Literature Review

All posts tagged with “Palliative Care Provider News | Utilization.”



Palliative care often comes late for veterans with COPD; use increases modestly

03/16/26 at 03:00 AM

Palliative care often comes late for veterans with COPD; use increases modestlyU.S. Medicine - The Voice of Federal Medicine, Atlanta, GA; by Mary Anne Dunkin; 3/13/26 Chronic obstructive pulmonary disease (COPD) is associated with substantial symptom burden, functional decline and frequent hospitalizations, making early palliative care an important component of comprehensive management. Yet, despite an increased focus by the VA on such care, new research suggested that many veterans with COPD still receive little or no palliative support—and, when they do, it often begins late in the course of illness. 

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Translating palliative care narratives into art: An arts-based knowledge translation pilot with young adult artists

03/16/26 at 03:00 AM

Translating palliative care narratives into art: An arts-based knowledge translation pilot with young adult artists Palliative Care and Social Practice; by Kristina A. Smith, Philippe Blanchard, Susan Law, and Kelli Stajduhar; 2/25/26 Objectives: This knowledge translation project explored arts-based approaches for translating palliative care narrative data into creative forms, examining the feasibility of converting research narratives into accessible art forms that could facilitate engagement with death-related topics. Results: Over 25 artistic works illustrating death and dying experiences were created. The collaborative translation process revealed that undergraduate artists could effectively interpret and visualize complex palliative care narratives through diverse artistic approaches. Course evaluations and informal feedback indicated that artists found the experience meaningful and challenging, and expressed interest in further exploration of death-related topics. Editor's Note: Go to this article and scroll down past "Results" to see photos of these artworks and their descriptions.

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A narrative review of attitudes and beliefs toward hospice and palliative care in South Asian Muslim communities

03/14/26 at 03:30 AM

A narrative review of attitudes and beliefs toward hospice and palliative care in South Asian Muslim communitiesJournal of Palliative Medicine; by Adeela Mushtaq, Mona Tareen, Renato V Samala, Susan B LeGrand; 2/26This article presents two case narratives illustrating reservations toward HPC [hospice and palliative care] in South Asian Muslim (SAM) communities, highlighting challenges and proposing strategies for culturally sensitive care. The first case demonstrates that, even with evidence-based and empathetic approaches, hesitancy toward HPC may persist. This underscores the need for (1) community-level initiatives leveraging religious and cultural platforms to educate and engage communities, and (2) greater awareness among healthcare professionals of these values to minimize conflict and reduce provider distress. In the second case, Islamic scholars were consulted regarding the use of sedative medicines at the end of life. They agreed such use is permissible under the principle of medical necessity, emphasized deference to medical expertise, and stressed preserving the patient's ability to recite the Shahadah (testimony of faith) in their final moments.

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"I don't get to feel this good very often:" Virtual reality intervention for veterans receiving end-of-life care

03/14/26 at 03:20 AM

"I don't get to feel this good very often:" Virtual reality intervention for veterans receiving end-of-life careJournal of Palliative Medicine; by Megan E Gately, Steven D Shirk, Anastasia Canell, Alexandra Laffer, Melanie Corle, Kristen Dillon; 2/26We explored the use of VR [virtual reality] with patients receiving inpatient HPC [hospice and palliative care]. Twenty-five veterans with complex medical and psychiatric comorbidities at a Veterans Affairs hospital participated. Data related to self-reported pain and well-being, as well as session feedback, were gathered. Despite some challenges with setup, 91% reported enjoyment, and 90% would participate again. Travel experiences were most popular, allowing reminiscence and touring of bucket-list destinations. Program feedback suggested improvements in anxiety, mood, and boredom.

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Webinar for free CME/CE credit: Determining prognosis in cancer and non-cancer diagnosis

03/13/26 at 03:00 AM

Webinar for free CME/CE credit: Determining prognosis in cancer and non-cancer diagnosis VITAS Healthcare; Press Release; for 3/18/26, 1pm EDT Supported by evidence-based data, this webinar will help physicians and healthcare professionals identify hospice-eligible patients with advanced illnesses, including cancer, cardiac disease, lung disease, dementia, liver disease, stroke, and HIV/AIDS. Attendees will explore trajectories of dying, functional decline, and factors that support accurate diagnoses and prognoses for cancer and other key diseases that lead to hospice referrals. ... Presented by Lauren Loftis, MD

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Sovereign Hospice guides Dallas-Fort Worth families through hospital discharge

03/13/26 at 03:00 AM

Sovereign Hospice guides Dallas-Fort Worth families through hospital discharge The Malone Telegram, Aubrey, TX; by Baaba Sampson; 3/12/26 Families facing hospital discharge for a loved one with a terminal illness often feel overwhelmed by the sudden shift in care responsibilities. Sovereign Hospice addresses this challenge by providing seamless coordination between hospital teams and home-based hospice services. The organization serves all counties within the Dallas-Fort Worth Metroplex, offering same-day admission and round-the-clock support.

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Palliative care for multiple sclerosis: Managing progressive disease with compassion

03/12/26 at 03:00 AM

Palliative care for multiple sclerosis: Managing progressive disease with compassion Ashland localtownpages, Aubrey, TX; by Press Services; 3/5/26 Multiple sclerosis presents unique challenges that require specialized support throughout the disease journey. Patients experience unpredictable symptoms including fatigue, pain, mobility issues, and cognitive changes. These symptoms shift and intensify over time, affecting daily life for both patients and their families. Sovereign Hospice addresses these complex needs through palliative care and hospice at home service across the Dallas-Fort Worth Metroplex.

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Why Florida’s Certificate of Need program works for hospice | Opinion

03/12/26 at 03:00 AM

Why Florida’s certificate of need program works for hospice | Opinion The Florida Times-Union; by Susan Ponder-Stansel; 3/11/26 Since the introduction of hospice care in the U.S. during the 1970s, Florida has been a leader in establishing high standards for licensing of hospice organizations who provide care in our state. This includes a certificate of need program that has a competitive process that is intentional, effective and disciplined. Through a competitive batching process under the program, hospice licenses are awarded only when providers can demonstrate unmet community need and prove they have the resources, staffing, infrastructure and expertise to meet that need reliably and over time. [Full access may be limited by paywall] 

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Palliative care and its importance on Block Island

03/11/26 at 03:00 AM

Palliative care and its importance on Block Island The Block Island Times, Block Island, RI; by Laurie Anderson, APRN-C, CDOE; 3/6/26 ... On Block Island, [Rhode Island,] palliative care is a cornerstone of a plan to allow residents to age in place. ... On Block Island, the importance of palliative care is magnified by geography. With no inpatient hospital and limited access to specialty services, island residents often rely on local care combined with strong coordination to meet complex health needs. ... One of the most meaningful local commitments to palliative and end-of-life care on Block Island is the Livesey Endowment for Palliative and End of Life Care, established through Block Island Health Services. ... In our small, close-knit island community, palliative care also serves a broader social purpose. It helps preserve independence, reduces unnecessary hospital transfers, and honors patients’ wishes to remain connected to their homes, families, and community. 

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Penn Medicine Collaborative providing holistic care to cancer patients

03/11/26 at 03:00 AM

Penn Medicine Collaborative providing holistic care to cancer patients healthleaders; by Christopher Cheney; 3/10/26 Key Takeaways:

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[United Kingdom] Specialist palliative care has the potential to reduce costs by up to £8,000 per person and improve quality of life, according to new research published in Palliative Medicine

03/11/26 at 03:00 AM

[United Kingdom] Specialist palliative care has the potential to reduce costs by up to £8,000 per person and improve quality of life, according to new research published in Palliative Medicine Innovation News Network; by Megan Traviss; 3/10/26 Led by researchers at King’s College London, the research considered two modes of palliative care for those living at home and for those in acute hospital settings. As well as significantly reducing the overall cost of care per person, specialist palliative care delivered at home and in the hospital was associated with improved quality of life for patients in their final months. Peter May, Senior Lecturer in Health Economics at King’s College London and lead author of the study, stated: “This is the first study to estimate the economic impact for England.

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Thyme Care launches Integrated Social Support model, bringing proactive oncology social work to 8 million Americans upon diagnosis

03/11/26 at 03:00 AM

Thyme Care launches Integrated Social Support model, bringing proactive oncology social work to 8 million Americans upon diagnosis PR Newswire, Nashville, TN; by Thyme Care; 3/5/26 Thyme Care today announced the public launch of its Integrated Social Support (ISS) model, a redesigned approach to oncology navigation that positions licensed master's-level social workers as the first to intervene when members experience barriers to navigating their cancer. The announcement coincides with National Social Work Month in March, recognizing the essential role social workers play in improving health outcomes. An estimated 44% of individuals affected by cancer experience psychosocial burdens, which are associated with poorer health, clinical, and economic outcomes for patients and caregivers. Thyme Care's ISS model flips the approach by making licensed social workers one of the first points of contact for social, emotional, and practical needs, assessing members from day one and throughout their journey ...

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C-TAC report: From metrics to momentum - accelerating the spread of community-based palliative care

03/11/26 at 02:00 AM

C-TAC report: From metrics to momentum - accelerating the spread of community-based palliative care The John A. Hartford Foundation, Washginton, DC; 3/4/26 The Coalition to Transform Advanced Care (C-TAC) and and The John A. Hartford Foundation (JAHF) have released a report, "From Metrics to Momentum: Accelerating the Spread of Community-Based Palliative Care." The report summarizes discussion from a September 2025 C-TAC national convening of clinical, policy, payer, and delivery system leaders that was focused on accelerating the spread of community-based palliative care and identifying meaningful approaches to measuring access. 

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Delivering palliative care in mental health nursing settings: A systematic review

03/10/26 at 03:00 AM

Delivering palliative care in mental health nursing settings: A systematic review Journal of Psychiatric and Mental Health Nursing; by Oladapo Akinlotan, Allen O'Connor, Ruben Seetharamdoo, Mo Ghoorun; 3/6/26 Palliative care can provide comfort, alleviate suffering, and improve quality of life; however, access to palliative care for people with mental illnesses at the end of their lives is extremely poor. As the need for palliative care is expected to rise significantly in the future, palliative care must be considered a global health priority. ...  Recommendations: Although care for people with complex mental illness is complex while dying, conversations around palliative care need to be as part of a therapeutic relationship and engagement. Also, palliative care staff have an important role in communicating end-of-life planning to patients' families and carers.

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Oncologist perspectives on timely hospice referral: A qualitative study

03/10/26 at 02:00 AM

Oncologist perspectives on timely hospice referral: A qualitative study American Journal of Hospice and Palliative Care; by Andrew Lynch, Andrea Altschuler, Joseph P Cosgrove, Hannah Whitehead, Corey Schwartz, Raymond Liu, Mina Chang; 3/7/26 Background: Late hospice referral rates are on the rise and are associated with negative outcomes at the end of life (EoL). Rates of late hospice referral vary drastically from oncologist to oncologist, and behavioral and psychological factors among individual oncologists have been identified as potential contributors to this variability. ...  Conclusions: Numerous factors independent of hospice eligibility were reported to influence hospice referral practices among oncologists. While some factors represent challenging cultural and social barriers to timely hospice referral, other system- and patient-specific barriers offer opportunities for potential interventions. 

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Hawaii Care Choices expands palliative care services to N. Hawaii

03/09/26 at 03:00 AM

Hawaii Care Choices expands palliative care services to N. Hawaii West Hawaii Today; Press Release; 3/8/26 Hawaii Care Choices has expanded of its Kupu Palliative Care Program into North Hawaii, “increasing access to compassionate, patient-centered care for individuals living with serious illness and the families who care for them,” according to a press release. Kupu Palliative Care is now available through a dedicated clinic space located within the North Hawaii Hospice office. This will extend palliative care services to those living in Hamakua, Waimea, as well as North and South Kohala. 

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Exploring the relationship between palliative care knowledge, health concerns, and education among seriously ill older adults and their family caregivers using survey and interview data: A novel approach

03/07/26 at 03:25 AM

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Why Baylor Scott & White opted for an access redesign

03/06/26 at 03:00 AM

Why Baylor Scott & White opted for an access redesign Becker's Hospital Review; by Kelly Gooch; 3/2/26 Dallas-based Baylor Scott & White Health, the largest nonprofit health system in Texas, has been undergoing a consumer-focused transformation aimed at expanding access. ... “One thing we heard consistently through all of that is just a need for more access,” Rob Watson, MD, chief clinical operations officer, told Becker’s. “Not just traditional access through what we would consider our large hospitals and clinics, but expanded options like digital and virtual as well as when they had an urgent need or an emergent need, more physical locations as well.”

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Investigating the role of occupational therapy in palliative care a literature review

03/06/26 at 03:00 AM

Investigating the role of occupational therapy in palliative care a literature review Home Healthcare Now; by Carlie Liseo, OTD, OTR/L and Daniel Martin, D.Sc., MS, OTR/L; March/April 2026 ... Three themes regarding the provision of occupational therapy (OT) services to palliative care (PC) patients were identified: engaging in meaningful activities to increase quality of life (QOL), symptom management and comfort, and supporting caregivers and client environments. OT can play a pivotal role in catering to PC clients’ needs by promoting occupational engagement, alleviating symptoms, and modifying environments. This review offers recommendations for OT service provision in palliative care, clarifying the profession’s role within multidisciplinary home healthcare teams.

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[Canada] New report released advancing equity in palliative and end-of-life care

03/06/26 at 02:00 AM

[Canada] New report released advancing equity in palliative and end-of-life care ehospice | BC Centre for Palliative Care, British Columbia; by the BCCPC Project Team: Rachel Carter, Eman Hassan, Simon Anderson, Grace Hu; 2/22/26 We’re pleased to share a new publication from the BC Centre for Palliative Care. This report distills key insights from a three-part Knowledge Exchange Series held in Spring 2025 that brought together people with lived experience, community organizations, clinicians, researchers, and system leaders across British Columbia. This Knowledge Exchange Series explored how health system services and community supports can work together to better meet the needs of underserved populations—highlighting both persistent gaps and promising paths forward. The report is supplemented with 12 population-specific chapters. [Read the full report]

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Outpatient curricular content for hospice and palliative medicine trainees: A national survey

03/05/26 at 03:00 AM

Outpatient curricular content for hospice and palliative medicine trainees: A national survey Journal of Pain and Symptom Management; by Harry J Han, Angelika Golebiowska, Emily N Hansen, Michelle Park, Victoria I Sweetnam, Christian T Sinclair, Jonathan C Yeh, Mary K Buss; 3/2/26, online ahead of print Context: More health systems are establishing outpatient palliative care (PC) programs, increasing demand for ambulatory PC clinicians. ... Little is known about the outpatient-specific knowledge and skills PC trainees should acquire for competent outpatient practice. Conclusion: This national survey identified foundational outpatient-focused educational topics for hospice and pallitive medical (HPM) learners and suggests that outpatient curricula prioritize deliberate education on the unique application of core PC skills in outpatient settings. This prioritized list provides education leaders a roadmap to enhance existing curricula and informs the development of outpatient educational resources that can be shared across institutions.

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Responsive emergency assessment and community team: an acute palliative medicine virtual ward with emergency department in-reach

03/05/26 at 02:00 AM

Responsive emergency assessment and community team: an acute palliative medicine virtual ward with emergency department in-reach BMJ Supportive & Palliative Care; by Emily Holdsworth and Clare Rayment; 3/2/26 Objectives: More than 50% of people who die in England and Wales use an ambulance at least once in their last 3 months of life, and around 50% attend the emergency department (ED). In Bradford, an estimated 1000 patients a year are not recognised as being within the last year of life and do not access palliative care services. ... Methods: We created the Responsive Emergency Assessment and Community Team (REACT), comprised of both ED palliative medicine in-reach and a community virtual ward. The virtual ward accepts patients as ‘step-down’ from the hospital and ‘step-up’ from primary care to avoid hospital admissions through intensive holistic support.

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Navigating end-of-life decisions with Islamic ethics

03/04/26 at 03:00 AM

Navigating end-of-life decisions with Islamic ethics WisconsinMuslimJournal.org; by Sandra Whitehead; 2/20/26 Medical College of Wisconsin Professor Aasim I. Padela, M.D., founder and president of the Initiative on Islam and Medicine, discussed Islamic bioethics during a January workshop on end-of-life decisions at the Islamic Society of Milwaukee. ... About 50 people attended the four-hour workshop, Islamic Bioethics & End-of-Life Healthcare Decisions, held Jan. 31 at the Islamic Society of Milwaukee. It featured experts with backgrounds in medicine, palliative care, hospice and Islam. Speakers made presentations and led discussions about practical steps, resources and strategies to help Muslims “transition from a state of uncertainty about end-of-life healthcare to thoughtful preparation for it,” a workbook given to participants stated.

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3 strategies to improve care access: McKinsey

03/04/26 at 03:00 AM

3 strategies to improve care access: McKinsey Becker's Hospital Review; by Kristin Kuchno; 3/3/26 With the U.S. physician shortage projected to surpass 137,000 by 2037, improving patient access cannot rely on pushing physicians to see more patients, according to a Feb. 26 McKinsey article. In McKinsey’s 2025 Physician Survey, 83% of physicians said they have seen patients delay care, with access barriers ranking among the top reasons. ... McKinsey outlines three additional strategies that when implemented together and in sequence — alongside efforts to reduce waste — can improve patient satisfaction and retention.

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Q&A: Why are more Americans under 50 years of age dying of colorectal cancer?

03/04/26 at 03:00 AM

Q&A: Why are more Americans under 50 years of age dying of colorectal cancer? Medscape; by Keith Mulvihill; 2/10/26 First, the good news: Fewer Americans younger than 50 years are dying from cancer vs just a decade ago — reflecting progress in prevention, early detection, and treatment. There is, however, one big exception. Colorectal cancer mortality has been steadily inching up, and the disease now stands as the leading cause of cancer death in this age group, up from the fifth-leading in the early 1990s. ... The outlier is colorectal cancer, where mortality has been rising by about 1% per year since 2005. And it’s a pattern seen in both men and women. ... [The researchers are asked,] "Can you offer some possible reasons for the declining mortality in most of the cancers you studied?" 

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