Literature Review
American Academy of Hospice and Palliative Medicine Announces Pierre M. Désy, MPH, CAE, as New Chief Executive Officer
08/25/25 at 03:00 AMAmerican Academy of Hospice and Palliative Medicine Announces Pierre M. Désy, MPH, CAE, as New Chief Executive OfficerIn late July, Pierre Désy, MPH, CAE became the new CEO of the American Academy of Hospice and Palliative Medicine. Désy recently served as CEO of the Society of Gynecologic Oncology (SGO) and the Foundation for Women's Cancer (FWC), where he led the development and implementation of strategic plans, revised bylaws, improved governance models, and advanced diversity and inclusion initiatives. Désy previously held executive leadership roles with the International Association of Oral and Maxillofacial Surgeons (IAOMS) and the Emergency Nurses Association (ENA). He has also served as a management consultant and coach, supporting healthcare associations and professionals in improving performance and achieving excellence. Désy said, "I am particularly energized to be part of an organization where I can bring together my public health background and decades of association management experience, and work alongside a team that shares my passion for building partnerships, advancing health equity, and supporting interdisciplinary collaboration to expand access to quality care. I am impressed by the work that has been accomplished by the Academy and look forward to working together to further its mission."Guest Editor Note, Ira Byock, MD: Mr. Désy’s public health background and substantial experience in executive roles of national specialty groups positions him well to lead AAHPM during this turbulent period in American healthcare. Hopefully, with his guidance the Academy will find ways to respond to the variability in access to and quality of hospice and palliative services and the widespread persistence of unmet needs among seriously ill and dying Americans.
Social relationships and end-of-life quality among older adults in the United States: The impacts of marital, kinship, and network ties
08/24/25 at 03:55 AMSocial relationships and end-of-life quality among older adults in the United States: The impacts of marital, kinship, and network tiesThe Journals of Gerontology; by Kafayat Mahmoud, Deborah Carr; 7/25We examine marital status differences in recent decedents’ end-of-life care and gender differences therein, and the role of other social ties (children, siblings, network members) in influencing the quality of end-of-life care. Divorced decedents fared poorly on multiple outcomes, being less likely than married or widowed persons to receive excellent care and to have personal care needs met. Divorced and widowed decedents were less likely to receive respectful treatment relative to married decedents. We found no significant gender differences in these patterns. Persons with more siblings and network members had superior pain management. Hospital patient advocates could also aid those who lack close kin at the end of life.
Guest Voice: What ‘It’s a Wonderful Life’ teaches us about living with MS
08/24/25 at 03:50 AMGuest Voice: What ‘It’s a Wonderful Life’ teaches us about living with MS Multiple Sclerosis News Today; by Donald Kushner, MD; 8/15/25 Donald Kushner, MD, is a retired physician, board certified in internal medicine and hospice and palliative care. He has been living with multiple sclerosis (MS) for more than 20 years and draws on his dual perspective as both doctor and patient to explore illness, identity, and adaptation. He’s writing a book about how people with chronic illness and their support systems can better understand — and talk to — each other. ... George’s story reminds me that resilience often shows up in ordinary moments. That the life we’ve built — even with detours — is still a life of worth.
BrightSpring taking modest approach to M&A in 2025
08/24/25 at 03:45 AMBrightSpring taking modest approach to M&A in 2025 Hospice News; by Jim Parker; 8/15/25 BrightSpring Health Services (Nasdaq: BTSG) is taking a slow and steady look at acquisition opportunities through the remainder of the year. The company is allowing the dust to settle on the divestiture of its community living business to Setiva for $835 million before once again investing heavily in acquisitions, according to CEO, President and Chairman Jon Rousseau. The divestiture is expected to close in the fourth quarter. But that doesn’t mean that BrightSpring is out of the market for deals.
Black and white older adults’ end-of-life experiences: Does hospice use mitigate racial disparities?
08/24/25 at 03:40 AMBlack and white older adults’ end-of-life experiences: Does hospice use mitigate racial disparities?The Journals of Gerontology; by Clifford Ross, Brina Ratangee, Emily Schuler, Zheng Lian, Benmun Damul, Deborah Carr, Lucie Kalousová; 7/25Racial disparities in end-of-life care are well documented, but less is known about how these inequalities shape assessments of death quality. Proxies for Black decedents reported higher perceived death quality than those for White decedents, despite evidence of greater structural disadvantage. However, perceived care concordance was significantly lower among Black decedents. Hospice care was associated with improved perceived death quality for Black decedents but not for Whites. When accounting for socioeconomic and death experience controls, hospice care did not moderate perceived care concordance.
Addressing hospice care Medicare fraud: Awareness and action
08/24/25 at 03:35 AMAddressing hospice care Medicare fraud: Awareness and actionInvestors Hangout; by Lucas Young; 8/18/25 The New York StateWide Senior Action Council (StateWide) is an impactful 53-year-old non-profit organization dedicated to assisting approximately 2.5 million senior citizens. Recently, they have spotlighted a concerning trend in their monthly Medicare Fraud identification: Hospice Care Medicare Fraud. This initiative is part of the Senior Medicare Patrol (SMP), which equips older adults and their caregivers with the knowledge to detect, prevent, and report healthcare fraud, errors, and abuse. StateWide administers this program for New York State, acting as a crucial resource for senior citizens across the region. [This article provides simple, clear facts for the public.]
Do you care about your legacy? 54% of Americans want to leave mark on the world
08/24/25 at 03:30 AMDo you care about your legacy? 54% of Americans want to leave mark on the world Study Finds, New York, NY; by StudyFindsAnalysis, reviewed by Steve Fink; 8/15/25 Getting older changes everything, including what we care about most. A new survey of 2,000 Americans reveals ...
Pennant Group expands through Amedisys acquisition
08/24/25 at 03:25 AMPennant Group expands through Amedisys acquisition Pulivarthi Group; 8/12/25In a significant shift within the healthcare landscape, the Pennant Group has announced its intention to acquire home health and hospice agencies presently owned by Amedisys and UnitedHealth. This move marks an essential strategic expansion into the Southeast U.S., a region already experiencing increasing demand for quality home health services. ... This post provides an in-depth analysis of the home health acquisition landscape while addressing key challenges such as reimbursement issues, staff retention, and access to care for vulnerable patients.
How to estimate your EHR implementation cost: Factors that impact your budget
08/24/25 at 03:20 AMHow to estimate your EHR implementation cost: Factors that impact your budget Joyrulez; by RickD32; 8/14/25 Implementing an EHR (Electronic Health Record) system is one of the most significant investments a healthcare organization can make. Beyond the obvious benefits of digital recordkeeping—such as improved patient care, streamlined workflows, and regulatory compliance—the financial implications of EHR implementation are considerable. Understanding the factors that influence costs is essential for accurate budgeting and successful project execution. This guide will break down the key considerations, providing insights into an ehr implementation cost breakdown, the roles involved, and hidden expenses that organizations often overlook.
Caregiver-reported barriers and facilitators to hospice enrollment for persons with dementia: A systematic review of qualitative evidence
08/24/25 at 03:15 AMCaregiver-reported barriers and facilitators to hospice enrollment for persons with dementia: A systematic review of qualitative evidencePalliative Medicine; by Oonjee Oh, Connie M Ulrich, Lauren Massimo, George Demiris; 7/25Despite the increasing prevalence of dementia, persons with dementia often receive suboptimal care near the end of life. Dementia caregivers experience intrapersonal, interpersonal, emotional, logistical, and physical challenges in ensuring quality end-of-life support for their loved one (e.g. limited understanding of end-stage dementia, gatekeeping providers, and family conflicts). The unique needs of caregivers caring for a seriously ill family member with dementia are not being fully addressed by the current available services and policies.
YoloCares: A caring coalition for California
08/24/25 at 03:10 AMYoloCares: A caring coalition for California The Davis Enterprise; by Craig Dresang; 8/15/25 In his closing remarks at a 2016 stakeholder meeting, hosted by the National Academy of Medicine, Dr. Victor Dzau (academy president) said, “We need a coalition, a movement, a critical mass. We need to work together so that the whole is greater than the sum of its parts. We need to come together to develop resources for policy and communication. We need to improve our communication — to patients and families, healthcare providers, government, and the public.” His words perfectly captured the founding spirit of the Coalition for Compassionate Care of California. ... The group is a small but mighty powerhouse that works closely with healthcare systems and providers, patient advocacy groups, professional associations and policy — and lawmakers to promote high-quality care for seriously ill Californians.Publisher's note: Thanks for your editorial Craig - and a shout out to Jennifer Ballentine and the strong work she and the Coalition are doing!
Palliative care plays an essential role in heart failure care
08/24/25 at 03:05 AMPalliative care plays an essential role in heart failure care Cardiovascular Business; by Michael Walter; 8/13/25 Palliative care should play a significant role in the day-to-day management of heart failure (HF) patients, according to new recommendations from the Heart Failure Society of America (HFSA). HF patients are associated with high mortality and a considerably worse quality of life, the group wrote. Care teams should be doing everything in their power to help patients control their symptoms and live the best lives possible. The HFSA guidance is available in full in the Journal of Cardiac Failure. ... “When using a guide, conversations are more likely to be feasible, acceptable and associated with positive experiences for both patients and clinicians,” the authors wrote.
Make a habit of two things...
08/24/25 at 03:00 AMMake a habit of two things - to help, or at least, to do no harm. ~Hippocrates
350 health groups urge Congress to extend Medicare telehealth
08/24/25 at 03:00 AM350 health groups urge Congress to extend Medicare telehealth MedCityNews; by Marissa Plescia; 8/14/25 A group of 350 organizations, including the American Academy of Hospice and Palliative Medicine, are urging Congress to make Medicare telehealth flexibilities introduced during the COVID-19 pandemic permanent, or at least extend them for two years. In a letter to congressional leaders, the organizations emphasize the importance of telehealth for Medicare beneficiaries, particularly those with chronic conditions or in rural areas, and highlight the potential impact on health care access and infrastructure. Guest Editor’s Note, Judi Lund Person: Unless there is Congressional action after the August recess to extend the hospice face-to-face requirement through telehealth, that option will conclude on September 30, 2025.
Today's Encouragement
08/23/25 at 03:55 AMMaybe some people just aren't meant to be in our lives forever. Maybe some people are just passing through. It's like some people just come through our lives to bring us something: a gift, a blessing, a lesson we need to learn. And that's why they're here. You'll have that gift forever. ~Danielle Steel
Ethical obligations to inform patients about use of AI tools
08/23/25 at 03:40 AMEthical obligations to inform patients about use of AI toolsJAMA; by Michelle M. Mello, Danton Char, Sonnet H. Xu2; 7/25When a health care organization decides to deploy an AI tool, it should decide whether notification or consent is ethically required. To decide that disclosure is not required at the point of care is not to conclude that organizations have no transparency obligations concerning their use of AI. Two complementary steps can help discharge these obligations. First, health care organizations’ websites and written materials distributed to patients should explain how the organization uses AI to deliver better, safer, more efficient care and protect staff well-being. This kind of transparency honors patients’ desire to know how their care may be affected by AI and may help some make decisions about where to seek care.
Exploring virtual reality as an intervention to improve symptom severity in hospice-eligible patients
08/23/25 at 03:35 AMExploring virtual reality as an intervention to improve symptom severity in hospice-eligible patientsAmerican Journal of Hospice and Palliative Care; by Hannah Maciejewski, Kathryn Levy, Catherine M Mann, Suzanne S Sullivan, Gina Schuster, Christopher W Kerr; 7/25Virtual reality (VR) as an intervention has appeared in the literature and in clinical settings across many different populations. To expand the use of this care option, it is worth considering the ways in which a VR application may benefit individuals with life-limiting illness in hospice and palliative care settings. The incorporation of VR as a therapy option may aid in symptom management and support people nearing the end of life in focusing on aspects of their overall well-being.
Improved outcomes and cost with palliative care in the Emergency Department: Case-control study
08/23/25 at 03:30 AMImproved outcomes and cost with palliative care in the Emergency Department: Case-control studyThe Western Journal of Emergency Medicine; Brandon Chalfin, Spencer M Salazar, Regina Laico, Susan Hughes, Patrick J Macmillan; 7/25This small pilot case-control study included a subset of all patients referred by emergency physicians and hospitalists for palliative care within 24 hours of registration, physically present in the ED. CONCLUSION: Embedding hybrid physicians in the ED significantly shortened hospital stays and reduced charges for seriously ill patients. A notable secondary outcome was that 26.5% of ED visits in the case group did not result in hospital admission, compared to all controls being admitted ... In addition, more cases than controls had a code status of comfort care at discharge ... These findings support the further exploration of integrating such physicians into ED settings to enhance patient care and optimize hospital resources.
Trends in hospice and palliative care consults initiated in the emergency department: An eight-year utilization analysis
08/23/25 at 03:25 AMTrends in hospice and palliative care consults initiated in the emergency department: An eight-year utilization analysisThe American Journal of Emergency Medicine; by Satheesh Gunaga, Abe Al-Hage, Alyssa Buchheister, Harish Neelam, Jessica Corcoran, Michael Welchans, Kirby Swan, Mahmoud Awada, Joseph Miller, Fabrice Mowbray; 8/25Emergency departments (EDs) play a central role in end-of-life care, yet the early integration of hospice and palliative care (HPC) is often underutilized. A total of 8,055 HPC consults were ordered for 6,370 unique patients. The average age was 78.1 years, with 56.4 % female and 75.0 % White. Of the cohort, 91.7 % were admitted, 5.3 % discharged home, and 53.2 % died in-hospital. HPC consults increased from 369 in 2016 to 1,355 in 2023 (367 % increase ... ). The ratio of hospice to palliative care consults reversed from 1.5:1 in 2016 to 1:1.9 in 2023.
Behavioral symptoms in patients with dementia are associated with care partner abusive behaviors
08/23/25 at 03:20 AMBehavioral symptoms in patients with dementia are associated with care partner abusive behaviorsJournal of Elder Abuse & Neglect; by Emily LeRolland, Francesca Falzarano, Karen L. Siedlecki; 8/25Abuse of older adults with dementia is an increasingly prevalent public health concern in the United States. The current study examined whether care recipient behavioral symptoms (e.g. aggressive or agitated behaviors) predicted abusive behaviors by care partners. Results indicate that most participants reported engaging in at least one abusive behavior toward their care recipient. Behavioral symptoms in care recipients were a significant predictor of abusive behavior perpetrated by the care partner, even after controlling for a large number of covariates. Care partner depressive symptoms significantly mediated the relationship between care recipient behavioral symptoms and care partner abusive behavior. Our results suggest that physician screening for depression in care partners and referral to appropriate resources may be one avenue for decreasing the risk of abuse toward care recipients.
The Faith Care Family Project: A pilot intervention for African American dementia family caregivers
08/23/25 at 03:15 AMThe Faith Care Family Project: A pilot intervention for African American dementia family caregiversAmerican Journal of Alzheimer's Disease and Other Dementias; Noelle L Fields, Ling Xu, Ishan C Williams, Fayron Epps, Samantha Tinker; 8/25The Faith Care Family (FCF) Project was a telephone based, volunteer-led intervention for African American Alzheimer’s disease and related dementias (AD/ADRD) family caregivers that was piloted in one predominantly African American church. Church volunteers indicated overall significant improvements knowledge of AD/ADRD after the training as well as after the intervention. Quantitative results indicated that caregivers increased their knowledge of dementia, reported improved coping skills, and reported increased positive aspects of caregiving. Feeling a connection, normalizing the challenges of caregiving, gaining or reinforcing knowledge, and sharing community resources were themes from qualitative interviews with the family caregivers.
Clinician and caregiver perspectives on managing dementia behaviors in hospice
08/23/25 at 03:10 AMClinician and caregiver perspectives on managing dementia behaviors in hospiceMedpage Today; by Elethia W. Tillman; 7/25New research reveals a gap in training and resources for managing behavioral and psychological symptoms of dementia (BPSD) in hospice settings, impacting both patient well-being and caregiver burden. Key points include:
[Iceland] Medication causes and treatment of delirium in patients with and without dementia
08/23/25 at 03:05 AM[Iceland] Medication causes and treatment of delirium in patients with and without dementiaBrain and Behavior; by Anita Elaine Weidmann, Rut Matthíasdóttir, Guðný Björk Proppé, Ivana Tadić, Pétur Sigurdur Gunnarsson, Freyja Jónsdóttir; 7/25This summary offers the most detailed summary of medication-related information for delirium in patients with and without dementia to support prescribing decisions. While the detailed results can be used to support a multicomponent approach to delirium care, they also support the call for categorizing delirium into distinct etiological subgroups. The effect of medication on gut microbiome diversity and composition should be considered.
Proportional sedation for persistent agitated delirium in palliative care-A randomized clinical trial
08/23/25 at 03:05 AMProportional sedation for persistent agitated delirium in palliative care-A randomized clinical trialJAMA Oncology; David Hui, Allison De La Rosa, Jaw-Shiun Tsai, Shao-Yi Cheng, Egidio Del Fabbro, Anita Thankam Thomas Kuzhiyil, Kendra Rowe, Ahsan Azhar, Thuc Nguyen, Michael Tang, Chien-An Yao, Hsien-Liang Huang, Jen-Kuei Peng, Wen-Yu Hu, Sonal Admane, Rony Dev, Minxing Chen, Patricia Bramati, Sanjay Shete, Eduardo Bruera; 7/25Neuroleptic and benzodiazepine medications are often considered for patients with persistent agitated delirium in the last days of life; however, the risk-to-benefit ratio of these medications is ill-defined and benzodiazepine medications have not been compared to placebo. The results of this randomized clinical trial indicate that proactive use of scheduled sedatives, particularly lorazepam-based regimens, may reduce persistent restlessness and/or agitation in patients with advanced cancer and delirium in the palliative care setting.
