Literature Review
All posts tagged with “Palliative Care Provider News | Utilization.”
Death, taxes, and talking to your parents: Why the conversation you’re avoiding might save your family
06/16/25 at 03:00 AMDeath, Taxes, and Talking to Your Parents: Why the conversation you’re avoiding might save your familyPsychology Today; by Nancy J. Kislin, LCSW, MFT; 6/11/25Key points:
Medicare Home Health Care is the ideal platform for home-based palliative care at the end of life
06/16/25 at 03:00 AMMedicare Home Health Care is the ideal platform for home-based palliative care at the end of lifeJournal of Palliative Medicine; by Tessa Jones and Sean Morrison, with Guest Editor note by Ira Byock, MD; 6/10/25Recognizing the central role of HH as a de facto means of providing home-based palliative care—and strategizing how to integrate palliative care principles and education into it—holds the potential to expand access to palliative care services and improve the quality of end of life for older Americans. The authors identify four main barriers to successfully integrating HH into the suite of palliative care delivery models. First, the HH workforce lacks training in fundamental palliative care. Second, the current lack of ongoing physician involvement in the HH setting. Third, reimbursement. Palliative care services are often excluded from traditional payment models, particularly in the HH setting. Lastly, financialization of the HH sector. They say that integration of palliative care within for-profit HH agencies may require a strategic emphasis on financial incentives.Guest Editor Note, Ira Byock, MD: This academic oped extends the drumbeat toward alternatives to hospice care. Overcoming barriers to home-based palliative care requires steps that are strikingly similar to those needed to make hospice programs successful. The authors repeatedly refer to HH interdisciplinary teams. In fact, home health is a multidisciplinary model of service delivery that lacks the clinical synergy of high-functioning interdisciplinary hospice teams.
Serious illness has mental health implications — palliative care can help
06/16/25 at 03:00 AMSerious illness has mental health implications — palliative care can help Becker's Behavioral Health; by Dr. Simeon Kwan and Dr. Rowland Pearsall; 6/12/25 ... As health plans and providers strive to deliver whole-person, value-based care, we must recognize that treating the body is only part of the equation. Mental and emotional well-being are critical dimensions of serious illness, and they demand more focused attention. Fortunately, we have a powerful but often underutilized ally: palliative care. ... According to multiple studies, up to 40% of patients with advanced cancer experience clinical depression. Anxiety and spiritual distress are also common, particularly when facing the unknown or confronting the loss of autonomy. For those managing progressive illnesses over time, mental health concerns can erode treatment adherence, accelerate physical decline, and strain family caregivers.
Nursing home is pressuring my mother-in-law to enter hospice
06/16/25 at 03:00 AMNursing home is pressuring my mother-in-law to enter hospiceAging Care - Caregiver Forum - End of Life - Questions; question posed by "concerned8"; 6/12/25 I am her Health Care Surrogate but as they won't declare her incompetent it has not come into effect. I believe the home's intent is to prevent me from making the decision regarding hospice and instead to pressure her to enter it in various ways. ... I am not anti-hospice and expect her to enter it in the near future, but want that to be my decision, not the home's (even if it's portrayed as hers). ... [An answer from another reader" Our family has only had bad experiences with three different hospice companies. Contrary to what most people believe, many patients are placed on hospice for free equipment and free services. I was told this by more than one hospice worker.Editor's Note: This post raises numerous troubling perceptions, with descriptions of poor hospice experiences.
Advancing Symptom Alleviation with Palliative Treatment (ADAPT): A qualitative study to understand how a nurse and social worker palliative telecare team improved quality of life in chronic illness
06/14/25 at 03:10 AMAdvancing Symptom Alleviation with Palliative Treatment (ADAPT): A qualitative study to understand how a nurse and social worker palliative telecare team improved quality of life in chronic illnessJournal of Applied Gerontology; Amy Ladebue, Juliana G. Barnard, Leah M. Haverhals, Brianne Morgan, Kelly Blanchard, Marilyn Sloan, David B. Bekelman; 5/25 The Advancing Symptom Alleviation with Palliative Treatment (ADAPT) trial found that a nurse and social worker palliative telecare team (providing care via phone) improved quality of life in older Veteran patients with chronic illness. Our objective was to describe clinician and patient experiences of ADAPT and how ADAPT influenced Veterans’ quality of life. We used thematic analysis on structured interviews with 36 randomly selected patients, semi-structured focus groups with nine palliative care intervention team clinicians, and clinical intervention summaries of 147 patients. ADAPT proved to be an effective model for most Veterans by improving Veterans’ health care delivery and navigation and promoting timely and holistic health care and teaching skills that improved wellbeing. ADAPT also helped to improve patient engagement and sense of agency.
[Canada] The discourse of medical assistance in dying and its relationship with hospice palliative care in Canada: An integrative literature review
06/14/25 at 03:05 AM[Canada] The discourse of medical assistance in dying and its relationship with hospice palliative care in Canada: An integrative literature reviewJournal of Advanced Nursing; Jennifer D Dorman, D Shelley Raffin Bouchal, Eric Wasylenko, Shane Sinclair; 5/25Three themes identified from the data were the relationship between MAiD [medical assistance in dying] and HPC [hospice pallaitive care], suffering in the context of MAiD, and moral distress and moral uncertainty in providing or not providing MAiD. The discourse around the relationship between MAiD and HPC is complex and contextual. Personal and professional understandings of end-of-life care differ and influence perspectives on how and whether MAiD and hospice palliative care can be reconciled. Findings consider how the concepts of end of life, MAiD, HPC, suffering, and moral distress influence and are influenced by the discourse of dying.
Healing hearts: How palliative care staff reunited a father with his daughters after nearly 40 years apart
06/13/25 at 03:00 AMHealing hearts: How palliative care staff reunited a father with his daughters after nearly 40 years apart The Daily Scan - Cancer; by Sondi Bruner; 11/25/24, published in our newsletter 11/25/24Leah Duval and Tanya Ellis don’t have many childhood memories of their father. They recall fragments, like his bright smile and building snowmen in the backyard. And then one day, when they were three and five years old, Glenn Ellis disappeared completely. As the girls grew up, they learned their father had schizophrenia, which they guessed played a large role in his disappearance. ... The family searched for years in the 1980s and never found him. The sisters had no choice but to move forward with their lives, though they never gave up hope that their father was still out there. ... Then, on May 14th 2024, nearly 40 years after their father vanished from their hometown in Ontario, Tanya received an unexpected phone call from across the country. It was from Siobhan Gallagher, a social worker at May’s Place Hospice in Vancouver, BC. She had a patient named Glenn Ellis, and he was looking for his daughters. [Click on the title's link to read this story.] ... “People can hold onto grudges for their entire life and they don’t allow healing to happen,” says Tanya. “Have an open heart and an open mind. Just let things go, because we’re just all humans trying to do the best we can in this world.”
My dad had an Advance Directive. He still had to fight to die
06/13/25 at 03:00 AMMy dad had an Advance Directive. He still had to fight to die Newsweek - My Turn; by Maggie Schneider Huston; 8/26/24, published in our newsletter 8/27/24My mom died peacefully. My dad died 72 days later, angry at the doctors for ignoring his wishes. ... Dad had heart surgery on December 20, 2023. An hour after the surgery ended, his vital systems started shutting down. A cascade of interventions, one after another, kept him alive. Four days later, he said: "Put me on hospice." The doctor dismissed this request, rolling his eyes and saying: "Everyone on a ventilator says that." On Christmas Day, my father asked for hospice again. He was in pain. He knew his recovery would be long and ultimately futile. He would never have an acceptable quality of life again. ... Dad's care team insisted palliative care was the same as hospice care, but he knew the difference. He wanted hospice care. Finally, they reluctantly agreed and called for a social worker to make arrangements. It wasn't necessary. Once they removed his treatment and relieved his pain, he died five hours later. ... Editor's Note: This article is not about Medical Aid in Dying (MAiD). It is about honoring Advance Directives, person-centered care with communications and actions related to "palliative" vs. "hospice" care. Pair this with other posts in our newsletter today, namely "Improving post-hospital care of older cancer patients."
Revolutionizing health in South Florida: The benefits of IV therapy and inclusive hospice care
06/11/25 at 03:00 AMRevolutionizing health in South Florida: The benefits of IV therapy and inclusive hospice care South Florida Reporter; by southfloridareporter.com; 6/8/25 ... South Florida is known for its multicultural population, making the expansion of hospice care to diverse groups particularly significant. Traditionally, certain cultural or community groups may have had hesitations or lacked access to hospice care due to language barriers, cultural misunderstandings, or lack of awareness. Increasingly, hospice organizations are focusing on outreach and education within these communities, breaking down barriers and encouraging patients and families to consider hospice as a valuable option for quality end-of-life care.
Summerlin Hospice and Palliative Care transforms hospice care in Las Vegas with comprehensive in-home services
06/10/25 at 03:00 AMSummerlin Hospice and Palliative Care transforms hospice care in Las Vegas with comprehensive in-home services East Coastsentinel; Press Release; 6/8/25 The healthcare industry is experiencing significant advancements as Summerlin Hospice and Palliative Care announces the expansion of comprehensive services that redefine compassionate end-of-life care throughout Nevada. ... The in-home care model provides comprehensive medical oversight, including pain management, regular health assessments, and specialized medical testing, all administered by trained healthcare professionals. This approach to hospice allows families to remain together while receiving the highest quality medical attention and emotional support throughout the care process.
SCI Waymart meets needs of aging incarcerated population by training inmates in hospice care
06/10/25 at 03:00 AMSCI Waymart meets needs of aging incarcerated population by training inmates in hospice care PBS WVIA News, NPR, Pittston, PA; by Lydia McFarlane; 6/8/25 Nurses and their inmate aides care for hospice patients. Some are bedridden, needing help with eating, changing and using the bathroom. The patients have recently signed do-not-resuscitate (DNR) forms. Some have just a few more months to live. The medium security prison's hospice unit looks like a nursing home. SCI Waymart is one of two prisons, along w ith SCI Laurel Highlands, in the Commonwealth that has a personal care unit. Waymart receives medical transfers from institutions across the state, making its population older than most of Pennsylvania’s state prisons. The average age of a Waymart inmate is 45.5, according to SCI Waymart’s superintendent, Mark Wahl. About 36% of inmates are over the age of 50, and 10% are over 65 out of a total of 1,122 as of April of this year, he said. Wahl said SCI Waymart averages one death per month.
Palliative care advocacy at the World Health Assembly 2025
06/10/25 at 03:00 AMPalliative care advocacy at the World Health Assembly 2025 ehospice; by Stephen Connor, Executive Director WHPCA; 6/5/25 Once again, palliative care advocates ensured that the voice of palliative care was heard at the premier event for global health, the World Health Assembly (WHA). The WHA is the governing body of the WHO where resolutions are passed that direct the Global Programme of Work for WHO. ... This year there were resolutions and actions involving non-communicable disease, cervical cancer, lung health, the pandemic response, mental health and social connection, the healthcare workforce, women’s health, universal health coverage, health emergencies, and so forth. WHO’s funding has been significantly reduced due to withdrawal of the US from WHO and global health funding generally. However, during the meeting other countries are stepping up to support WHO.
Implementing palliative care in nursing homes: A podcast with Connie Cole, Kathleen Unroe, and Cari Levy
06/10/25 at 03:00 AMImplementing palliative care in nursing homes: A podcast with Connie Cole, Kathleen Unroe, and Cari Levy GeriPal; podcast by Connie Cole, Kathleen Unroe and Cari Levy; 6/5/25 Consider this: the majority of the 1.4 million adults residing in U.S. nursing homes grapple with serious illnesses, and roughly half experience dementia. Many also suffer from distressing symptoms like pain. In addition, about 25% of all deaths in the United States occur within these facilities. Despite these substantial needs, specialized palliative care beyond hospice is rare in nursing homes. Furthermore, only about half of nursing home residents nearing the end of life receive hospice care. So, how can we improve palliative care for individuals in nursing homes? [This] podcast explores this crucial question with three leading experts: Connie Cole, Kathleen Unroe, and Cari Levy.
Fostering a team-based approach to elevate neuro-oncology care
06/10/25 at 03:00 AMFostering a team-based approach to elevate neuro-oncology care CancerNetwork; by Sylvia Kurz, MD, PhD; 6/9/25 Sylvia Kurz, MD, PhD, spoke with CancerNetwork® about the importance of collaborating with multiple disciplines to elevate the level of care and meet the needs of patients with brain tumors.
Understanding hospice care: Eligibility, cost and purpose
06/10/25 at 03:00 AMUnderstanding hospice care: Eligibility, cost and purpose Emmanuel Hospice; 6/5/25 How do you want to live? It may be surprising to learn that’s the first question Emmanuel Hospice asks every new patient. Isn’t hospice about dying? While hospice is often associated with death, Melissa Wedberg will tell you it’s more about living, especially at Emmanuel Hospice, where she serves as vice president of community relations. With more than a decade in the hospice industry, Wedberg has spent years dispelling this and many other myths. Despite having roots in the U.S. dating back to the 70s, there remains a lot of mystery about hospice. Common questions Wedberg hears include: What is hospice and who’s eligible? How does hospice work? How is hospice paid for? Editor's note: This simple question jumps to the core of person-centered care, "How do you want to live?"
Death literacy is fostering positive conversations about the end
06/09/25 at 03:00 AMDeath literacy is fostering positive conversations about the end Counterpunch; by Caren Martineau; 5/30/25 “[D]eath literacy is defined as the knowledge and skills that make it possible to understand and act upon the end-of-life and death care options,” according to a 2024 article in the journal Palliative Care and Social Practice, and its four foundational pillars: knowledge, skills, experiential learning, and social action. ... The U.S. Census named 2024 as the start of “Peak 65,” a period that will last through 2027. Around 4.1 million Americans are expected to turn 65 each year from 2024 to 2027 (approximately 11,000 a day). By 2030, all baby boomers will be 65 or older. Implications of “Peak 65” include:
Nurse Elaine Gillard and her lifelong calling for caring
06/09/25 at 03:00 AMNurse Elaine Gillard and her lifelong calling for caring New York Amsterdam News; by Leyrian Colón Santiago; 6/5/25 Treating patients with dignity and with an awareness of the disparities that Black people face in accessing health care were the two main reasons Elaine Gillard decided to become a nurse 14 years ago. ... According to a 2024 analysis, Black-American New Yorkers experienced the lowest health system performance in the state compared to white individuals. For Gillard, a 41-year-old native of Staten Island and a nurse at VNS Health Care, the disparities affecting the Black-American population were what inspired her to focus her nursing career on hospice care. ... Gillard believes that being a Black nurse and caring for patients from Black-American communities helps foster greater trust in the health care system.
Sister Grace spent her life helping the homeless. Now in hospice, she reflects on legacy and lessons
06/09/25 at 03:00 AMSister Grace spent her life helping the homeless. Now in hospice, she reflects on legacy and lessons WXXI News NPR, Rochester, NY; by Gino Fanelli; 6/6/25Sister Grace Miller smiles as she props herself up in her hospice bed and gently teases her strands of chestnut brown hair. “How does my hair look?” she asks. It’s the type of remark one would expect from Miller. Sister Grace is many things: a radical compassionate, a devout follower of the Catholic faith, a civil disruptor, and a wielder of a sharp, slightly sardonic wit. ... The 89-year-old champion for the homeless and destitute is dying, in hospice care at a congregation home on Carter Street. But her spirit is alive and well. “I would fight with them over whatever, whatever the people needed,” Miller said, referring to the county and city administrations she often tangled with over the years. “I would fight for the people. ... She said it was, ultimately, an undying, uncompromising commitment to the work she does as a fierce and fearless advocate for the poor.
A World War II hero is facing his final battle - with Medicare | PennLive letters
06/09/25 at 02:00 AMA World War II hero is facing his final battle - with Medicare | PennLive letters PennLive Patriot News; by PenLive Letters to the Editor; 6/5/25 “Is this how one treats a 100-year-old World War II Army veteran?” I am such, having defended my country in the Philippines and then as one of the first GIs to step on Japan’s shores when it surrendered. Today, I am a widower, living alone under hospice care in the same small, comfortable home my wife and I cherished for so many years. My health condition has deteriorated dramatically, due to the ravages of ESRD, bladder cancer, anemia, high blood pressure, depression, and loss of balance. I am mostly bedridden, waiting for the inevitable. And yet, just now, I have received a Notice of Discharge from hospice because of an “extended prognosis,” literally meaning in lay terms that, “I’m living too long for hospice and Medicare purposes.” They argue that I’m now able enough medically to make it on my own without hospice care! ... I know I have only weeks, perhaps a month to live, but their rejoinder is simply, “Thank you for your service, but get out of our sight.”Editor's note: Click here for a similar related article and my editor's note, Dementia patient discharged from hospice over Medicare requirement. Here’s why it happened. (One of our "most read" Sunday posts.) These cases are too common. Basic communication, information, and coordinated care planning can mitigate much of the distress and pain. How does this dynamic play out with the patients and families you serve?
Palliative care for patients with end-stage renal disease-An examination of unmet needs and experiencing problems
06/07/25 at 03:30 AMPalliative care for patients with end-stage renal disease-An examination of unmet needs and experiencing problemsJournal of Hospice & Palliative Nursing; Darawad, Muhammad W. PhD, RN; Reinke, Lynn F. PhD, ANP-BC, FPCN, FAAN; Khalil, Amani PhD, RN; Melhem, Ghaith Bani PhD, RN; Alnajar, Malek MSN, CNS, RN; June 2025Patients with end-stage renal disease face numerous physical, emotional, and financial burdens, necessitating palliative care (PC) interventions. This cross-sectional study ... revealed that 64.7% of participants experienced significant challenges, primarily financial difficulties (78.5%), autonomy concerns (68.8%), and a need for information (68.0%). More than half (51.9%) reported needing PC [palliative care], particularly for managing fatigue (78.3%), pain (79.8%), and depression (72.9%). Unmet needs were common (47.6%), with the most notable gaps in financial support (52.5%) and information provision (50%). These findings underscored the urgent need for tailored PC interventions for end-stage renal disease patients, particularly in addressing symptom management, psychosocial and spiritual support, financial support, and information deficits, to enhance their quality of life.
Implementing palliative care in nursing homes: A podcast with Connie Cole, Kathleen Unroe, and Cari Levy
06/06/25 at 03:00 AMImplementing palliative care in nursing homes: A podcast with Connie Cole, Kathleen Unroe, and Cari LevyGeriPal podcast; by Eric Widera, Alex Smith; 6/5/25The need for better palliative care in nursing homes is significant. Consider this: the majority of the 1.4 million adults residing in U.S. nursing homes grapple with serious illnesses, and roughly half experience dementia. Many also suffer from distressing symptoms like pain. In addition, about 25% of all deaths in the United States occur within these facilities. Despite these substantial needs, specialized palliative care beyond hospice is rare in nursing homes. Furthermore, only about half of nursing home residents nearing the end of life receive hospice care. So, how can we improve palliative care for individuals in nursing homes? Today’s podcast explores this crucial question with three leading experts: Connie Cole, Kathleen Unroe, and Cari Levy.
Rosen introduces bipartisan bills to expand access to palliative care, hospice care
06/06/25 at 03:00 AMRosen introduces bipartisan bills to expand access to palliative care, hospice careJacky Rosen, U.S. Senator for Nevada, Washington, DC; 6/5/25 U.S. Senator Jacky Rosen, co-founder and co-chair of the bipartisan Senate Comprehensive Care Caucus, announced the introduction of a pair of bipartisan bills to expand access to palliative and hospice care. The Expanding Access to Palliative Care Act with Senators Barrasso (R-WY), Baldwin (D-WI), and Fischer (R-NE) would establish a demonstration project through Medicare to expand access to palliative care at the time of diagnosis of serious illness or injury. The Improving Access to Transfusion Care for Hospice Patients Act with Senators Barrasso (R-WY) and Baldwin (D-WI) would carve out payment for transfusion services within the Medicare hospice benefit, allowing for separate billing to Medicare for transfusions. This would improve access to hospice care for patients who rely on transfusion care to maintain quality of life.
Hawai'i Pacific University alumni join forces to build a pioneering palliative care team for student excellence
06/05/25 at 03:00 AMHawai'i Pacific University alumni join forces to build a pioneering palliative care team for student excellence Special to The 'Ohana - HPU's Daily News, Honolulu, HI; 6/3/25 A group of HPU alumni from the nursing, social work, public health and business administration programs ... will be working towards steering a newly established palliative care team at HPU to assist nursing students, social workers and public health students to play an important role in understanding palliative care, hospice and communication with family and survivors. The team will play a role in setting up clinical placements in the community at St. Francis Palliative Care Units and Hospice, to give our nursing students invaluable hands-on experience in providing compassionate care for patients with serious and life-limiting illnesses. HPU Assistant Professor Joy Bliss, Ph.D., will also be designing simulations for “effective listening and communication skills,” to enhance student’s performance and skills in grief and this specialty of nursing. ... This initiative is not only an opportunity to strengthen the clinical training of nursing students, but also an essential step forward in improving the availability and quality of palliative care in Hawaiʻi.
Hospice provider MiraSol Health launches new Behavioral Health Program
06/05/25 at 03:00 AMProvider MiraSol Health launches new Behavioral Health Program Hospice News; by Jim Parker; 6/3/25 MiraSol Health has launched a new behavioral health program designed to amplify emotional and psychological support for its hospice and palliative care patients. Branded as Rays of Hope Behavioral Health, the program offers individual and group therapy sessions, both in person and via a secure telehealth platform. Through Rays of Hope, MiraSol’s licensed therapists will help address anticipatory grief, caregiver stress, loss and other struggles that patients and families face during a time of chronic, serious or terminal illness.
10 Signs death is near for dementia patients
06/04/25 at 03:00 AM10 Signs death is near for dementia patients The Healthy; by Dr. Patricia Varacollo, DO; 6/2/25 For families and caregivers, recognizing the final stages of dementia can be difficult, but understanding the signs can help ensure comfort and dignity in a loved one's last days. Dr. Koncilja highlights these key indicators that may suggest the end of life is near: