Literature Review
All posts tagged with “Clinical News | Advanced Illness Management News.”
Death Matters: The bedside vigil (Part 2) — after death arrives
09/17/26 at 03:00 AMDeath Matters: The bedside vigil (Part 2) — after death arrivesSequim Gazette, Sequim, WA; by Jeanette Stehr-Green and Astrid Raffinpeyloz; 9/16/26The bedside vigil is the act of sitting by a dying person during their final hours or days, holding space for them with a loving presence, and tending to their needs. The vigil can provide comfort and companionship to the dying person. It can offer meaning and peace to all involved. The undertaking, however, does not end with the loved one’s last breath. Immediately following the death, the vigil enters a new stage, one that allows time to honor the moment but also attend to the practical steps that must follow. ...
For families facing the unthinkable, NPHI launches new Guide to help navigate a child’s serious illness
09/17/26 at 03:00 AMFor families facing the unthinkable, NPHI launches new Guide to help navigate a child’s serious illness National Partnership for Healthcare and Hospice Innovation (NPHI), Washington, DC; Press Release; 9/14/26 ... Fewer than one in 10 children who die in the United States receive hospice care, underscoring an important opportunity to better support families facing a child’s serious illness. The National Partnership for Healthcare and Hospice Innovation (NPHI), the national voice for nonprofit hospice and advanced illness care, recently released the Advanced Pediatric Care™ Patient & Caregiver Guide — a free national resource created by pediatric hospice and palliative care experts from nonprofit providers across the country to give families something the system has never reliably given them: national clear, trustworthy guidance when a child is seriously ill. [Download the Guide]
The critical competencies hospice leaders must build for value-based care success | part one
09/17/26 at 02:00 AMThe critical competencies hospice leaders must build for value-based care cuccess | part one Teleios Collaborative Network (TCN); podcast hosted by Chris Comeaux with Dr. Jessica Hubbs; 9/16/26 Value-based care isn’t just changing how hospice gets paid—it’s redefining what hospice leaders must be capable of delivering. In Part One of The Critical Competencies Hospice Leaders Must Build for Value-Based Care Success, host Chris Comeaux sits down with Dr. Jessica Hubbs, Chief Clinical Officer at Advanced Care Innovations, to explore the accelerating shift from fee-for-service healthcare toward models built around outcomes, total cost of care, and coordinated care delivery. Dr. Hubbs explains why emerging models such as LEAD (Long-term Enhanced ACO Design) matter to hospice and palliative care leaders—and why the movement upstream into serious illness and home-based care could represent both a competitive headwind and an extraordinary opportunity.
Hospice Foundation of America receives Partner of the Year Award from Penn State College of Medicine
09/15/26 at 03:15 AMHospice Foundation of America receives Partner of the Year Award from Penn State College of MedicineHospice Foundation of America, Washington, DC; Press Release, Cindy Bramble; 9/11/26 Hospice Foundation of America (HFA) was named 2026 Partner of the Year by the Penn State University College of Medicine [Thursday, 9/10]. The award recognizes HFA’s significant contributions to a National Institutes of Health funded research initiative, the Project Talk Trial, which studied how to best engage communities across the U.S. in advance care planning. ... With its vast national network, HFA connected PSU College of Medicine researchers to community organizations across the country to bring advance care planning conversations to 1,799 people in 78 communities across 32 states and the District of Columbia. Project Talk Trial is the largest research study of its kind.Editor's Note: Congratulations, Hospice Foundation of America! We thank you for your longstanding, innovative leadership to improve hospice care throughout our nation.
Perceived importance of good death components among patients with advanced cancer and family caregivers
09/15/26 at 03:00 AMPerceived importance of good death components among patients with advanced cancer and family caregivers JAMA Network; by Hammoda Abu-Odah, PhD, Gulbeyaz Can, PhD, Sotirios Plakas, PhD, Juanjuan Zhao, PhD, Xixi Wang, MSN, Alexandros Stergiou, MSc(c), Ourania Govina, PhD, Kimya Kilicaslan, PhD, Bahar Ozdemir, MD, Matthew J. Allsop, PhD, Mitsunori Miyashita, PhD, Alex Molassiotis, PhD, Janelle Yorke, PhD, and Frances Kam Yuet Wong, PhD; 9/14/26Importance: Although the concept of a good death is central to palliative care policy and practice, empirical evidence is largely derived from high-income Western or single-country contexts, limiting cross-setting relevance.Objective: To determine the importance of good death components, compare priorities across settings, and examine patient–caregiver differences and setting-by-role interactions. ... Conclusions and Relevance: In this cross-sectional study, patients with advanced cancer and family caregivers across 5 settings shared a broad aspiration for a good death, but priorities varied across settings. Emotional peace, dignity, and family connection were consistently highly valued. These findings suggest that culturally sensitive palliative care models should recognize both shared end-of-life priorities and setting-specific meanings of a good death.
Free webinar for physicians and healthcare professionals: Reducing hospital readmissions and length of stay in advanced illness patients
09/15/26 at 03:00 AMFree webinar for physicians and healthcare professionals: Reducing hospital readmissions and reducing Hospital Readmissions and Length of stay in advanced illness patients VITAS Healthcare; Press Release; 9/14/26
Enhancing quality of life for terminally ill veterans during the COVID-19 pandemic and beyond
09/15/26 at 03:00 AMEnhancing quality of life for terminally ill veterans during the COVID-19 pandemic and beyond Medscape | Federal Practitioner; by Denise Kresevic, PhD, RN, APN-BC, Marilyn Swanson, DNP, RN, FNP-C, Muralidhar Pallaki, MD, Bridgette Wasil, MSN, RN CHPN, Rosalie Diaz, PsyD, and Christopher J. Burant, PhD; 9/14/26 Background: Honoring individualized preferences for end-of-life interventions for veterans is a priority for families and caregivers. Medications used to treat symptoms such as pain, anxiety, and delirium may also result in sedation, making it difficult to balance comfort while minimizing sedation. ... Conclusions: The See Me, Hear Me, Comfort Me model may help hospice teams better align end-of-life care with individual preferences. ...
The dark side of full patient autonomy
09/15/26 at 03:00 AMThe dark side of full patient autonomy Medscape; by Lisa O'Mary; 9/14/26 Paternalism is out. Shared decision-making is in. But some communication and ethics experts say medicine is veering far too much toward full patient autonomy. A new review in the journal Health Communication found that clear delivery, active listening, and empathy were associated with patient trust. Obvious? Probably. But here’s the twist: The authors also found that paternalistic styles didn’t always harm trust — and even aided shared decision-making in some situations, particularly in contexts such as emergency care, serious illness, and end-of-life decisions.
[Hospice bereavement director] A non-anxious presence: Red Cross volunteer supports Flight 93 families and responders
09/14/26 at 03:00 AM[Hospice bereavement director] A non-anxious presence: Red Cross volunteer supports Flight 93 families and responders American Red Cross; video interview with Patti Anewalt, PhD; 9/1/26 [Dr. Patti Anewalt is the retired director of Hospice and Community Care's Pathways Center for Grief and Loss, Mount Joy / Lancaster, Pensylvania. Of note, her hospice organization supported her volunteer time in this crucial Red Cross disaster mental health role.] When Patti Anewalt first learned about the terrorist attacks on Sept. 11, 2001, she immediately sensed her phone might ring. At the time, Patti was an American Red Cross volunteer in Central Pennsylvania and an experienced grief counselor [whose PhD was in trauma]. As coworkers gathered around televisions to watch events unfold, she told her boss she thought she would be called to respond. She was right. The next day, Patti was deployed to Somerset County, Pennsylvania, where United Flight 93 crashed near Shanksville ... For two weeks, she worked alongside fellow Red Cross volunteers, supporting victims' families, disaster workers and responders as they navigated one of the most tragic moments in American history. ... As family members arrived in Pennsylvania, many visited the crash site for the first time. Some were unsure whether they even wanted to go. ... "Whenever we're teaching in hospice, we say we're a non-anxious presence at a very difficult time in people's lives," she said. "The role I had there was no different than my day role at hospice because it's just being a non-anxious presence to people who are in the worst time in their lives and being present for them." ...Editor's Note: Many readers know Patti--both as faithful friend and for her prolific leadership teaching about trauma, grief, and hospice organization's appropriate (and not appropriate) responses to community tragedies, especially in the years following 9/11. Patti led NHPCO's professional Bereavement Group to be the most active, growing group during her 6-year volunteer tenure. Patti was a regular reader of our newsletter until her well-deserved, recent retirement.
[Pakistan] Existential loneliness and spiritual well-being as predictor of hope among patient with chronic illness
09/12/26 at 03:00 AMTime is of the essence: evaluating short-term prognosis tools in cancer and non-cancer patients
09/10/26 at 03:00 AMTime is of the essence: evaluating short-term prognosis tools in cancer and non-cancer patients Journal of Pain and Symptom Management; by Kayla Sheehan, Navasuja Kumar, Julia Pudar, Susan Duong, Megan Bricely, Mohamman Alhameed, Mohammed Kabeto, Donglin Zeng, Adam Marks; 8/27/26 Accurate end-of-life prognostication supports patient, family, clinician, and health system decision-making. The Palliative Prognostic Index (PPI), Palliative Performance Scale (PPS), and Short-Term Prognosis Signs (SPS) have been used in palliative care populations, particularly advanced cancer (1-3), but their utility for short-term prognostication in non-cancer patients is less established.
Beyond the bottle: a whole person approach to pain management for veterans enrolled in inpatient hospice
09/10/26 at 02:00 AMBeyond the bottle: a whole person approach to pain management for veterans enrolled in inpatient hospice Medscape; by Tracy Shamas, APRN, MSN, ACHPN, Andrea Ruskin, MD, HEC-C, and Alexandra Laffer, PhD; 9/9/26 Background: ... Veterans Affairs inpatient hospice units are uniquely positioned to implement non-pharmacological pain interventions due to longer lengths of stay and broader resources compared to Medicare GIP-regulated settings. This quality improvement project aims to support the uptake and utilization of non-pharmacological pain management interventions for veterans receiving inpatient hospice care. ... Conclusions: Initial findings show that veterans with pain at end-of-life express interest in holistic non-pharmacological options, and integrating these approaches is feasible within inpatient hospice care. ...
When lung cancer spreads to the liver: what to expect
09/09/26 at 03:00 AMWhen lung cancer spreads to the liver: what to expect Everyday Health; by Ashley Welch, medically reviewed by Tingting Tan, MD, PhD; 9/8/26 Liver metastasis from lung cancer occurs when cancer cells from the tumor in the lung travel to the liver. Also known as stage 4, it’s the most advanced stage of lung cancer. ...
When the end of life feels like a beginning: a hospice encounter raises questions medicine can't answer
09/09/26 at 03:00 AMWhen the end of life feels like a beginning: a hospice encounter raises questions medicine can't answerBroadview; by Ralph Klose; 9/8/26 As a retired neuropsychologist and longtime hospice companion, I often wonder what can still be measured at the end of life — and what cannot. ... Magda had lived in the hospice for three months. A former violinist, she rarely spoke about her past. But her hands still moved in gentle arcs, as if drawing invisible phrases from the air. ... One afternoon, I entered her room and paused. The air felt different — not cold, not scented, but bright. The blinds were closed. No sunlight entered. And still, the space around her shimmered faintly, like a curtain of breath. Her skin looked translucent. Her lips moved, but no sound came. Later, as I sat quietly at her bedside, a nurse whispered, “She’s speaking with someone.” There was no theology in her gestures. No visions of angels. But something had changed — as if a second world had unfolded beside the first, not replacing it, but resting gently alongside. ...
Central Illinois nursing home fined $25K by state after resident's death
09/08/26 at 03:00 AMCentral Illinois nursing home fined $25K by state after resident's death Pekin Daily Times, Perioa, IL; by Zach Roth; 9/6/26 A Canton nursing home was fined $25,000 after a resident died last year after being taken off medication that was prescribed to prevent blood clots. ... On March 31, 2025, a verbal order was given to stop providing Xarelto because the woman began hospice care one month prior. ... The care plan noted that she had a history of strokes and that medication needed to be provided as ordered by her doctor. ... The hospice's owner said that the power of attorney had contacted them after the woman had died asking about the medication situation, noting that they hadn't seen anything to show that her Xarelto had been discontinued. The hospice owner also said that they hadn't received an order from a hospice physician or nurse to discontinue it. Editor's Note: Details are more complex than space allows in the short summary above. A verbal order to stop a medication, without a documented physician directive or clear communications with the family, is a quiet risk hiding in plain sight at hospice transitions — one that can hasten death rather than ease it. Deprescribing has its place in end-of-life care, but only through structured, physician-ordered, shared decision-making. Does your hospice's process protect against this, or could it happen to one of your patients tomorrow?
Inpatient palliative care utilization in gynecological malignancies: a national inpatient study
09/08/26 at 03:00 AMInpatient palliative care utilization in gynecological malignancies: a national inpatient study Medscape; by Lydia Francis, LF and Benjamin Easow, MD; 9/3/26 Conclusions: Only 1 in 6 hospitalizations for gynecological malignancies had documented palliative care, reflecting underutilization in a population with substantial supportive care needs. Palliative care concentration among older, higher-acuity admissions suggests late referral rather than early integration. These findings support timely palliative care expansion in gynecological malignancies to improve symptom management and goal-concordant care.
Sorrow, unpermitted: A narrative review of grief in chronic liver disease
09/05/26 at 03:35 AMWhen end-of-life becomes the beginning of new life: Application of the Society of Critical Care Medicine Clinical Practice Guidelines on Adult End-of-Life Care in the ICU to the setting of donation after circulatory death
09/05/26 at 03:25 AMWhen end-of-life becomes the beginning of new life: Application of the Society of Critical Care Medicine Clinical Practice Guidelines on Adult End-of-Life Care in the ICU to the setting of donation after circulatory deathCritical Care Explorations; by Ian M. Oppenheim, Rita N. Bakhru, Carolina B. Maciel, Katharina M. Busl, on behalf of the Donor Care Unit Network for Optimizing Recovery (DONOR) GroupThe recently published Society of Critical Care Medicine Guidelines on Adult End-of-Life Care in the ICU provide a detailed and well-thought-out approach to a vital component of critical care, although they explicitly refrain from discussing how they may apply to organ donation. As representatives of the Donor Care Unit Network for Optimizing Recovery (DONOR), a group of intensivists experienced in managing donation after circulatory death (DCD), we wish to endorse equal delivery of high-quality end-of-life (EOL) care for organ donors. Although some logistical differences must be addressed, the EOL recommendations outlined in the Guidelines are still applicable to patients being evaluated for or undergoing DCD. Recent accounts of unacceptable patient care in the setting of DCD highlight a critical threat to patient welfare and public trust. Our mandate is clear: implement and audit protocols that guarantee dignity and symptom control while demonstrating that DCD remains wholly consistent with a compassionate, honorable, and fulfilling EOL.
National Alliance VP: palliative care should occur throughout continuum
09/04/26 at 03:00 AMNational Alliance VP: palliative care should occur throughout continuum Hospice News; podcast hosted by Jim Parker with Katie Wehri; 9/3/26 Palliative care should be offered via home health, but not only through home health. This is according to Katie Wehri, vice president for regulatory affairs, quality and compliance at the National Alliance for Care at Home. The U.S. Centers for Medicare and Medicaid Services recently clarified in a proposed rule that palliative care is available via the home health benefit. Hospice News recently sat down with Wehri on the Elevate podcast to discuss the implications of this clarification for providers, as well as other avenues CMS could consider to expand palliative care.
Evasiveness in everyday hospital palliative care practice: a focused ethnography
09/04/26 at 03:00 AMEvasiveness in everyday hospital palliative care practice: a focused ethnography Journal of Clinical Nursing; by Carolien van Leussen, Evelien Kuip, Renske Kruizinga, Els van Wijngaarden; 9/2/26 Conclusion: This study shows how evasiveness in hospital-based palliative care is produced and sustained through biomedical routines, organizational pressures and professional and personal orientations. These factors make it difficult to realize the holistic ideals of palliative care in everyday practice. As a result, patients' fears, uncertainties and end-of-life wishes often remain insufficiently explored, whereas organizational routines shape what is considered appropriate and possible in clinical interactions.
Hospice Savannah launches Georgia Care Innovators to unite growing family of services
09/04/26 at 01:00 AMHospice Savannah launches Georgia Care Innovators to unite growing family of services WJCL-22 ABC, Savannah, GA; by Emma Hamilton; 9/3/26 After more than 45 years of providing end-of-life care, Hospice Savannah has launched Georgia Care Innovators, a new organizational identity to reflect its expanding range of healthcare and community services. Hospice Savannah will continue operating under its established name as a central part of the organization. ... “Our story has never been defined by a single service,” said Kathleen Benton, president and CEO of Georgia Care Innovators. “It’s been defined by listening to our community, recognizing unmet needs and asking how we can help.” ... The Georgia Care Innovators family includes:
Alzheimer’s blood test gets FDA clearance, but not CMS coverage
09/03/26 at 03:00 AMAlzheimer’s blood test gets FDA clearance, but not CMS coverage Inside Health Policy, Washington, DC; by Jessica Karins; 9/2/26 A blood test aiming to help with early identification of Alzheimer’s disease, including in primary care settings, by detecting buildup in the brain of the key Alzheimer’s biomarker amyloid beta plague, has been cleared by FDA, but the test and others in its category are not yet covered by CMS or any Medicare Administrative Contractors, its developer confirmed, with MACs having to make an individual determination for each patient of whether payment for the test is appropriate.
Beloved celebrities who opened up about their battles with dementia
09/02/26 at 03:00 AMBeloved celebrities who opened up about their battles with dementia MSN; by Travis Reeed; 8/31/26 Dementia and Alzheimer’s disease have affected people from many walks of life, including some of the most recognizable figures in entertainment, politics, and culture. Their experiences helped bring greater attention to memory loss, cognitive decline, and the challenges faced by families and caregivers. From Hollywood legends to celebrated musicians and political leaders, these individuals continued to leave lasting legacies despite their health struggles. Their stories also helped encourage public conversations about conditions that were once poorly understood or rarely discussed openly. [Click on the slides to see personalized stories of Tony Bennett, Sally Kirkland, Ronald Reagan, Sean Connery, Margaret Thatcher, Rita Hayworth, and Jimmy Stewart.]
Palliative care is about living better — not giving up
09/02/26 at 03:00 AMPalliative care is about living better — not giving up Patch, Westport, CT; by Hartford HealthCare, featuring Dr. Sara Dost; 8/31/26 For many patients and families, the words palliative care can be difficult to hear. Some assume it means treatment has stopped. Others confuse it with hospice care or believe it is only appropriate during the final stages of life. But according to Dr. Sara Dost of Hartford HealthCare's Cancer Institute at St. Vincent's Medical Center, palliative care is about something much different: helping people feel better and live as fully as possible while facing a serious illness. “I like to call palliative care supportive care,” Dr. Dost said. “We help patients deal with side effects, decision-making and the challenges that can come with a serious illness. Think of us as an extra layer of support.”
The death I feared, and the peace I found
09/01/26 at 03:00 AMThe death I feared, and the peace I found Gillette News Record; by Michelle Mathal; 8/29/26 ... From the dreaded day my brother was diagnosed, to two years later when my parents tragically died in a car accident and I surfaced from the glacial water knowing I had to live to be his caregiver, to grieve alone. ... We enrolled in hospice earlier than most because Tomas was falling and losing movement in his left hand. ... No one told me that caring for a dying person would be so intimate. When I dressed him in the morning, I realized we had the same hands and feet, big enough that we should’ve been a foot taller. No one told me about the deep trust between caregiver and patient. It is a sacred pact not bound by blood, but an understanding that we would be seen at our most vulnerable and sensitive times, but not judge each other for these moments, but respect one another despite them.
