Literature Review

How caregivers can prepare for a loved one’s final days AARP; by Paul Wynn; 9/28/26 When Dr. Chris Kerr’s mother was dying, he had the kind of experience that can change the way a doctor thinks about death. Kerr had spent decades caring for people at the end of life as a palliative care doctor in the Buffalo, New York, area. But when his mother, Shirley, became seriously ill, he experienced death through the lens of a son and a caregiver... “My lasting memory of my mother is her strong connection to her parents,” says Kerr, author of Death Is But a Dream and chief medical officer of Hospice and Palliative Care Buffalo. “It took me a while, but I realized that I had to stop trying to play doctor and just be there for her.”

At the bedside: clinician grief Core IM; podcast by Dr. Margot Hedlin, Dr. Danai Papadatou, Dr. Tamar Schiff and Dr. Jafar Al-Mondhiry; 9/8/26... "I can’t share his name, but I can tell you what he taught me about grief. I met this patient a few months after graduating from medical school, and by that point he was already dying. ... I grieved for this man the way I’ve grieved for many patients: I found a supply closet to cry in for a few minutes before my pager went off. But in the years since, years in which I worked at the epicenter of the COVID pandemic, worked nights at a cancer hospital, and suffered personal loss, I’ve found that grief is too large to be stuffed in a supply closet: when left unaddressed, it keeps coming back, in ways and places that I couldn’t predict."

Palliative care conversations can enhance support for patients with advanced cancer Oncology Nurse Advisor; by Megan Garlapow, PhD; 9/22/26 Palliative care and hospice address different points along the trajectory of serious illness, and clinicians can improve patient and family understanding by clearly distinguishing the 2 services and using direct, supportive language, according to a presentation at ONS Bridge 2026 by Meg Krasne, MD, MPH, clinical expert and instructor at Dana-Farber Cancer Institute and Harvard Medical School. ... She described palliative care as a specialized medical discipline centered on symptom management, coping, and medical decision-making. Rather than representing a transition away from active treatment, palliative care can function as an additional layer of support throughout the course of serious illness. 

Capstone University offering Clinical Pastoral Education for hospice and palliative care chaplaincy NEWSnet; Press Release; 9/18/26 Capstone University [in University Place, WA] now offers clinical pastoral education (CPE) with a specific focus on hospice and palliative care chaplaincy. This transformative program centers on spiritual caregiving in response to aging, serious illness, dying, and bereavement. It enables chaplains to deepen their ability to provide culturally responsive, patient-led spiritual care to individuals and families throughout the end-of-life experience. 

Effective palliative care for hospice transitionsJAMA Internal Medicine; by May Hua, MD, MS, Miguel Cid, MPH, Claire Barshied, PhD, Rachel C. Shelton, ScD, MPH, Grace Hu, MPH, Natasha Stekl, MPH, Carrie Brill, BS5; Elise C. Carey, MD, and R. Sean Morrison, MD; 9/14/26 Question: What factors impact the ability of palliative care teams to affect hospice use for patients with metastatic cancer?Findings: In this qualitative study across 6 sites with interviews among 93 clinicians and patients, institutions with high and low performance in hospice use exhibited substantive differences in the relationship between palliative care and oncology teams. At high-performing sites, the relationship was characterized by mutual trust and respect, warmth and familiarity, and empathy for each other, while at low-performing sites, the relationship was characterized by a lack of trust and familiarity as well as negative regard for each other.Meaning: These findings suggest that the relationship between palliative care and oncology teams is a modifiable factor that could affect care delivery and patient outcomes.

Medicine on screen: 10 films doctors may want to rewatch Medscape; by Medscape's editorial team; 8/24/26 Cinema has long portrayed medicine through many different lenses: from the perspectives of doctors and patients to those of friends and family, whether set in hospital wards or research laboratories. This curated selection of classic and contemporary films explores care, illness, and hospital life from strikingly different angles — some realistic, some visionary, and others deeply unsettling. Together, they aim to refocus attention on medicine not only as a science, but as a profoundly human experience. 10 Films Every Doctor Should (Re)Watch:

Priorities for advancing palliative care for Amyotrophic Lateral Sclerosis: a consensus report from a palliative care for ALS working group in the United States Muscle & Nerve; by Kara E. Bischoff, Yaowaree L. Leavell, Jessica M. Besbris, Christi Lero, Kelsey Noble, Astrid Grouls, Jerome Kurent, Benzi M. Kluger, Steven Z. Pantilat, Ambereen K. Mehta, on behalf of the International Neuropalliative Care Society's Palliative Care for ALS Working Group; 8/31/2026 The Palliative Care for ALS Working Group was formed within the International Neuropalliative Care Society, consisting of interprofessional ALS and palliative care clinicians, researchers, advocates, and patients and care partner representatives who are committed to improving palliative care for people living with ALS. The group engaged in a strategic planning process to determine what is needed to advance palliative care for people with ALS over the next 3–5 years. This report outlines the core recommendations from that strategic planning process. Recommendations are divided into five sections: (1) clinician education, (2) clinical service expansion, (3) research, (4) public awareness, and (5) policy change. Editor's Note: ALS is an especially devastating, demanding disease for patients, caregivers and families, for your clinical staff and volunteers. What disease-specific education and resources do you provide? How many ALS patients have your organization served in "x" years? Do you partner in any way with your regional ALS association? For non-clinical leaders, an important, easy distinction for you to remember the clinical, deeply personal differences between ALS versus ALZ: 

Chaplains describe comforting families during Hawk Fire evacuations KOLO-8 ABC News Now, Reno, NV; by Noah Bond; 8/28/26 The Great Basin Chaplain Corps deployed 17 chaplains across evacuation sites during the Hawk and Bug fires, logging more than 466 hours of service at shelters, according to Chaplain Dana Sater, VOAD liaison and team lead for Northern Nevada corps. ... Sater said the corps logged 466.5 hours of service for the fires at evacuation centers, in addition to chaplains serving in hospitals, hospice, fire departments and with CERT through the Washoe County Sheriff’s Office. ... Blackburn said chaplains also coordinated evacuation for a hospice family to the Lawrence J. Weiss Hospice Guest House, ...

Why Hospice Austin is training frontline staff on specialized dementia care KXAN Austin, TX; by Avery Travis; 8/26/26 A Central Texas hospice service received national recognition for investing in dementia-specific training and certification for frontline caregivers, as the impact of dementia grows in the United States. According to Hospice Austin and Austin Palliative Care, it recently became the only hospice organization in the country to be named to the National Council of Certified Dementia Practitioners' Memory Care Excellence Network. Diana Wagner, the Director of Education and Training at Hospice Austin and Austin Palliative Care, spoke to KXAN's Avery Travis and Will DuPree about the nuance needed to care for someone with dementia at the end of their life. ... Wagner said her team worked to certify more than 70% of their frontline staff in dementia care.

Spirituality and religiosity in end-of-life decision-making in intensive care units: a systematic review of preferences, ethical framing, and meaning-making Cureus; by Dimitrios G. Apostolakis, Nikiforos V. Angelopoulos, Spiros Georgakis, Fotios Tatsis, Foteini Veroniki, Konstantinos Stamatis, Georgios Papathanakos, Mary Gouva, Vasilios Koulouras; 8/25/26 End-of-life decision-making in intensive care units (ICUs) is a complex and ethically challenging process shaped not only by clinical factors but also by patients' values, cultural contexts, and spiritual or religious beliefs. ...  [Spirituality] demonstrated a multidimensional role, facilitating acceptance of death, promoting support for palliative care in some contexts, and contributing to meaning-making during the end-of-life process. Cultural and contextual factors moderated these relationships, and the provision of spiritual care by healthcare professionals was associated with less aggressive end-of-life care. ... Integrating spiritual assessment and culturally sensitive spiritual care into routine clinical practice may enhance shared decision-making and improve alignment between treatment decisions and patients' values, preferences, and goals of care.