Literature Review
All posts tagged with “Hospice Provider News | Utilization.”
Struggling rural Nebraska hospitals find 'lifeline' in emergency model
02/04/26 at 03:00 AMStruggling rural Nebraska hospitals find 'lifeline' in emergency model Lincoln Journal Star, Lincoln, NE; by Julie Anderson; 1/31/26 ... In Garden County, which spans 2,000 square miles in Nebraska's eastern Panhandle and numbers about 2,000 residents, the stream of patients coming into the hospital side of Garden County Health Services in Oshkosh had dwindled to a trickle in recent years. According to a recent count, inpatient admissions at the hospital averaged .07 per day and daily swing bed admissions averaged .05. "They can be few and far between," said Sam Pennington, Garden County's CEO. ... Pennington said hospice care was another concern of residents, so he also plans to try to arrange that under some available options.
National policy framework for Pediatric Palliative Care Homes
02/04/26 at 03:00 AMNational policy framework for Pediatric Palliative Care Homes National Center for Pediatric Palliative Care Homes; email and webpage; 2/3/26The NCPPCH recently formally released its National Policy Framework for Pediatric Palliative Care Homes, and has begun early engagement with key national partners. This framework is intended to help policymakers at the state and federal level better understand the structural, licensing, and reimbursement pathways needed to support Pediatric Palliative Care Centers nationwide. Review the Policy Framework and Executive Summary here: https://www.ncppch.org/national-policy-framework.
CAPC tools and events to help address disparities and improve outcomes
02/04/26 at 02:00 AMCAPC tools and events to help address disparities and improve outcomes Center to Advance Palliative Care (CAPC); email and webpage; 2/2/26 February 2026 marks 100 years of Black History Month. As we reflect on a century of honoring the history and contributions of Black Americans, CAPC’s Project Equity initiative focuses on turning that reflection into action by providing practical tools, innovative practices, and training to help palliative care teams effectively advance health equity for patients living with serious illness.
How to responsibly use AI in palliative care and hematologic malignancies
02/03/26 at 03:00 AMHow to responsibly use AI in palliative care and hematologic malignancies CancerNetwork; podcast by Ram Prakash Thirugnanasambandam, MBBS; 2/2/26 In a conversation with CancerNetwork®, Ram Prakash Thirugnanasambandam, MBBS, discussed the evolving roles that artificial intelligence (AI)–based tools may play in palliative care and the management of different hematologic malignancies. ... According to Thirugnanasambandam, implementing AI into one’s workflow may help accurately predict disease subtypes and burdens among patients with leukemia, lymphoma, or multiple myeloma. ... Thirugnanasambandam also discussed some of the ethical considerations surrounding the growth of AI-based tools, highlighting information privacy concerns and potentially biased datasets as notable issues with these platforms. Although AI may assist with decision-making, Thirugnanasambandam stated that it ultimately cannot replace a human’s nuanced clinical judgment and empathy.
End-of-life care statistics by care, conditions and illness (2026)
02/03/26 at 03:00 AM[Worldwide] End-of-life care statistics by care, conditions and illness (2026) Market.us Media; by Samruddhi Yardi; 2/2/26 Each year, an estimated 56.8 million people, including 25.7 million in the last year of life, are in need of palliative care. Worldwide, only about 14% of people who need palliative care currently receive it. ... As society continues to grapple with evolving views on life and death, the commitment to compassionate, personalized, and respectful end-of-life care remains paramount. Embracing this philosophy ensures that every individual is allowed a dignified and meaningful conclusion to their life’s journey.
CMS announces $50 billion Rural Health Transformation Program: What providers and states need to know
02/03/26 at 03:00 AMCMS announces $50 billion Rural Health Transformation Program: What providers and states need to know JD Supra; by Margia Corner, Alexandria Foster, Kendall Kohlmeyer; 2/2/26On December 29, 2025, the Centers for Medicare & Medicaid Services (“CMS”) announced that it will distribute award amounts to all 50 states under the first year of the Rural Health Transformation Program (the “Program”). ... The Program’s $50 billion in funds will be allocated over five years, with $10 billion available each year beginning in 2026. ... Under Public Law 119-21, funding must be distributed to states as follows: ...
Los Angeles County hospice industry under scrutiny for suspected Medicare fraud
02/03/26 at 03:00 AMLos Angeles County hospice industry under scrutiny for suspected Medicare fraud Santa Monica Observer, Santa Monica, CA; by Chet McSnark; 2/1/26 With 2,000 hospice agencies, Los Angeles County has more than 36 states combined and 30x more than Florida and New York. ... Recent reports indicate that the county accounts for approximately 18% of the nation's total Medicare billing for these services, despite representing only about 2.5% of the U.S. population. According to statements from CMS Administrator Dr. Mehmet Oz ... has estimated that fraudulent activity in Los Angeles County hospice and home health care could amount to roughly $3.5 billion annually. Federal data shows the county hosts nearly 1,923 hospice providers, a number that exceeds the total in many other states combined.
Protecting patients at the end of life why CON still matters - part 2
02/02/26 at 03:00 AMProtecting patients at the end of life why CON still matters - part 2 Teleios Collaborative Network (TCN); podcast hosted by Chris Comeaux with Paul A. Ledford and Tim Rogers; 1/30/26 In Part Two of Protecting Patients at the End of Life: Why CON Still Matters, host Chris Comeaux continues the conversation with two of the nation’s most respected hospice policy leaders—Paul A. Ledford, President & CEO of the Florida Hospice & Palliative Care Association, and Tim Rogers, President & CEO of the Association for Home & Hospice Care of North Carolina. This episode moves beyond regulatory theory and into the real-world patient and family experience—especially in states without hospice Certificate of Need (CON) laws. Drawing on decades of leadership, personal stories of loved ones in hospice, and data-informed insights, Paul and Tim explore what families actually face when hospice markets are oversaturated, fragmented, or poorly regulated.
Drivers of disease-specific end-of-life disparities
02/02/26 at 03:00 AMDrivers of disease-specific end-of-life disparities Hospice News; by Holly Vossel; 1/30/26 ... Racial and ethnic disparities persist among underserved patient populations with dementia, who have a stronger likelihood of dying without awareness or access to hospice, recent research has found. Clinicians may play a vital role in moving the needle forward. Nearly 260, 000 Black, Hispanic and white Medicare decedents with dementia-related conditions were recently examined in a new study, which was published in the Journal of the American Medical Association (JAMA) Health Forum. Editor's Note: We posted this study in our Saturday Research newsletter, 12/27/25, End-of-life care for older adults with dementia by race and ethnicity and physicians’ role. This article gives more practical descriptions and applications for its results.
Retired VA Nurse shares what she learned from over 10,000 dying veterans
02/02/26 at 03:00 AMRetired VA Nurse shares what she learned from over 10,000 dying veteransTampa Bay 28-ABC, Tampa Bay, FL; by Wendy Ryan; 1/30/26“Everything I've learned that has really mattered, I learned from the dying. Perspectives shift dramatically as death approaches. The day before you're given a terminal diagnosis, you take your life for granted. The day after, you wake up,” said Deborah Grassman, reading her book ‘Soul Injury.’ For over three decades as a VA hospice nurse practitioner, Deborah Grassman helped over 10,000 veterans take their final breath in peace. In those sacred moments, she began to see something they all carried. She calls it a “Soul Injury”, a wound that quietly haunts you. ...
Concurrent care and equity: Addressing palliative care gaps for African American men in rural communities with a serious respiratory illness
01/31/26 at 03:35 AMConcurrent care and equity: Addressing palliative care gaps for African American men in rural communities with a serious respiratory illnessAmerican Journal of Hospice & Palliative Medicine; by Cathy L. Campbell; 12/25Hospice and palliative care are often hard to access for African Americans (AA) living in rural areas with serious respiratory illnesses. Under the Medicare Hospice Benefit, patients must stop curative or life-sustaining treatments for their terminal illness, which limits options for concurrent care. This is a major challenge for AA men, whose average life expectancy is 67.8 years—about 10 years shorter than the national average. They also experience more care transitions in the last 6 months of life compared to White and Hispanic patients. These frequent transitions show how fragmented the health system is and how it often fails AA families. Using intersectionality and a vignette, this paper explores how overlapping factors—lived experience as AA man, rural location, and serious illness—affect access to palliative care.
Patients with terminal blood cancer stress need for transfusion access in hospice care, survey finds
01/30/26 at 03:00 AMPatients with terminal blood cancer stress need for transfusion access in hospice care, survey findsHematology Advisor; by Joantahn Goodman, MPhil; 1/28/26 Patients with blood cancer eligible for hospice care emphasize the importance of access to transfusion over other services, according to research published in JAMA Network Open. The survey-based study confirms that, among patients with an estimated life expectancy of 6 months or less, routine hospice services are perceived of less value than transfusion access — suggesting that palliative transfusion availability should be incorporated into hospice care universally, the authors noted in their report.
Hospice telehealth once again endangered as federal shutdown looms
01/30/26 at 03:00 AMHospice telehealth once again endangered as federal shutdown looms Hospice News; by Jim Parker; 1/28/26 The prospect of another government shutdown could result in the expiration of COVID-era telehealth flexibilities. The government experienced a lengthy shutdown in November 2025, which ended with the passing of the Continuing Appropriations Act of 2026. That bill not only funded the government through Jan. 30, but it also extended the telehealth flexibilities to that date. Now, a further extension sits in limbo as congressional lawmakers spar along partisan lines. If a new shutdown occurs, it would likely be partial, according to Logan Hoover, vice president of policy and government relations for the National Alliance for Care at Home.
VITAS Healthcare to be featured on CNBC's Now We Know! with Steve Guttenberg – airing January 31
01/30/26 at 03:00 AMVITAS Healthcare to be featured on CNBC's Now We Know! with Steve Guttenberg – airing January 31 1045 TheDan.com, Delray Beach, FL; by Now We Know!; 1/29/26The upcoming episode of Now We Know! with Steve Guttenberg, airing Saturday, January 31 at 11a ET on CNBC, will feature VITAS Healthcare, the nation’s leader in hospice and palliative care dedicated to improving quality of life for seriously ill patients and their families. ... Hosted by actor, author, and businessman, Steve Guttenberg, this unique platform inspires the next generation of knowledge seekers and viewers around the country.
California revokes 280 hospice licenses in fraud fight; Congressional hearing set
01/30/26 at 02:00 AMCalifornia revokes 280 hospice licenses in fraud fight; Congressional hearing set Hospice News; by Holly Vossel; 1/28/26 California Gov. Gavin Newsom (D) has provided an update on how the state is tackling fraudulent activity in the hospice space amid rising federal concerns. More than 280 licenses have been revoked among new hospice operators entering the state during the last two years, the governor reported on Tuesday. ... CMS Administrator Dr. Mehmet Oz and other agency officials visited hospices in California and Nevada earlier this month, pledging greater efforts to combat fraud.
Lifespark’s COMPLETE Senior Living Model sets new standard for senior living innovation
01/29/26 at 03:00 AMLifespark’s COMPLETE Senior Living Model sets new standard for senior living innovation Business Wire, Minneapolis, MN; Press Release; 1/27/26 Lifespark, a complete senior health company managing more than 50 senior living communities in Minnesota and Wisconsin, has unveiled its COMPLETE Senior Living (CSL) model with plans for significant growth in 2026. The CSL model integrates four key components: Lifespark Senior Living Management, SPARK Growth and Wellness led by Dr. Bill Thomas, Lifespark Medical Group, and Lifespark Hospice.
Protecting patients at the end of life: Why CON still matters / part one, with Tim Rogers and Paul A. Ledford
01/29/26 at 03:00 AMProtecting patients at the end of life: Why CON still matters / part one, with Tim Rogers and Paul A. Ledford Teleios Collaborative Network (TCN); podcast/video hosted by Chris Comeaux with Time Rogers and Paul A. Ledford; 1/28/26 Certificate of Need (CON) laws remain one of the most debated—and misunderstood—regulatory frameworks in healthcare. In this in-depth conversation, Chris Comeaux is joined by two of the nation’s most respected Hospice association leaders: Paul A. Ledford, President & CEO of the Florida Hospice & Palliative Care Association, and Tim Rogers, President & CEO of the Association for Home & Hospice Care of North Carolina.
What home-based care consumers really want
01/28/26 at 03:00 AMWhat home-based care consumers really want Hospice News; by Jim Parker; 1/27/26In interviews conducted by Cozy Home Community with patients and family members who received home-based care, six key themes emerged as factors that influence their perceptions of care — education, navigation, community and fit, families serving as health care “quarterbacks” and the importance of emotional intelligence and empathy.
I will be a window in your home. ~ David Tasma to a young Cicely Saunders
01/28/26 at 12:00 AMRemembering the Holocaust with little-known story about a Jewish refugee and Cicely Saunders: Honoring the International Holocaust Remembrance Day - 80th Anniversary of the liberation of Auschwitz
Changing the story data tells about Black health
01/27/26 at 03:00 AMChanging the story data tells about Black health The Seattle Medium, Seattle, WA; by Joseph Williams; 1/26/26 When it comes to the health of Black Americans, the numbers don’t lie. ... Last August, Word In Black launched its Insights & Research Division, a data-focused department centered on the perspectives, priorities, and lived experiences of Black Americans. The goal is straightforward: find out what Black people think about the issues affecting them most, analyze the results, and use those insights to reshape the narrative.
[United Kingdom] Hospice to support additional 1,000 patients
01/27/26 at 03:00 AM[United Kingdom] Hospice to support additional 1,000 patients BBC News; by Greig Watson; 1/25/26 A service to look after terminally ill people is to be expanded across much of Nottinghamshire after a new contract was awarded. Newark-based Beaumond House Hospice Care will lead on the creation of a new End of Life Referral Hub and make its Hospice at Home service available across Newark, Sherwood, Mansfield, Ashfield and Bassetlaw. The service is currently provided to about 200 patients across Newark and Sherwood but from April 2026 it will care for an additional 1,000 patients a year in their place of choice. ... Macmillan Cancer Support's End-of-Life Care Fund is providing the £1.8m of funding to support the expansion.Editor's Note: Recent hospice coverage from the United Kingdom has largely focused on service reductions. This announcement offers welcome news, signaling expanded access to end-of-life care for more patients. We hope this growth is accompanied by continued commitment to high-quality, person-centered care for patients and families.
Stroke survivors in DFW find new hope with Sovereign Hospice Home Care
01/27/26 at 03:00 AMStroke survivors in DFW find new hope with Sovereign Hospice Home Care Holliston Town News, Aubrey, TX; by Sovereign Hospice; 1/26/26 Stroke survivors and their families often encounter unexpected challenges ... Sovereign Hospice in Aubrey, Texas, addresses these complex needs through targeted palliative care programs designed specifically for post-stroke complications. ... Post-stroke pain affects approximately 30% of survivors, manifesting as headaches, muscle spasticity, or neuropathic sensations. Fatigue represents another common issue, with many patients reporting exhaustion after minimal activity. Depression occurs in roughly one-third of stroke survivors, creating additional barriers to recovery.
World Hospice and Palliative Care Day theme suggestions 2026
01/27/26 at 02:00 AMWorld Hospice and Palliative Care Day theme suggestions 2026 World Hospice and Palliative Care Association (WHPCA); 1/26/26 World Hospice and Palliative Care Day (WHPCD) is celebrated and marked each year on the second Saturday of October. [This] year, it will be on 10 October 2026. Each year, the WHPCA team gives a lot of thought to the theme, which is used the world over to advocate for better palliative care services for people living with palliative care needs. The WHPCA invites you to share suggestions for the theme for the coming year, 2026. ... If your suggestion is selected, we can share your name and picture on our digital platforms, giving you a shout-out for your brilliant contribution.
Patients' perceptions of autonomy in palliative care: Two patient interview exemplars
01/23/26 at 03:00 AMPatients' perceptions of autonomy in palliative care: Two patient interview exemplars Palliative Care and Social Practice; by Kristen Tulloch, Julia Acordi Steffen, John P Rosenberg; 1/19/26 Results: Four themes were identified: (a) my involvement in healthcare decisions, (b) change to my autonomy during illness progression, (c) self-assessing my abilities to exercise autonomy and (d) my coping mechanisms for loss of autonomy. Palliative care patients perceived and managed their autonomy amidst their illnesses, revealing a sense of loss of autonomy extending beyond healthcare into many daily activities. Participants wished to exercise autonomy in nuanced ways, varying in intensity across many aspects of their lives, underscoring the importance of recognising and respecting individuals' wishes for autonomy.Editor's Note: The authors’ focus on coping with loss of autonomy is essential. As illness progresses, autonomy can erode not only in medical decisions but across daily life, identity, and meaning—losses that are too often overlooked in clinical care. The frequently misapplied “Five Stages of Grief” can further blur this reality, reducing complex, personal experiences to linear expectations not supported by contemporary grief research. Understanding how patients adapt to loss of autonomy is foundational to truly person-centered palliative care.
Advance care planning in patients nearing the end of life: A pre-intervention study of racial disparities and provider factors
01/22/26 at 03:00 AMAdvance care planning in patients nearing the end of life: A pre-intervention study of racial disparities and provider factors Journal of General Internal Medicine | Springer; by Vedha Penmetcha BA, Mia Marcotte BA, Yashaswani Chauhan MD, Malathi Srinivasan MD, Adrian M. Bacong PhD, Amelia Sattler MD; 1/19/26 The pre-intervention study of Advance Care Planning (ACP) in patients nearing the end of life highlighted significant racial disparities and the impact of provider factors on ACP documentation. The study found that Asian patients were least likely to have ACP documentation in their charts, and minorities who had ACP conversations were less likely to have documentation. This suggests that ACP conversations are often not documented in the electronic health records of these patients, indicating a need for targeted interventions to improve ACP documentation rates. The study also revealed that providers may struggle to identify who and when to engage in ACP conversations, which can be a barrier to effective ACP.
