Literature Review
All posts tagged with “Research News.”
First person profile: Betty Ferrell, PhD, RN
03/09/24 at 03:05 AMFirst person profile: Betty Ferrell, PhD, RNCancer, by Mary Beth Nierengarten; 2/24Dr Ferrell has built her career on the belief that palliative care should be offered from the time of cancer diagnosis rather than just as end-of-life care.Publisher's note: Honoring our heros...
Digital ‘communication bridge’ for seniors with aphasia is $13M closer to reality
03/08/24 at 03:00 AMDigital ‘communication bridge’ for seniors with aphasia is $13M closer to reality McKnights Senior Living; by Aaron Dorman; 3/5/24 An upcoming research program will examine the potential for telehealth and wearable sensors to address a specific and nasty form of aphasia. The University of Chicago was awarded $13.2 million by the National Institutes of Health to study the disease, as part of its five-year Communication Bridge Research Program. The university recently announced the grant windfall and has begun reaching out to potential participants for a clinical trial.
“Dying with a smile, just knowing that somebody’s listened to me”: End-of-life care and medical assistance in dying in Canadian prisons
03/02/24 at 03:40 AM“Dying with a smile, just knowing that somebody’s listened to me”: End-of-life care and medical assistance in dying in Canadian prisonsOMEGA - Journal of Death and Dying, by Jessica Shaw, Peter Driftmier; 3/24Medical assistance in dying (MAiD) has been legal in Canada since 2016 and some incarcerated patients who are at the end of their lives are eligible for the procedure. Interviews with nine incarcerated men at a federal penitentiary in Canada provide insight into some of the ways that people who are navigating aging and end-of-life in prison think about MAiD.
Knowledge gaps in end-of-life family caregiving for persons living with dementia: A study of hospice clinician perspectives
03/02/24 at 03:35 AMKnowledge gaps in end-of-life family caregiving for persons living with dementia: A study of hospice clinician perspectivesAmerican Journal of Hospice and Palliative Medicine, by Meghan McDarby, David Russell, Lori King, Elissa Kozlov, Elizabeth A Luth; 5/23More than 35% of hospice care recipients 65 and older have a dementia diagnosis. Yet family care partners of persons living with dementia report feeling unprepared to address their hospice recipient's changing needs nearing end of life. Hospice clinicians may have unique insight into the knowledge needs of family care partners and strategies for end-of-life dementia caregiving.
Close but not close enough: How distance caregiving is associated with hospice family caregiver hospice communication experiences
03/02/24 at 03:30 AMClose but not close enough: How distance caregiving is associated with hospice family caregiver hospice communication experiencesHealth Communication, by Lauren T Starr, Karla Washington, Kyle Pitzer, Debra Parker Oliver, George Demiris; 3/24Half of hospice family caregivers report having unmet information needs, which can contribute to poor pain and symptom management, emergency department use, and hospice disenrollment for care-recipients and to caregiver strain and stress. Effective communication between hospice teams and family caregivers is critical yet communication inadequacies persist. Despite the growing prevalence of distance caregiving, including in hospice care, and the relationship between caregiver proximity and communication effectiveness, little is known about how caregiver proximity is associated with caregiver perceptions of hospice communication.
Case histories of significant advances: Cicely Saunders and the modern hospice movement
03/02/24 at 03:25 AMCase histories of significant advances: Cicely Saunders and the modern hospice movementHarvard Business School, by Amar Bhide, Srikant Datar; 2/25/24This Case history describes the role of Dame Cicely Saunders (1918- 2005) in shaping the modern hospice movement. It is narrated in the first person through the words of her brother, Christopher Saunders (1926-2024) as told to one of the authors of this paper.
Oncologist perceptions of racial disparity, racial anxiety, and unconscious bias in clinical interactions, treatment, and outcomes
03/02/24 at 03:20 AMOncologist perceptions of racial disparity, racial anxiety, and unconscious bias in clinical interactions, treatment, and outcomesJournal of the National Comprehensive Cancer Network, by Alexandrina Balanean, Emily Bland, Ajeet Gajra, Yolaine Jeune-Smith, Andrew J Klink, Harlen Hays, Bruce A Feinberg; 2/24Cancer spares no demographic or socioeconomic group; it is indeed the great equalizer. But its distribution is not equal; when structural discrimination concentrates poverty and race, zip code surpasses genetic code in predicting outcomes. Compared with White patients in the United States, Black patients are less likely to receive appropriate treatment and referral to clinical trials, genetic testing, or palliative care/hospice.
Private equity's plot against older Americans
03/02/24 at 03:15 AMPrivate equity's plot against older AmericansJournal of the American Geriatrics Society, by James Webster MD MS; 2/24/24Over the past several decades more than 140 private equity investment firms have acquired entities in major components of healthcare in the United States... Private Equity firms have undertaken acquisitions of financially or administratively distressed hospitals, nursing homes, physician practices especially emergency care and medical specialties, hospices, home care agencies, physical therapy and rehabilitation operations, ambulance services, and nursing registries... Of particular importance for older Americans, Private Equity firms currently own a significant percentage of U.S. nursing homes; estimates range from 5% to 11%, and a rapidly increasing percentage of hospice and home care agencies. All three are important sources of seniors' care. Why should we be concerned about these issues considering all of the other current challenges to the medical system?...
Hospice fraud: Predicting ability and intent
03/02/24 at 03:10 AMHospice fraud: Predicting ability and intentIllness, Crisis & Loss, by Laura M. Waters, Patricia Moyle Wright; 2/28/24Hospice fraud is a growing concern around the world. Yet, little attention has been given to the study of hospice fraud in the extant literature.
Palliative medicine fellows’ discussions, perceptions, and training regarding medical cannabis
03/02/24 at 03:05 AMPalliative medicine fellows’ discussions, perceptions, and training regarding medical cannabisJournal of Pain and Sympotom Management, by Dylan R. Sherry MD, Rushad Patell MD, Harry J. Han MD, Laura E. Dodge ScD MPH, Ilana M. Braun MD, Mary K. Buss MD MPH; 2/27/24Medical cannabis is increasingly considered for palliation of pain, nausea/vomiting, anorexia, and other symptoms. We aimed to determine whether training in hospice and palliative medicine (HPM) adequately prepares fellows to counsel patients about medical cannabis.
Saturday Newsletters
03/02/24 at 03:00 AMSaturday NewslettersResearch literature is the focus of Saturday newsletters - enjoy!
Ethics at the end of life in the newborn intensive care unit: Conversations and decisions
02/24/24 at 03:35 AMEthics at the end of life in the newborn intensive care unit: Conversations and decisionsSeminars in Fetal and Neonatal Medicine, by Mark R. Mercurio, Lynn Gillam; 6/23The unexpected birth of a critically ill baby raises many ethical questions for neonatologists. Some of these are obviously ethical questions, about whether to attempt resuscitation, and, if the baby is resuscitated and survives, whether to continue life sustaining interventions. Other ethical decisions are more related to what to say rather than what to do. Although less obvious, they are equally as important, and may also have far-reaching ramifications... This may serve as a helpful guide for ethical deliberation, and helpful scripting for parental discussion, in similar cases.
Pain management education for rural hospice family caregivers: A pilot study with embedded implementation evaluation
02/24/24 at 03:30 AMPain management education for rural hospice family caregivers: A pilot study with embedded implementation evaluationAmerican Journal of Hospice & Palliative Medicine, by Lauren T. Starr, PhD, MBE, RN; Karla T. Washington, PhD, MSW; JoAnn Jabbari, MSN, RN; Jacquelyn J. Benson, PhD, MA; Debra Parker Oliver, PhD, MSW; George Demiris, PhD, FACMI; John G. Cagle, PhD, MSW; 7/23Assessing and managing hospice patients’ pain is a common source of anxiety among hospice familycaregivers, especially caregivers in rural communities who face special challenges including distance, limited access, and concerns about opioid misuse... A multisite clinical trial of Ready2Care is warranted; however, its success may require more effective recruitment and retention strategies for rural caregiver participants.
What aspects of quality of life are important from palliative care patients’ perspectives? A framework analysis to inform preference‑based measures for palliative and end‑of-life settings
02/24/24 at 03:25 AMWhat aspects of quality of life are important from palliative care patients’ perspectives? A framework analysis to inform preference‑based measures for palliative and end‑of-life settingsThe Patient - Patient-Centered Outcomes Research, by Nikki McCaffrey, Julie Ratcliffe, David Currow, Lidia Engel, Claire Hutchinson; 11/23Existing, popular, preference-based outcome measures such as the EQ-5D do not incorporate the most important, patient-valued, quality-of-life domains in the palliative and end-of-life settings. Development of a new, more relevant and comprehensive preference-based outcome measure could improve the allocation of resources to patient-valued services and have wide applicability internationally.
Clinician perception of likelihood of death in the next year is associated with 1-Year mortality and hospice use among older adults receiving home health care
02/24/24 at 03:20 AMClinician Perception of Likelihood of Death in the Next Year Is Associated With 1-Year Mortality and Hospice Use Among Older Adults Receiving Home Health CareJournal of Palliative Medicine, by Zainab Toteh Osakwe, Evan Bollens-Lund, Yihan Wang, Christine S Ritchie, Jennifer M Reckrey, Katherine A Ornstein; 2//12/24HHC clinician perception of patients' risk of death or decline is associated with 1-year mortality. A better understanding of HHC patients at high risk for mortality can facilitate improved care planning and identification of homebound older adults who may benefit from hospice.
Drugs, delirium, and ethics at the end of life
02/24/24 at 03:15 AMDrugs, delirium, and ethics at the end of lifeJournal of the American Geriatric Society, by Columba Thomas, MD; Yesne Alici, MD; William Breitbart, MD; Eduardo Bruera, MD; Liz Blackler, MBE, LCSW-R; Daniel P. Sulmasy MD, PhD; 1/24For older persons with delirium at the end of life, treatment involves complextrade-offs and highly value-sensitive decisions. The principles of beneficence,nonmaleficence, respect for autonomy, and justice establish important parametersbut lack the structure necessary to guide clinicians in the optimal management ofthese patients. We propose a set of ethical rules to guide therapeutics—the canonsof therapy—as a toolset to help clinicians deliberate about the competing concernsinvolved in the management of older patients with delirium at the end of life.
Patient navigator intervention to improve palliative care outcomes for Hispanic patients with serious noncancer illness: A randomized clinical trial
02/24/24 at 03:10 AMPatient navigator intervention to improve palliative care outcomes for Hispanic patients with serious noncancer illness: A randomized clinical trialJAMA Internal Medicine, by Stacy M Fischer, Sung-Joon Min, Danielle M Kline, Kathleen Lester, Wendolyn Gozansky, Christopher Schifeling, John Himberger, Joseph Lopez, Regina M Fink; 2/12/24In this randomized clinical trial, a culturally tailored patient navigator intervention did not improve QOL for patients. However, the intervention did increase ACP engagement, AD documentation, and hospice utilization in Hispanic persons with serious medical illness.
Disparities in the geographic distribution of palliative care specialists in 2022
02/24/24 at 03:05 AMDisparities in the geographic distribution of palliative care specialists in 2022Journal of General Internal Medicine, by Julia L Frydman, Karen McKendrick, Yingtong Chen, Jonathan Wun, Nathan E Goldstein, R Sean Morrison, Laura P Gelfman; 2/12/24In 2022, the number of HPM board-certified clinicians was 8,935 (6,448 = physicians (72.2%); 2,487 = NPs (27.8%)), which represents 0.7% of the NP workforce and 0.6% of the physician workforce... Our study highlights the uneven geographic distribution of board-certified HPM clinicians, which depends on state, metropolitan status, and area-level SES.
Saturday Newsletters
02/24/24 at 03:00 AMSaturday NewslettersResearch literature is the focus of Saturday newsletters - enjoy!
Kim Mooney-Doyle awarded nearly $500,000 to study communication needs in families of seriously ill children
02/19/24 at 03:00 AMKim Mooney-Doyle awarded nearly $500,000 to study communication needs in families of seriously ill childrenThe Elm of the University of Maryland, by Mary Therese Phelan; 2/15/24Kim Mooney-Doyle, PhD, RN, CPNP-AC, assistant professor at the University of Maryland School of Nursing (UMSON), has been awarded a two-year R21 grant of $460,000 from the National Institute of Nursing Research (NINR) to research how understanding family communication during serious pediatric illness, from the perspective of adolescent siblings and parents, provides opportunities to prevent long-term distress.
Individual socioeconomic factors have a greater impact on end-of-life care outcomes than regional factors
02/17/24 at 03:45 AMIndividual socioeconomic factors have a greater impact on end-of-life care outcomes than regional factorsJournal of Palliative Medicine, by William H. Gansa, Hannah Kleijwegt, Melissa Aldridge, Claire Ankuda; 2/24High quality of care at the end of life may be more associated with individual socioeconomic factors than regional indicators, including degrees of rurality. Clinicians should strive to recognize the interplay of individual characteristics and regional indicators to provide more personalized care.Publisher's note: Also see https://www.liebertpub.com/doi/10.1089/jpm.2023.0163.
Palliative sedation: ethics in clinical practice guidelines - systematic review
02/17/24 at 03:40 AMPalliative sedation: ethics in clinical practice guidelines - systematic reviewBJM Supportive & Palliative Care, by Martyna Tomczyk, Cécile Jaques, Ralf J Jox; 8/23Effective cooperation between palliative care clinicians and ethicists should be encouraged, in order to integrate in particular the crucial ethical issues of continuous deep sedation until death when developing or updating clinical practice guidelines on palliative sedation.
The administrative burden on palliative academic physicians
02/17/24 at 03:35 AMThe administrative burden on palliative academic physiciansJournal of Pain and Symptom Management, by Rida Khan, Michael Tang, Ahsan Azhar, Eduardo Bruera; 1/24Every faculty member spends annually an approximate average of 5,300 minutes on administrative activities (approximately the equivalent of 29 consults plus 133 follow-ups). Using the department net average per encounter, the approximate value of these encounters is $36, 936 for each faculty member (about 11 clinical days)... We recommend that regulatory agencies and institutions work together to better regulate this list of tasks and their frequency.
Perspectives on transfusions for hospice patients with blood cancers: A survey of hospice providers
02/17/24 at 03:30 AMPerspectives on transfusions for hospice patients with blood cancers: A survey of hospice providersJournal of Pain and Symptom Management, by Helen P Knight, Caitlin Brennan, Susan Lysaght Hurley, Anna J Tidswell, Melissa D Aldridge, Kimberly S Johnson, Edo Banach, James A Tulsky, Gregory A Abel, Oreofe O Odejide; 1/24We received 113 completed surveys (response rate = 23.5%). Of the cohort, 2.7% reported that their agency always offers transfusions, 40.7% reported sometimes offering transfusions, and 54.9% reported never offering transfusions... Most respondents (76.6%) identified lack of transfusion access in hospice as a barrier to hospice enrollment for blood cancer patients. The top intervention considered as "very helpful" for increasing enrollment was additional reimbursement for transfusions (72.1%).
Health care costs associated with hospice use for people with dementia in the US
02/17/24 at 03:25 AMHealth care costs associated with hospice use for people with dementia in the USHealth Affairs, by Melissa D Aldridge, Lauren J Hunt, Krista L Harrison, Karen McKendrick, Lihua Li, R Sean Morrison; 9/23Policy makers in the US are increasingly concerned that greater use of the Medicare hospice benefit by people with dementia is driving up costs... For community-dwelling people with dementia, Medicare costs were lower for those who used hospice than for those who did not, whether hospice enrollment was in the last three days ($2,200) or last three months ($7,200) of life, primarily through lower inpatient care costs in the last days of life...