Literature Review
All posts tagged with “Palliative Care Provider News | Utilization.”
The effect of race on patterns of care and utilization of palliative interventions in patients with lung cancer
02/23/26 at 03:00 AMThe effect of race on patterns of care and utilization of palliative interventions in patients with lung cancer Holistic Integrative Oncology; by Calvin Walker, Jr., Zeytun Guyo, Davin Means, Martlin Emeasoba, Samantha Robinson, Mohammod Mahmudur Rahman, Kingsley Nnawuba & Hanna Jensen; 2/6/26 ... Results: Altogether 2,048 (1,660 white and 388 black) patients were included in the study with other races excluded due to low sample sizes. Black patients were younger, more male, had higher rates of current tobacco use, and utilized Medicaid more often than their white counterparts. Black patients also had more comorbidities while having less family history of cancer, were diagnosed with more advanced stages of cancer, and had more active cancer status in follow-up. ...
Hospice use after ICU admission increased across the US from 2011–2023
02/23/26 at 02:00 AMHospice use after ICU admission increased across the US from 2011–2023 Medical Xpress; by Boston University School of Medicine, edited by Gaby Clark; 2/19/26 ... In a new study from Boston University Chobanian & Avedisian School of Medicine, researchers have found that more older adults in the U.S. are being discharged to hospice after an ICU stay than in the past, and this increase happened even as overall short-term death rates stayed stable. This research is the first to quantify hospice use after ICU stays on a national scale, and suggests a real shift in how end-of-life care is delivered to the seriously ill. These findings appear online in the Annals of the American Thoracic Society.
Too late to help? Disparities in palliative and hospice care among veterans with pancreatic cancer—A 10-year retrospective study at a VA medical center
02/21/26 at 03:15 AMToo late to help? Disparities in palliative and hospice care among veterans with pancreatic cancer—A 10-year retrospective study at a VA medical centerJournal of Clinical Oncology; by Jonathan Blackmon, Mirza Mashaal Khan, Rahul Reddy Tirumalareddy, Zohair Siddiqui, Saurin Chokshi, Alva Bowen Weir III; 1/26Pancreatic cancer is characterized by high symptom burden, rapid progression, and poor prognosis. ASCO [American Society of Clinical Oncology] guidelines recommend palliative care consultation at diagnosis or within 8–12 weeks. Despite guideline recommendations, many patients with pancreatic cancer did not receive timely palliative or hospice care. Delays were more pronounced among rural and Black patients, highlighting persistent disparities in access. These findings support the implementation of a quality improvement initiative at the Memphis VA to standardize early palliative care referrals for high-risk populations.
[UK] Parental experiences of perinatal loss, with a focus on hospice provision: A thematic analysis
02/21/26 at 03:10 AM[UK] Parental experiences of perinatal loss, with a focus on hospice provision: A thematic analysisPalliative & Supportive Care; Rhiannon Latham, Katrina Williams, Keeley Guest, Fauzia Paize, Robyn Lotto; 1/26Perinatal palliative care (PPC) offers holistic support to families of babies with life-limiting conditions, addressing emotional, psychological, and practical needs alongside ensuring dignity for the baby. Five key themes were identified [in this study]: the significance of language used by healthcare professionals when discussing the baby's condition; the importance of timely introduction to hospice care; recognition that grief is a personal and evolving process; the role of shared experiences in building relationships; and the importance of creating lasting memories. Findings highlight the importance of improving healthcare professionals' communication skills and integrating multidisciplinary palliative care services early in the care pathway. Parents expressed gratitude for the hospice support, particularly the opportunity to spend quality time with their baby and make lasting memories.
Cindy Mensik on hospice care: When to shift focus?
02/20/26 at 03:00 AMCindy Mensik on hospice care: When to shift focus? Investors Hangout; by Lucas Young; 2/17/26 Families in Texas City, TX, are facing a critical decision as loved ones enter the later stages of life. A recent article featuring insights from hospice care expert Cindy Mensik outlines when it’s time to pivot from aggressive treatment methods to hospice care. The reality is stark: this shift isn’t about surrendering; it’s about prioritizing comfort and quality of life during challenging times.
Comparison of patients seen by an embedded social worker and nurse practitioner palliative care model in hospital medicine versus referral-based specialty palliative care and their acute care utilization outcomes
02/19/26 at 03:00 AMComparison of patients seen by an embedded social worker and nurse practitioner palliative care model in hospital medicine versus referral-based specialty palliative care and their acute care utilization outcomes Journal of Palliative Medicine; by Laura P Gelfman, Li Zeng, Keisha Bergland, Elizabeth Rizzo, Cheyenne Higgins, Claire Doucette, Krishna Chokshi, Emily Chai; 2/17/26 Background: Hospitalized patients with serious illness often face delayed or limited access to palliative care. Embedded hospital primary palliative care (HPPC), led by social workers and nurse practitioners, may deliver more timely, needs-based support compared with referral-based specialty palliative care (SPC). Conclusions: An embedded SW/NP-led palliative care model in hospital medicine improves access, reduces acute care use, and is sustainable over time. This approach supports timely, culturally sensitive, needs-based palliative care and may be scalable for hospital-based delivery.
[England] Almost one in three people in England die without the basic care they need
02/18/26 at 03:00 AM[England] Almost one in three people in England die without the basic care they need Medical Xpress; by King's College London, edited by Lisa Lock; 2/16/26 About 170,000 people in England every year spend their final days in pain, distress or without vital support that should be available to everyone at the end of life. These are the findings of the first major study in more than a decade to estimate unmet palliative care needs among people at the end of life. The paper was led by researchers at King's College London and Hull York Medical School, University of Hull, with contributions from the University of Edinburgh and was published in the Journal of Health Services Research & Policy.
How to plan for a ‘good death,’ according to a VCU researcher
02/18/26 at 03:00 AMHow to plan for a ‘good death,’ according to a VCU researcher VCU News, Virginia Commonwealth University; by Madeline Reinsel; 2/16/26 People talk a lot more about death than dying. That’s according to Yifan Lou, Ph.D., a Virginia Commonwealth University School of Social Work assistant professor who studies how expectations around death and end-of-life care differ across cultures. ... “My job is really trying to understand different populations and then help design a policy and health care system that can support their value of the good death.” Planning for a good death requires patients and families to make decisions around hospice care, pain management, quality of life, financial affairs and long-term care, ideally alongside a social worker.
Psychosocial oncology: The Omega Project
02/17/26 at 03:00 AMPsychosocial oncology: The Omega Project Taylor & Francis | Death Studies; by Matthew Loscalzo and Linda A. Klein; 2/14/26This article reports on an interview with J. William Worden that focuses initially on the Omega Project (1968–1986) that studied end-of-life care. Worden explains the four phases of the project with specific populations, goals, and key concepts that emerged. The discussion then shifts to the development of psychosocial oncology and palliative care. Finally, Worden offers some thoughts on the development of the hospice movement in the United States, the role of religion in coping with mortality, coping with personal loss, and his advice to new medical or graduate students just starting out.
Geographic and sociodemographic disparities in access to hospice in Pennsylvania
02/17/26 at 03:00 AMGeographic and sociodemographic disparities in access to hospice in Pennsylvania American Journal of Hospice and Palliative Medicine; by Jacob Whitman, PhD, Dylan Nagy, MS, Harsheni Sudakar, BSPH, Coleman Drake, PhD, Lindsay Sabik, PhD, and Yael Schenker; 2/14/26 online ahead of print Results: In total, 2.3 million Pennsylvanians, or 17% of the state population, reside in census tracts classified as cold spots. Cold spots were concentrated in rural and socioeconomically disadvantaged regions. Compared with other tracts, cold spot tracts were lower income, less educated, older, more reliant on public insurance, and less racially diverse. Patterns were consistent when restricting to high quality hospice and nonprofit hospices. Conclusion: Geographic disparities in hospice access compound existing sociodemographic inequities. Addressing these inequities will require efforts to expand high-quality hospice availability in underserved communities.
Sociodemographic disparities and impact of palliative care utilization during end-of-life hospitalizations in patients with gastric cancer
02/14/26 at 03:35 AMSociodemographic disparities and impact of palliative care utilization during end-of-life hospitalizations in patients with gastric cancerJournal of Palliative Medicine; by James Lee, Jasmine Lee, Rahul Tripathi, David Stein, Ballakur Rao, Daniel Jamorabo, Lisa Fisher; 1/26Gastric cancer is frequently diagnosed at an advanced stage and is associated with high symptom burden. Among 13,435 weighted hospitalizations [among gastric cancer patients who died during hospitalization] ..., 57.6% received palliative care. Black patients had 32% lower odds of receiving palliative care than White patients ... Higher palliative care use was associated with greater income, large hospitals, urban teaching hospitals, and private/other insurance. In adjusted analyses, palliative care was linked to a $36,240 reduction in hospital charges ..., with no significant difference in LOS [length of stay]. Palliative care was associated with higher odds of DNR status ... and lower odds of CPR, mechanical ventilation, transfusion, and vasopressor use.
[Republic of Korea] P-1080. Multidrug-resistant organism status and its association with hospice use and end-of-life care patterns in patients with advanced cancer referred palliative care
02/14/26 at 03:00 AM[Republic of Korea] P-1080. Multidrug-resistant organism status and its association with hospice use and end-of-life care patterns in patients with advanced cancer referred palliative careOpen Forum Infectious Diseases; by Jeong-Han Kim, Jiwon Yu, Ye Sul Jeung, Shin Hye Yoo, Jin-ah Sim, Bhumsuk Keam; 1/26Multidrug-resistant organisms (MDRO) are increasingly prevalent and may contribute to more aggressive healthcare utilization near the end-of-life, particularly among patients with advanced cancer receiving palliative care (PC). MDRO status was associated with significantly lower use of community-based hospice care, including inpatient hospice ... and home hospice ... It was also linked to more frequent deaths in tertiary hospitals ... and higher intensive care unit admissions ... and renal replacement therapy ... Medical costs were consistently higher in the MDRO group across all end-of-life trajectory before death.
El Paso's Veterans Cafe helps give community to those who served
02/13/26 at 03:00 AMEl Paso's Veterans Cafe helps give community to those who served News*Talk 96.3 fm 1290 am; by Grizz; 2/12/26 On a quiet Saturday, something special is happening over coffee in El Paso. Hospice El Paso’s Veteran Café is proving that sometimes the most powerful form of support doesn’t come from a clinic or an office, but from a shared table, a familiar story, and the simple act of being welcomed. The pop-up café, sponsored by Hospice El Paso, is designed specifically for veterans from all branches of service. While it may look like a casual coffee gathering on the surface, its purpose runs much deeper. The café offers veterans a place to connect, talk, laugh, and support one another in a low-pressure environment where no one is expected to have the right words or any answers at all.
[Global] UCLA report reveals a significant global palliative care gap among children
02/13/26 at 03:00 AM[Global] UCLA report reveals a significant global palliative care gap among children UCLA Health, Los Angeles, CA; by University of California, Los Angeles (UCLA) - Health Sciences; 2/10/26 Nearly all the world’s 10.6 million children experiencing serious health-related suffering (SHS) live in low- and middle-income countries with little to no access to palliative care specialized care for their illness, according to a comprehensive new report published in The Lancet Child & Adolescent Health. ... The findings reveal a dramatic shift: most children in need of palliative care now live longer with severe, chronic illness, fundamentally changing the type of services needed and extending the duration of these services. ...
Hawaiʻi Care Choices is expanding services, care options to North Hawaiʻi this month
02/12/26 at 03:00 AMHawaiʻi Care Choices is expanding services, care options to North Hawaiʻi this month Big Island Now; Press Release; 2/11/26 Hawaiʻi Care Choices is expanding its palliative care program to North Hawaiʻi, ... Beginning this month, the Kupu Palliative Care Program will be available through a dedicated clinic space within the North Hawaiʻi Hospice office, extending palliative care services to residents of Hāmākua, Waimea, North Kohala, and South Kohala. ... “This partnership with Hawaiʻi Care Choices expands the support available to our community,” said Faye Mitchell, executive director of North Hawaiʻi Hospice. ... “We are both honored and excited to bring Kupu Palliative Care to North Hawaiʻi and to work with a trusted organization that shares our values of compassion, dignity, and community,” said Brenda Ho, CEO of Hawaiʻi Care Choices.
New Jersey's new Community-Based Palliative Care Medicaid (CBPC)
02/12/26 at 03:00 AMNew Jersey's new Community-Based Palliative Care Medicaid (CBPC) State of New Jersey - Department of Human Services - Division of Medical Assistance & Health Services; email and website notifications; 2/9/26 Community-Based Palliative Care is a benefit available to NJ Family Care members, starting April 1, 2026. The benefit was signed into the law by Governor Murphy on December 21, 2023, underscoring the state's commitment to supporting residents facing serious illness. Community-Based Palliative Care (CBPC) is designed to support people living with serious health conditions by helping manage symptoms, coordinating care, and making the healthcare system easier to navigate. You can receive CBPC while continuing your current treatments. CBPC is not hospice; a terminal diagnosis is not required. It is designed to give you extra support alongside the care you already receive.
Tell us more: Episode 3-Shirley Otis-Green
02/11/26 at 03:00 AMTell us more: Episode 3-Shirley Otis-GreenJournal of Palliative Medicine; by Shirley Otis-Green, MSW, MA, ACSW, LCSW, OSW-CE, FNAP, FAOSW, Yilong Peng, MD, William E. Rosa, PhD, MBE, APRN, and Richard E. Leiter, MD, MA; 2/9/26 The Journal of Palliative Medicine’s “Tell Us More: The Palliative Care Oral History Project,” seeks to tell the story of Hospice and Palliative Care through informal interviews with pivotal leaders in the field. In each episode, hosts Drs. Ricky Leiter and Billy Rosa, along with research assistant Dr. Yilong Peng, sit down with an HAPC luminary and do what our field does best—ask questions, listen, and reflect. In the third episode, Drs. Leiter and Rosa interviewed Ms. Shirley Otis-Green, founder of Collaborative Caring and a pioneer in palliative social work. What follows is a transcript of their conversation, edited lightly for clarity.
CommonSpirit Health at Home’s ‘aggressive’ hospice growth strategy for 2026 and beyond
02/11/26 at 03:00 AMCommonSpirit Health at Home’s ‘aggressive’ hospice growth strategy for 2026 and beyond Hospice News; by Jim Parker; 2/10/26 Continuing its de novo- and joint venture-based blueprint for growth, home health and hospice provider CommonSpirit Health at Home is also setting plans in motion to engage patients further upstream for earlier hospice enrollment, when appropriate. CommonSpirit Health at Home is the home-based care arm of the nonprofit health system CommonSpirit Health, which operates more than 2,200 care sites across 24 states. Hospice News caught up with CommonSpirit Health at Home CEO Trisha Crissman at the Home Care 100 conference in Scottsdale, Arizona to discuss CommonSpirit Health at Home’s strategic plans for 2026, as well as the top trends and market forces shaping the hospice community.
Community Hospice & Palliative Care unveils Advanced Cardiac Care Program
02/10/26 at 02:00 AMCommunity Hospice & Palliative Care unveils Advanced Cardiac Care Program Hospice News; by Jim Parker; 2/9/26 Florida-based Community Hospice & Palliative Care has launched an Advanced Cardiac Care Program to serve patients and families wrestling with heart disease. The hospice, an affiliate of Alivia Care, designed the program in collaboration with the American Heart Association (AHA) and the National Partnership for Healthcare and Hospice Innovation. It will provide a suite of services specifically designed for patients with cardiac conditions.
Why patient flow will decide hospital performance in 2026
02/10/26 at 02:00 AMWhy patient flow will decide hospital performance in 2026 Healthcare Business Today | Clinical Care | Patient Experience; by Russel Graney, 2/7/26 ... Why 2026? Health systems are entering a period where demand accelerates, reimbursement pressure tightens, and building new capacity becomes a distant solution. That’s why the next phase of performance will not be decided by who hires faster or cuts deeper, but by who moves patients through the system better. ...
[Canada] The quiet web of care: Hospitals, hospice, paramedics and community working as one
02/10/26 at 01:00 AM[Canada] The quiet web of care: Hospitals, hospice, paramedics and community working as one The Millstone; Mississippi Mills area, Canada; 1/25/26 When we think about care, most of us picture the hospital: rooms, nurses, doctors, the moment a life changes. But real care in North Lanark is not anchored to a single building. It’s a living web the Mississippi River Health Alliance — Almonte General Hospital, Carleton Place & District Memorial Hospital, Fairview Manor, and Lanark County Paramedic Service — working alongside Home Hospice North Lanark and Houle Healthcare so neighbors can get the right help at the right time, in the place that matters most. ... They are parts of the same journey, passing the baton back and forth so patients, families and neighbors are not left to navigate alone.Editor's Note: Pair this with today's post, "Why patient flow will decide hospital performance in 2026."
Spreading the principles of palliative care to all corners
02/09/26 at 03:00 AMSpreading the principles of palliative care to all corners Health Affairs; by Jessica Nutik Zitter; 2/2/26 My daughter Sasha is a first-year medical student. ... Most recently, she has been envisioning herself as a palliative care physician. She tells me it may be the only specialty that will allow her to practice her values. As a long-time palliative care physician who has acted as an evangelist for the specialty, I surprised myself with a reflexive response. “I’m not sure that’s the best choice for you,” I said. ... Something needs to change—for our patients and for ourselves. ... I propose several strategies ...
Effectiveness and impact of telehealth-integrated palliative care for persons living with dementia and their caregivers
02/07/26 at 03:05 AMEffectiveness and impact of telehealth-integrated palliative care for persons living with dementia and their caregiversTelemedicine & e-Health; by Brooke Worster, Lizabeth Kaminoff, Amina Mason, Laura Pontiggia, Kayla Madden, Mackenzie Kemp, Amanda Guth, Nina Diamond, Allison Herens, Kristin Rising, Jeannette Kates; 12/25 In 2024, an estimated 6.9 million Americans aged 65 and older were living with Alzheimer’s disease (AD), the most common form of dementia. Palliative care (PC) can improve quality of life (QOL) and reduce nonbeneficial care, yet persons living with dementia (PLWD) remain underserved. The intervention group [in this study] received up to two telehealth visits with a PC specialist, the patient (if able), and a caregiver (if participating). The intervention group had significantly fewer emergency department visits and hospitalizations but no differences in QOL or caregiver burden.
Personalized palliative care shows signs of improving quality of life for children with advanced cancer
02/06/26 at 03:00 AMPersonalized palliative care shows signs of improving quality of life for children with advanced cancer American Association for the Advancement of Science (AAAS), EurekAlert!; by Mass General Brigham; 2/4/26How to reduce suffering in children with advanced cancer remains an ongoing but urgent question. A Mass General Brigham-led study examined whether systematically surveying children with advanced cancer and their parents about their symptoms and quality of life, providing feedback to children, families, and clinicians—and acting on that information by implementing personalized palliative care—could improve patients’ experiences. Their findings, published in the Journal of Clinical Oncology, suggest that integrating feedback along with response by specialized pediatric palliative care (SPPC) has the potential to improve children’s quality of life.