Literature Review
All posts tagged with “Palliative Care Provider News | Utilization.”
[Global] Top designs revealed in buildner’s Fourth Annual Hospice – Home for the Terminally Ill competition
10/14/25 at 03:00 AM[Global] Top designs revealed in buildner’s Fourth Annual Hospice – Home for the Terminally Ill competition ArchDaily; 10/13/25 Buildner has announced the results of its fourth annual Hospice - Home for the Terminally Ill international architecture ideas competition. This global call for ideas continues to explore how architecture can support end-of-life care with empathy, dignity, and contextual sensitivity. The competition invited architects and designers to move beyond clinical requirements and envision spaces that offer emotional warmth, social connection, and a profound sense of place. ... An international jury reviewed the submissions for their design clarity, emotional resonance, and architectural depth.
The Exec: Hamilton Medical Center CMO on incremental successes in change management
10/14/25 at 03:00 AMThe Exec: Hamilton Medical Center CMO on incremental successes in change management HealthLeaders; by Christopher Cheney; 10/13/25 In healthcare, attempts to make changes quickly at a grand scale are often unsuccessful, this CMO says. The primary element of success in change management is to pursue a strategy that emphasizes small and incremental changes, according to [Ricard Perez] the new CMO of Hamilton Medical Center in Dalton, Georgia. ... If you are going to be affecting people's daily work lives, your best bet for success is to make sure that those people have some representation at the table," Perez says. "Once you have stakeholders at the table, they can become advocates and catalysts for change because they will have an intricate understanding of why change needs to happen."
Palliative care remains underused among young adults with advanced cancer in U.S.
10/13/25 at 03:00 AMPalliative care remains underused among young adults with advanced cancer in U.S. American Cancer Society, Chicago, IL; 10/10/25 Although palliative care use has increased over time among young adults with advanced cancers in the United States, new research led by the American Cancer Society (ACS) found that utilization still remains very low. Palliative care focuses on improving the quality of life for individuals with serious or life-limiting illnesses. ... Researchers, led by Kewei (Sylvia) Shi, MPH, at the American Cancer Society, used the National Cancer Database to identify patients aged 18-39 who were newly diagnosed with stage-IV cancers. ... The study included a total of 76,666 patients. The percentage receiving any palliative care increased from 2.0% in 2010 to 4.8% in 2023.
Care that never gives up - in honour of World Hospice & Palliative Care Day 2025
10/13/25 at 03:00 AMCare that never gives up - in honour of World Hospice & Palliative Care Day 2025 The Morung Express; by Dr. Victoria Seb, MBBS, PDGDM, FIPM; 10/10/25 Quoting the Father of Medicine, Hippocrates, himself : ‘To cure sometimes, to relieve often, to comfort always’, these timeless words echo deeply the realm of palliative care, reminding us that the heart of healthcare lies not only in curing disease but in easing suffering and preserving dignity. The World Hospice & Palliative Care Day 2025 theme “Achieving the Promise: Universal Access to Palliative Care” calls to action for communities, healthcare systems and policy makers to ensure that palliative care is not a privilege but a universal right – accessible to every person, everywhere. ... In an era marked by medical advancement and increased life expectancy, the demand for holistic, compassionate care at the end of life has never been greater. Yet, despite its proven benefits, access to palliative care remains limited worldwide. The need for palliative care is urgent and growing, especially as populations age and chronic diseases become more prevalent.
Bridging gaps in palliative care for undocumented immigrants using the social determinants of health framework
10/11/25 at 03:45 AMBridging gaps in palliative care for undocumented immigrants using the social determinants of health frameworkAmerican Journal of Hospice and Palliative Medicine; by Lisa Cross, Rachael Salguero; 9/25Systemic policies and inequities, rather than immigration status itself, create barriers to health. In the United States, an estimated 11 million individuals live without legal authorization, a population that faces profound challenges in accessing equitable care. These barriers pose particular difficulties for palliative care nurses in recognizing and addressing the needs of undocumented immigrants. Identifying nursing interventions in this manner aligns with the overarching goals of the American Nurses Association and reflects the principles of ethical compassionate palliative nursing.
Beyond bars: Evaluating end-of-life care and surrogate decision-making for hospitalized incarcerated persons
10/11/25 at 03:40 AMBeyond bars: Evaluating end-of-life care and surrogate decision-making for hospitalized incarcerated personsJournal of Palliative Medicine; by Zack Watson, Julie Brown, Abhinav Vyas, Stacey Tillman, Sumi Misra, Rajiv Agarwal, Cheryl Gatto, Allison McCarthy, Mohana Karlekar; 9/25Incarcerated persons (IPs) retain the constitutional right to health care, yet they face unique challenges in accessing palliative care (PC) and designating surrogates, especially when incapacitated. We present two cases of hospitalized IPs with life-limiting illnesses who experienced significant barriers in identifying and engaging surrogates. Both cases underscore the effect of delays in communication with surrogates and restricted end-of-life (EOL) visitation due to correctional policies. These delays limited the delivery of optimal interdisciplinary PC and bereavement support. Despite clear legal guidance under the Tennessee Health Care Decisions Act, misinformation and procedural ambiguity among medical and correctional staff impeded timely and appropriate care.
Evaluation of a flexible artist-facilitated storytelling intervention on a palliative care unit
10/11/25 at 03:35 AMEvaluation of a flexible artist-facilitated storytelling intervention on a palliative care unitJournal of Pain and Symptom Management; by Kyle J. Drouillard, Regine Krechowicz, Kim Kilpatrick, Shirley H. Bush, Cory J. Ingram, Kaitlyn Boese, Jaya Rastogi, Jessica Roy, Carol Wiebe, Jenny McMaster, Claudia Hampel, Sarina Isenberg; 9/25A professional storyteller facilitated sessions with patients, caregivers, and healthcare professionals on a palliative care unit, starting with an open-ended question (e.g., “What story do you want to tell?”). From 18 sessions, patients (n=6), caregivers (n=8), and healthcare professionals (n=6), found the storytelling session acceptable, appropriate, feasible, meaningful and worthwhile. The storyteller perceived participants as enthusiastic and appreciative. Patient and caregiver stories described the palliative care unit as a calm site of reflection, and framed illness as a journey. Healthcare professionals’ stories reflected pride in and gratitude for their work.
[Brazil] Integrating holistic communication into psychedelic-assisted therapies in hospice and palliative care: An approach based on Peplau's theory
10/11/25 at 03:05 AM[Brazil] Integrating holistic communication into psychedelic-assisted therapies in hospice and palliative care: An approach based on Peplau's theoryJournal of Holistic Nursing; by Ana Cláudia Mesquita Garcia, Felipe Teixeira, Lucas Oliveira Maia; 9/25 Psychedelic-assisted therapy (PAT) has shown promising results in alleviating psychological and existential suffering among individuals with serious illnesses. This article explores the application of Peplau's Theory of Interpersonal Relations (PTIR) as a foundation for holistic communication in PAT, particularly in hospice and palliative care. We examine how PTIR's core concepts (person, health, environment, and nursing) along with its articulation of therapeutic roles, phases of the nurse–patient relationship, and the concept of anxiety as a signal of unmet needs, can be integrated into PAT's preparation, dosing, and integration phases. Drawing on a fictional case study involving a patient with advanced cancer, we illustrate how nurses can use PTIR to support emotional processing, foster insight, and promote personal growth during psilocybin-assisted therapy.
Conspiracy of verticals: Rethinking healthcare models with Peter Benjamin
10/10/25 at 03:00 AMConspiracy of verticals: Rethinking healthcare models with Peter Benjamin Teleios collaborative Network (TCN); video/podcast hosted by Chris Comeaux with Peter Benjamin; 10/8/25 In this conversation, Peter Benjamin and Chris Comeaux discuss the impact of COVID-19 on mortality rates, particularly the concept of 'death pull forward' and its implications for Hospice Care. Peter highlights the significant role of assisted living facilities in Hospice days and explores macro trends in healthcare, emphasizing the shift from vertical to horizontal care models. The discussion also covers the evolution of Palliative Care, frail elderly practices, and institutional special needs plans (iSNPs), while stressing the importance of measuring quality of care, particularly in pain management.
Bipartisan group of N.Y. legislators urge Hochul to sign bill preventing for-profit hospice expansion
10/10/25 at 03:00 AMBipartisan group of N.Y. legislators urge Hochul to sign bill preventing for-profit hospice expansion Spectrum News 1, Northern New York; by Susan Arbetter; 10/9/25 Because hospice care doesn’t provide curative treatment, for-profit companies, including private equity firms, are swiftly entering the field because they can make a lot of money. It hasn’t worked out well. In New York state, there are 39 not-for-profit hospice programs and two for-profit. There are those who point to the state’s low hospice utilization rate and say the answer is to open the state up to more for-profit hospice. State Sen. Liz Krueger, a Democrat from Manhattan, and state Assemblyman Brian Maher, a Republican from the Hudson Valley, both strongly disagree.
For this doctor, LGBTQ+ care is about the mission and the moment
10/10/25 at 02:00 AMFor this doctor, LGBTQ+ care is about the mission and the moment American Medical Association (AMA); by Timothy M. Smith; 10/8/25 ... [Shail Maing, MD] is a hematology-oncology and palliative care physician at Dana-Farber Cancer Institute (DFCI), in Boston, where she is also the inaugural DFCI Network health equity and inclusion liaison. In addition to her work caring for patients, Dr. Maingi’s passion is advocacy, particularly on health inequities for LGBTQ+ patients. She was the founding chair of the American Academy of Hospice and Palliative Medicine’s LGBTQ Special Interest Group. “We’re living in a very diverse world, with much more acceptance and acknowledgement that health care is for everybody—that there are differences that are unexplored, and we can't pretend everybody has the same set of needs,” said Dr. Maingi ...
The expanding role of family medicine in Alzheimer's Disease and other dementias
10/09/25 at 03:00 AMThe expanding role of family medicine in Alzheimer's Disease and other dementias Patient Care; by Grace Halsey; 10/7/25 [From the 2025 Family Medicine Experience conference] Family medicine's unique position in dementia management spans initial diagnosis through end-of-life care. ... Dementia Staging: Clinical Assessment and Hospice EligibilityFor practical bedside assessment and hospice determination, the Functional Assessment Staging Tool (FAST) proves particularly valuable.1 The FAST scale includes 7 main stages, progressing from no impairment (stage 1) through severe dementia requiring total care (stage 7). Stage 7 breaks down further into substages (7a-7f) that capture specific functional losses including ambulation, independent sitting, smiling, and head control. Eligibility for hospice care generally requires FAST stage 7c or beyond, indicating ... [continue reading this important criteria] Editor's Note: Leaders must understand hospice eligibility criteria when setting census goals, guiding teams, and communicating with families. Getting it wrong risks fraudulent billing, angry caregivers when live discharges occur, or too little care that comes too late. Getting it right ensures dignity, humanity, and meaningful final moments amid dementia's long goodbyes—true measures of compassionate hospice dementia care.
Telepalliation creates a sense of security: A qualitative study of patients with cancer receiving palliative care
10/09/25 at 03:00 AMTelepalliation creates a sense of security: A qualitative study of patients with cancer receiving palliative carePalliative Medicine; by Jarl Voss Andersen Sigaard, Elisabet Dortea Ragnvaldsdóttir Joensen, Una Rósa Birgisdóttir, Helle Spindler, Birthe Dinesen; 10/7/25 ... The aim of this study was to explore patients' experiences with the functionality of the Telepalliation program while receiving specialized palliative care. ... Results: Four key themes emerged: "Sense of coherence," "Telepal platform," "Roles of spouse/partner and relatives," and "Cross-sector collaboration." The program improved patients' sense of security and coherence by enhancing communication with healthcare professionals. ... The platform also successfully integrated relatives into the care process. Editor's Note: While this research was conducted in Denmark, it surely resonates with patient care in the US. Reference articles in the uncertainties of government shutdowns, legislative needs to extend telehealth, and more:
Timing matters: Impact of early advance care planning conversations on hospice utilization in outpatient oncology
10/09/25 at 03:00 AMTiming matters: Impact of early advance care planning conversations on hospice utilization in outpatient oncologyJCO Oncology Practice, An American Society of Clinical Oncology Journal; by Lydia Mills, Malia Albin, Ami Gorsky-Zabukovic, Liz Hutchison, Molly Mendenhall, and Robyn Tibert; 10/7/25 Results: 53% of physicians interviewed defined [Advance Care Planning] ACP as hospice, end-of-life, or code status conversations. This group of providers preferred waiting to conduct ACP discussions until later in a patient’s disease trajectory. However, 33% of physicians interviewed viewed ACP as broader discussions, to include patients’ values, goals and preferences for EOL care. These physicians stated they engage in ACP conversations as early as the first or second visit, especially with patients who have Stage IV disease or have a poor prognosis, introducing hospice as a potential option and revisiting these discussions throughout the course of treatment. PI data showed that providers who engage in early and consistent ACP discussions have a 17% higher hospice enrollment rate compared to their peers.
Wisconsin rarely grants compassionate release as aging, ailing prisoners stress systems
10/08/25 at 03:00 AMWisconsin rarely grants compassionate release as aging, ailing prisoners stress systems Wisconsin Watch; by Mario Koran and Sreejita Patra; 10/7/25 Increased use of compassionate release could ease costs and crowding with minimal risks to public safety, experts say. But it remains off limits to many prisoners. ... Wisconsin grants few applicants compassionate release, leaving many severely ill inmates in short-staffed prisons that often struggle to meet health care needs. Wisconsin courts approved just 53, or 11%, of 489 compassionate release petitions they received between January 2019 and June 2025 — about eight petitions a year, Corrections data show. Courts approved just five of 63 petitions filed in all of 2024.
Living with injustice: Gary Tyler had his life taken away, yet managed to claw it back.
10/07/25 at 03:00 AMLiving with injustice: Gary Tyler had his life taken away, yet managed to claw it back. The Progressive Magazine; by Bill Lueders; 10/6/25 Just as I sat down to write this review of former death row inmate Gary Tyler’s memoir, I noticed that its publication date is the fifty-first anniversary of the day that upended his life: October 7, 1974. This undoubtedly deliberate timing, like the book itself, serves to help close the circle around Tyler’s remarkable—at times, almost unbelievable—life journey. That was the day Tyler, then a sixteen-year-old Black youth, was arrested for the shooting death of a thirteen-year-old white boy at their high school in Destrehan, Louisiana, about twenty-five miles from New Orleans. He was taken into custody and beaten so severely that he was left with permanent physical scars, as well as psychological ones. Police and prosecutors ignored and withheld evidence of his innocence, and suborned perjury by threatening witnesses. One witness, Natalie Blanks, was told she would be charged as an accessory to murder and miss out on her baby’s life if she didn’t falsely testify that she saw Tyler fire a gun from inside a bus. Stitching Freedom: A True Story of Injustice, Defiance, and Hope in Angola Prison is, for much of its first half especially, an intensely bleak book.Editor's Note: See previous significant posts in our newsletter about Gary Tyler and this transformative hospice program at Angola Prison.
Life lessons from a palliative care psychologist - and how to support a dying loved one
10/07/25 at 03:00 AMLife lessons from a palliative care psychologist - and how to support a dying loved one HELLO! onMSN; by Pilar Hernán; 10/5/25 ... Psychological support becomes a fundamental pillar for providing comprehensive and humane care, from managing emotional pain to adapting to the new reality. MD Anderson Cancer Centre psycho-oncologist Fátima Castaño helps us understand the process, explaining how we can support a loved one in palliative or end of life care, and shares the powerful life lessons she has learned through her work.
Milton Village Open House builds community to support caregivers of individuals with Alzheimer's, dementia, or other cognitive conditions
10/07/25 at 03:00 AMMilton Village Open House builds community to support caregivers of individuals with Alzheimer's, dementia, or other cognitive conditions GreatNews.Life; by Lauren Grasham; 10/6/25 To help healthcare providers better understand the numerous resources available, Milton Village hosted an open house on Tuesday, September 30. Milton Village is a collaborative effort between Milton Adult Day Services (a program of the Center for Hospice Care) and Alzheimer’s & Dementia Services of Northern Indiana (a REAL Services program) to provide comprehensive care and support to individuals living with Alzheimer’s or other cognitive conditions and their caregivers. “Inviting healthcare providers to see our facility and learn more about our programs is a great way to help them understand our unique model,” said Sarah Youngs, director of Milton Adult Day Services. “As providers tour the facility and hear how our guests engage in the programming, it’s so satisfying to see them recognize what this can mean for their patients and the patients’ caregivers.”
'Traffic light care model will help generations'
10/07/25 at 03:00 AM'Traffic light care model will help generations'BBC News, West Midlands, England; by Chloe Hughes; 10/6/25 A man with a neuromuscular condition has said that a model of care developed in Shropshire to help patients like him will benefit future generations. ... Part of his care has involved using the Oswestry model developed by Prof Tracey Willis from the Robert Jones and Agnes Hunt Orthopaedic Hospital (RJAH) and her husband, Prof Derek Willis, Severn Hospice's medical director. It uses a "traffic light system" to help neuromuscular teams identify key stages in a patient's journey, in which hospice involvement would improve their quality of life. ... Patients are identified as green, amber or red.
Healthcare AI in the United States — navigating regulatory evolution, market dynamics, and emerging challenges in an era of rapid innovation
10/06/25 at 03:00 AMHealthcare AI in the United States — navigating regulatory evolution, market dynamics, and emerging challenges in an era of rapid innovation The National Law Review; by Nadia de la Houssaye, Andrew R. Lee, Jason M. Loring, Graham H. Ryan of Jones Walker LLP; 10/2/25 The use of artificial intelligence (AI) tools in healthcare continues to evolve at an unprecedented pace, fundamentally reshaping how medical care is delivered, managed, and regulated across the United States. As 2025 progresses, the convergence of technological innovation, regulatory adaptation (or lack thereof), and market shifts has created remarkable opportunities and complex challenges for healthcare providers, technology developers, and federal and state legislators and regulatory bodies alike. ...
Stamford-area seniors can now enjoy free daytime care
10/06/25 at 03:00 AMStamford-area seniors can now enjoy free daytime care Evergreen, Stamford, CT; by Evergreen Daytime Senior Care and CT Hospice; 10/3/25Thanks to a groundbreaking Medicare initiative, seniors living with dementia now qualify for benefits that help cover the cost of adult daytime care. Designed to improve quality of life, the GUIDE (Guiding an Improved Dementia Experience) Model, offered by Connecticut Hospice's Stand By Me program, features a full range of valuable services, including care coordination, caregiver education, and an annual respite benefit for up to 25 free days at adult day centers like Evergreen Daytime Senior Care. ... "We're excited to partner with Evergreen to provide high-quality adult day services to families enrolled in the GUIDE Model program," explained Mark Olynciw, GUIDE Program Manager at Connecticut Hospice. "Having trusted partners like Evergreen ensures our families have excellent options for their respite benefits."
How palliative care supports families emotionally and physically
10/06/25 at 03:00 AMHow palliative care supports families emotionally and physically Elevated Magazines; 10/3/25 People often feel lost when someone they love is diagnosed with a serious illness. The shift in daily routines, the constant medical appointments, and the uncertainty about the future can feel overwhelming. Palliative care steps in to ease this transition, offering medical expertise and guidance that helps families adjust to new roles and responsibilities. Having a care team that understands both medical needs and the emotional burden can make a significant difference.
Surgeon perspectives on palliative care: Are we the barrier to better care?
10/04/25 at 03:35 AMSurgeon perspectives on palliative care: Are we the barrier to better care?The Journal of Clinical Ethics; Sean J Donohue, Baddr A Shakhsheer, Peter Phung, Anthony W Kim, Monica Zell, Sean C Wightman; Fall 25Surgeons face numerous perioperative challenges when caring for patients with life-threatening or chronic diseases. Palliative care has been associated with an average reduction of $3,237 per admission, as well as reduction in emergency department visits, hospital admissions, and hospital length of stay. For patients within the intensive care setting, palliative interventions have shown a 26 percent relative risk reduction in intensive care unit length of stay and overall alignment of patients' and families' goals of care. It remains pervasive in surgical culture that operative intervention and palliation are mutually exclusive and occur sequentially, rather than concurrently. Preoperative palliative care consultations in surgical patients occur less than 1 percent of the time. Preoperative palliative care may serve to help explore, clarify, and document quality-of-life values and preferences, in hopes of better promoting goal-concordant care.
Not everything is delirium at the end of life: A case report
10/04/25 at 03:15 AMNot everything is delirium at the end of life: A case reportAnnals of Palliative Medicine; by Daniel Gilbey, Eduardo Bruera, Patricia S Bramati; 9/25In this report, we highlight the challenges faced by clinical teams diagnosing and managing delirium, in particular when a language barrier is present. Case description: A patient in his late sixties with low English proficiency with a metastatic neuroendocrine tumor was transferred to a palliative care unit on non-invasive bilevel ventilation. He appeared to become delirious and agitated, trying to remove the face mask, wriggling in bed, and tapping the bedrails. Haloperidol and lorazepam were required when non pharmacological interventions failed to calm him down. The following morning, the patient was able to explain that the positive-pressure facemask was suffocating him and that he could not breathe. So, he was transitioned to high-flow oxygen via nasal cannula, and within a few hours, his respiratory distress significantly improved, and he regained his previous self.
[UK] From living well to dying well with dementia: The significance of an expanded understanding of loss for end-of-life care
10/04/25 at 03:05 AM[UK] From living well to dying well with dementia: The significance of an expanded understanding of loss for end-of-life carePalliative Care and Social Practice; by Joseph M Sawyer, Paul Higgs; 9/25As rates of dementia increase, the need for care is clear. Understanding what this looks like and how people might orientate the narratives and practices of care against a universally relatable version of success is less clear cut yet seems crucial if we are to progress towards an ideal of care that allows for a 'good' or 'dignified' death with palliative care. With this as a central focus, the paper examines the orientating principles that govern the current approach to dementia care. We map the evolution in academic theory from deficit-based models of care that identify impairments as a means to building resources to counter them, towards capacity-oriented approaches that focus on accommodating the new experiences that dementia brings. Where conventionally dementia has been viewed through the reductionist lens of being either a biological or social challenge to which there should be a matching solution, it is perhaps more useful to look at it from the inside out, to learn the lessons that dementia and its associated vulnerabilities may hold for humanity.
