Literature Review
All posts tagged with “Clinical News | Disease Specific.”
Social determinants of death anxiety in patients with advanced cancer receiving outpatient palliative care
07/25/26 at 03:20 AM“A lot of the times, patients really don’t know what questions to ask:” Communication perspectives of Black patients with advanced lung cancer
07/25/26 at 03:10 AM[Italy] Fever in a palliative care setting: Clinical insights and implications from a prospective observational cohort study
07/25/26 at 03:05 AM[Italy] Fever in a palliative care setting: Clinical insights and implications from a prospective observational cohort studyPalliative Medicine; by Stefania Cheli, Elena Angeli, Oscar Corli, Sofia Dinegro, Agostino Zambelli, Tania Carta, Romina Shazivari, Michaela Smolikova, Paolo Franceschi, Francesco Molà, Yara Silva Cruzeiro, Emilio Clementi, Andrea Gori; 5/26Fever is a frequent but complex symptom in adults with a limited prognosis, arising from multifactorial causes beyond infection. The study was conducted in an inpatient hospice palliative care unit within the Luigi Sacco Hospital in Milan, Italy (January and December 2024). Fever occurred in 40% of patients, with a median onset of 5.5 days after admission. In 39.7% of cases, fever was attributed to infections, mainly catheter-associated urinary tract infection. Its strong association with medical devices highlights the need for proportional, personalised interventions that primarily consider prognosis, symptom relief, and quality of life.
H.R.9703 - Improving access to transfusion care for hospice patients act of 2026
07/21/26 at 03:00 AMH.R.9703 - Improving access to transfusion care for hospice patients act of 2026 U.S. Congress.gov, House Ways and Means Committee; sponsored by Rep. Debbie Dingell (D-MI-6); bill introduced 7/15/26 H.R. 9703: To require the Center for Medicare and Medicaid Innovation to test allowing blood transfusions to be paid separately from the Medicare hospice all-inclusive per diem payment.
Emotional and ethical impacts on healthcare professionals performing cardiopulmonary resuscitation
07/18/26 at 03:40 AMEmotional and ethical impacts on healthcare professionals performing cardiopulmonary resuscitationAmerican Journal of Hospice & Palliative Medicine; by Patrick J. Macmillan, Susan Hughes, Dumindra Gurusinghe, Allison Go, Chase Lancaster, Iris Price; 6/26Many studies exist outlining poor outcomes related to cardiopulmonary resuscitation (CPR) administered to patients who are elderly and/or have comorbid medical conditions with sudden cardiac arrest. Studies show only 10% of patients with out-of-hospital cardiac arrest and initial asystole survive until they reach the hospital. Less than 5% survive until hospital discharge with good neurologic function. This study presents data that suggests that there is an association between moral distress and performing CPR on individuals who are elderly with multiple comorbid medical conditions. More than sixty percent of our respondents were challenged emotionally during these types of code situations, and a similar number of healthcare workers felt the code could be considered unethical.
Toward home cancer care—Reducing time toxicity for the right patients with prostate cancer
07/18/26 at 03:30 AMBreast-directed palliative radiotherapy in metastatic and inoperable locally advanced breast cancer: From clinical efficacy to psychosocial impact
07/18/26 at 03:25 AMReach of palliative care in Parkinson disease-Progress and gaps after a national team-based implementation project
07/18/26 at 03:20 AMReach of palliative care in Parkinson disease-Progress and gaps after a national team-based implementation projectNeurology in Clinical Practice; by Sandhya Seshadri, Umer Akbar, Peggy Auinger, Nicole Andrea Lessard, Megan Dini, Sally A. Norton, Hillary D. Lum, Jodi Summers Holtrop, Janis M. Miyasaki, Christina L. Vaughan, Benzi M. Kluger; 6/26While clinical trials demonstrate PC [palliative care] improves quality of life for PWP [people with Parkinson disease] and carepartners, little is known about the impact of PC on their experiences of receiving care in real-world settings. At COEs [Parkinson's Foundation US-based Centers of Excellence], [surveyed] PWP reported significant increases in non-motor symptom (NMS) assessment ... and pain management ... Emotional and spiritual needs were addressed more frequently ... Advance care planning (ACP) discussions [and documentation] rose ... Communication ratings and knowledge of PC were high (>85%) and stable across surveys.
[Spain] Post-recurrence management of malignant glial brain tumors: Therapeutic strategies, evidence and limitations, palliative care, terminal sedation, and end-of-life considerations
07/18/26 at 03:05 AM[Iran] Prerequisites and challenges of the role played by death doula for supporting patients with cancer in end-of-life (EOL) stages: Qualitative study
07/18/26 at 03:00 AMWhen technology meets its limits: Integrating Medical Aid in Dying with withdrawal of a left ventricular assist device
07/18/26 at 03:00 AMVITAS medical director: improve hospice referrals for cancer patients
07/17/26 at 03:00 AMVITAS medical director: improve hospice referrals for cancer patients Hospice News; by Jim Parker; 7/16/26 Hospice utilization among some cancer patients is leveling off and slowing growth, but healthcare providers and medical educators can adopt certain strategies to move the needle. This is according to Dr. Ileana Leyva, regional medical director for VITAS Healthcare. ... Neuro-degenerative, lung and cardiac diseases are gaining more prominence among hospice diagnoses. In 2024, senile degeneration of the brain was the most common terminal diagnosis among Medicare decedents at 9%, followed by Alzheimer’s at 6%, according to the National Alliance for Care at Home. Chronic obstructive pulmonary disease rounded out the top three at 4.2%. Lung cancer was the 11th most common diagnosis that year, at 2.1%, the highest rate for any form of cancer. Hospice News spoke with Leyva about the barriers that prevent cancer patients from accessing hospice sooner and what stakeholders can do to drive improvement.
Cardiologists treating increasingly complex patients as America ages
07/16/26 at 03:00 AMCardiologists treating increasingly complex patients as America ages Medscape; by Sarah Amandolare; 7/14/26 ... Heart failure (HF) affects 15%-20% of adults over 80, according to the American Heart Association/American College of Cardiology/Heart Failure Society of America Guideline for the Management of Heart Failure. HF with preserved ejection fraction (HFpEF), which becomes more likely after age 80, is related to other common conditions of aging, including hypertension, chronic kidney disease, diabetes, and obesity. “Almost by definition, most people that have HFpEF have multiple comorbidities,” Hummel said. “You have to account for a lot of them when you’re thinking about how to help the patient best.” This population also has higher chances of developing dementia and frailty, which affect 35% of adults age 90 and older and 31% of octogenarians, respectively. Older adults hospitalized for HF also have a high likelihood of polypharmacy; 68% take 10 or more medicines.
Early palliative care for people with primary malignant brain tumors: A systematic review
07/11/26 at 03:25 AMEarly 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.
Palliative care for older adults with hip fracture: An explanatory sequential mixed-methods study
07/11/26 at 03:20 AMPalliative 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.
[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 AMThe hidden cost of cancer's end: how financial strain shapes final months of care
07/08/26 at 03:00 AMThe 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?
Addressing the emotional and psychologic toll of a cancer diagnosis
07/08/26 at 03:00 AMAddressing the emotional and psychologic toll of a cancer diagnosis Cancer Therapy Advisor; by Sabrina Martinez, MS and Jason L. Harris; 7/7/26 Patients with cancer experience distress not only from receiving a jarring diagnosis, but also a treatment regimen that can be difficult and debilitating, additional challenges to relationships that might be fraught already, significant financial stress, and the reality of death. Many also experience thoughts of fear of recurrence, stress, depression, anxiety, self-consciousness, and loneliness. The mental and emotional burden of cancer can be as difficult as enduring the disease itself. We spoke with oncologists and experts in psycho-oncology to get their perspectives on delivering “bad” news, working with loved ones and caregivers, resources for those involved in the patient’s cancer journey, and survivorship issues that should be addressed.
7 ways palliative care can help people with ATTR-CM
07/06/26 at 03:00 AM7 ways palliative care can help people with ATTR-CMEveryday Health; by Abby McCoy, RN; 7/3/26 Transthyretin cardiac amyloidosis (ATTR-CM), a rare type of heart failure, can cause symptoms that affect more than just your heart, and many of them can lower your quality of life. But palliative care, or care meant to provide symptom relief, comfort, and support, can help you live better with this condition. ... Here’s how your palliative care team can help you manage life with ATTR-CM and feel your best.
Epidural and intrathecal catheter use at the end of life for cancer pain
06/27/26 at 03:35 AMPalliative care involvement for pediatric hematopoietic cell transplant patients can enhance comfort-focused care at end of life without shortening survival duration
06/27/26 at 03:25 AMComparison of end-of-life care utilization among patients with and without documented goals of care
06/27/26 at 03:10 AMFamily caregivers' perspectives on challenges and support needs in hospital-based palliative care for persons living with dementia
06/24/26 at 03:00 AMFamily caregivers' perspectives on challenges and support needs in hospital-based palliative care for persons living with dementia Baylor Medicine | Texas Medical Center Documents ; by Jung Kwak, Anita Chary, Sarah Stayer, Kwaku Duah Oppong, Sumin Yoon, Snehal Patel, and Elizabeth A Kvale; originally pub 11/17/25, reposted online 6/23/26Palliative care needs of hospitalized persons living with dementia (PLWD) and their family caregivers remain poorly understood. ... Thematic analysis of interviews revealed three themes: the value of palliative care in navigating end-of-life uncertainty in dementia, uncoordinated and reactive care during hospitalization, and lack of guidance for post-hospital transitions. While caregivers valued palliative care for emotional and decision-making support, findings underscore the need for earlier integration and improved coordination across hospital teams to better support families.
Dying patients shouldn’t have to choose between dialysis care and comfort
06/23/26 at 03:00 AMDying patients shouldn’t have to choose between dialysis care and comfort The Boston Globe, Boston, MA; by Patricia Ramsden; 6/22/26 ... Medicare currently requires most end-stage kidney failure patients to choose between dialysis and hospice benefits. ... People dying from other terminal illnesses do not face this harsh choice. For several years, Dialysis Clinic, Inc. (DCI), the only national not-for-profit dialysis organization, has collaborated with not-for-profit hospice organizations to offer concurrent palliative dialysis and hospice care to selected patients in Tennessee and Western Pennsylvania. A 2026 collaboration between DCI and Care Dimensions, the largest hospice provider in the state, expanded that model to Eastern Massachusetts. However, this innovative program, relying on philanthropic funding, remains available only to a few patients.
