 6 | pages = 831–870 | date = December 2018 | pmid = 30391049 | doi = 10.1016/j.jpainsymman.2018.09.008 | s2cid = 53217269 | doi-access = free }}</ref> Historically, palliative care services were focused on individuals with incurable [[cancer]], but this framework is now applied to other diseases, including severe [[heart failure]],<ref>{{Cite web|title=Heart failure – palliative care: MedlinePlus Medical Encyclopedia|url=https://medlineplus.gov/ency/patientinstructions/000365.htm|website=medlineplus.gov|language=en|access-date=30 April 2020|archive-date=3 August 2019|archive-url=https://web.archive.org/web/20190803010857/https://medlineplus.gov/ency/patientinstructions/000365.htm|url-status=live}}</ref> [[chronic obstructive pulmonary disease]], [[multiple sclerosis]] and other [[Neurodegenerative Diseases|neurodegenerative]] conditions.<ref>{{cite journal | vauthors = Foley P, Hampton J, Hampton A, Hampton R, Oleksy D, Oliver D, Weller BJ | title = Lesley's story: a case report, and discussion of challenges faced in end-of-life care for progressive neurological disease | journal = Practical Neurology | volume = 12 | issue = 4 | pages = 244–248 | date = August 2012 | pmid = 22869768 | doi = 10.1136/practneurol-2012-000263 | s2cid = 38747721 }}</ref> Forty million people each year are expected to need palliative care, with approximately 78% of this population living in low and middle income countries. However, only 14% of this population is able to receive this kind of care, with a majority in high-income countries, making this an important sector to pay attention to.<ref>{{cite journal | vauthors = Atreya S, Sinha A, Kumar R | title = Integration of primary palliative care into geriatric care from the Indian perspective | journal = Journal of Family Medicine and Primary Care | volume = 11 | issue = 9 | pages = 4913–4918 | date = September 2022 | pmid = 36505579 | pmc = 9731086 | doi = 10.4103/jfmpc.jfmpc_399_22 | doi-access = free }}</ref>

Palliative care can be initiated in a variety of care settings, including emergency rooms, hospitals, hospice facilities, or at home.<ref>{{cite web|title=Hospice and Palliative Medicine Specialty Description|publisher=American Medical Association|url=https://www.ama-assn.org/specialty/hospice-and-palliative-medicine-specialty-description|access-date=22 October 2020|archive-date=27 October 2020|archive-url=https://web.archive.org/web/20201027214423/https://www.ama-assn.org/specialty/hospice-and-palliative-medicine-specialty-description|url-status=live}}</ref> For some severe disease processes, [[Specialty (medicine)|medical specialty]] [[professional organizations]] recommend initiating palliative care at the time of diagnosis or when disease-directed options would not improve a patient's [[prognosis]]. For example, the [[American Society of Clinical Oncology]] recommends that patients with advanced cancer should be "referred to interdisciplinary palliative care teams that provide inpatient and outpatient care early in the course of disease, alongside active treatment of their cancer" within eight weeks of diagnosis.<ref name="National Consensus Project for Quality Palliative Care 2018"/>

Appropriately engaging palliative care providers as a part of patient care improves overall symptom control, quality of life, and family satisfaction of care while reducing overall healthcare costs.<ref>{{cite journal | vauthors = Dy SM, Apostol C, Martinez KA, Aslakson RA | title = Continuity, coordination, and transitions of care for patients with serious and advanced illness: a systematic review of interventions | journal = Journal of Palliative Medicine | volume = 16 | issue = 4 | pages = 436–445 | date = April 2013 | pmid = 23488450 | doi = 10.1089/jpm.2012.0317 | hdl-access = free | hdl = 2027.42/140114 }}</ref><ref>{{cite journal | vauthors = Fawole OA, Dy SM, Wilson RF, Lau BD, Martinez KA, Apostol CC, Vollenweider D, Bass EB, Aslakson RA | title = A systematic review of communication quality improvement interventions for patients with advanced and serious illness | journal = Journal of General Internal Medicine | volume = 28 | issue = 4 | pages = 570–577 | date = April 2013 | pmid = 23099799 | pmc = 3599019 | doi = 10.1007/s11606-012-2204-4 }}</ref>

=== Palliative care vis-à-vis hospice care ===
{{See also|Hospice and palliative medicine|Hospice care in the United States}}

The distinction between palliative care and hospice differs depending on global context. In the United States, the term ''hospice'' refers specifically to a benefit provided by the federal government since 1982. Hospice care services and palliative care programs share similar goals of mitigating unpleasant symptoms, controlling pain, optimizing comfort, and addressing psychological distress. Hospice care focuses on comfort and psychological support and curative therapies are not pursued.<ref>{{Cite web |title=History of Hospice |url=https://www.nhpco.org/hospice-care-overview/history-of-hospice/ |access-date=2023-01-12 |website=NHPCO |language=en-US}}</ref> Under the Medicare Hospice Benefit, individuals certified by two physicians to have less than six months to live (assuming a typical course) have access to specialized hospice services through various insurance programs ([[Medicare (United States)|Medicare]], [[Medicaid]], and most [[health maintenance organizations]] and [[Health insurance in the United States|private insurers]]). An individual's hospice benefits are not revoked if that individual lives beyond a six-month period. In the United States, in order to be eligible for hospice, patients usually forego treatments aimed at cure, unless they are minors. This is to avoid what is called concurrent care, where two different clinicians are billing for the same service. In 2016 a movement began to extend the reach of concurrent care to adults who were eligible for hospice but not yet emotionally prepared to forego curative treatments.<ref>{{Cite web |title=Medicare Care Choices Model (MCCM): The First Two Years {{!}} CMS |url=https://www.cms.gov/newsroom/fact-sheets/medicare-care-choices-model-mccm-first-two-years |access-date=2023-01-12 |website=www.cms.gov}}</ref>

Outside the United States, the term [[hospice]] usually refers to a building or institution that specializes in palliative care. These institutions provide care to patients with end of life and palliative care needs. In the common vernacular outside the United States, hospice care and palliative care are synonymous and are not contingent on different avenues of funding.<ref name="Sibson_2005">{{cite book|title=Handbook of Palliative Care| vauthors = Sibson K, Craig F, Goldman A |publisher=Blackwell Publishing Ltd|year=2005|isbn=978-0-470-75587-7|pages=295–316|chapter=Palliative Care for Children|doi=10.1002/9780470755877.ch15 }}</ref> Over 40% of all dying patients in the United States currently undergo hospice care.<ref name="NHPCO" /> Most of the hospice care occurs at a home environment during the last weeks/months of their lives. Of those patients, 86.6% believe their care is "excellent".<ref name="NHPCO">{{Cite news|title=Hospice Facts & Figures|url=https://www.nhpco.org/research/|website=NHPCO|language=en-US|access-date=12 May 2020|archive-date=21 June 2020|archive-url=https://web.archive.org/web/20200621183013/https://www.nhpco.org/research/|url-status=live}}</ref> Hospice's philosophy is that death is a part of life, so it is personal and unique. Caregivers are encouraged to discuss death with the patients and encourage spiritual exploration (if they so wish).<ref>{{Cite journal| vauthors = Werner D |date=31 January 2011|title=Communicating About Health: Current Issues and Perspectives, by Athena du Pre|journal=Health Communication|volume=26|issue=1|page=110|doi=10.1080/10410236.2011.527626|s2cid=143078786|issn=1041-0236}}</ref>

== History ==
{{Globalize|section|US|date=July 2022}}
The field of palliative care grew out of the hospice movement, which is commonly associated with Dame [[Cicely Saunders]], who founded [[St. Christopher's Hospice]] for the terminally ill in 1967,<ref name="Clark_2007">{{cite journal | vauthors = Clark D | title = From margins to centre: a review of the history of palliative care in cancer | journal = The Lancet. Oncology | volume = 8 | issue = 5 | pages = 430–438 | date = May 2007 | pmid = 17466900 | doi = 10.1016/S1470-2045(07)70138-9 }}</ref> and [[Elisabeth Kübler-Ross]] who published her seminal work "[[Kübler-Ross model|On Death and Dying]]" in 1969.{{citation needed|date=August 2022}} In 1974, [[Balfour Mount]] coined the term "palliative care".<ref name="Clark_2007" /> and [[Paul Henteleff]] became the director of a new "terminal care" unit at [[Saint Boniface Hospital]] in Winnipeg.<ref>{{Cite web|date=29 May 2019|title=Why Quality of Life Matters, Even in Your Final Hours|website=The Walrus|url=https://thewalrus.ca/death-why-quality-of-life-matters-even-in-your-final-hours/|access-date=29 June 2021|archive-date=29 June 2021|archive-url=https://web.archive.org/web/20210629132333/https://thewalrus.ca/death-why-quality-of-life-matters-even-in-your-final-hours/|url-status=live}}</ref> In 1987, Declan Walsh established a palliative medicine service at the [[Cleveland Clinic]] Cancer Center in Ohio which later expanded to become the training site of the first palliative care clinical and research fellowship as well as the first acute pain and palliative care inpatient unit in the United States.<ref>{{cite journal | vauthors = LeGrand SB, Walsh D, Nelson KA, Davis MP | title = A syllabus for fellowship education in palliative medicine | journal = The American Journal of Hospice & Palliative Care | volume = 20 | issue = 4 | pages = 279–289 | date = July 2003 | pmid = 12911073 | doi = 10.1177/104990910302000410 | s2cid = 25125235 }}</ref> The program evolved into The Harry R. Horvitz Center for Palliative Medicine which was designated as an international demonstration project by the [[World Health Organization]] and accredited by the [[European Society for Medical Oncology]] as an Integrated Center of Oncology and Palliative Care.<ref>{{cite journal | vauthors = Goldstein P, Walsh D, Horvitz LU | title = The Cleveland Clinic Foundation Harry R. Horvitz Palliative Care Center | journal = Supportive Care in Cancer | volume = 4 | issue = 5 | pages = 329–333 | date = September 1996 | pmid = 8883225 | doi = 10.1007/bf01788838 | s2cid = 5322289 }}</ref>

Women have played a central role in the historical development of palliative care, particularly through their work in hospice settings, which helped expand services beyond oncology to encompass frail elderly patients.<ref>{{Cite web |last=Silbermann M, Baider L, Saleem A, Gafer N, Tang L, Fadhil AR, Rassouli M, Hassan A, Fernandez-Ortega P, Brant J, Kebudi R, Respini D, Muckaden M.A |date=2018 |title=The overwhelming contribution of women to the development and establishment of palliative care as a recognized medical specialty |url=https://britishjournalofcancerresearch.com/the-overwhelming-contribution-of-women-to-the-development-and-establishment-of-palliative-care-as-a-recognized-medical-specialty |access-date=2025-09-27 |website=British Journal of Cancer Research |language=en}}</ref> These contributions established the foundation for geriatric palliative care as a distinct and expanding domain of global health.

Advances in palliative care have since inspired a dramatic increase in hospital-based palliative care programs. Notable research outcomes forwarding the implementation of palliative care programs include:

* Evidence that hospital palliative care consult teams are associated with significant hospital and overall health system cost savings.<ref>{{cite journal | vauthors = Morrison RS, Penrod JD, Cassel JB, Caust-Ellenbogen M, Litke A, Spragens L, Meier DE | title = Cost savings associated with US hospital palliative care consultation programs | journal = Archives of Internal Medicine | volume = 168 | issue = 16 | pages = 1783–1790 | date = September 2008 | pmid = 18779466 | doi = 10.1001/archinte.168.16.1783 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Kelley AS, Deb P, Du Q, Aldridge Carlson MD, Morrison RS | title = Hospice enrollment saves money for Medicare and improves care quality across a number of different lengths-of-stay | journal = Health Affairs | volume = 32 | issue = 3 | pages = 552–561 | date = March 2013 | pmid = 23459735 | pmc = 3655535 | doi = 10.1377/hlthaff.2012.0851 }}</ref>
* Evidence that palliative care services increase the likelihood of dying at home and reduce symptom burden without impacting on caregiver grief among the vast majority of Americans who prefer to die at home.<ref>{{cite journal | vauthors = Gomes B, Calanzani N, Curiale V, McCrone P, Higginson IJ | title = Effectiveness and cost-effectiveness of home palliative care services for adults with advanced illness and their caregivers | journal = The Cochrane Database of Systematic Reviews | issue = 6 | article-number = CD007760 | date = June 2013 | volume = 2022 | pmid = 23744578 | pmc = 4473359 | doi = 10.1002/14651858.CD007760.pub2 }}</ref>
* Evidence that providing palliative care in tandem with standard oncologic care among patients with advanced cancer is associated with lower rates of depression, increased quality of life, and increased length of survival compared to those receiving standard oncologic care<ref name="Early palliative care for patients">{{cite journal | vauthors = Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, Dahlin CM, Blinderman CD, Jacobsen J, Pirl WF, Billings JA, Lynch TJ | title = Early palliative care for patients with metastatic non-small-cell lung cancer | journal = The New England Journal of Medicine | volume = 363 | issue = 8 | pages = 733–742 | date = August 2010 | pmid = 20818875 | doi = 10.1056/NEJMoa1000678 | s2cid = 1128078 | doi-access = free }}</ref><ref name="ReferenceA">{{cite journal |vauthors=Hoerger M, Wayser GR, Schwing G, Suzuki A, Perry LM |date=June 2019 |title=Impact of Interdisciplinary Outpatient Specialty Palliative Care on Survival and Quality of Life in Adults With Advanced Cancer: A Meta-Analysis of Randomized Controlled Trials |journal=Annals of Behavioral Medicine |volume=53 |issue=7 |pages=674–685 |doi=10.1093/abm/kay077 |pmc=6546936 |pmid=30265282}}</ref> and may even prolong survival.<ref name="Early palliative care for patients"/>

Over 90% of US hospitals with more than 300 beds have palliative care teams, yet only 17% of rural hospitals with 50 or more beds have palliative care teams.<ref>America's Care of Serious Illness: A State-by-State Report Card on Access to Palliative Care in Our Nation's Hospitals. Center to Advance Palliative Care and the National Palliative Care Research Center. September 2019.</ref> [[Hospice and palliative medicine]] has been a board certified sub-specialty of medicine in the United States since 2006. Additionally, in 2011, The [[Joint Commission]] began an Advanced Certification Program for Palliative Care that recognizes hospital inpatient programs demonstrating outstanding care and enhancement of the quality of life for people with serious illness.<ref>"Advanced Certification for Palliative Care Programs". Joint Commission. 30 April 2014. Retrieved 17 August 2014.</ref>

== Practice of palliative care ==
{{Further|End-of-life care}}Medications used in palliative care can be common medications but used for a different indication based on established practices with varying degrees of evidence.<ref>{{cite journal |vauthors=Currow D, Agar MR, Abernethy AP |date=2011 |title=Tackling the Challenges of Clinical Trials in Palliative Care |url=http://adisonline.com/pharmaceuticalmedicine/Abstract/2011/25010/Tackling_the_Challenges_of_Clinical_Trials_in.2.aspx |url-status=live |journal=Pharm Med |volume=25 |issue=1 |pages=7–15 |doi=10.1007/bf03256842 |s2cid=34967878 |archive-url=https://web.archive.org/web/20120111162932/http://adisonline.com/pharmaceuticalmedicine/Abstract/2011/25010/Tackling_the_Challenges_of_Clinical_Trials_in.2.aspx |archive-date=11 January 2012 |access-date=1 June 2011}}</ref> Examples include the use of antipsychotic medications, anticonvulsants, and morphine. Routes of administration may differ from acute or chronic care, as many people in palliative care lose the ability to swallow. A common alternative route of administration is subcutaneous, as it is less traumatic and less difficult to maintain than intravenous medications. Other routes of administration include sublingual, intramuscular and transdermal. Medications are often managed at home by family or nursing support.<ref>{{cite web |title=Palliative Medications |url=http://www.caresearch.com.au/caresearch/ProfessionalGroups/NursesHubHome/Clinical/MedicationManagement/PalliativeMedications/tabid/1554/Default.aspx |url-status=live |archive-url=https://web.archive.org/web/20110220102234/http://www.caresearch.com.au/caresearch/ProfessionalGroups/NursesHubHome/Clinical/MedicationManagement/PalliativeMedications/tabid/1554/Default.aspx |archive-date=20 February 2011 |access-date=28 October 2010 |work=Caresearch: Palliative care knowledge network}}</ref>

Palliative care interventions in care homes may contribute to lower discomfort for residents with dementia and to improve family members' views of the quality of care.<ref name="Hall_2011">{{cite journal |vauthors=Hall S, Kolliakou A, Petkova H, Froggatt K, Higginson IJ |date=March 2011 |title=Interventions for improving palliative care for older people living in nursing care homes |journal=The Cochrane Database of Systematic Reviews |volume=2011 |issue=3 |article-number=CD007132 |doi=10.1002/14651858.CD007132.pub2 |pmc=6494579 |pmid=21412898}}</ref> However, higher quality research is needed to support the benefits of these interventions for older people dying in these facilities.<ref name="Hall_2011" /><ref>{{cite journal |vauthors=Bajwah S, Oluyase AO, Yi D, Gao W, Evans CJ, Grande G, Todd C, Costantini M, Murtagh FE, Higginson IJ |date=September 2020 |title=The effectiveness and cost-effectiveness of hospital-based specialist palliative care for adults with advanced illness and their caregivers |journal=The Cochrane Database of Systematic Reviews |volume=2020 |issue=9 |article-number=CD012780 |doi=10.1002/14651858.CD012780.pub2 |pmc=8428758 |pmid=32996586}}</ref>

High-certainty evidence supports the finding that implementation of home-based end-of-life care programs may increase the number of adults who will die at home and slightly improve patient satisfaction at a one-month follow-up.<ref name="Shepperd_2021">{{cite journal |vauthors=Shepperd S, Gonçalves-Bradley DC, Straus SE, Wee B |date=March 2021 |title=Hospital at home: home-based end-of-life care |journal=The Cochrane Database of Systematic Reviews |volume=3 |issue=3 |article-number=CD009231 |doi=10.1002/14651858.CD009231.pub3 |pmc=8092626 |pmid=33721912}}</ref> The impact of home-based end-of-life care on caregivers, healthcare staff, and health service costs are uncertain.<ref name="Shepperd_2021" />

=== Pain, distress, and anxiety ===
{{See also|Analgesic|Psychologist}}
{{See also|Distress in cancer caregiving}}
For many patients, end of life care can cause emotional and psychological distress, contributing to their total suffering.<ref>{{cite journal | vauthors = Strang P, Strang S, Hultborn R, Arnér S | title = Existential pain—an entity, a provocation, or a challenge? | journal = Journal of Pain and Symptom Management | volume = 27 | issue = 3 | pages = 241–250 | date = March 2004 | pmid = 15010102 | doi = 10.1016/j.jpainsymman.2003.07.003 | doi-access = free }}</ref> An interdisciplinary palliative care team consisting of a mental health professional, [[social worker]], [[Mental health counselor|counselor]], as well as spiritual support such as a [[chaplain]], can play important roles in helping people and their families cope using various methods such as counseling, visualization, cognitive methods, drug therapy and [[Relaxation technique|relaxation therapy]] to address their needs. Palliative pets can play a role in this last category.<ref>Kathryn Batson et al. "The Effect of a Therapy Dog on Socialization and Physiological Indicators of Stress in Persons Diagnosed with Alzheimer's Disease" in 'Companion Animals in Human Health' Editors – Cindy C. Wilson and Dennis C. Turner, Sage Publications 1998, {{ISBN|0-7619-1062-X}}</ref>

'''Total pain'''

In the 1960s, hospice pioneer [[Cicely Saunders]] first introduced the term "total pain" to describe the heterogenous nature of pain.<ref>{{Cite journal| vauthors = Saunders C |date=14 February 1964|title=Care of patients suffering from terminal illness at St Joseph's Hospice, Hackney, London|journal=Nursing Mirror|pages=vii–x}}</ref>  This is the idea that a patient's experience of total pain has distinctive roots in the physical, psychological, social and spiritual realm but that they are all still closely linked to one another. Identifying the cause of pain can help guide care for some patients, and impact their quality of life overall.<ref name="Rome_2011">{{cite journal | vauthors = Rome RB, Luminais HH, Bourgeois DA, Blais CM | title = The role of palliative care at the end of life | journal = The Ochsner Journal | volume = 11 | issue = 4 | pages = 348–352 | date = 2011 | pmid = 22190887 | pmc = 3241069 }}</ref>

==== Physical pain ====

Physical pain can be managed using pain medications as long as they do not put the patient at further risk for developing or increasing medical diagnoses such as heart problems or difficulty breathing.<ref name="Rome_2011" /> Patients at the end of life can exhibit many physical symptoms that can cause extreme pain such as dyspnea<ref>{{Cite web|title=Palliative care – shortness of breath: MedlinePlus Medical Encyclopedia|url=https://medlineplus.gov/ency/patientinstructions/000471.htm|website=medlineplus.gov|language=en|access-date=30 April 2020|archive-date=5 June 2020|archive-url=https://web.archive.org/web/20200605103924/https://medlineplus.gov/ency/patientinstructions/000471.htm|url-status=live}}</ref> (or difficulty breathing), coughing, [[xerostomia]] (dry mouth), nausea and vomiting, constipation, fever, [[delirium]], and excessive oral and pharyngeal secretions ("[[Death rattle|Death Rattle]]").<ref>{{cite journal | vauthors = Blinderman CD, Billings JA | title = Comfort Care for Patients Dying in the Hospital | journal = The New England Journal of Medicine | volume = 373 | issue = 26 | pages = 2549–2561 | date = December 2015 | pmid = 26699170 | doi = 10.1056/NEJMra1411746 | doi-access = free }}</ref>
Radiation is commonly used with palliative intent to alleviate pain in patients with cancer. As an effect from radiation may take days to weeks to occur, patients dying a short time following their treatment are unlikely to receive benefit.<ref name="pmid32592442">{{cite journal | vauthors = Kain M, Bennett H, Yi M, Robinson B, James M | title = 30-day mortality following palliative radiotherapy | journal = Journal of Medical Imaging and Radiation Oncology | volume = 64 | issue = 4 | pages = 570–579 | date = August 2020 | pmid = 32592442 | doi = 10.1111/1754-9485.13073 | s2cid = 220119083 }}</ref>

==== Psychosocial pain and anxiety ====

Once the immediate physical pain has been dealt with, it is important to remember to be a compassionate and empathetic caregiver that is there to listen and be there for their patients. Being able to identify the distressing factors in their life other than the pain can help them be more comfortable.<ref name="Kelley_2015">{{cite journal | vauthors = Kelley AS, Morrison RS | title = Palliative Care for the Seriously Ill | journal = The New England Journal of Medicine | volume = 373 | issue = 8 | pages = 747–755 | date = August 2015 | pmid = 26287850 | pmc = 4671283 | doi = 10.1056/nejmra1404684 }}</ref> When a patient has their needs met then they are more likely to be open to the idea of hospice or treatments outside comfort care. Having a psychosocial assessment allows the medical team to help facilitate a healthy patient-family understanding of adjustment, coping and support. This communication between the medical team and the patients and family can also help facilitate discussions on the process of maintaining and enhancing relationships, finding meaning in the dying process, and achieving a sense of control while confronting and preparing for death.<ref name="Rome_2011" /> For adults with anxiety, medical evidence in the form of high-quality randomized trials is insufficient to determine the most effective treatment approach to reduce the symptoms of anxiety.<ref>{{cite journal | vauthors = Salt S, Mulvaney CA, Preston NJ | title = Drug therapy for symptoms associated with anxiety in adult palliative care patients | journal = The Cochrane Database of Systematic Reviews | volume = 5 | issue = 6 | article-number = CD004596 | date = May 2017 | pmid = 28521070 | pmc = 6481598 | doi = 10.1002/14651858.CD004596.pub3 }}</ref>

==== Spirituality ====

Among spiritual persons, spirituality is typically considered a fundamental component of palliative care. Hospice facilities where palliative care is administered usually have available chaplains.

According to the Clinical Practice Guidelines for Quality Palliative Care, spirituality is a "dynamic and intrinsic aspect of humanity" and has been associated with "an improved quality of life for those with chronic and serious illness", especially for patients who are living with incurable and advanced illnesses of a chronic nature.<ref name="dupeRef1">{{cite journal | vauthors = Silva RS, Caldeira S, Coelho AN, Apóstolo JL | title = Forgiveness facilitation in palliative care: a scoping review | journal = JBI Evidence Synthesis | volume = 18 | issue = 11 | pages = 2196–2230 | date = November 2020 | pmid = 32813428 | doi = 10.11124/JBISRIR-D-19-00286 | s2cid = 221179683 }}</ref><ref>{{cite journal | vauthors = Puchalski CM, Vitillo R, Hull SK, Reller N | title = Improving the spiritual dimension of whole person care: reaching national and international consensus | journal = Journal of Palliative Medicine | volume = 17 | issue = 6 | pages = 642–656 | date = June 2014 | pmid = 24842136 | pmc = 4038982 | doi = 10.1089/jpm.2014.9427 }}</ref><ref>{{cite journal | vauthors = Thuné-Boyle IC, Stygall JA, Keshtgar MR, Newman SP | title = Do religious/spiritual coping strategies affect illness adjustment in patients with cancer? A systematic review of the literature | journal = Social Science & Medicine | volume = 63 | issue = 1 | pages = 151–164 | date = July 2006 | pmid = 16427173 | doi = 10.1016/j.socscimed.2005.11.055 }}</ref> Spiritual beliefs and practices can influence perceptions of pain and distress, as well as quality of life among advanced cancer patients.<ref name="Kelley_2015" /> Spiritual needs are often described in literature as including loving/being loved, forgiveness, and deciphering the meaning of life.<ref>McSherry W, Smith J. Spiritual care. In: McSherry W, McSherry R, Watson R, editors. In care in nursing – principles, values and skills. New York: Oxford University Press, 2012;117–31.</ref><ref name="dupeRef2">{{cite journal | vauthors = Vilalta A, Valls J, Porta J, Viñas J | title = Evaluation of spiritual needs of patients with advanced cancer in a palliative care unit | journal = Journal of Palliative Medicine | volume = 17 | issue = 5 | pages = 592–600 | date = May 2014 | pmid = 24745870 | pmc = 4012638 | doi = 10.1089/jpm.2013.0569 }}</ref>

Most spiritual interventions are subjective and complex.<ref>{{cite journal | vauthors = Weathers E, McCarthy G, Coffey A | title = Concept Analysis of Spirituality: An Evolutionary Approach | journal = Nursing Forum | volume = 51 | issue = 2 | pages = 79–96 | date = April 2016 | pmid = 25644366 | doi = 10.1111/nuf.12128 | doi-access = free }}</ref><ref name="dupeRef1" /> Many have not been well evaluated for their effectiveness, however tools can be used to measure and implement effective spiritual care.<ref name="dupeRef1" /><ref name="dupeRef2" /><ref>{{cite journal | vauthors = Candy B, Jones L, Varagunam M, Speck P, Tookman A, King M | title = Spiritual and religious interventions for well-being of adults in the terminal phase of disease | journal = The Cochrane Database of Systematic Reviews | issue = 5 | article-number = CD007544 | date = May 2012 | pmid = 22592721 | doi = 10.1002/14651858.CD007544.pub2 }}</ref>

==== Nausea and vomiting ====

Nausea and vomiting are common in people who have advanced terminal illness and can cause distress. Several [[antiemetic]] pharmacologic options are suggested to help alleviate these symptoms. For people who do not respond to first-line medications, [[levomepromazine]] may be used, however there have been insufficient clinical trials to assess the effectiveness of this medication.<ref>{{cite journal | vauthors = Cox L, Darvill E, Dorman S | title = Levomepromazine for nausea and vomiting in palliative care | journal = The Cochrane Database of Systematic Reviews | issue = 11 | article-number = CD009420 | date = November 2015 | volume = 2017 | pmid = 26524693 | pmc = 6481825 | doi = 10.1002/14651858.CD009420.pub3 }}</ref> [[Haloperidol]] and [[droperidol]] are other medications that are sometimes prescribed to help alleviate nausea and vomiting, however further research is also required to understand how effective these medications may be.<ref>{{cite journal | vauthors = Murray-Brown F, Dorman S | title = Haloperidol for the treatment of nausea and vomiting in palliative care patients | journal = The Cochrane Database of Systematic Reviews | volume = 2020 | issue = 11 | article-number = CD006271 | date = November 2015 | pmid = 26524474 | pmc = 6481565 | doi = 10.1002/14651858.CD006271.pub3 }}</ref><ref>{{cite journal | vauthors = Storrar J, Hitchens M, Platt T, Dorman S | title = Droperidol for treatment of nausea and vomiting in palliative care patients | journal = The Cochrane Database of Systematic Reviews | issue = 11 | article-number = CD006938 | date = November 2014 | volume = 2014 | pmid = 25429434 | pmc = 7265628 | doi = 10.1002/14651858.CD006938.pub3 }}</ref>

==== Hydration and nutrition ====

Many terminally ill people cannot consume adequate food or drink. Providing medically assisted food or drink to prolong their life and improve the quality of their life is common, however there have been few high quality studies to determine best practices and the effectiveness of these approaches.<ref>{{cite journal | vauthors = Buchan EJ, Haywood A, Syrmis W, Good P | title = Medically assisted hydration for adults receiving palliative care | journal = The Cochrane Database of Systematic Reviews | volume = 2023 | issue = 12 | article-number = CD006273 | date = December 2023 | pmid = 38095590 | pmc = 10720602 | doi = 10.1002/14651858.CD006273.pub4 }}</ref><ref>{{cite journal | vauthors = Good P, Richard R, Syrmis W, Jenkins-Marsh S, Stephens J | title = Medically assisted nutrition for adult palliative care patients | journal = The Cochrane Database of Systematic Reviews | volume = 2014 | issue = 4 | article-number = CD006274 | date = April 2014 | pmid = 24760679 | pmc = 7388544 | doi = 10.1002/14651858.CD006274.pub3 }}</ref>

==== Symptom assessment ====
{{anchor|ESAS}}
One instrument used in palliative care is the ''Edmonton Symptom Assessment Scale'' (ESAS), which consists of eight [[visual analog scale]]s (VAS) ranging from 0–10, indicating the levels of [[pain]], activity, [[nausea]], [[Depression (mood)|depression]], [[anxiety]], [[drowsiness]], [[appetite]], sensation of [[well-being]], and sometimes [[shortness of breath]].<ref name="ontario">[https://www.cancercare.on.ca/common/pages/UserFile.aspx?fileId=13262 Edmonton Symptom Assessment System (ESAS)] {{Webarchive|url=https://web.archive.org/web/20170731000248/https://www.cancercare.on.ca/common/pages/UserFile.aspx?fileId=13262|date=31 July 2017}} from Cancer Care Ontario. Revised 2005 February</ref><ref name="Bruera1991">{{cite journal |vauthors=Bruera E, Kuehn N, Miller MJ, Selmser P, Macmillan K |date=1991 |title=The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients |journal=Journal of Palliative Care |volume=7 |issue=2 |pages=6–9 |doi=10.1177/082585979100700202 |pmid=1714502 |s2cid=26165154}}</ref> A score of 0 indicates absence of the symptom, and a score of 10 indicates the worst possible severity.<ref name="ontario" /> The instrument can be completed by the patient, with or without assistance, or by nurses and relatives.<ref name="Bruera1991" />

=== Pediatric palliative care ===
{{See also|Analgesic|Psychologist}}
Pediatric palliative care is family-centered, specialized medical care for children with serious illnesses that focuses on mitigating the physical, emotional, psychosocial, and spiritual suffering associated with illness to ultimately optimize quality of life.

Pediatric palliative care practitioners receive specialized training in family-centered, developmental and age-appropriate skills in communication and facilitation of shared decision making; assessment and management of pain and distressing symptoms; advanced knowledge in care coordination of multidisciplinary pediatric caregiving medical teams; referral to hospital and [[Ambulatory care|ambulatory]] resources available to patients and families; and psychologically supporting children and families through illness and [[Grief|bereavement]].<ref name="Faull_2005">{{Cite book|title=Handbook of palliative care|date=2005|publisher=Blackwell Pub| vauthors = Faull C, Carter Y, Daniels L |isbn=978-0-470-75587-7|edition=2nd|location=Malden, MA|oclc=212125356}}</ref>

==== Symptoms assessment and management of children ====
As with palliative care for adults, symptom assessment and management is a critical component of pediatric palliative care as it improves quality of life, gives children and families a sense of control, and prolongs life in some cases.<ref name="Sibson_2005" /> The general approach to assessment and management of distressing symptoms in children by a palliative care team is as follows:

* Identify and assess symptoms through history taking (focusing on location, quality, time course, as well as exacerbating and mitigating stimuli). Symptoms assessment in children is uniquely challenging due to communication barriers depending on the child's ability to identify and communicate about symptoms. Thus, both the child and caregivers should provide the [[Medical history|clinical history]]. With this said, children as young as four years of age can indicate the location and severity of pain through visual mapping techniques and metaphors.<ref>{{cite journal | vauthors = Savedra MC, Tesler MD, Holzemer WL, Wilkie DJ, Ward JA | title = Pain location: validity and reliability of body outline markings by hospitalized children and adolescents | journal = Research in Nursing & Health | volume = 12 | issue = 5 | pages = 307–314 | date = October 1989 | pmid = 2798951 | doi = 10.1002/nur.4770120506 }}</ref>
* Perform a thorough [[Physical examination|exam]] of the child. Special attention to the child's behavioral response to exam components, particularly in regards to potentially [[Pain management in children|painful stimuli]]. A commonly held myth is that premature and neonatal infants do not experience pain due to their immature pain pathways, but research demonstrates pain perception in these age groups is equal or greater than that of adults.<ref>{{cite journal | vauthors = Anand KJ, Hickey PR | title = Pain and its effects in the human neonate and fetus | journal = The New England Journal of Medicine | volume = 317 | issue = 21 | pages = 1321–1329 | date = November 1987 | pmid = 3317037 | doi = 10.1097/00132586-198808000-00042 }}</ref><ref>{{Cite book|title=Pain in infants, children, and adolescents|date=2003|publisher=Lippincott Williams & Wilkins| vauthors = Schechter N, Berde CB, Yaster M |isbn=978-0-7817-2644-3|edition=2nd|location=Philadelphia|oclc=808596673}}</ref> With this said, some children experiencing intolerable pain present with 'psychomotor inertia', a phenomenon where a child in severe chronic pain presents overly well behaved or depressed.<ref>{{cite journal | vauthors = Gauvain-Piquard A, Rodary C, Rezvani A, Serbouti S | title = The development of the DEGR(R): A scale to assess pain in young children with cancer | journal = European Journal of Pain | volume = 3 | issue = 2 | pages = 165–176 | date = June 1999 | pmid = 10700346 | doi = 10.1053/eujp.1999.0118 | s2cid = 14580922 }}</ref> These patients demonstrate behavioral responses consistent with pain relief when titrated with [[morphine]]. Finally, because children behaviorally respond to pain atypically, a playing or sleeping child should not be assumed to be without pain.<ref name="Sibson_2005" />
* Identify the place of treatment ([[Tertiary referral hospital|tertiary]] versus local hospital, [[intensive care unit]], home, [[hospice]], etc.).
* Anticipate symptoms based on the typical disease course of the [[Medical diagnosis|hypothesized diagnosis]].
* Present treatment options to the family proactively, based on care options and resources available in each of the aforementioned care settings. Ensuing management should anticipate [[Transitional care|transitions]] of palliative care settings to afford seamless continuity of service provision across health, education, and social care settings.
* Consider both pharmacologic and non-pharmacologic treatment modalities (education and mental health support, administration of hot and cold packs, [[massage]], [[play therapy]], [[Distraction|distraction therapy]], [[hypnotherapy]], [[physical therapy]], [[occupational therapy]], and [[Alternative medicine|complementary therapies]]) when addressing distressing symptoms. [[Respite care]] is an additional practice that can further aid alleviating the physical and mental pain from the child and their family. By allowing the caregiving to ensue by other qualified individuals, it allows the family time to rest and renew themselves<ref>{{Cite journal|last=Committee on Bioethics|date=August 2000|title=Palliative Care for Children|journal=American Academy of Pediatrics}}</ref>
* Assess how the child perceives their symptoms (based on personal views) to create individualized care plans.
* After the implementation of therapeutic interventions, involve both the child and family in the reassessment of symptoms.<ref name="Sibson_2005" />

The most common symptoms in children with severe chronic disease appropriate for palliative care consultation are weakness, fatigue, pain, poor appetite, weight loss, agitation, lack of mobility, shortness of breath, nausea and vomiting, constipation, sadness or depression, drowsiness, difficulty with speech, headache, excess secretions, anemia, pressure area problems, anxiety, fever, and mouth sores.<ref>{{cite journal | vauthors = Wolfe J, Grier HE, Klar N, Levin SB, Ellenbogen JM, Salem-Schatz S, Emanuel EJ, Weeks JC | title = Symptoms and suffering at the end of life in children with cancer | journal = The New England Journal of Medicine | volume = 342 | issue = 5 | pages = 326–333 | date = February 2000 | pmid = 10655532 | doi = 10.1056/NEJM200002033420506 | doi-access = free }}</ref><ref>{{cite book | vauthors = ((World Health Organization)) | year = 2012 | title = The selection and use of essential medicines: report of the WHO Expert Committee, March 2011 (including the 17th WHO model list of essential medicines and the 3rd WHO model list of essential medicines for children) | publisher = World Health Organization | location = Geneva | author-link = World Health Organization | hdl = 10665/44771 | id = WHO technical report series;965 | hdl-access=free | isbn = 978-92-4-120965-6 | issn = 0512-3054 }}</ref> The most common end of life symptoms in children include shortness of breath, cough, fatigue, pain, nausea and vomiting, agitation and anxiety, poor concentration, skin lesions, swelling of the extremities, [[Epileptic seizure|seizures]], poor appetite, difficulty with feeding, and diarrhea.<ref>{{Cite journal| vauthors = Stockman JA |date=Jan 2008|title=Symptoms Affecting Children With Malignancies During the Last Month of Life: A Nationwide Follow-up|journal=Yearbook of Pediatrics|language=en|volume=2008|pages=448–449|doi=10.1016/S0084-3954(08)70519-0}}</ref><ref>{{cite journal | vauthors = Drake R, Frost J, Collins JJ | title = The symptoms of dying children | journal = Journal of Pain and Symptom Management | volume = 26 | issue = 1 | pages = 594–603 | date = July 2003 | pmid = 12850642 | doi = 10.1016/S0885-3924(03)00202-1 | doi-access = free }}</ref> In older children with neurologic and neuromuscular manifestations of disease, there is a high burden of anxiety and depression that correlates with disease progression, increasing disability, and greater dependence on carers.<ref>{{cite journal | vauthors = Hilton T, Orr RD, Perkin RM, Ashwal S | title = End of life care in Duchenne muscular dystrophy | journal = Pediatric Neurology | volume = 9 | issue = 3 | pages = 165–177 | date = May 1993 | pmid = 8352847 | doi = 10.1016/0887-8994(93)90080-V }}</ref> From the caregiver's perspective, families find changes in behavior, reported pain, lack of appetite, changes in appearance, talking to God or angels, breathing changes, weakness, and fatigue to be the most distressing symptoms to witness in their loved ones.<ref>{{cite journal | vauthors = Pritchard M, Burghen E, Srivastava DK, Okuma J, Anderson L, Powell B, Furman WL, Hinds PS | title = Cancer-related symptoms most concerning to parents during the last week and last day of their child's life | journal = Pediatrics | volume = 121 | issue = 5 | pages = e1301–e1309 | date = May 2008 | pmid = 18450873 | doi = 10.1542/peds.2007-2681 | s2cid = 207160955 }}</ref>

As discussed above, within the field of adult palliative medicine, validated symptoms assessment tools are frequently utilized by providers, but these tools lack essential aspects of children's symptom experience.<ref>{{cite journal | vauthors = Woodgate RL, Degner LF, Yanofsky R | title = A different perspective to approaching cancer symptoms in children | journal = Journal of Pain and Symptom Management | volume = 26 | issue = 3 | pages = 800–817 | date = September 2003 | pmid = 12967729 | doi = 10.1016/S0885-3924(03)00285-9 | doi-access = free | author-link = Roberta Woodgate }}</ref> Within pediatrics, there is not a comprehensive symptoms assessment widely employed. A few symptoms assessment tools trialed among older children receiving palliative care include the Symptom Distress Scale, and the Memorial Symptom Assessment Scale, and Childhood Cancer Stressors Inventory.<ref>{{cite journal | vauthors = Hinds PS, Quargnenti AG, Wentz TJ | title = Measuring symptom distress in adolescents with cancer | journal = Journal of Pediatric Oncology Nursing | volume = 9 | issue = 2 | pages = 84–86 | date = April 1992 | pmid = 1596393 | doi = 10.1177/104345429200900238 | s2cid = 34253777 }}</ref><ref>{{cite journal | vauthors = Collins JJ, Byrnes ME, Dunkel IJ, Lapin J, Nadel T, Thaler HT, Polyak T, Rapkin B, Portenoy RK | title = The measurement of symptoms in children with cancer | journal = Journal of Pain and Symptom Management | volume = 19 | issue = 5 | pages = 363–377 | date = May 2000 | pmid = 10869877 | doi = 10.1016/S0885-3924(00)00127-5 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Hockenberry-Eaton M, Manteuffel B, Bottomley S | title = Development of two instruments examining stress and adjustment in children with cancer | journal = Journal of Pediatric Oncology Nursing | volume = 14 | issue = 3 | pages = 178–185 | date = July 1997 | pmid = 9260409 | doi = 10.1016/S1043-4542(97)90054-0 }}</ref> Quality of life considerations within pediatrics are unique and an important component of symptoms assessment. The Pediatric Cancer Quality of Life Inventory-32 (PCQL-32) is a standardized parent-proxy report which assesses cancer treatment-related symptoms (focusing mainly on pain and nausea). But again, this tool does not comprehensively assess all palliative are symptoms issues.<ref name="pmid9591169">{{cite journal | vauthors = Varni JW, Katz ER, Seid M, Quiggins DJ, Friedman-Bender A, Castro CM | title = The Pediatric Cancer Quality of Life Inventory (PCQL). I. Instrument development, descriptive statistics, and cross-informant variance | journal = Journal of Behavioral Medicine | volume = 21 | issue = 2 | pages = 179–204 | date = April 1998 | pmid = 9591169 | doi = 10.1023/a:1018779908502 | s2cid = 23995360 }}</ref><ref>{{Cite report |title=Pediatric Quality of Life Inventory 4.0 Generic Core Scales| vauthors = Varni JW, Seid M, Kurtin PS|date=2001 |doi = 10.1037/t54487-000}}</ref> Symptom assessment tools for younger age groups are rarely utilized as they have limited value, especially for infants and young children who are not at a developmental stage where they can articulate symptoms.

==== Communication with children and families ====
Within the realm of pediatric medical care, the palliative care team is tasked with facilitating family-centered communication with children and their families, as well as multidisciplinary pediatric caregiving medical teams to forward coordinated medical management and the child's quality of life.<ref name="Communicating with children and fam">{{cite journal | vauthors = Levetown M | title = Communicating with children and families: from everyday interactions to skill in conveying distressing information | journal = Pediatrics | volume = 121 | issue = 5 | pages = e1441–e1460 | date = May 2008 | pmid = 18450887 | doi = 10.1542/peds.2008-0565 | doi-access = free }}</ref> Strategies for communication are complex as the pediatric palliative care practitioners must facilitate a shared understanding of and consensus for goals of care and therapies available to the sick child amongst multiple medical teams who often have different areas of expertise. Additionally, pediatric palliative care practitioners must assess both the sick child and their family's understanding of complex illness and options for care, and provide accessible, thoughtful education to address knowledge gaps and allow for informed decision making. Finally, practitioners are supporting children and families in the queries, emotional distress, and decision making that ensues from the child's illness.

Many frameworks for communication have been established within the medical literature, but the field of pediatric palliative care is still in relative infancy. Communication considerations and strategies employed in a palliative setting include:

* '''Developing supportive relationships with patients and families.''' An essential component of a provider's ability to provide individualized palliative care is their ability to obtain an intimate understanding of the child and family's preferences and overall character. On initial consultation, palliative care providers often focus on affirming a caring relationship with the pediatric patient and their family by first asking the child how they would describe themself and what is important to them, communicating in an age and developmentally cognizant fashion. The provider may then gather similar information from the child's caregivers. Questions practitioners may ask include 'What does the child enjoy doing? What do they most dislike doing? What does a typical day look like for the child?' Other topics potentially addressed by the palliative care provider may also include familial rituals as well as spiritual and religious beliefs, life goals for the child, and the meaning of illness within the broader context of the child and their family's life.<ref name="Faull_2005" />
* '''Developing a shared understanding of the child's condition with the patient and their family.''' The establishment of shared knowledge between medical providers, patients, and families is essential when determining palliative goals of care for pediatric patients. Initially, practitioners often elicit information from the patient ''and'' child to ascertain these parties' baseline understanding of the child's situation.<ref name="Garwick_1995">{{cite journal | vauthors = Garwick AW, Patterson J, Bennett FC, Blum RW | title = Breaking the news. How families first learn about their child's chronic condition | journal = Archives of Pediatrics & Adolescent Medicine | volume = 149 | issue = 9 | pages = 991–997 | date = September 1995 | pmid = 7655604 | doi = 10.1001/archpedi.1995.02170220057008 }}</ref> Assessing for baseline knowledge allows the palliative care provider to identify knowledge gaps and provide education on those topics. Through this process, families can pursue informed, shared medical decision making regarding their child's care. A framework often employed by pediatric palliative care providers is 'ask, tell, ask' where the provider asks the patient and their family for a question to identify their level of comprehension of the situation, and then subsequently supplements the family's knowledge with additional expert knowledge.<ref name="Garwick_1995" /><ref name="baile">{{cite journal | vauthors = Baile WF, Buckman R, Lenzi R, Glober G, Beale EA, Kudelka AP | title = SPIKES-A six-step protocol for delivering bad news: application to the patient with cancer | journal = The Oncologist | volume = 5 | issue = 4 | pages = 302–311 | date = 2 March 2000 | pmid = 10964998 | doi = 10.1634/theoncologist.5-4-302 | doi-access = free }}</ref> This information is often conveyed without jargon or euphemism to maintain trust and ensure understanding. Providers iteratively check for comprehension of this knowledge supplementation by asking questions related to previous explanations, as information retention can be challenging when undergoing a stressful experience.<ref name="Garwick_1995" />
* '''Establishing meaning and dignity regarding the child's illness.''' As part of developing a shared understanding of a child's illness and character, palliative providers will assess both the child and their family's symbolic and emotional relationship to disease. As both the somatic and psychologic implications of illness can be distressing to children, palliative care practitioners look for opportunities to establish meaning and dignity regarding the child's illness by contextualizing disease within a broader framework of the child's life.<ref name="Chochinov_2012">{{Cite book|title=Dignity therapy: final words for final days | vauthors = Chochinov HM |date=2012|publisher=Oxford University Press|isbn=978-0-19-517621-6|location=Oxford|oclc=714030350}}</ref><ref name="Cassell_2004">{{Cite book|title=The nature of suffering and the goals of medicine | vauthors = Cassell EJ | date=2004|publisher=Oxford University Press|isbn=1-60256-743-3|edition=2nd|location=New York|oclc=173843216}}</ref> Derived from the fields of [[Harvey Chochinov|dignity therapy]] and [[William Breitbart|meaning-centered psychotherapy]], the palliative care provider may explore the following questions with the sick child and their family:
** What gives your life meaning, worth, or purpose?
** Where do you find strength and support?
** What inspires you?
** How do you like to be thought of?
** What are you most proud of?
** What are the particular things you would like your family to know or remember about you?
** When was the last time you laughed really hard?
** Are you frightened by all of this? What, in particular, are you most frightened of?
** What is the meaning of this (illness) experience for you? Do you ever think about why this happened to you?<ref name="Chochinov_2012" /><ref name="Cassell_2004" />
* '''Assessing preferences for decision making.''' Medical decision making in a pediatric setting is unique in that it is often the child's legal guardians, not the patient, who ultimately consent for most medical treatments. Yet within a palliative care setting, it is particularly consequential to incorporate the child's preferences within the ultimate goals of care. Equally important to consider, families may vary in the level of responsibility they want in this decision-making process.<ref name="Hinds_2004">{{cite journal | vauthors = Hinds PS | title = The hopes and wishes of adolescents with cancer and the nursing care that helps | journal = Oncology Nursing Forum | volume = 31 | issue = 5 | pages = 927–934 | date = September 2004 | pmid = 15378093 | doi = 10.1188/04.ONF.927-934 | s2cid = 46005587 }}</ref> Their preference may range from wanting to be the child's sole decision makers, to partnering with the medical team in a shared decision making model, to advocating for full deferral of decision-making responsibility to the clinician.<ref name="Hinds_2004" /> Palliative care providers clarify a family's preferences and support needs for medical decision making by providing context, information, and options for treatment and medical palliation. In the case of critically ill babies, parents are able to participate more in decision making if they are presented with options to be discussed rather than recommendations by the doctor. Utilizing this style of communication also leads to less conflict with doctors and might help the parents cope better with the eventual outcomes.<ref>{{Cite journal |date=2021-03-09 |title=Parents are meaningfully involved in decisions on the care of their critically ill baby when they are given options not recommendations |url=https://evidence.nihr.ac.uk/alert/parents-meaningfully-involved-care-decisions-critically-ill-baby-when-given-options-not-recommendations/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/alert_45227|s2cid=242477064 |url-access=subscription }}</ref><ref>{{cite journal | vauthors = Marlow N, Shaw C, Connabeer K, Aladangady N, Gallagher K, Drew P | title = End-of-life decisions in neonatal care: a conversation analytical study | journal = Archives of Disease in Childhood. Fetal and Neonatal Edition | volume = 106 | issue = 2 | pages = 184–188 | date = March 2021 | pmid = 32943530 | doi = 10.1136/archdischild-2020-319544 | s2cid = 221788612 | url = http://www.open-access.bcu.ac.uk/9943/8/End-of-life%20decisions%20in%20neonatal%20care.pdf }}</ref>
* '''Optimizing the environment for effective conversations around prognosis and goals of care.''' Essential to facilitating supportive, clear communication around potentially distressing topics such as prognosis and goals of care for seriously ill pediatric patients is optimizing the setting where this communication will take place and developing informed consensus among the child's caregiving team regarding goals and options for care. Often, these conversations occur within the context of family meetings, which are formal meetings between families and the child's multidisciplinary medical team. Prior to the family meeting, providers often meet to discuss the child's overall case, reasonably expected prognosis, and options for care, in addition to clarifying specific roles each provider will take on during the family meeting. During this meeting, the multidisciplinary medical team may also discuss any legal or ethical considerations related to the case. Palliative care providers often facilitate this meeting and help synthesize its outcome for children and their families. Experts in optimized communication, palliative care providers may opt to hold the family meeting in a quiet space where the providers and family can sit and address concerns during a time when all parties are not constrained. Additionally, parents' preferences regarding information exchange with the sick child present should be clarified.<ref>{{cite journal | vauthors = Mack JW, Grier HE | title = The Day One Talk | journal = Journal of Clinical Oncology | volume = 22 | issue = 3 | pages = 563–566 | date = February 2004 | pmid = 14752081 | doi = 10.1200/JCO.2004.04.078 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Mack JW, Hilden JM, Watterson J, Moore C, Turner B, Grier HE, Weeks JC, Wolfe J | title = Parent and physician perspectives on quality of care at the end of life in children with cancer | journal = Journal of Clinical Oncology | volume = 23 | issue = 36 | pages = 9155–9161 | date = December 2005 | pmid = 16172457 | doi = 10.1200/JCO.2005.04.010 }}</ref> If the child's guardians are resistant to disclosing information in front of their child, the child's provider may explore parental concerns on the topic. When excluded from family meetings and moments of challenging information exchange, adolescents, in particular, may have challenges with trusting their medical providers if they feel critical information is being withheld. It is important to follow the child's lead when deciding whether to disclose difficult information. Additionally, including them in these conversations can help the child fully participate in their care and medical decision making.<ref name="Communicating with children and fam"/><ref name="Hinds_2004"/><ref>{{cite journal | vauthors = Snethen JA, Broome ME, Knafl K, Deatrick JA, Angst DB | title = Family patterns of decision-making in pediatric clinical trials | journal = Research in Nursing & Health | volume = 29 | issue = 3 | pages = 223–232 | date = June 2006 | pmid = 16676342 | doi = 10.1002/nur.20130 }}</ref> Finally, it is important to prioritize the family's agenda while additionally considering any urgent medical decisions needed to advance the child's care.
* '''Supporting emotional distress.''' A significant role of the pediatric palliative care provider is to help support children, their families, and their caregiving teams through the emotional stress of illness. Communication strategies the palliative care provider may employ in this role are asking for permission when engaging with potentially distressing conversations, naming emotions witnessed to create opportunities to discuss complex emotional responses to illness, actively listening, and allowing for invitational silence.<ref>{{cite journal | vauthors = Back AL, Bauer-Wu SM, Rushton CH, Halifax J | title = Compassionate silence in the patient-clinician encounter: a contemplative approach | journal = Journal of Palliative Medicine | volume = 12 | issue = 12 | pages = 1113–1117 | date = December 2009 | pmid = 19698026 | pmc = 2939848 | doi = 10.1089/jpm.2009.0175 }}</ref> The palliative care provider may iteratively assess the child and family's emotional responses and needs during challenging conversations. At times, the medical team may be hesitant to discuss a child's prognosis out of fear of increasing distress. This sentiment is not supported by the literature; among adults, end of life discussions are not associated with increased rates of anxiety or depression.<ref>{{cite journal | vauthors = Wright AA, Zhang B, Ray A, Mack JW, Trice E, Balboni T, Mitchell SL, Jackson VA, Block SD, Maciejewski PK, Prigerson HG | title = Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment | journal = JAMA | volume = 300 | issue = 14 | pages = 1665–1673 | date = October 2008 | pmid = 18840840 | pmc = 2853806 | doi = 10.1001/jama.300.14.1665 }}</ref> Though this topic is not well studied in pediatric populations, conversations about prognosis have the potential to increase in parental hope and peace of mind.<ref>{{cite journal | vauthors = Mack JW, Joffe S | title = Communicating about prognosis: ethical responsibilities of pediatricians and parents | journal = Pediatrics | volume = 133 | issue = Suppl 1 | pages = S24–S30 | date = February 2014 | pmid = 24488537 | doi = 10.1542/peds.2013-3608E | doi-access = free }}</ref>
* '''SPIKE framework.''' This is a framework that is designed to assist healthcare workers deliver bad news.<ref name="baile" /> The acronym stands for: setting, perception, invitation, knowledge, empathy, and summarize/strategy. When giving bad news it is important to consider the setting, which considers the environment in which the healthcare provider is delivering the news including privacy, sitting, time, and the inclusion of family members. What to say should also be considered, as well as rehearsed. It is important to understand how a patient is receiving the information by asking open ended questions and asking them to repeat what they learned in their own words, which is perception aspect of the framework. The healthcare provider should seek an invitation from the patient to disclose additional information before doing so in order to prevent overwhelming or distressing the patient further. In order to ensure the patient understands what is being told, knowledge must be used. This includes speaking in a way that the patient will understand, using simple words, not being excessively blunt, giving information in small chunks and checking in with the patient to confirm that they understand, and not providing poor information that may not be completely true. In order to alleviate some of a patient's distress it is crucial to be empathetic in the sense of understanding how a patient is feeling and the reactions they are having. This can allow one to change how they are delivering information, allow the patient to have time to process the information, or console them if needed. Connecting with patients is an important step in delivering bad news; maintaining eye contact proves that the healthcare provider is present and the patient and family has their full attention. Furthermore, the provider may make a connection by touching the patients shoulder or hand, giving them a physical connection to know that they are not alone.<ref>{{Cite web|title=John Hausdorff, MD|url=https://pub.hematology.org/Thehematologist/Authors/7455.aspx|date=1 July 2017|website=pub.hematology.org|language=en-US|access-date=12 May 2020|archive-date=4 July 2020|archive-url=https://web.archive.org/web/20200704214145/https://pub.hematology.org/Thehematologist/Authors/7455.aspx|url-status=live}}</ref><ref>{{Cite book| vauthors = du Pre A |title=Communicating About Health: Current Issues and Perspectives|publisher=Oxford University Press|year=2017|isbn=978-0-19-027568-6|location=New York, New York|pages=208–209|chapter=Social Support, Family Caregivers, and End of Life}}</ref> Finally, it is important to summarize all the information given in order to ensure the patient fully understands and takes away the major points. Additionally, patients who have a clear plan for the future are less likely to feel anxious and uncertain, but it is important to ask people if they are ready for that information before providing them with it.<ref>{{cite journal | vauthors = Saraiya B, Bodnar-Deren S, Leventhal E, Leventhal H | title = End-of-life planning and its relevance for patients' and oncologists' decisions in choosing cancer therapy | journal = Cancer | volume = 113 | issue = 12 Suppl | pages = 3540–3547 | date = December 2008 | pmid = 19058149 | pmc = 2606925 | doi = 10.1002/cncr.23946 }}</ref><ref>{{cite journal | vauthors = O'Leary KJ, Kulkarni N, Landler MP, Jeon J, Hahn KJ, Englert KM, Williams MV | title = Hospitalized patients' understanding of their plan of care | journal = Mayo Clinic Proceedings | volume = 85 | issue = 1 | pages = 47–52 | date = January 2010 | pmid = 20042561 | pmc = 2800283 | doi = 10.4065/mcp.2009.0232 }}</ref>

=== Geriatric palliative care ===
{{See also|Analgesic|Psychologist}}

==== Overview ====
With the transition in the population toward lower child mortality and lower death rates, countries around the world are seeing larger elderly populations. In some countries, this means a growing burden on national resources in the shape of social security and health care payments. As aging populations put increasing pressure on existing resources, long-term palliative care for patients' non-communicable, chronic conditions has emerged as a necessary approach to increase these patient's quality of life, through prevention and relief by identifying, assessing, and treating the source of pain and other psychosocial and spiritual problems.<ref>{{cite journal | vauthors = Kar SS, Subitha L, Iswarya S | title = Palliative care in India: Situation assessment and future scope | journal = Indian Journal of Cancer | volume = 52 | issue = 1 | pages = 99–101 | date = 2015 | pmid = 26837989 | doi = 10.4103/0019-509x.175578 | doi-access = free }}</ref>

The global rise in life expectancy and the aging of populations have increased the need for palliative approaches in geriatric medicine.<ref>{{Cite web |title=Global average life expectancy has more than doubled since 1900 |url=https://ourworldindata.org/data-insights/global-average-life-expectancy-has-more-than-doubled-since-1900 |access-date=2025-09-27 |website=Our World in Data |language=en}}</ref><ref>{{Cite web |title=Ageing and health |url=https://www.who.int/news-room/fact-sheets/detail/ageing-and-health |access-date=2025-09-27 |website=www.who.int |language=en}}</ref> Older adults frequently experience multiple chronic illnesses, frailty, and cognitive decline, resulting in complex care needs that extend beyond disease-specific treatments.<ref>{{Cite web |date=September 2021 |title=Older Adults - Health and age-related changes |url=https://www.apa.org/pi/aging/resources/guides/older |access-date=2025-09-27 |website=American Psychological Association}}</ref> Geriatric palliative care addresses physical, psychosocial, and spiritual suffering in this population, emphasizing quality of life, autonomy, and dignity during the final stages of life.<ref name="SchelinFurstRasmussenHedman2023">{{Cite journal |last1=Schelin |first1=Maria E. C. |last2=Fürst |first2=Carl Johan |last3=Rasmussen |first3=Birgit H. |last4=Hedman |first4=Christel |date=2023 |title=Increased patient satisfaction by integration of palliative care into geriatrics-A prospective cohort study |journal=PLOS One |volume=18 |issue=6 |article-number=e0287550 |doi=10.1371/journal.pone.0287550 |doi-access=free |issn=1932-6203 |pmc=10286968 |pmid=37347730 |bibcode=2023PLoSO..1887550S }}</ref> Expanding access remains challenging due to uneven resource distribution, shortages of trained professionals, and limited policy prioritization.<ref>{{Cite journal |last1=Stiel |first1=Stephanie |last2=Krause |first2=Olaf |last3=Berndt |first3=Carolin Sophie |last4=Ewertowski |first4=Helen |last5=Müller-Mundt |first5=Gabriele |last6=Schneider |first6=Nils |date=December 2020 |title=Caring for frail older patients in the last phase of life: Challenges for general practitioners in the integration of geriatric and palliative care |journal=Zeitschrift für Gerontologie und Geriatrie |volume=53 |issue=8 |pages=763–769 |doi=10.1007/s00391-019-01668-3 |issn=1435-1269 |pmid=31828367}}</ref>

==== Distinct challenges in older populations ====
Prognostication in older adults is often uncertain due to multi-morbidity and gradual functional decline, complicating the timing of palliative interventions.<ref name="JacobsonMayMorrison2022">{{Cite journal |last1=Jacobson |first1=Mireille |last2=May |first2=Peter |last3=Morrison |first3=R. Sean |date=2022-01-04 |title=Improving Care of People With Serious Medical Illness-An Economic Research Agenda for Palliative Care  |journal=JAMA Health Forum |volume=3 |issue=1 |pages=e214464 |doi=10.1001/jamahealthforum.2021.4464 |issn=2689-0186 |pmc=11210404 |pmid=36218864}}</ref> Care delivery is further challenged by fragmented health and social care systems, where reimbursement models frequently favor acute interventions over longitudinal, supportive care. These structural issues contribute to delayed referrals and underutilization of palliative services in older populations.<ref name="RajabaleeJosephTapper2023">{{Cite journal |last1=Rajabalee |first1=Nafiisah B. M. H. |last2=Joseph |first2=Augustin |last3=Tapper |first3=Corey X. |date=August 2023 |title=Global Geriatric Palliative Care |journal=Clinics in Geriatric Medicine |volume=39 |issue=3 |pages=465–473 |doi=10.1016/j.cger.2023.05.002 |issn=1879-8853 |pmid=37385697}}</ref>

==== Integration into healthcare systems ====
Efforts to better integrate palliative care into geriatric medicine have expanded since PC's formal recognition by the [[World Health Organization]] (WHO) in 1990, with emerging models emphasizing early incorporation of palliative principles into routine care for older adults.<ref>{{Cite journal |last1=Tripodoro |first1=Vilma A. |last2=Bouësseau |first2=Marie-Charlotte |last3=Connor |first3=Stephen R. |last4=Centeno |first4=Carlos |date=2025-08-14 |title=35 Years of Palliative Care Progress: What Lies Ahead for Society Engagement? |url=https://www.sciencedirect.com/science/article/pii/S0885392425007638 |journal=Journal of Pain and Symptom Management |volume=70 |issue=5 |pages=e291–e298 |doi=10.1016/j.jpainsymman.2025.08.003 |pmid=40818829 |issn=0885-3924|url-access=subscription }}</ref> In countries such as Germany and the Netherlands, specialized geriatric palliative care programs have been established to bridge hospital, nursing home, and community-based care settings.<ref>{{Cite journal |last1=Loosen |first1=Sven H. |last2=Krieg |first2=Sarah |last3=Eschrich |first3=Johannes |last4=Luedde |first4=Mark |last5=Krieg |first5=Andreas |last6=Schallenburger |first6=Manuela |last7=Schwartz |first7=Jacqueline |last8=Neukirchen |first8=Martin |last9=Luedde |first9=Tom |last10=Kostev |first10=Karel |last11=Roderburg |first11=Christoph |date=2022-11-12 |title=The Landscape of Outpatient Palliative Care in Germany: Results from a Retrospective Analysis of 14,792 Patients  |journal=International Journal of Environmental Research and Public Health |volume=19 |issue=22 |article-number=14885 |doi=10.3390/ijerph192214885 |doi-access=free |issn=1660-4601 |pmc=9691170 |pmid=36429604}}</ref><ref>{{Cite journal |last1=van Velzen |first1=N. |last2=Brom |first2=L. |last3=van der Vorst |first3=M. J. D. L. |last4=Kiers |first4=M. L. |last5=Wagemans |first5=M. F. M. |last6=Kazimier |first6=H. |last7=Boddaert |first7=M. S. A. |last8=Raijmakers |first8=N. J. H. |last9=Stoppelenburg |first9=A. |date=2025-01-23 |title=Development of specialist palliative care in Dutch hospitals between 2014 and 2020: a repeated survey  |journal=BMC Palliative Care |volume=24 |issue=1 |page=20 |doi=10.1186/s12904-025-01657-x |doi-access=free |issn=1472-684X |pmc=11755811 |pmid=39849515}}</ref>

Research indicates that embedding palliative care into geriatrics improves patient satisfaction, reduces unnecessary hospitalizations, and enhances the quality of end-of-life experiences.<ref name="SchelinFurstRasmussenHedman2023"/> This has led professional societies, including the European Association for Palliative Care (EAPC) and the [[American Geriatrics Society]] (AGS), to call for systematic integration of palliative frameworks into geriatric training and practice.<ref>{{Cite journal |last1=Van den Block |first1=Lieve |last2=de Nooijer |first2=Kim |last3=Pautex |first3=Sophie |last4=Pivodic |first4=Lara |last5=Van Den Noortgate |first5=Nele |last6=Nicholson |first6=Caroline |last7=Szczerbińska |first7=Katarzyna |last8=Pereira |first8=Sandra Martins |last9=Tiberini |first9=Rebecca |last10=Hanratty |first10=Barbara |last11=Miranda |first11=Rose |date=2025-09-01 |title=A European Association for Palliative Care White Paper defining an integrative palliative, geriatric, and rehabilitative approach to care and support for older people living with frailty and their family carers: a 28-country Delphi study and recommendations |journal=eClinicalMedicine |volume=87 |article-number=103403 |doi=10.1016/j.eclinm.2025.103403 |pmid=40838200 |pmc=12362020 |issn=2589-5370}}</ref><ref>{{Cite web |title=Mission & Vision {{!}} American Geriatrics Society |url=https://www.americangeriatrics.org/about-us/mission-vision |access-date=2025-09-27 |website=www.americangeriatrics.org |language=en}}</ref>

==== Policy frameworks and global perspectives ====
Policy initiatives around geriatric palliative care vary widely across countries. In some European nations, palliative care is formally embedded into national aging strategies, while in others, services remain fragmented and underfunded.<ref>{{Cite journal |last1=Clark |first1=David |last2=Baur |first2=Nicole |last3=Clelland |first3=David |last4=Garralda |first4=Eduardo |last5=López-Fidalgo |first5=Jesús |last6=Connor |first6=Stephen |last7=Centeno |first7=Carlos |date=April 2020 |title=Mapping Levels of Palliative Care Development in 198 Countries: The Situation in 2017  |journal=Journal of Pain and Symptom Management |volume=59 |issue=4 |pages=794–807.e4 |doi=10.1016/j.jpainsymman.2019.11.009 |issn=1873-6513 |pmc=7105817 |pmid=31760142}}</ref> The WHO has called for universal access to palliative care, highlighting disparities in access for older adults worldwide.<ref>{{Cite web |title=Palliative care |url=https://www.who.int/news-room/fact-sheets/detail/palliative-care |access-date=2025-09-27 |website=www.who.int |language=en}}</ref>

Cross-national comparisons show significant differences in implementation. High-income countries such as the United Kingdom and Canada have more established frameworks like the ''Ambitions for Palliative and End of Life Care'', which includes funding mechanisms supporting interdisciplinary geriatric palliative care teams.<ref>{{Cite web |last=England |first=N. H. S. |title=NHS England » Ambitions for palliative and end of life care |url=https://www.england.nhs.uk/eolc/ambitions/ |access-date=2025-09-27 |language=en-US}}</ref><ref>{{Cite web |last=Canada |first=Health |date=2018-12-04 |title=Framework on Palliative Care in Canada |url=https://www.canada.ca/en/health-canada/services/health-care-system/reports-publications/palliative-care/framework-palliative-care-canada.html |access-date=2025-09-27 |website=www.canada.ca}}</ref> In contrast, low- and middle-income countries face persistent challenges including workforce shortages, limited opioid availability, and minimal policy support, leading to widespread unmet need among older populations.<ref name="RajabaleeJosephTapper2023" />

==== Economic considerations and evaluations in geriatric palliative care ====
The economics of geriatric palliative care have become increasingly important as healthcare systems confront the financial implications of population aging. Older adults  account for a disproportionate share of medical expenditures in their final years, much of it directed toward aggressive treatments with limited benefit.<ref name="JacobsonMayMorrison2022"/> Understanding how palliative care influences both cost and patient outcomes is central to effective policy and resource allocation.

===== Challenges in economic evaluation =====
Economic evaluations in palliative and end-of-life care face methodological challenges distinct from those in curative medicine. Common issues include narrow cost perspectives, short time horizons, difficulties defining control groups, and limited generalizability across settings.<ref name="FischerBednarzSimon2024">{{Cite journal |last1=Fischer |first1=Claudia |last2=Bednarz |first2=Damian |last3=Simon |first3=Judit |date=January 2024 |title=Methodological challenges and potential solutions for economic evaluations of palliative and end-of-life care: A systematic review  |journal=Palliative Medicine |volume=38 |issue=1 |pages=85–99 |doi=10.1177/02692163231214124 |issn=1477-030X |pmc=10798028 |pmid=38142280}}</ref> These obstacles are amplified in geriatric settings, where multi-morbidity, frailty, and variable trajectories complicate the definition of intervention and control groups.

The standard use of [[Quality-adjusted life year|Quality-Adjusted Life Years]] (QALYs) in cost effectiveness analysis has also been debated. Traditional QALY instruments, such as the [[EQ-5D]], may overlook domains central to palliative care, including dignity, existential well-being, and symptom burden.<ref name="PACE2017">{{Cite journal |last1=Wichmann |first1=Anne B. |last2=Adang |first2=Eddy Mm |last3=Stalmeier |first3=Peep Fm |last4=Kristanti |first4=Sinta |last5=Van den Block |first5=Lieve |last6=Vernooij-Dassen |first6=Myrra Jfj |last7=Engels |first7=Yvonne |last8=PACE |date=April 2017 |title=The use of Quality-Adjusted Life Years in cost-effectiveness analyses in palliative care: Mapping the debate through an integrative review  |journal=Palliative Medicine |volume=31 |issue=4 |pages=306–322 |doi=10.1177/0269216316689652 |issn=1477-030X |pmc=5405846 |pmid=28190374}}</ref> To address this, researchers have proposed modifying time valuations and incorporating domain-specific or capability-based measures such as ICECAP-SCM to better capture end-of-life quality.<ref name="FischerBednarzSimon2024" />

===== Evidence on cost and value =====
Growing empirical evidence supports that palliative care can reduce costs or yield cost offsets, especially in acute care environments. A large meta-analysis of hospital palliative care consultations estimated an average reduction in direct hospital costs of USD 3,237 per patient, with greater savings in cancer cases and those with multiple co-morbidities.<ref>{{Cite journal |last1=May |first1=Peter |last2=Normand |first2=Charles |last3=Cassel |first3=J. Brian |last4=Del Fabbro |first4=Egidio |last5=Fine |first5=Robert L. |last6=Menz |first6=Reagan |last7=Morrison |first7=Corey A. |last8=Penrod |first8=Joan D. |last9=Robinson |first9=Chessie |last10=Morrison |first10=R. Sean |date=2018-06-01 |title=Economics of Palliative Care for Hospitalized Adults With Serious Illness: A Meta-analysis  |journal=JAMA Internal Medicine |volume=178 |issue=6 |pages=820–829 |doi=10.1001/jamainternmed.2018.0750 |issn=2168-6114 |pmc=6145747 |pmid=29710177}}</ref> A narrative review likewise reported that home-based palliative care consistently lowers hospitalization rates and emergency visits, although many studies measure cost outcomes alone and omit formal cost-utility analyses.<ref>{{Cite journal |last1=Luta |first1=Xhyljeta |last2=Ottino |first2=Baptiste |last3=Hall |first3=Peter |last4=Bowden |first4=Joanna |last5=Wee |first5=Bee |last6=Droney |first6=Joanne |last7=Riley |first7=Julia |last8=Marti |first8=Joachim |date=2021-06-23 |title=Evidence on the economic value of end-of-life and palliative care interventions: a narrative review of reviews |journal=BMC Palliative Care |volume=20 |issue=1 |page=89 |doi=10.1186/s12904-021-00782-7 |doi-access=free |issn=1472-684X |pmc=8223342 |pmid=34162377}}</ref>

Community and home-based models demonstrate similar economic advantages. These care avenues have been associated with lower hospitalization rates and improved patient satisfaction.<ref name="SchelinFurstRasmussenHedman2023"/> A multi-country economic evaluation reported that early integration of palliative services into primary and long-term care improved cost efficiency without compromising patient outcomes.(CITE)<ref name="PACE2017" /> Modeling studies suggest that scaling community-based programs for older adults could reduce national health expenditures by up to 15 percent over a decade, primarily through reduced acute care utilization and improved coordination of chronic care.<ref>{{Cite journal |last1=Xie |first1=Feng |last2=Zhou |first2=Ting |last3=Humphries |first3=Brittany |last4=Neumann |first4=Peter J. |date=2024-06-01 |title=Do Quality-Adjusted Life Years Discriminate Against the Elderly? An Empirical Analysis of Published Cost-Effectiveness Analyses |url=https://www.sciencedirect.com/science/article/pii/S1098301524001268 |journal=Value in Health |volume=27 |issue=6 |pages=706–712 |doi=10.1016/j.jval.2024.03.011 |pmid=38548176 |issn=1098-3015|url-access=subscription }}</ref>

===== Remaining research gaps =====
Despite these findings, the literature remains limited by short time horizons, a narrow healthcare system perspective, and a lack of standardized outcome measures. Few evaluations consider caregiver burden or broader societal costs. Scholars have called for a coordinated research agenda that strengthens the evidence base for geriatric palliative care economics and ensures models balance efficiency with dignity and quality at the end of life<ref name="JacobsonMayMorrison2022" />

==Ethics==
{{excerpt|End-of-life ethics}}

== In religions ==
The doctrine of the Catholic Church accepts and supports the use of palliative care.<ref>{{Cite web |date=2023-08-03 |title=Magisterial teaching on end-of-life issues - Texas Catholic Conference |url=https://txcatholic.org/magisterial-teaching-on-end-of-life-issues/ |access-date=2024-07-12 |archive-url=https://web.archive.org/web/20230803011349/https://txcatholic.org/magisterial-teaching-on-end-of-life-issues/ |archive-date=3 August 2023 }}</ref> Many of the largest religions in the world likewise endorse the practice.<ref>{{cite journal | vauthors = Grove G, Lovell M, Best M | title = Perspectives of Major World Religions regarding Euthanasia and Assisted Suicide: A Comparative Analysis | journal = Journal of Religion and Health | volume = 61 | issue = 6 | pages = 4758–4782 | date = December 2022 | pmid = 35092533 | pmc = 9569313 | doi = 10.1007/s10943-022-01498-5 }}</ref><ref>{{cite journal | vauthors = Kinzbrunner BM | title = Jewish medical ethics and end-of-life care | journal = Journal of Palliative Medicine | volume = 7 | issue = 4 | pages = 558–573 | date = August 2004 | pmid = 15353100 | doi = 10.1089/jpm.2004.7.558 }}</ref>

== In society ==

=== Certification and training for services ===

In most countries, hospice care and palliative care is provided by an interdisciplinary team consisting of [[physician]]s, [[clinical pharmacy|pharmacists]], [[registered nurses|nurses]], [[nursing assistants]], [[social worker]]s, [[hospice chaplain|chaplain]]s, and caregivers. In some countries, additional members of the team may include certified nursing assistants and home healthcare aides, as well as volunteers from the community (largely untrained but some being skilled medical personnel), and housekeepers.

In the United Kingdom, Palliative Medicine specialist training is delivered alongside Internal Medicine stage two training over an indicative four years. Entry into Palliative medicine training is possible following successful completion of both a foundation programme and a core training programme. There are two core training programmes for Palliative Medicine training:<ref>{{Cite web |title=Specialist Training in Palliative Medicine UK |url=https://www.jrcptb.org.uk/specialties/palliative-medicine |website=Joint Royal College of Physicians Training Board}}</ref>

* Internal Medical Training (IMT)
* Acute Care Common Stem - Internal Medicine (ACCS-IM)

In the United States, the physician sub-specialty of [[hospice and palliative medicine]] was established in 2006<ref>American Board of Medical Specialties, [http://www.abms.org/News_and_Events/downloads/NewSubcertPalliativeMed.pdf ABMS Establishes New Subspecialty Certificate in Hospice and Palliative Medicine] {{webarchive|url=https://web.archive.org/web/20101116144358/http://abms.org/News_and_Events/downloads/NewSubcertPalliativeMed.pdf |date=16 November 2010 }}, 6 October 2006, Retrieved 11 September 2010.</ref> to provide expertise in the care of people with life-limiting, advanced disease, and [[catastrophic injury]]; the relief of distressing symptoms; the coordination of interdisciplinary care in diverse settings; the use of specialized care systems including hospice; the management of the imminently dying patient; and legal and ethical decision making in end of life care.<ref>American Board of Medical Specialties, [http://www.boardcertifieddocs.com/pdf/Resources_guide_physicians.pdf ABMS Guide to Physician Specialties] {{Webarchive|url=https://web.archive.org/web/20170731025601/https://www.boardcertifieddocs.com/pdf/Resources_guide_physicians.pdf |date=31 July 2017 }}, 2011, p. 2, Retrieved 11 September 2010.</ref>

Caregivers, both family and [[voluntary caregiver|volunteers]], are crucial to the palliative care system. Caregivers and people being treated often form lasting friendships over the course of care. As a consequence caregivers may find themselves under severe emotional and physical strain. Opportunities for caregiver [[respite care|respite]] are some of the services hospices provide to promote caregiver well-being. Respite may last a few hours up to several days (the latter being done by placing the primary person being cared for in a [[nursing home]] or inpatient hospice unit for several days).<ref>{{cite journal | vauthors = Thayyil J, Cherumanalil JM | title = Assessment of status of patients receiving palliative home care and services provided in a rural area-kerala, India | journal = Indian Journal of Palliative Care | volume = 18 | issue = 3 | pages = 213–218 | date = September 2012 | pmid = 23440060 | pmc = 3573477 | doi = 10.4103/0973-1075.105693 | series = 18 | doi-access = free }}</ref>

In the US, board certification for physicians in palliative care was through the [[American Board of Hospice and Palliative Medicine]]; recently this was changed to be done through any of 11 different speciality boards through an [[American Board of Medical Specialties]]-approved procedure. Additionally, board certification is available to [[Osteopathic medicine in the United States|osteopathic physicians]] ([[Doctor of Osteopathic Medicine|D.O.]]) in the United States through four medical specialty boards through an [[American Osteopathic Association Bureau of Osteopathic Specialists]]-approved procedure.<ref>{{cite web|title=Specialties & Subspecialties|url=http://www.osteopathic.org/inside-aoa/development/aoa-board-certification/Pages/specialty-subspecialty-certification.aspx|publisher=American Osteopathic Association|access-date=23 September 2012|archive-url=https://web.archive.org/web/20150813083503/http://www.osteopathic.org/inside-aoa/development/aoa-board-certification/Pages/specialty-subspecialty-certification.aspx|archive-date=13 August 2015}}</ref> More than 50 fellowship programs provide one to two years of specialty training following a primary residency. In the [[United Kingdom]] palliative care has been a full specialty of medicine since 1989 and training is governed by the same regulations through the [[Royal College of Physicians]] as with any other medical speciality.<ref>{{cite web|url=http://www.aahpm.org/certification/default/index.html|title=American Academy of Hospice and Palliative Medicine|author=American Academy of Hospice|author2=Palliative Medicine|publisher=Aahpm.org|access-date=21 November 2014|archive-date=23 April 2014|archive-url=https://web.archive.org/web/20140423074541/http://www.aahpm.org/certification/default/index.html|url-status=live}}</ref> Nurses, in the United States and internationally, can receive continuing education credits through Palliative Care specific trainings, such as those offered by [[End-of-Life Nursing Education Consortium]] (ELNEC).<ref>{{cite journal | vauthors = Ferrell BR, Virani R, Grant M, Rhome A, Malloy P, Bednash G, Grimm M | title = Evaluation of the End-of-Life Nursing Education Consortium undergraduate faculty training program | journal = Journal of Palliative Medicine | volume = 8 | issue = 1 | pages = 107–114 | date = February 2005 | pmid = 15662179 | doi = 10.1089/jpm.2005.8.107 }}</ref>

The Tata Memorial Centre in Mumbai has offered a physician's course in palliative medicine since 2012, the first one of its kind in the country.

=== Regional variation in services ===
{{See also|Hospice care in the United States}}
In the United States, hospice and palliative care represent two different aspects of care with similar philosophies, but with different payment systems and location of services. Palliative care services are most often provided in acute care hospitals organized around an interdisciplinary consultation service, with or without an acute inpatient palliative care unit. Palliative care may also be provided in the dying person's home as a "bridge" program between traditional US home care services and hospice care or provided in long-term care facilities.<ref>{{cite web |publisher=Agency for Healthcare Research and Quality |url=https://innovations.ahrq.gov/profiles/home-palliative-care-allows-more-patients-die-home-leading-higher-satisfaction-and-lower |title=In-Home Palliative Care Allows More Patients to Die at Home, Leading to Higher Satisfaction and Lower Acute Care Utilization and Costs |date=3 April 2013 |access-date=9 July 2013 |archive-date=14 March 2020 |archive-url=https://web.archive.org/web/20200314094231/https://innovations.ahrq.gov/profiles/home-palliative-care-allows-more-patients-die-home-leading-higher-satisfaction-and-lower |url-status=live }}</ref> In contrast over 80% of hospice care in the US is provided at home with the remainder provided to people in long-term care facilities or in free standing hospice residential facilities. In the UK hospice is seen as one part of the speciality of palliative care and no differentiation is made between 'hospice' and 'palliative care'.

In the UK palliative care services offer inpatient care, home care, day care and outpatient services, and work in close partnership with mainstream services. Hospices often house a full range of services and professionals for children and adults. In 2015 the UK's palliative care was ranked as the best in the world "due to comprehensive national policies, the extensive integration of palliative care into the ''[[National Health Service]]'', a strong hospice movement, and deep community engagement on the issue".<ref>{{cite news|title=Quality of Death Index 2015: Ranking palliative care across the world|url=http://www.economistinsights.com/healthcare/analysis/quality-death-index-2015|access-date=8 October 2015|work=The Economist Intelligence Unit|date=6 October 2015|postscript=none|archive-date=17 June 2020|archive-url=https://web.archive.org/web/20200617220416/https://perspectives.eiu.com/|url-status=live}}; {{cite news|title=UK end-of-life care 'best in world'|url=https://www.bbc.co.uk/news/health-34415362|access-date=8 October 2015|work=BBC|date=6 October 2015|archive-date=11 April 2020|archive-url=https://web.archive.org/web/20200411212841/https://www.bbc.co.uk/news/health-34415362|url-status=live}}</ref>

In 2021 the UK's National Palliative and End of Life Care Partnership published their six ambitions for 2021–26. These include fair [[Health equity|access to end of life care]] for everyone regardless of who they are, where they live or their circumstances, and the need to maximise comfort and wellbeing. Informed and timely conversations are also highlighted.<ref>{{Cite web |date=May 2021 |title=Ambitions for Palliative and End of Life Care: A national framework for local action 2021-2026 |url=https://www.england.nhs.uk/wp-content/uploads/2022/02/ambitions-for-palliative-and-end-of-life-care-2nd-edition.pdf |access-date=20 April 2022 |website=National Palliative and End of Life Care Partnership}}</ref>

=== Acceptance and access ===

The focus on a person's quality of life has increased greatly since the 1990s. In the United States today, 55% of hospitals with more than 100 beds offer a palliative-care program,<ref>Center to Advance Palliative Care, www.capc.org</ref> and nearly one-fifth of community hospitals have palliative-care programs.<ref>{{cite book |author=Lynn, Joanne |title=Sick to death and not going to take it anymore!: reforming health care for the last years of life |publisher=[[University of California Press]] |location=Berkeley |date=2004 |page=[https://archive.org/details/sicktodeathnotgo00joan/page/72 72] |isbn=978-0-520-24300-2 |url-access=registration |url=https://archive.org/details/sicktodeathnotgo00joan }}</ref> A relatively recent development is the palliative-care team, a dedicated health care team that is entirely geared toward palliative treatment.

Physicians practicing palliative care do not always receive support from the people they are treating, family members, healthcare professionals or their social peers. More than half of physicians in one survey reported that they have had at least one experience where a patient's family members, another physician or another health care professional had characterized their work as being "[[euthanasia]], murder or killing" during the last five years. A quarter of them had received similar comments from their own friends or family member, or from a patient.<ref>{{cite journal | vauthors = Goldstein NE, Cohen LM, Arnold RM, Goy E, Arons S, Ganzini L | title = Prevalence of formal accusations of murder and euthanasia against physicians | journal = Journal of Palliative Medicine | volume = 15 | issue = 3 | pages = 334–339 | date = March 2012 | pmid = 22401355 | pmc = 3295854 | doi = 10.1089/jpm.2011.0234 }}</ref>

Despite significant progress that has been made to increase access to palliative care within the United States and other countries, many countries have not yet considered palliative care as a public health problem, and therefore do not include it in their public health agenda.<ref>{{Cite journal |last=Sepúlveda |first=Cecilia |last2=Marlin |first2=Amanda |last3=Yoshida |first3=Tokuo |last4=Ullrich |first4=Andreas |date=2002-08-01 |title=Palliative Care: The World Health Organization's Global Perspective |url=https://www.jpsmjournal.com/article/S0885-3924(02)00440-2/fulltext |journal=Journal of Pain and Symptom Management |language=English |volume=24 |issue=2 |pages=91–96 |doi=10.1016/S0885-3924(02)00440-2 |issn=0885-3924 |pmid=12231124}}</ref> Resources and cultural attitudes both play significant roles in the acceptance and implementation of palliative care in the health care agenda. A study identified the current gaps in palliative care for people with severe [[Mental health|mental illness]] (SMI's). They found that due to the lack of resources within both mental health and [[End-of-life care|end of life]] services people with SMI's faced a number of barriers to accessing timely and appropriate palliative care. They called for a multidisciplinary team approach, including [[advocacy]], with a point of contact co-ordinating the appropriate support for the individual. They also state that [[End-of-life care|end of life]] and [[Mental health|mental health care]] needs to be included in the training for professionals.<ref>{{Cite journal |date=28 February 2022 |title=How to improve end-of-life care for people with mental illness |url=https://evidence.nihr.ac.uk/alert/how-to-improve-end-of-life-care-for-people-with-severe-mental-illness/ |access-date=4 July 2022 |website=NIHR Evidence |doi=10.3310/alert_49015 |s2cid=247180312 |language=en-GB |archive-date=23 June 2022 |archive-url=https://web.archive.org/web/20220623142001/https://evidence.nihr.ac.uk/alert/how-to-improve-end-of-life-care-for-people-with-severe-mental-illness/ |url-status=live |url-access=subscription }}</ref><ref name="Edwards_2021">{{cite journal | vauthors = Edwards D, Anstey S, Coffey M, Gill P, Mann M, Meudell A, Hannigan B | title = End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study) | journal = Palliative Medicine | volume = 35 | issue = 10 | pages = 1747–1760 | date = December 2021 | pmid = 34479457 | pmc = 8637363 | doi = 10.1177/02692163211037480 }}</ref>

A review states that by restricting referrals to palliative care only when patients have a definitive time line for death, something that the study found to often be inaccurate, can have negative implications for the patient both when accessing [[End-of-life care|end of life care]], or being unable to access services due to not receiving a time line from medical professionals. The authors call for a less rigid approach to referrals to palliative care services in order to better support the individual, improve quality of life remaining and provide more holistic care.<ref name="Petrova_2021">{{cite journal | vauthors = Petrova M, Wong G, Kuhn I, Wellwood I, Barclay S | title = Timely community palliative and end-of-life care: a realist synthesis | journal = BMJ Supportive & Palliative Care | date = December 2021 | volume = 14 | issue = e3 | pages = e2423–e2437 | pmid = 34887313 | doi = 10.1136/bmjspcare-2021-003066 | s2cid = 245013480 | doi-access = free | pmc = 11671952 }}</ref><ref>{{Cite journal |date=26 April 2022 |title=End of life care should not wait for prediction of death |url=https://evidence.nihr.ac.uk/alert/end-of-life-care-should-not-wait-for-prediction-of-death/ |access-date=4 July 2022 |website=NIHR Evidence |doi=10.3310/post_50369 |s2cid=249936671 |language=en-GB |archive-date=5 July 2022 |archive-url=https://web.archive.org/web/20220705190956/https://evidence.nihr.ac.uk/alert/end-of-life-care-should-not-wait-for-prediction-of-death/ |url-status=live |url-access=subscription }}</ref>

Many people with chronic pain are stigmatized and treated as opioid addicts. Patients can build a tolerance to drugs and have to take more and more to manage their pain. The symptoms of chronic pain patients do not show up on scans, so the doctor must go off trust alone. This is the reason that some wait to consult their doctor and endure sometimes years of pain before seeking help.<ref>{{cite journal | vauthors = Dubin RE, Kaplan A, Graves L, Ng VK | title = Acknowledging stigma: Its presence in patient care and medical education | journal = Canadian Family Physician | volume = 63 | issue = 12 | pages = 906–908 | date = December 2017 | pmid = 29237624 | pmc = 5729132 }}</ref>

==== Disparities in access ====
Access to palliative care is not distributed equally across populations, with disparities observed based on race, ethnicity,<ref name="Johnson2013">{{cite journal | vauthors = Johnson KS | title = Racial and ethnic disparities in palliative care | journal = Journal of Palliative Medicine | volume = 16 | issue = 11 | pages = 1329–1334 | date = November 2013 | pmid = 24073685 | pmc = 3822363 | doi = 10.1089/jpm.2013.9468 }}</ref><ref name="Barzagan-Hejasi-2021">{{cite journal | vauthors = Bazargan M, Bazargan-Hejazi S | title = Disparities in Palliative and Hospice Care and Completion of Advance Care Planning and Directives Among Non-Hispanic Blacks: A Scoping Review of Recent Literature | journal = The American Journal of Hospice & Palliative Care | volume = 38 | issue = 6 | pages = 688–718 | date = June 2021 | pmid = 33287561 | pmc = 8083078 | doi = 10.1177/1049909120966585 }}</ref> and socioeconomic status.<ref name="WachtermanSommers2021">{{cite journal | vauthors = Wachterman MW, Sommers BD | title = Dying Poor in the US-Disparities in End-of-Life Care | journal = JAMA | volume = 325 | issue = 5 | pages = 423–424 | date = February 2021 | pmid = 33528526 | doi = 10.1001/jama.2020.26162 }}</ref> Research has shown that marginalized groups are less likely to receive timely and comprehensive palliative care services, leading to differences in end-of-life experiences. These disparities stem from [[structural inequality]] in healthcare, financial barriers, cultural differences, and [[societal racism]] within medical institutions.<ref>{{cite journal | vauthors = Nelson KE, Wright R, Peeler A, Brockie T, Davidson PM | title = Sociodemographic Disparities in Access to Hospice and Palliative Care: An Integrative Review | journal = The American Journal of Hospice & Palliative Care | volume = 38 | issue = 11 | pages = 1378–1390 | date = November 2021 | pmid = 33423532 | pmc = 8514114 | doi = 10.1177/1049909120985419 }}</ref> Disparities in palliative care may also be influenced by provider-patient racial discordance, as studies suggest that increasing racial and ethnic concordance between patients and healthcare providers could improve trust, shared decision-making, and end-of-life care outcomes.<ref>{{Cite journal |last1=Collons |first1=Danielle |last2=Florez |first2=Narjust |last3=Petrillo |first3=Laura |last4=Dhawan |first4=Natasha |last5=Gray |first5=Tamryn F. |date=2023-10-01 |title=Palliative Care for All? An Assessment of Racial and Ethnic Disparities Research With Solutions |url=https://www.jpsmjournal.com/article/S0885-3924(23)00570-5/fulltext |journal=Journal of Pain and Symptom Management |language=English |volume=66 |issue=4 |pages=e521–e523 |doi=10.1016/j.jpainsymman.2023.06.014 |issn=0885-3924 |pmid=37364736}}</ref>

===== Racial and ethnic disparities =====
Studies have found that racial and ethnic minorities, particularly Black, Hispanic, and [[Indigenous peoples|Indigenous]] populations, have lower access to palliative care compared to White patients.<ref name="Johnson2013" /> Non-Hispanic Black individuals, for example, are significantly less likely to enroll in hospice services or complete advance care planning documents, which can lead to more aggressive medical interventions at the end of life rather than comfort-focused care.<ref name="Barzagan-Hejasi-2021" /> Contributing factors include mistrust of the medical system, differences in communication about end-of-life care, and provider biases that may affect the type of recommendations given to minority patients.<ref name="Johnson2013" />

===== Socioeconomic disparities =====
Lower-income individuals are less likely to receive palliative care services, often facing greater barriers due to financial constraints, lack of [[Insurance in the United States|insurance coverage]], and limited healthcare infrastructure in low-income and rural areas.<ref name="WachtermanSommers2021" /> Those living in [[poverty]] have higher rates of unmanaged symptoms and may be more likely to receive care in emergency settings rather than through specialized palliative care programs. Economic disparities in healthcare access contribute to differing end-of-life experiences, with wealthier individuals more likely to receive personalized, home-based palliative care services.<ref name="WachtermanSommers2021" />

== In media ==
Palliative care was the subject of the 2018 Netflix short documentary, ''[[End Game (2018 film)|End Game]]'' by directors [[Rob Epstein]] and Jeffrey Friedman<ref>{{Cite news|url=https://decider.com/2018/05/07/end-game-on-netflix-stream-it-or-skip-it/|title=Stream It Or Skip It: 'End Game' On Netflix, A Short Documentary About Dying Gracefully|date=7 May 2018|work=Decider|access-date=10 April 2020|language=en|archive-date=30 April 2019|archive-url=https://web.archive.org/web/20190430061424/https://decider.com/2018/05/07/end-game-on-netflix-stream-it-or-skip-it/|url-status=live}}</ref> about terminally ill patients in a San Francisco hospital and features the work of palliative care physician, [[BJ Miller]]. The film's executive producers were [[Steven Ungerleider]], [[David C. Ulich]] and [[Shoshana R. Ungerleider]].<ref>{{Cite news|url=https://www.forbes.com/sites/rimmaboshernitsan/2018/08/29/how-this-doctor-is-bringing-human-connection-back-to-end-of-life-care/#3ad05f6d6208|title=How This Doctor Is Bringing Human Connection Back to End-of-Life Care|date=29 August 2018|work=Forbes|access-date=10 April 2020|language=en|archive-date=26 June 2020|archive-url=https://web.archive.org/web/20200626200756/https://www.forbes.com/sites/rimmaboshernitsan/2018/08/29/how-this-doctor-is-bringing-human-connection-back-to-end-of-life-care/#3ad05f6d6208|url-status=live}}</ref>

In 2016, an open letter<ref>{{Cite web|date=16 January 2016|title=Thank you letter to David Bowie from a palliative care doctor|url=https://blogs.bmj.com/spcare/2016/01/15/a-thank-you-letter-to-david-bowie-from-a-palliative-care-doctor/|url-status=live|website=British Medical Journal Supportive & Palliative Care|access-date=30 December 2021|archive-date=28 December 2021|archive-url=https://web.archive.org/web/20211228221124/https://blogs.bmj.com/spcare/2016/01/15/a-thank-you-letter-to-david-bowie-from-a-palliative-care-doctor/}}</ref> to the singer [[David Bowie]] written by a palliative care doctor, [[Mark Taubert|Professor Mark Taubert]], talked about the importance of good palliative care, being able to express wishes about the last months of life, and good tuition (nutrition?) and education about end of life care generally. The letter went viral after David Bowie's son [[Duncan Jones]] shared it.<ref>{{Cite news|date=18 January 2016|title=David Bowie's son shares powerful letter|url=https://edition.cnn.com/2016/01/18/entertainment/david-bowie-son-letter-feat/index.html|access-date=30 December 2021|archive-date=28 December 2021|archive-url=https://web.archive.org/web/20211228221119/https://edition.cnn.com/2016/01/18/entertainment/david-bowie-son-letter-feat/index.html|url-status=live}}</ref> The letter was subsequently read out by the actor [[Benedict Cumberbatch]] and the singer [[Jarvis Cocker]] at public events.<ref>{{Cite news|date=6 June 2016|title=Benedict Cumberbatch read out a letter to Bowie by a palliative care doctor|work=Wales Online|url=https://www.walesonline.co.uk/news/news-opinion/benedict-cumberbatch-read-out-welsh-11424522|access-date=30 December 2021|archive-date=28 December 2021|archive-url=https://web.archive.org/web/20211228221121/https://www.walesonline.co.uk/news/news-opinion/benedict-cumberbatch-read-out-welsh-11424522|url-status=live}}</ref>

== Research ==

Research funded by the UK's [[National Institute for Health and Care Research]] (NIHR) has addressed these areas of need.<ref>{{Cite journal |date=2022-03-31 |title=End of life care: research highlights the importance of conversations and need for equal access |url=https://evidence.nihr.ac.uk/collection/end-of-life-care-research-highlights-the-importance-of-conversations-and-need-for-equal-access/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/collection_49245 |s2cid=247873633|url-access=subscription }}</ref> Examples highlight inequalities faced by several groups and offers recommendations. These include the need for close partnership between services caring for people with severe mental illness,<ref>{{Cite journal |date=2022-02-28 |title=Team work and proactive healthcare could help people with severe mental illness receive good end-of-life care |url=https://evidence.nihr.ac.uk/alert/how-to-improve-end-of-life-care-for-people-with-severe-mental-illness/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/alert_49015 |s2cid=247180312 |archive-date=23 June 2022 |access-date=5 July 2022 |archive-url=https://web.archive.org/web/20220623142001/https://evidence.nihr.ac.uk/alert/how-to-improve-end-of-life-care-for-people-with-severe-mental-illness/ |url-status=live |url-access=subscription }}</ref><ref name="Edwards_2021a">{{cite journal |vauthors=Edwards D, Anstey S, Coffey M, Gill P, Mann M, Meudell A, Hannigan B |date=December 2021 |title=End of life care for people with severe mental illness: Mixed methods systematic review and thematic synthesis (the MENLOC study) |journal=Palliative Medicine |volume=35 |issue=10 |pages=1747–1760 |doi=10.1177/02692163211037480 |pmc=8637363 |pmid=34479457}}</ref> improved understanding of barriers faced by [[Romanichal|Gypsy, Traveller and Roma]] communities,<ref>{{Cite journal |date=2021-12-17 |title=A highly personalised approach to end of life care is needed to help Gypsy, Traveller and Roma communities |url=https://evidence.nihr.ac.uk/alert/personalised-end-of-life-care-essential-travelling-communities/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/alert_48747 |s2cid=245290694|url-access=subscription }}</ref><ref>{{cite journal |vauthors=Dixon KC, Ferris R, Kuhn I, Spathis A, Barclay S |date=February 2021 |title=Gypsy, Traveller and Roma experiences, views and needs in palliative and end of life care: a systematic literature review and narrative synthesis |journal=BMJ Supportive & Palliative Care |volume=14 |pages=bmjspcare–2020–002676 |doi=10.1136/bmjspcare-2020-002676 |pmid=33619223 |s2cid=231992307}}</ref> the provision of flexible palliative care services for children from [[Ethnic groups in the United Kingdom|ethnic minorities]] or deprived areas.<ref name="pmid25085264">{{cite journal |vauthors=Hardelid P, Dattani N, Gilbert R |date=August 2014 |title=Estimating the prevalence of chronic conditions in children who die in England, Scotland and Wales: a data linkage cohort study |journal=BMJ Open |volume=4 |issue=8 |article-number=e005331 |doi=10.1136/bmjopen-2014-005331 |pmc=4127921 |pmid=25085264}}; {{lay source|template=cite web|title=Most children with life-limiting conditions still die in hospital, not home or hospice|url=https://evidence.nihr.ac.uk/alert/most-children-life-limiting-conditions-die-in-hospital-not-home-hospice/|date=2021-07-20|language=en|doi=10.3310/alert_46991|s2cid=242843746}}</ref><ref>{{cite journal |vauthors=Gibson-Smith D, Jarvis SW, Fraser LK |date=December 2020 |title=Place of death of children and young adults with a life-limiting condition in England: a retrospective cohort study |journal=Archives of Disease in Childhood |volume=106 |issue=8 |pages=780–785 |doi=10.1136/archdischild-2020-319700 |pmc=8311108 |pmid=33355156}}</ref>

Other research suggests that giving nurses and pharmacists easier access to [[Electronic health records in England|electronic patient records]] about prescribing could help people manage their symptoms at home.<ref>{{Cite journal |date=2021-06-15 |title=Nurses and pharmacists are key to improving access to end of life medicines for people being cared for at home |url=https://evidence.nihr.ac.uk/alert/nurses-pharmacists-improve-access-end-of-life-medicines/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/alert_46494 |s2cid=241904445|url-access=subscription }}</ref><ref>{{cite journal |vauthors=Latter S, Campling N, Birtwistle J, Richardson A, Bennett MI, Ewings S, Meads D, Santer M |date=September 2020 |title=Supporting patient access to medicines in community palliative care: on-line survey of health professionals' practice, perceived effectiveness and influencing factors |journal=BMC Palliative Care |volume=19 |issue=1 |article-number=148 |doi=10.1186/s12904-020-00649-3 |pmc=7517636 |pmid=32972414 |doi-access=free }}</ref> A named professional to support and guide patients and carers through the healthcare system could also improve the experience of care at home at the end of life.<ref>{{Cite journal |date=2020-09-16 |title=Terminally ill patients and their families may need more help to manage their medicines |url=https://evidence.nihr.ac.uk/alert/terminally-ill-patients-and-their-families-may-need-more-help-to-manage-their-medicines/ |journal=NIHR Evidence |type=Plain English summary |language=en |publisher=National Institute for Health and Care Research |doi=10.3310/alert_41179 |s2cid=242429298|url-access=subscription }}</ref><ref>{{cite journal |vauthors=Wilson E, Caswell G, Latif A, Anderson C, Faull C, Pollock K |date=May 2020 |title=An exploration of the experiences of professionals supporting patients approaching the end of life in medicines management at home. A qualitative study |journal=BMC Palliative Care |volume=19 |issue=1 |article-number=66 |doi=10.1186/s12904-020-0537-z |pmc=7216477 |pmid=32393231 |doi-access=free }}</ref> A synthesised review looking at palliative care in the UK created a resource showing which services were available and grouped them according to their intended purpose and benefit to the patient. They also stated that currently in the UK palliative services are only available to patients with a timeline to death, usually 12 months or less. They found these timelines to often be inaccurate and created barriers to patients accessing appropriate services. They call for a more holistic approach to end of life care which is not restricted by arbitrary timelines.<ref>{{Cite journal |date=2022-04-26 |title=End of life care should not wait for prediction of death |url=https://evidence.nihr.ac.uk/alert/end-of-life-care-should-not-wait-for-prediction-of-death/ |journal=NIHR Evidence |type=Plain English summary |language=en-GB |publisher=National Institute for Health and Care Research |doi=10.3310/post_50369 |access-date=2022-07-04 |s2cid=249936671 |archive-date=5 July 2022 |archive-url=https://web.archive.org/web/20220705190956/https://evidence.nihr.ac.uk/alert/end-of-life-care-should-not-wait-for-prediction-of-death/ |url-status=live |url-access=subscription }}</ref><ref>{{cite journal |vauthors=Petrova M, Wong G, Kuhn I, Wellwood I, Barclay S |date=December 2021 |title=Timely community palliative and end-of-life care: a realist synthesis |journal=BMJ Supportive & Palliative Care |volume=14 |issue=e3 |pages=bmjspcare–2021–003066 |doi=10.1136/bmjspcare-2021-003066 |pmid=34887313 |s2cid=245013480|doi-access=free |pmc=11671952 }}</ref>

== See also ==
* [[Health Advocate]]
* [[Health care reform]]
* [[Health insurance]]
* [[Health Insurance Innovations]]

== References ==
{{Reflist}}

== External links ==
{{wikibooks|Internal Medicine|Palliative Care}}

{{Medicine}}
{{Healthcare}}
{{Portal bar | Medicine}}
{{Authority control}}

[[Category:Palliative care| ]]
[[Category:Hospice]]