Literature Review
It takes considerable knowledge to...
01/18/26 at 03:00 AMIt takes considerable knowledge just to realize the extent of your own ignorance. ~Thomas Sowell
Sunday newsletters
01/18/26 at 03:00 AMSunday newsletters focus on headlines and top read stories of the last week (in order) - enjoy!
Baptist Health and Hosparus Health expand hospice and palliative care partnership to Southern Indiana
01/18/26 at 03:00 AMBaptist Health and Hosparus Health expand hospice and palliative care partnership to Southern Indiana Hosparus Health, Louisville, KY; Press Release; 1/14/26 Hosparus Health and its palliative care affiliate, Pallitus Health Partners, in collaboration with Baptist Health, announce the expansion of their innovative partnership to Southern Indiana. As of January 2, 2026, Pallitus Health Partners is offering palliative care consultations for patients at Baptist Health Floyd in New Albany. The program focuses on supporting patients and families facing serious illness by providing expert symptom management, helping them plan for the future, and connecting them with broader care options, including hospice when appropriate.
Today's Encouragement
01/17/26 at 03:55 AMThe meaning of life is to find your gift. The purpose of life is to give it away. ~Pablo Picasso
New voices, shared vision: How emerging research scholars are supporting HPNA's research priorities
01/17/26 at 03:55 AMNew voices, shared vision: How emerging research scholars are supporting HPNA's research prioritiesJournal of Hospice & Palliative Nursing; by Jyotsana Parajuli, Kristin Levoy, Avery C Bechthold, Lyndsay Degroot, C Robert Bennett, Shena Gazaway, Heather Coats; 12/25Evidence-based practice is critical to providing high-quality hospice and palliative nursing care. Professional organizations, such as the Hospice and Palliative Nurses Association (HPNA), play a critical role in shaping the future of the hospice and palliative nursing field by identifying gaps in the science and fostering collaborative research efforts to inform evidence-based practices. One such driver is the tri-annual HPNA Research Agenda, which outlines key research priorities in hospice and palliative nursing, ultimately aiming to accelerate translation of research into practice and practice improvements. In this article, 6 emerging research scholars in the field and present and former co-chairs of the HPNA Emerging Research Scholar Special Interest Group reflect on the experiences that led them to pursue research careers in hospice and palliative nursing. Through a process of collective self-assessment, these scholars articulated their shared progress toward addressing the research priorities outlined in the 2023-2026 HPNA Research Agenda as a means of generating insights to direct future research efforts in the field.
Existential communication with patients and families: A qualitative exploration of multidisciplinary oncology clinicians’ experiences
01/17/26 at 03:50 AMExistential communication with patients and families: A qualitative exploration of multidisciplinary oncology clinicians’ experiencesAmerican Journal of Hospice & Palliative Medicine; by Megan Miller, William E. Rosa, Haley Buller, Meghan McDarby, Alix Youngblood, Betty R. Ferrell; 12/25Existential concerns are inherent in serious illness and at the end of life, yet communication to address such concerns can be challenging. Themes across clinicians’ experiences of existential communication with patients and families included existential questions, guilt/regret, fears about the future, grief, preparing for death, values and goals of care, spiritual concerns, and letting go. Meaningful experiences included bearing witness; providing emotional support and information; easing suffering; learning and growing; and the honor of accompanying patients and families through the end of life. Challenges included discomfort when talking about death; facing denial; being unable to “fix it”; resistance to palliative care among oncology team members, patients, and families; fear of saying the wrong thing; navigating conflicting values; responding to spiritual concerns; barriers to inclusive, high-quality care; and struggling with emotions.
Neuropalliative care in movement disorders
01/17/26 at 03:45 AMNeuropalliative care in movement disordersContinuum: Lifelong Learning in Neurology; by Benzi M Kluger; 12/25Over the past decade, significant progress has been made to advance palliative care approaches for patients with Parkinson disease and other movement disorders. This population has significant palliative care needs that are poorly met under traditional models of care, including nonmotor symptom management, advance care planning, psychosocial support, spiritual and existential support, care partner support, and timely referrals for specialist and end-of-life palliative care (hospice). Clinical trials demonstrate that specialist palliative care can improve many patient and family outcomes. Neurologists can use the five-pillars framework (nonmotor symptoms, advance care planning, psychosocial and spiritual support, care partner support, and timely involvement of specialist palliative care) to systematically address common sources of suffering that are poorly recognized in traditional models of care. This framework can be integrated into previsit screening forms and note templates to improve the detection of palliative issues.
Improving palliative care knowledge and intentions among Great Plains American Indians: Efficacy results from a randomized clinical trial testing a culture-centric palliative care message
01/17/26 at 03:40 AMRural-urban differences in the prevalence of chronic pain among adult cancer survivors
01/17/26 at 03:35 AMAll hands on deck: A case report of an interdisciplinary team preventing elder financial abuse at a skilled nursing facility
01/17/26 at 03:30 AMAll hands on deck: A case report of an interdisciplinary team preventing elder financial abuse at a skilled nursing facilityCureus; by Grace Yi, Nicholas S. Cho, Karen Galvez-Maquindang, Christine Sun, Navid Darouian; 12/25Elder financial abuse (EFA) is a common but under-reported form of maltreatment among elderly individuals. This case describes an 84-year-old woman with cognitive deficits residing in a skilled nursing facility (SNF), who was exploited by a purported friend who took funds, important documents, and attempted to designate herself as the patient’s power of attorney. The situation was quickly identified by the multidisciplinary care team at the SNF and mitigated through early action and collaboration. The case emphasizes the importance of multidisciplinary efforts to identify at-risk patients and the establishment of protocols surrounding abuse identification and reporting to protect elderly patients from financialexploitation and preserve their autonomy, dignity, and quality of life.
A peer support intervention for Black family caregivers of persons living with dementia: A feasibility study
01/17/26 at 03:25 AMA peer support intervention for Black family caregivers of persons living with dementia: A feasibility studyJournal of the American Geriatrics Society; by Karen O Moss, Alai Tan, Abraham A Brody, Karen Bullock, Kathy D Wright, Kimberly Johnson, Mary Beth Happ; 12/25Black family caregivers of older adults living with dementia are at high risk for physical, spiritual, and psychosocial challenges. Culturally responsive interventions are needed to address disparities in this population. The purpose of this National Institute on Aging Stage Model 1A study was to test the feasibility, acceptability, and fidelity of the Peer Support for Black Family Caregivers of Persons Living with Dementia (Pair 2 Care) intervention. Pair 2 Care is a culturally responsive, non-judgmental, flexible, co-designed virtual peer support intervention in which former caregivers are paired as peer mentors with current caregivers for 6 months. On average, participants rated their overall Pair 2 Care satisfaction as very high (4.6/5).
Caregivers’ positive emotional language predicts their depression trajectories after dementia caregiving ends
01/17/26 at 03:20 AMCaregivers’ positive emotional language predicts their depression trajectories after dementia caregiving ends The Journals of Gerontology; by Jenna L Wells, Julian A Scheffer, Suzanne M Shdo, Claire I Yee, Kevin J Grimm, Alissa B Sideman, Bruce L Miller, Jennifer M Merrilees, Katherine L Possin, Robert W Levenson; 12/25There are striking differences among caregivers of people with dementia in their health and well-being during active caregiving and after caregiving has ended. A key factor influencing caregiver health is the emotional quality of the caregiver-care recipient relationship, which may be reflected in the emotional language caregivers use when describing this relationship. Caregivers who use more positive words when describing their connection with the care recipient may be more resilient, underscoring the potential role of positive emotional qualities of the caregiving relationship in preserving caregivers’ mental health after caregiving ends.
Preparedness as a bridge: How religious coping shapes acceptance of death in dementia caregiving
01/17/26 at 03:15 AMPreparedness as a bridge: How religious coping shapes acceptance of death in dementia caregivingClinical Gerontologist; by L. Blake Peeples, Lauren Chrzanowski, Benjamin T. Mast; 12/25This study examined the role of religious coping and preparedness in shaping caregivers’ acceptance of death following the loss of a care recipient with Alzheimer’s disease or related dementias. Bivariate analyses indicated that both positive and negative religious coping were significantly associated with greater preparedness, and preparedness was strongly related to acceptance. Findings suggest that interventions focused on religious coping enhance preparedness which improves caregivers’ acceptance in the bereavement process.
Prevalence rate of depression in palliative and hospice care: A narrative review
01/17/26 at 03:10 AMPrevalence rate of depression in palliative and hospice care: A narrative reviewJournal of Social Work in End-of-Life & Palliative Care; by Reid M. JacobsDepression is a common but not universal experience among individuals receiving hospice and palliative care. Though much research exists on depression in this population, there is little consensus on the actual prevalence rate, with estimates varying drastically. This is due, in part, to non-standardized definitions of what constitutes depression, variance based on assessment methods and tools, and the presence of somatic symptoms that may be due to physical illness and not depression, thus distorting the prevalence rate in this population. Depression can cause significant negative consequences for individuals and those who care for them, robbing them of precious time, increasing suffering, and decreasing overall quality of life. This narrative review seeks to understand depression’s prevalence among people living with severe and life limiting illness based on the existing literature.
[Norway] Conceptual barriers to palliative sedation: Insights from focus group interviews with specialist palliative care professionals
01/17/26 at 03:05 AMDevelopment of a mortality prediction model for incarcerated adults to identify palliative care needs
01/17/26 at 03:05 AMDevelopment of a mortality prediction model for incarcerated adults to identify palliative care needsJournal of General Internal Medicine; by W. James Deardorff, Alexandra K. Lee, Kaiwei Lu, Bocheng Jing, W. John Boscardin, Michele DiTomas, John Dunlap, Brie A. Williams, Sei J. Lee, Alexander K. Smith; 12/25The United States prison population has seen a rapid rise in the number of older adults, with roughly 14% of male prisoners and 9% of female prisoners aged 55 years or older in 2020. Incarcerated adults experience accelerated aging, leading to reduced life expectancy and higher rates of chronic medical conditions, functional impairments, and mental health conditions compared with non-incarcerated persons. For individuals with advanced age, multimorbidity, and/or serious illness, advance care planning discussions, palliative care, and hospice services are crucial for improving quality of life and ensuring medical care that is consistent with an individual’s values and goals. As the number of incarcerated adults with limited life expectancy increases, there is a clear need for a systematic way to identify individuals who may most benefit from these services. Our 2-year mortality prediction model for adults within the California prison system performed well on measures of discrimination, calibration, and classification. The model can be used to flag individuals at higher risk for mortality for consideration of advance care planning interventions, palliative care and hospice referrals, and compassionate release.
Saturday newsletters
01/17/26 at 03:00 AMSaturday newsletters focus on headlines and research - enjoy!
[Spain] The ethical challenge of negative compassion: How excessive empathy in end-of-life care affects decision-making and patient autonomy
01/17/26 at 03:00 AMSurvival variation and predictors of length of stay in U.S. hospice patients: A retrospective cohort study
01/17/26 at 03:00 AMSolomon Center’s groundbreaking palliative care law and policy initiative drives nationwide reforms
01/16/26 at 03:00 AMSolomon Center’s groundbreaking palliative care law and policy initiative drives nationwide reforms Yale Law School; Press Release; 1/15/26 The Solomon Center for Health Law and Policy at Yale Law School has established the country’s first comprehensive interdisciplinary initiative dedicated to palliative medical care, law, and policy — a pathbreaking effort that is already shaping reforms for patients of all ages. ... The work is supported by a first-of-its kind open-access research platform for palliative care policy across the states, developed by the Center, and in collaboration with partners at Yale School of Medicine, Yale School of Public Health, Yale School of Nursing, and Mount Sinai’s nationally renowned Center to Advance Palliative Care.
Executive Personnel Changes - 1/16/26
01/16/26 at 03:00 AMExecutive Personnel Changes - 1/16/26
US health expenditures rapidly accelerating
01/16/26 at 03:00 AMUS health expenditures rapidly accelerating Hospice News; by Jim Parker; 1/14/26 ... Rising health care utilization is the most significant driver of the spending increases, according to CMS. One key factor is that utilization is bouncing back from declines that occurred during the COVID-19 pandemic, according to Micah Hartman, a statistician in the National Health Statistics Group with the Office of the Actuary at CMS. Population growth was also a factor. ... By payer type, private health insurance saw the largest rate of spending growth at 8.8%, followed by Medicare at 7.8% and Medicaid at 6.6%. Out-of-pocket spending rose by 5.9%. ... Hospice care saves Medicare roughly $3.5 billion for patients in their last year of life, according to a joint report from the National Hospice and Palliative Care Organization (NHPCO), the National Association for Home Care & Hospice (NAHC) and NORC at the University of Chicago.
Heart to Heart Hospice expands service in Oklahoma
01/16/26 at 03:00 AMHeart to Heart Hospice expands service in Oklahoma Cision PR Newswire, Plano, TX; Press Release; 1/13/26 Heart to Heart Hospice, one of the country's largest private providers of hospice care, has expanded its presence in Oklahoma with the recent acquisition of an agency in Oklahoma City. Heart to Heart Hospice of Oklahoma City is now open and serving patients and families across Central Oklahoma. ... his is Heart to Heart's second location in Oklahoma following its expansion into Southeastern Oklahoma with the opening of its Durant site in 2024.
Tri-Cities Chaplaincy Hospice House
01/16/26 at 03:00 AMTri-Cities Chaplaincy Hospice House Tri-Cities Area Journal of Business, Kennewick, WA; Press Release; 1/15/26 Tri-Cities Chaplaincy has completed a remodel of its Hospice House in Kennewick. The 15,000-square-foot facility provides hospice inpatient care, including symptom management, respite for family caregivers and routine care ... The remodel addressed cosmetic and functional updates to all 10 patient rooms, including added technology for point-of-care charting. Several new spaces were added, including a fireside room, waiting area, larger collaborative nurses station and an interfaith chapel. ... A primary goal of the remodel also was to establish a homelike environment with a less clinical feel while still providing quality end-of-life care.
Retirement for Beth Dorsk: Her day is her own
01/16/26 at 03:00 AMRetirement for Beth Dorsk: Her day is her own Jewish News; by Terri Denison; 1/15/26 A Virginia Beach native, Beth Koonan Dorsk retired as a hospice nurse in 2025. She agreed to share with Jewish News some of her reasons for retiring and how it’s working out.
