Literature Review
All posts tagged with “Research News | Journal Article.”
First-ever global ranking of palliative care: 2025 World Map under the new WHO framework
08/12/25 at 03:00 AMFirst-ever global ranking of palliative care: 2025 World Map under the new WHO framework Journal of Pain and Symptom Management; by Vilma A. Tripodoro, Jesús Fernando López Fidalgo, Juan José Pons, Stephen R. Connor, Eduardo Garralda, MA, Fernanda Bastos, Álvaro Montero, Laura Monzón Llamas, Ana Cristina Béjar, Daniela Suárez, Carlos Centeno; 8/7/25 This is the fourth edition of mapping global palliative care development and the first to introduce a country ranking using the new WHO framework. Covering 201 countries, the findings reveal deep inequities and highlight priority areas for action. The Global Development Score enables the creation of tailored strategies, supporting advocacy, policy, and investment to expand access and reduce serious health-related suffering worldwide. [To view the map, open the source article and scroll down to Figure 3.]
Communication and end-of-life care in dementia: insights from a close family member working in healthcare
08/12/25 at 03:00 AMCommunication and end-of-life care in dementia: insights from a close family member working in healthcare British Journal of Community Nursing; by Jennifer M Hadley; 7/31/25 There is very little documented evidence on the experiences of healthcare professionals caring for their own family outside of their role. This article explores the differences in the care received as the author shares her perspectives of caring for her mother, who was diagnosed with dementia. The author reflects on the care received and the impact of communication, as well as the ethical limitations of caring for a member of her own family. Significant references to communication barriers already exist within the literature, relating to end-of-life conversations. The presence of a relative who has a healthcare background may further impact the communication approach of healthcare professionals.
[Netherlands] Voluntarily stopping eating and drinking as a self-chosen path for end of life
08/09/25 at 03:55 AM[Netherlands] Voluntarily stopping eating and drinking as a self-chosen path for end of lifeWorld Medical Journal; Gert van Dijk, Veelke Derckx, Alexander de Graeff; 6/25Moving into the future, it is likely that doctors and other healthcare providers will be confronted more often with patients who would like to explore options for controlling their end of life care. They should correctly inform patients about the various clinical care options, including VSED [voluntarily stopping eating and drinking], and carefully guide them in the event of a decision to choose VSED. If healthcare providers have conscientious objections in providing care to people who choose VSED, then care must be transferred to a healthcare provider who is willing to provide the necessary care.
Palliative delays associated with increased length of stay in older traumatic brain injury patients
08/09/25 at 03:50 AMPalliative delays associated with increased length of stay in older traumatic brain injury patientsThe Journal of Trauma & Acute Care Surgery; by Sarah A Hatfield, Parima Safe, Cleo Siderides, Anjile An, Cassandra V Villegas, Nicole Goulet, Robert J Winchell, Elizabeth Gorman; 7/25Trauma Quality Improvement Program guidelines recommend early goals of care discussions (≤72 hours) for older patients with severe injuries. Patients (55 years or older) with moderate to severe TBI [traumatic brain injury] ... were retrospectively identified at a level I trauma center (2020-2022). Conclusions: Delayed PI [palliative intervention] is associated with increased LOS [length of stay] in older TBI patients, with no survival difference compared with early PI. Palliative interventions should be introduced early to reduce morbidity in patients with potential poor prognosis.
Sex and racial/ethnic differences in end-of-life care in decedents with lung cancer in Texas
08/09/25 at 03:50 AMSex and racial/ethnic differences in end-of-life care in decedents with lung cancer in TexasJournal of Palliative Medicine; by Myrna Katalina Serna, Efstathia Polychronopoulou, Aimee Rodriguez, Anjali Ramachandran, Margaret Goodrich, Sean O'Mahoney, Mukaila Raji, Yong-Fang Kuo; 7/25The lung cancer five-year survival rate is lower for Texans compared with the national average. We assessed sex and racial/ethnic differences in end-of-life care among decedents with lung cancer in Texas [and found that] ... males had more health care utilization and less hospice enrollment. Non-Hispanic Blacks and Hispanics had more health care utilization and less hospice enrollment ... Billed ACP [advance care planning] was low across all groups.
End-of-life course and subspecialty palliative care involvement for children on mechanical circulatory support: Five-center retrospective cohort study from the United States, 2015–2020
08/09/25 at 03:40 AMEnd-of-life course and subspecialty palliative care involvement for children on mechanical circulatory support: Five-center retrospective cohort study from the United States, 2015–2020Pediatric Critical Care Medicine ; by Vazquez Colon, Zasha; Robinson, Lorelei; Lopez-Colon, Dalia; Joong, Anna; Waldman, Elisha; Delgado-Corcoran, Claudia; May, Lindsay J.; Cousino, Melissa K.; Peng, David M.; Lukich, Stevan; Blume, Elizabeth D.; Machado, Desiree S.; M. Moynihan, Katie; 7/25Objectives: To characterize end-of-life (EOL) care and subspecialty palliative care (SPC) involvement in children with heart disease supported on mechanical circulatory support (MCS), including ventricular assist devices (VADs) and extracorporeal membrane oxygenation (ECMO). Most pediatric deaths after MCS occur soon after discontinuation of devices while receiving invasive therapies in ICUs. SPC teams were involved in less than half of the cases, with only 21% being consulted early. SPC was associated with more ACP [advance care planning] and less CPR at EOL.
Creating user personas to represent the needs of dementia caregivers who support medication management at home: Persona development and qualitative study
08/09/25 at 03:35 AMCreating user personas to represent the needs of dementia caregivers who support medication management at home: Persona development and qualitative studyJMIR Aging; by Anna Jolliff, Priya Loganathar, Richard J Holden, Anna Linden, Himalaya Patel, Jessica R Lee, Aaron Ganci, Noll Campbell, Malaz Boustani, Nicole E Werner; 7/25Caregiver-assisted medication management plays a critical role in promoting medication adherence and quality of life for people living with Alzheimer disease or related dementias (ADRD). Caregivers in this study demonstrated a range of characteristics and values that informed their approach to medication management. They used a combination of technology-based strategies and strategies situated in their physical environments to manage medications. The personas created can be used to inform interventions, such as digital tools, that address caregivers' unmet needs.
End-of-life care planning among older Vietnamese and Filipino Americans: A qualitative analysis
08/09/25 at 03:30 AMEnd-of-life care planning among older Vietnamese and Filipino Americans: A qualitative analysisJournal of Gerontological Social Work; Carson M. De Fries, My Ngoc To, Peiyuan Zhang, Emerson Ea, Fei Sun, Bei Wu, Sue E. Levkoff, Kaipeng Wang; 7/25Racial and ethnic disparities in end-of-life (EOL) care planning persist, particularly due to limited knowledge of culturally sensitive practices among older Vietnamese and Filipino Americans – two of the largest Southeast Asian American subgroups. Thematic analysis ... revealed a shared belief in the importance of EOL care planning in both groups, driven by the desire to honor personal wishes, reduce burden on family, and minimize conflict. Participants also expressed distrust in healthcare systems and emphasized the influence of family dynamics on EOL decisions. Notable differences emerged: Vietnamese participants more often described cultural practices that encouraged open conversations about death, while Filipino participants cited cultural taboos that hindered such discussions.
Working through grief: Exploring the relationship between organizational support on employee engagement, satisfaction, and loyalty
08/09/25 at 03:15 AMWorking through grief: Exploring the relationship between organizational support on employee engagement, satisfaction, and loyaltyTransdisciplinary Journal of Management; Katie N. Hansen; 7/25For most people, work and grief are unavoidable, meaning the majority of employees will work while grieving. Over the past several decades, employer grief responses have been more strategic than human-focused, leaving the bereaved under-supported. The most significant finding [of this study] is a decline in how engaged, loyal, and satisfied employees feel post-loss. Statistical analysis confirms that bereavement leave, reintegration accommodations, and provided support impact employee engagement, loyalty, and satisfaction, with positive and moderate to high associations existing between several variables. Finally, the results suggest the quality of an employer’s response and support for grieving employees remains insufficient, as the majority of respondents felt the need to take leave in excess of the bereavement leave provided, were not granted flexible work accommodations, and post-loss workloads did not meet their needs.
Ethics of overtreatment and undertreatment in older adults with cancer
08/09/25 at 03:05 AMEthics of overtreatment and undertreatment in older adults with cancerBMC Medical Ethics; by Clark DuMontier, William Dale, Anna C. Revette, Jane Roberts, Ameya Sanyal, Neha Perumal, Eric C. Blackstone, Hajime Uno, Mary I. Whitehead, Lewis Mustian, Tammy T. Hshieh, Jane A. Driver, Gregory A. Abel; 7/25This modified Delphi study convened a panel of experts in biomedical ethics and reached consensus that the principles of beneficence, non-maleficence, and autonomy are related to our previously proposed definitions of over- and undertreatment in older adults with cancer. The panel also reached consensus that, in most cases, it is unethical to make a treatment recommendation without (1) formal assessment of patient frailty (e.g., via a geriatric assessment) and (2) the opportunity for a patient to share their values, goals, and/or preferences. The panel did not reach consensus regarding the relationship between justice and over-/undertreatment; however, the panel concluded that justice applies to undertreatment when an oncologist withholds potentially beneficial cancer treatment in an older patient based on their age alone.
Demystifying dying in end-of-life-care: A phenomenological perspective
08/07/25 at 03:00 AMDemystifying dying in end-of-life-care: A phenomenological perspective Death Studies; by Elisabet Sernbo, Magnus Weber, Charlotta Öhrling, Stina Nyblom; 8/26/25 This article focuses on experiences of the process of dying. The empirical material consists of interviews with patients in palliative care and their significant others. The analysis draws attention to the lived experiences of the participants - embedded in time, identities, social relations, and everyday lives - and to how the possibility of sense-making is conditioned by the lifeworld. ... [This] needs to be understood as reorienting work: supporting people when their lines become disrupted or need to be altered. This requires a display of radical empathy ...
[Sweden] Ethical reflection: The palliative care ethos and patients who refuse information
08/02/25 at 03:55 AM[Sweden] Ethical reflection: The palliative care ethos and patients who refuse informationPalliative Care & Social Practice; Joar Björk; 7/25Situations wherein a patient refuses potentially important information present tricky ethical challenges for palliative care staff. Taken as a whole, the palliative care ethos seems to recommend a strategy of using communication skills and time to try to get information across to the patient without forcing things. The recommendation is nuanced and highly contextualised, which increases its validity for clinical practice. Some meta-ethical questions are discussed regarding the use of the palliative care ethos as a source of guidance in ethically challenging clinical situations.
The treatment of chemotherapy-induced peripheral neuropathy: A review of current management options and a potential role for scrambler therapy
08/02/25 at 03:45 AMThe treatment of chemotherapy-induced peripheral neuropathy: A review of current management options and a potential role for scrambler therapyFrontiers in Pain Research; by Hassan Aboumerhi, Henry Vucetic, Andrew Gruenzel, Bahar Moftakhar, Mona Gupta, Santosh K Rao, Michael D Staudt; 7/25Chemotherapy-induced peripheral neuropathy (CIPN) presents a growing medical and financial burden on patients and the healthcare system alike. This has been treated with conservative and interventional care limited by efficacy, side effects, and lack of coverage. As such, there is an unmet treatment need for effective non-invasive or minimally invasive therapies for the treatment of CIPN. Scrambler therapy (ST) is a peripheral, non-invasive neuromodulation technique, which uses transcutaneous electrical stimulation to modulate pain signals. ST has shown mixed results in clinical trials; while some patients report symptom relief, more robust evidence is required before it can be widely recommended.
Expanding the conceptualization of bereavement in the perinatal period
08/02/25 at 03:35 AMExpanding the conceptualization of bereavement in the perinatal periodThe Journal of Obstetric, Gynecologic & Neonatal Nursing; by Rana Limbo, Natasha Nurse-Clarke; 7/25Contemporary definitions of perinatal loss encompass a range of involuntary and unintended pregnancy outcomes, including miscarriage (loss of pregnancy before 20 weeks gestation; Mayo Clinic, 2023), ectopic pregnancy (fertilized egg implanted outside the uterus), stillbirth (the birth of a fetus who shows no signs of life at or after 20 weeks gestation; Gregory et al., 2022), and neonatal death (the death of a live-born fetus within the first 28 days of life; National Center for Health Statistics, 2024). The loss of a pregnancy or fetus or the death of a newborn is an event, and perinatal bereavement is the emotional response to that event. The need for perinatal palliative care, which refers to care provided to families who receive a life-limiting fetal diagnosis, has also emerged as a critical component in supporting families through these losses (Limbo & Wool, 2016).
Pitfalls of large language models in medical ethics reasoning
08/02/25 at 03:35 AMPitfalls of large language models in medical ethics reasoningnpj Digital Medicine; by Shelly Soffer, Vera Sorin, Girish N. Nadkarni, Eyal Klang; 7/25 Large language models (LLMs), such as ChatGPT-o1, display subtle blind spots in complex reasoning tasks. We illustrate these pitfalls with lateral thinking puzzles and medical ethics scenarios. Our observations indicate that patterns in training data may contribute to cognitive biases, limiting the models’ ability to navigate nuanced ethical situations. Recognizing these tendencies is crucial for responsible AI deployment in clinical contexts.
Challenges in effective communication for end-of-life decision making in clinical practice
08/02/25 at 03:25 AMChallenges in effective communication for end-of-life decision making in clinical practiceHospital Practice; by Anish Bhardwaj; 7/25Decisions on end-of-life (EOL) care are a complex process that involves multiple stakeholders including patients, their families, and healthcare providers. Myriad factors play a role in making these decisions, such as desires of the patient and surrogates, advance directives, the patient's health condition, expectations about the disease course and prognosis, metaphysical beliefs about life and death, spiritual and socio-cultural backgrounds and views, quality of life considerations, legal connotations, costs of care, and nuances surrounding organ donation and procurement. This treatise utilizes three real-life examples to highlight the complexity and debate surrounding these decisions, especially in terms of interface of medicine and legal process, especially when a patient is in coma or a vegetative state and decisions transfer to surrogates.
Evaluating the role of palliative care in emergency department opioid use among advanced cancer patients
08/02/25 at 03:20 AMEvaluating the role of palliative care in emergency department opioid use among advanced cancer patientsSupportive Care in Cancer; by Joel Nortey, Shiyun Zhu, Andrew Lynch, Hannah Whitehead, Nirmala Ramalingam, Raymond Liu; 7/25 Patients with advanced cancer often experience severe symptoms that significantly impact their quality of life, leading to frequent emergency department [ED] visits for pain management. These visits not only diminish patient quality of life, but also impose substantial costs on the healthcare system. Our study highlights the significant role that PC can play in reducing ED utilization for pain management needs among advanced cancer patients, improving quality of life and alleviating healthcare burdens.
Finding the communication sweet spot: Strategies promoting personhood in conversations between individuals with dementia and their family members
08/02/25 at 03:20 AMFinding the communication sweet spot: Strategies promoting personhood in conversations between individuals with dementia and their family membersJournal of Family Communication; by R. Amanda Cooper, Chizobam Nweke, Hannah Brocksmith; 7/25... this study explored the various ways through which family members promote the personhood of their loved ones with dementia. Personhood was promoted by reminding the people with dementia of their identities, encouraging them to share their thoughts, assessing and adjusting to their conversational needs, and cultivating relational connections with them. Some behaviors were inconsistent with the tenets of person-centered communication and involved underaccommodation or overaccommodation. The findings reveal potential strategies and pitfalls of promoting personhood within the family caregiving context.
Effect of a multi-component palliative care intervention on goals of care discussions for critical patients in the emergency department
08/02/25 at 03:10 AMEffect of a multi-component palliative care intervention on goals of care discussions for critical patients in the emergency departmentInternal & Emergency Medicine; by Julia Murray, Zacharia Grami, Katherine Benson, Christopher Hritz, Samantha Lawson, Corita Reilley Grudzen, Allison Cuthel, Lauren Talanda-Fath Southerland; 7/25Goals of care (GOC) discussions are vital to understanding patients' values and preferences during serious illness, but they occur infrequently during Emergency Department (ED) care. We report a single site sub-study of a stepped wedge pragmatic trial of a multi-component intervention of primary palliative care in the ED (PRIM-ER), focused on GOC conversations. The intervention did not change the proportion of patients receiving a GOC conversation in the ED ... [however patients] presenting with a cancer-related complaint ... or a respiratory emergency ... were associated with increased odds of a GOC conversation occurring. Of the 60 GOC conversations that occurred, 76.7% ... resulted in a change in code status, patient care plans, hospice, or updated advance care planning documents. While the intervention did not increase this secondary outcome of GOC conversations, the discussions that did occur frequently impacted ED care.Assistant Editor's note: This study concluded that the intervention employed in the ED did not increase the proportion of patients receiving GOC conversations. Yet the study also concluded that almost 77% of the patients who DID receive the conversation had a change in code status, care plan, hospice or advance care planning documents. This study clearly reminds us that GOC conversations, employed even in the ED, can help patients embrace a palliative approach to care when faced with serious illness.
Telemedicine special registrations for controlled substances
08/02/25 at 03:00 AMTelemedicine special registrations for controlled substancesJAMA Health Forum; by Jacob T. Kannarkat, John Torous, Joseph T. Kannarkat; 7/25Since the COVID-19 pandemic, the requirement for in-person evaluation of patients prior to the prescribing of controlled substances via telehealth, as established by the Ryan Haight Online Pharmacy Consumer Protection Act (Ryan Haight Act), has remained provisionally held. The Drug Enforcement Agency (DEA) previously proposed rulemaking to reintroduce the in-person patient evaluation requirement, as some unscrupulous clinicians and companies took advantage of this deregulated environment to overprescribe controlled substances. However, these flexibilities were extended through December 31, 2025, after the public voiced concerns over possible care disruptions in a landscape increasingly dependent on telehealth. Now, the DEA aims to compromise on prescribing flexibility with more practical enforcement measures.
The effects of private equity ownership in U.S. nursing homes quality and financial performance: A systematic review
08/02/25 at 03:00 AMThe effects of private equity ownership in U.S. nursing homes quality and financial performance: A systematic reviewHealth Policy; by Gregory N. Orewa, Aizhan Karabukayeva, Rohit Pradhan, Itopa Jimoh, Robert Weech-Maldonado; 7/25Private equity (PE) investment in U.S. nursing homes has increased significantly over the past two decades. The emergence of this novel ownership model has prompted concerns regarding its effects on nursing home performance, especially quality... Across studies, PE ownership was linked to higher number of deficiencies, increased hospitalization rates, and higher mortality, although some improvements in care processes were noted. Financial outcomes showed initial financial gains but long-term challenges, primarily due to high debt loads... Findings suggest that PE strategies may prioritize short-term profitability, which may compromise quality of care in some instances. These findings highlight the need for financial transparency, and reimbursement models that incentivize long-term quality.
Financial performance of rural and urban nursing homes: A comparative analysis
08/02/25 at 03:00 AMFinancial performance of rural and urban nursing homes: A comparative analysisThe Journal of Rural Health; by Gregory N. Orewa, Rohit Pradhan, Akbar Ghiasi, Shivani Gupta, Robert Weech-Maldonado; 7/25The financial sustainability of nursing homes is increasingly critical as the aging US population continues to grow. Rural facilities often encounter more significant economic challenges than urban counterparts. This study investigates the disparities in financial performance between rural and urban nursing homes in the United States, emphasizing the influence of organizational and environmental factors. A comprehensive understanding of these differences is necessary for the implementation of effective policy and management interventions... Rural nursing homes had lower operating margins than urban facilities in unadjusted models. However, after adjusting for organizational factors such as size, occupancy, and payer mix, the rural–urban difference was no longer significant. Environmental factors, including population demographics and income levels, contributed to financial disparities. COVID-19 exacerbated financial challenges, disproportionately affecting rural facilities... Financial disparities between rural and urban nursing homes are not solely due to geographical location, but also stem from structural challenges. These insights have significant policy implications suggesting that addressing reimbursement rates, operational efficiency, and resource allocation is crucial to ensure the financial sustainability and quality care for aging populations.
[India] Challenges and ethical considerations of palliative care in Indian prisons
08/02/25 at 03:00 AM[India] Challenges and ethical considerations of palliative care in Indian prisonsJournal of Pain and Symptom Management; by Swapnil Kumar Barasker, Pankaj Singhai, Maya Nair, Deepali Kumar; 8/25The landscape of palliative care (PC) in India is still nascent, and when applied to the prison setting, it becomes a terrain fraught with unique challenges. There is a dearth of region-specific perspectives on end-of-life care (EOLC) and PC in Indian prisons. In Indian prisons, EOLC is complicated by issues such as overcrowding, inadequate medical facilities, and the societal neglect of incarcerated individuals, yet the need for it remains largely unrecognized... Prison deaths are frequently associated with brutality or neglect, but statistics reveal that most deaths occur due to natural causes such as ischemic heart disease, pneumonia, cancer, and liver and kidney disorders. Despite many prisoners having chronic illnesses, they often lack regular follow-ups and access to appropriate care due to insufficient medical staff and infrastructure.
Estimating the number of services & patients receiving specialized palliative care globally in 2025
08/01/25 at 03:00 AMEstimating the number of services & patients receiving specialized palliative care globally in 2025 Journal of Pain and Symptom Management; by Stephen R Connor, Eduardo Garralda, Vilma A Tripodoro, Carlos Centeno; 7/28/25 online ahead of print ... In 2025, the estimated number of specialized palliative care service delivery teams worldwide reached approximately 33,700 - representing a 32.7% increase from the 25,000 identified in 2017. Service delivery expanded across all WHO regions except Africa. The estimated number of patients served rose from 7 million in 2017 to approximately 10.4 million in 2025. This figure represents roughly 14% of the total global need for palliative care. ... Despite notable growth in service availability, significant disparities persist, particularly in low- and middle-income countries. While over half of the need appears to be met in high-income countries, only 4.4% is addressed by specialist provision in low and middle-income countries.
System wide goals of care implementation: A podcast with Ira Byock, Chris Dale, and Matt Gonzales
07/30/25 at 03:00 AMSystem wide goals of care implementation: A podcast with Ira Byock, Chris Dale, and Matt GonzalesGeriPal podcast; by Eric Widera, Alex Smith, Ira Byock, Chris Dale, Matt Gonzales; 7/24/25Most health care providers understand the importance of goals-of-care conversations in aligning treatment plans with patients’ goals, especially for those with serious medical problems. And yet, these discussions often either don’t happen or at least don’t get documented. How can we do better? In today’s podcast, we sit down with Ira Byock, Chris Dale, and Matthew Gonzales to discuss a multi-year healthcare system-wide goals of care implementation project within the Providence Health Care System. Spanning 51 hospitals, this initiative [found] an increase from 7% to 85% in goals of care conversation documentation for patients who were in an ICU for 5 or more days. How did they achieve this? Our guests will share insights into the project’s inception and the strategies that drove its success, including:
