Literature Review



[Canada] Palliative care is a fundamental human right

07/12/26 at 03:10 AM

[Canada] Palliative care is a fundamental human right TroyMedia; by Rebecca Vachon; 7/6/26 ... Despite the fact that everyone dies, and despite the fact that something like 180,000 Canadians and their families interact with some form of end-of-life care in a year, I keep confronting the perception that palliative care is a niche issue, not one of broad interest. But this reaction only underscores the poll's findings: namely that many Canadians continue to misunderstnad what palliative care is and isn't. On a more positive note, however, when Canadians do understand it, palliative care is, in fact, identified as a priority issue.

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Dignity therapy: What matters most in end-of-life care?

07/12/26 at 03:05 AM

Dignity therapy: What matters most in end-of-life care? Medscape; by Irene Salvetti, MD; 7/7/26 ... Many patients, especially in advanced stages of illness, express the fear of no longer being themselves, of becoming a burden, or of losing their sense of meaning, role, and memory. In these experiences, suffering is not merely physical but also related to identity, relationships, and spirituality. The way patients perceive themselves as viewed by others is an important determinant of their sense of dignity. Dignity therapy was developed to give voice to this often-overlooked aspect of the experience of illness. ...  Harvey Max Chochinov introduced dignity therapy as a brief psychotherapeutic intervention for individuals with advanced or terminal illness, with the goal of preserving a sense of personal dignity during times of frailty, dependence, and the approach of death.

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The hidden cost of cancer's end: how financial strain shapes final months of care

07/12/26 at 03:00 AM

The hidden cost of cancer's end: how financial strain shapes final months of care Fred Hutch Cancer Center, University of Washingon, Seattle, WA; by D. Moosavi; 6/25/26 ... Previous Fred Hutch research has shown that people with cancer are more than twice as likely to file for bankruptcy, and nearly twice as likely to experience what researchers call an “adverse financial event,” compared with people who don’t have cancer. But most of that earlier work focused on financial hardship as an outcome caused by cancer. This study flips the question: once someone is already dealing with financial strain, what happens to the care they receive as their illness progresses?Publisher's note: This study also notes Fred Hutch researchers are already exploring this idea through an ongoing study called CREDIT, which is testing whether connecting patients with advanced cancer to financial navigation services can improve their care and reduce unnecessary emergency room and hospital use. Could hospices do something similar?

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DOWNLOAD E-BOOK: A History of Care - 250 Years of American Need, Service and Hope

07/12/26 at 03:00 AM

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Sunday newsletters

07/12/26 at 03:00 AM

Sunday newsletters focus on headlines and top read stories of the last week (in order) - enjoy!

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A bad day of camping is still better than...

07/12/26 at 03:00 AM

A bad day of camping is still better than a good day at work... Unless you get eaten by a bear, then I'd say it's a tie!

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Implementation of a serious illness conversation program in a health system: A retrospective observational study

07/11/26 at 03:40 AM

Implementation of a serious illness conversation program in a health system: A retrospective observational studyJournal of Palliative Medicine; by Glen Varns, Abbey Sidebottom, Katy Hentges, Sandra Castro-Pearson, Jan Richardson, Emily Downing; 6/26Serious illness conversation (SIC) is a structured conversation framework designed to improve shared decision making and promote goal-concordant care with patients anticipating end-of-life care decisions. Objective: Examine reach, timeliness, and quality of SIC implementation across a health system after implementation of a SIC Program (SICP) [and] examine factors associated with SIC completion for eligible patients. Factors associated with SIC included palliative care visits ... , a primary care provider in the system ... , and an inpatient admission with discharge to home care ... Patients with dementia ... were less likely to have SIC. Conclusion: Systemwide implementation of an SICP engaged [only] half of eligible patients; many of those had multiple documented conversations prior to death.

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The doctor will see you now--or will they? Theorizing AI’s impact on Black patients and providers in health care

07/11/26 at 03:35 AM

The doctor will see you now--or will they? Theorizing AI’s impact on Black patients and providers in health careSocial Currents; by Adia Harvey Wingfield, Tyrell Spencer; 6/26As far as recent innovation practices go, artificial intelligence (AI) represents one of the major disruptions reshaping various aspects of human life. Health care is perhaps one of the industries where AI stands to be most transformative, particularly as it is increasingly used to diagnose illnesses, assist in creating treatment plans, reduce human error, and offer routine patient services. Yet despite its rapid growth, AI technology still reflects human biases and perceptions, allowing it to replicate existing inequalities. These inequalities could take on particular significance given persistent occupational stratification and increasing racial diversity. In this paper, we theorize how the growing reliance on AI in the US health care system will affect Black care providers and patients.

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Impact of specialized pediatric palliative care on bereaved parents' mental and physical health

07/11/26 at 03:30 AM

Impact of specialized pediatric palliative care on bereaved parents' mental and physical healthJournal of Pain & Symptom Management; by Claudia Delgado-Corcoran, Huong D. Meeks, Sarah E. Wawrzynski, Barry P. Markovitz, Brandy Harman, Jasmine R. Masih, Kuan Li, Mark Harousseau, Dominic Moore, Jacob Wilkes, Stefanie G. Ames; 6/26Pediatric death can lead to long-term adverse effects on parents’ health. [In this study] of 776 deceased children linked to 773 mothers and 711 fathers, 36.1% received a SPPC [specialized pediatric palliative care] consultation prior to death. Higher rates of mental and physical health burden were observed in mothers than fathers across all time points. Lack of SPPC was associated with increased risks for new mental and physical health burden for mothers within 12 months after the child’s death ... Conclusions: Bereaved parents, especially mothers, experienced new mental and physical health burden up to 24 months after a child’s death.

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Early palliative care for people with primary malignant brain tumors: A systematic review

07/11/26 at 03:25 AM

Early palliative care for people with primary malignant brain tumors: A systematic reviewJournal of Palliative Medicine; by Jennifer C. Hall, Connor Barrett, Soren Christensen, Juliet Dalton, Samantha Kaplan, Christopher A. Jones, Margaret O. Johnson; 6/26In some populations with advanced cancers, early palliative care (ePC) has been shown to improve quality of life (QoL) and reduce aggressive interventions, but its role and timing in primary malignant brain tumors (PMBT) remains poorly defined. Definitions of ePC varied with “early” defined relative to diagnosis, treatment milestones, or death. Across studies, a minority of patients received PC (15%–40%), with most referrals occurring late in the disease course. Earlier PC was associated with reduced aggressiveness of EoL care, decreased health care utilization, and, in some cases, longer survival. Evidence suggests ePC for PMBT is infrequently implemented yet feasible and may reduce aggressive EoL care and improve outcomes. 

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Palliative care for older adults with hip fracture: An explanatory sequential mixed-methods study

07/11/26 at 03:20 AM

Palliative care for older adults with hip fracture: An explanatory sequential mixed-methods studyJournal of Pain & Symptom Management; by Daniel I Hoffman, Sydney Moore, Amanda J Reich, Christina Sheu, Mengyuan Ruan, Masami Tabata-Kelly, Kate Sciacca, Tamryn F Gray, Daniel Dohan, Charlotta Lindvall, Zara Cooper; 6/26After hip fracture, older adults experience burdensome treatments and high mortality; they may therefore benefit from palliative care (PC). Among 1,433 hip fracture admissions, GOCC [goals of care conversations], hospice discussions, and specialty PC were documented in view on their role in GOCC. Conclusion: Limited standardization, role uncertainty, and cultural factors limited PC documentation and delivery, highlighting opportunities to strengthen PC integration in surgical care.

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Experiences of end-of-life care among incarcerated individuals: A qualitative interpretative meta-analysis

07/11/26 at 03:15 AM

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Outcomes for hospitalized patients with comfort measures only orders

07/11/26 at 03:10 AM

Outcomes for hospitalized patients with comfort measures only ordersJournal of Palliative Medicine; by Gina Piscitello, Donna Durant, Tami Minnier, Marika Haranis, Robert M Arnold, Jane Schell; 6/26Clinicians place comfort measures only (CMO) orders for hospitalized patients at the end-of-life when a decision has been made to focus on patient comfort and allow the natural dying process to occur. Our primary aim was to assess the associations of specialty palliative consults (SPC) or documented goals of care conversations (GOCC) with in-hospital mortality among patients with CMO orders. Of 6,789 hospitalized patients with CMO orders ... seventy-three percent died in-hospital, and 22% were discharged with hospice. SPC placed anytime during hospital admission were associated with lower in-hospital mortality ... and higher discharge with hospice ... In contrast, documented GOCC anytime during admission were associated with higher in-hospital mortality ...  and lower discharge with hospice ...

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[Hong Kong SAR] Digital self-management of symptoms and quality of life for patients with advanced cancer-A randomized clinical trial

07/11/26 at 03:05 AM

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Survival variation and predictors of length of stay in US hospice patients

07/11/26 at 03:05 AM

Survival variation and predictors of length of stay in US hospice patientsInternational Perspectives and Future Directions for Practice, Research, and Policy; by Ian Duncan, Xiyue Liao, Terri Maxwell; 6/26End-of-life (EOL) patients in the US Medicare program represent a large and growing population, as well as a disproportionate share of Medicare’s costs. Survival of patients in hospice is, however, highly variable, implying an opportunity for improved management by enhancing the prediction of survival. Actuaries, health economists, policy analysts, and health services researchers have studied expenditures at the EOL for Medicare decedents for many years, finding that survival at EOL is highly variable. We discuss the utilization of hospice benefits for patients at the EOL in the United States.

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Today's Encouragement

07/11/26 at 03:00 AM

Once you carry your own water, you will learn the value of every drop.  ~African proverb

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An end-of-life care approach defining a new standard of care

07/11/26 at 03:00 AM

An end-of-life care approach defining a new standard of careJAMDA; by David N. Hoffman; 6/26The Institute for Healthcare Improvement (IHI) Leadership Alliance established an End-of-Life Care/Ending-Life Care Accelerator to define a continuum of care for patients as they progress from curative care, to palliative care, to hospice care, to final care planning, including ending life care interventions such as Medical Aid in Dying (MAiD), Voluntarily stopping eating and drinking (VSED), and palliative sedation. This accelerator defined as its goal the task of breaking down barriers between care providers which has been illuminated by research recently conducted by the Completed Life Initiative (CLI). CLI’s research efforts in this area started with an ongoing examination of nationwide hospice organization policies to provide referral for active intervention at the end of life. That effort was refocused on the widespread noncompliance of California and Washington state hospice organizations with a state law requirement to post on the organizations website a list of interventions made available by the hospice organization.

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[Italy] The Integrated Palliative Outcome Scale (IPOS): A tool for assessing needs and shaping individualized care plans in hospice settings

07/11/26 at 03:00 AM

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Saturday newsletters

07/11/26 at 03:00 AM

Saturday newsletters focus on headlines and research - enjoy!

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Executive Personnel Changes - 7/10/26

07/10/26 at 03:00 AM

Executive Personnel Changes - 7/11/26

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Reynolds creates Iowa Medicaid fraud task force

07/10/26 at 03:00 AM

Reynolds creates Iowa Medicaid fraud task force Insurance Newsnet; by Marissa Payne; 7/9/26 Gov. Kim Reynolds signed an executive order Wednesday [7/8] creating a new task force geared toward eliminating Medicaid fraud, waste and abuse, joining in the federal government's crackdown on potential misuse of public assistance programs. Reynolds signed the order establishing the Iowa Medicaid Fraud Elimination Task Force, which the Republican governor's office says will seek to ensure funds are used to support Iowans who qualify for benefits. "Safeguarding federal programs like Medicaid from bad actors requires accountability at every point in the process, from member eligibility verification to provider enrollment and billing," Reynolds said in a statement. 

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From Iowa City to the Rockies: How one social work graduate built a career on connection

07/10/26 at 03:00 AM

From Iowa City to the Rockies: How one social work graduate built a career on connection Iowa University College of Liberal Arts and Sciences, School of Social Work; 6/25/26 Since earning her bachelor's degree in social work from Iowa in 2010, Amanda Hebel has spent 15 years helping people navigate life's challenges—from hospice care to rehabilitation services across Colorado. ... Her senior year also brought her practicum placement in hospice care, and it’s where her education became a career. Having lost both of her parents before starting college, Hebel entered the placement with a depth of understanding that shaped how she showed up for patients from day one. The hands-on work—grief counseling, difficult conversations, navigating complex family dynamics—translated directly into the skills she'd carry into the workforce.

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'Labor of love:' Longtime Hospice of Dubuque leader retires

07/10/26 at 03:00 AM

'Labor of love:' Longtime Hospice of Dubuque leader retires Telegraph Herald, Dubuque, IA; by Elizabeth Kelsey; 7/8/26 When Lavonne Noel was hired as financial coordinator for Hospice of Dubuque in 1990, she was simply looking for a part-time job while she raised her young children. Little did the Dubuque resident know that she would spend the next 36 years working for the local nonprofit, including 15 as its executive director. Noel retired recently from Hospice of Dubuque after a career she described as “the greatest privilege of my professional life.” ... Hospice of Dubuque Financial Director Jackie Brehm is currently serving as interim executive director while officials conduct a search for Noel’s permanent replacement. Noel has every confidence Hospice of Dubuque will continue to thrive under new leadership.

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The Joint Commission Home Health Accreditation

07/10/26 at 03:00 AM

The Joint Commission Home Health Accreditation U.S. Department of Health and Human Services | FederalRegister.gov; Announcemen; scheduled to be published on 7/10/26  The Federal Register announced on July 9, 2026 that the application from The Joint Commission for continued CMS approval of its Home Health Agency (HHA) accreditation program has been approved by CMS. The approval is applicable from March 31, 2026 through March 31, 2032. 

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Deep summer is when laziness ...

07/10/26 at 03:00 AM

Deep summer is when laziness finds respectability. ~ Sam Keen

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