Literature Review

Home-based psilocybin-assisted therapy for a patient with advanced cancer: A case reportPalliative & Supportive Care; by Houman Farzin, Benjamin Koren, Héléna Ferrier, Justin J Sanders, Nicolas Garel; 10/25 Psychospiritual distress affects many patients with cancer, contributing to diminished quality of life, decreased survival and a desire for hastened death. The current standard of care, which primarily consists of antidepressants and psychotherapy, has demonstrated only modest benefits. Psilocybin-assisted therapy (PAT) has shown evidence of rapid, durable, and significant effects on measures of both depression and anxiety in this patient population. A 51-year-old man diagnosed with metastatic lung cancer, referred to palliative care (PC) with a prognosis of less than 6 months, experienced depression and anxiety in the context of demoralization and existential distress. PAT was well tolerated, with significant decreases in both anxiety and depression [and] the patient subjectively reported a sustained reduction in suffering and improved well-being at 2 months post-intervention. 

Opportunities to improve end-of-life care in assisted living: Results from a national survey of administrators The Journal of the Post-Acute and Long-Term Care Medical Association; by Emmanuelle Belanger, PhD, Nicole Rosendaal, MSc, Michelle L. Rogers, PhD, Tamara A. Sequeira, RN, MSN, Kali S. Thomas, PhDe ∙ Joan M. Teno, MD, MS, Susan L. Hayes, MPAf, Xiao (Joyce) Wang, PhD, Pedro L. Gozalo, PhDa, David M. Dosa, MD, MPHh, Melissa A. Clark, PhD; 11/9/25 Among 4796 eligible assisted living communities invited, 2084 administrators completed the survey from all 48 targeted states, a response rate of 43.4%. ... This national study of administrators highlights important opportunities to improve end-of-life care both as part of assisted living care processes for dying residents and through collaboration with hospice. These novel survey measures will help determine how end-of-life care processes vary along state regulations and shape residents' outcomes.

Home-based care providers reap benefits of palliative care – but broader adoption hinges on reformHome Health Care News; by Joyce Famakinwa; 11/10/25 Home-based providers are seeing tangible benefits from incorporating palliative care services as part of their offerings, but adoption of palliative service lines has remained limited. However, reimbursement and regulatory reform, as well as electronic medical record (EMR) enhancements, can accelerate broader adoption of palliative services. In the process, at-home care providers that diversify into palliative care services can differentiate themselves from their peers and improve the quality of care. For Dr. Kurt Merkelz, chief medical officer at Compassus, the combination of home health and palliative care is a net positive for providers.

NCPA and USC launch first publicly available tool to identify pharmacy shortage areas across America National Community Pharmacists Association (NCPA), Alexandria, VA; Press Release; 11/4/25 The National Community Pharmacists Association (NCPA), in collaboration with the University of Southern California (USC), unveiled an interactive, user-friendly pharmacy shortage area mapping tool available to the general public for the first time. Previously accessible only to select individuals and organizations, the public [can now] identify pharmacy shortage areas and understand access challenges in their local communities. ... The mapping tool reveals that approximately one in eight U.S. neighborhoods — representing millions of Americans — persistently lack convenient access to pharmacy services. In rural areas and underserved urban communities, the problem is far more severe, with some states and counties experiencing shortage rates approaching 50 percent.

Care of the dying patient: Maximizing compassionate care on the battlefield Military Medicine; by Kathryn B Muir, Jeremy Edwards, Rebeccah Dindinger, Benjamin Ingram, Benjamin Baker; 11/9/25... Palliative care has also been employed throughout history on the battlefield and is a vital component of compassionate care for dying patients. Unfortunately, its use on the battlefield is an unpalatable topic with little formal documentation. ... We must prepare now to reduce the pain and suffering of dying patients on the battlefield and potentially mitigate the degree of moral injury sustained by the personnel managing those casualties. Consider ...

TRUE Palliative Care launches as California strengthens commitment to compassionate care under SB 403 Pal Item, San Diego, CA; by TRUE Palliative Care; 10/28/25 Following California’s landmark decision to make the End of Life Option Act permanent under Senate Bill 403, a new chapter of compassionate healthcare has begun. Today, palliative care pioneer Dr. Bob Uslander announced the official launch of TRUE Palliative Care (TPC), an evolution of in-home, whole-person care designed to support patients and families living with serious or chronic illness, long before hospice begins.

[United Kingdom] Petition to save hospice beds going to Number 10 BBC News; Phil Shepka; 11/3/25 Families and MPs campaigning for beds to be saved at a hospice are to hand a petition with more than 15,000 signatures to Number 10 Downing Street. Nine inpatient beds at the Cambridge-based Arthur Rank Hospice are expected to close after the trust that operates nearby Addenbrooke's Hospital removed funding. ... Among those planning to attend Downing Street trip include those whose loved ones were cared for by the hospice. The funding cuts, announced last month, amount to £829,000 a year and will reduce the hospice's inpatient unit bed capacity from 21 to 12. 

Enhancing end-of-life quality metrics: The role of palliative care in a community oncology practice.JCO Oncology Practice; by Katherine Baker, Aaron J. Lyss, Larry Edward Bilbrey, L. Johnetta Blakely, Casey Chollet-Lipscomb, Natalie R. Dickson, Leah Owens, Sandhya Mudumbi; 10/25As value-based payment (VBP) models expand in oncology, care teams adopt innovative strategies to improve outcomes, enhance patient experience, and meet evolving quality metrics (QMs). End-of-life care is one area where timely access to hospice remains inconsistent—especially in rural and underserved communities—and often outside oncology practices' direct control. Additionally, advances like immunotherapy, which may be well tolerated near end-of-life, challenge the hospice model as the sole supportive care option. NCCN and ASCO guidelines recommend early palliative care in advanced cancers, and many community oncology practices now integrate palliative care-to provide longitudinal, goal-concordant care that supports quality of life throughout treatment. Including palliative care receipt in end-of-life QMs offers a more nuanced, equitable way to evaluate care, ensuring patients receive needed support regardless of geography or treatment stage.

Palliative care legislation exploding at state level, but policy gaps remain, study reveals McKnights Home Care: by Adam Healy; 10/27/25 States are becoming increasingly focused on palliative care. Since 2009, the number of palliative care-related bills introduced at the state level has grown at a rapid pace, according to a new study published in JAMA Network Open. ... Of the 819 bills introduced between 2009 and 2023, roughly 30% were eventually passed into law. ... Bills related to palliative care quality and public awareness bills were the most likely to pass, it found. Meanwhile, relatively few bills governing palliative care workforce, clinical skill building and patient rights passed during the study period.

WHO strengthens palliative care across the eastern Mediterranean to improve quality of life fundsforNGOs; Press Release; 10/29/25 The Seventy-second session of the WHO Regional Committee for the Eastern Mediterranean marked a historic step forward for health systems in the Region, as Member States endorsed resolution EM/RC72/R.4 on palliative care. The decision represents a transformative commitment to support individuals living with life-limiting illnesses, chronic conditions, and frailty, ensuring that care extends beyond treatment to dignity and compassion. ... [While] 2.4 million people in the Region need palliative care each year, less than 1% currently receive it. ... The resolution calls for countries to integrate palliative care into national health strategies, guarantee access to essential medicines such as oral opioids, and incorporate palliative care education into health professional training.

Hospice organizations: 5 tips for building a direct-to-consumer campaign McKnights Home Care; by Andrew Robinson; 10/22/25 [... Why] are so many hospice organizations so reliant on waiting for families to find you through referrals? Referrals usually come too late. And families are left scrambling to make sense of their options. This is why direct-to-consumer marketing is not only appropriate, it’s essential. Here are five tips on how to effectively create and execute hospice direct-to-consumer marketing.

After her son’s painful death, a Cheshire mother highlights Connecticut’s pediatric hospice gap New Haven Register, Norwalk, CT; by Cris Villalonga-Vivoni; 10/26/25 Carolyn Torello believes that no parent should outlive their children, yet that became her reality. ...  As his condition worsened, the family faced his impending death without the support of pediatric palliative or hospice care. No provider, she said, seemed to know how to help or where to begin. He died at 15 years old in 2021. ... In 2020, an estimated 7,800 children in Connecticut were living with complex medical conditions that limited their life expectancy and could have benefited from palliative or hospice care, according to data from the National Survey of Children's Health. ... Torello thinks that if Michael had access to hospice care, he could have died with greater dignity, and their family could have focused on simply being together. ... Efforts to create a more formalized pediatric palliative care system have been underway since 2024, led by a state-commissioned working group that will make recommendations to the legislature on potential reforms.

Correctional health and oncologist perspectives on strategies to improve cancer care in US prisons-A qualitative studyJAMA Network Open; by Christopher R. Manz, Brett Nava-Coulter, Emma Voligny, Daniel A. Gundersen, Alexi A. Wright; 10/25Individuals diagnosed with cancer while incarcerated in US prisons have worse mortality than nonincarcerated individuals. In this qualitative study of clinicians delivering cancer care for incarcerated individuals, participants identified pragmatic strategies to improve cancer screening and treatment that address most identified barriers to care in US prisons. Application of these strategies may be associated with mitigation of disparities in cancer survival for incarcerated individuals. Participants identified strategies to improve care addressing nearly all previously identified barrier themes, including strategies for (1) conducting screening in prisons; (2) bringing cancer treatment into prisons and centralizing care; (3) using telehealth, navigators, and early oncologist involvement to improve care coordination; (4) improving communication and social support; (5) improving symptom management, access to palliative medicine, and end-of-life care; and (6) delivering patient-centered care. Strategies require implementation by prisons, prison clinicians, oncologists, oncology practices, and policymakers.