“There is No Communication”: A Qualitative Examination of Deaf Signers’ Experiences With Advance Care Planning
SAGE Journals » Journal of Palliative Care
by Caroline Cerilli, Gabrielle Katz, Angelo E. Volandes, Aretha Delight Davis, Michael K. Paasche-Orlow, Tyler G. James, Michael M. McKee
2d ago
Journal of Palliative Care, Ahead of Print. Objective(s): Deaf American Sign Language (ASL) users are subject to health care disparities resulting from communication and language barriers. Currently, few resources on advance care planning and end-of-life care exist in ASL. This study explores Deaf ASL users’ perceptions and experiences with end-of-life care and advance care planning. Methods: Semi-structured 1:1 interviews with Deaf signers were translated, and transcribed into English by a bilingual researcher. Investigators inductively coded transcripts and identified themes of barriers, fac ..read more
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Hospices and Emergency Preparedness Planning: A Scoping Review of the Literature
SAGE Journals » Journal of Palliative Care
by Janna E. Baker Rogers
2w ago
Journal of Palliative Care, Ahead of Print. Objective. Palliative and end-of-life care, as provided by hospices, are important elements of a healthcare response to disasters. A scoping review of the literature was conducted to examine and synthesize what is currently known about emergency preparedness planning by hospices. Methods. A literature search of academic and trade publications was conducted through 6 publication databases, following Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines when applicable. Publications were selected and findings were organized into ..read more
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Post-graduate Course in Palliative Medicine: Experiences from an E-Learning-Based Pilot Program, a Mixed Methods Study
SAGE Journals » Journal of Palliative Care
by Annamarja Lamminmäki, Minna Hökkä, Outi Hirvonen, Eeva Rahko, Tiina Saarto, Juho Lehto
1M ago
Journal of Palliative Care, Ahead of Print. Objective: To study whether E-learning methods are feasible in the post-graduate education of palliative medicine. Methods: A mixed-methods study. Evaluations from pilot course attendees were analyzed numerically and answers to open-ended questions about E-learning were analyzed using inductive content analysis. A national pilot E-learning-based post-graduate course in palliative medicine with 24 participating physicians in Finland. The evaluation of teaching modules and different aspects of the course was achieved from the participants through numer ..read more
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Cancer Decedents’ Hospital End-of-Life Care Documentation: A Retrospective Review of Patient Records
SAGE Journals » Journal of Palliative Care
by L. Russell, R. Howard, M. Street, C. E. Johnson, D. Berry, E. Flemming-Judge, S. Brean, L. William, J. Considine
1M ago
Journal of Palliative Care, Ahead of Print. Objective: International standards of end-of-life care (EOLC) intend to guide the delivery of safe and high-quality EOLC. Adequately documented care is conducive to higher quality of care, but the extent to which EOLC standards are documented in hospital medical records is unknown. Assessing which EOLC standards are documented in patients’ medical records can help identify areas that are performed well and areas where improvements are needed. This study assessed cancer decedents’ EOLC documentation in hospital settings. Methods: Medical records of 24 ..read more
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Is Low Volume Drainage of Ascites Associated With Improved Survival in Digestive System Cancer Patients With Malignant Ascites?—A Retrospective Cohort Study
SAGE Journals » Journal of Palliative Care
by Shunya Hoshino, Yusuke Takagi, Takeo Fukagawa, Keiji Sano, Nobuhiko Seki, Yojiro Hashiguchi, Etsuko Aruga
1M ago
Journal of Palliative Care, Ahead of Print. Objectives: To determine whether the volume of paracentesis for malignant ascites in acute care hospital wards is associated with survival and symptom relief. Methods: Patients with malignant ascites caused by digestive system cancer who underwent paracentesis between January 2010 and April 2022 were retrospectively analyzed from medical records. Collected data included the drainage volume per paracentesis procedure, survival time from the first paracentesis procedure, symptoms, and adverse events. According to the volume per paracentesis procedure ..read more
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Nationwide Survey on Caregiver Burden When Supporting Terminal Cancer Patients with Dementia: Bereaved Family Members’ Perspective
SAGE Journals » Journal of Palliative Care
by Ayumi Takao, Harue Arao, Sena Yamamoto, Miwa Aoki, Katsuyasu Kouda, Tatsuya Morita, Yoshiyuki Kizawa, Satoru Tsuneto, Yasuo Shima, Kento Masukawa, Mitsunori Miyashita
1M ago
Journal of Palliative Care, Ahead of Print. ObjectiveThe prevalence of dementia and cancer has increased in recent years. The presence of dementia complicates the care of terminal cancer patients and affects their family caregivers. However, palliative care research seldom focuses on the family caregivers of patients with terminal cancer and dementia. This study aimed to evaluate the degree and factors of caregiver burden in cancer patients with dementia who died in hospice palliative care units. Methods: A nationwide cross-sectional survey was conducted among bereaved family members of patien ..read more
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“It's Not Just the Seizures”: Brain Tumor Caregivers’ Experiences and Educational Needs in Out-of-Hospital Seizure Management
SAGE Journals » Journal of Palliative Care
by Deborah Ejem, Macy Stockdill, Rebecca Edwards, J. Nicholas Dionne-Odom, Richard Taylor, Walter Baehr, L. Burt Nabors, Marie Bakitas, Paula Warren
2M ago
Journal of Palliative Care, Ahead of Print. Objective: Family caregivers (FCGs) of persons with primary brain tumors (PBTs) report high levels of distress related to concerns about out-of-hospital seizures. This study aims to explore their experiences and needs with seizure management. Methods: Semi-structured interviews were held with 15 FCGs of persons with PBTs, both those who have and those who have not experienced a seizure, to elicit their concerns about out-of-hospital seizure management and related information needs. A qualitative descriptive study using thematic analysis was conducted ..read more
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The Final Frontier: Palliative Care in Space is an Inevitability
SAGE Journals » Journal of Palliative Care
by Sheryn Tan, Vienna Tran, Brandon Stretton, Aashray Gupta, Joshua Kovoor, Stephen Bacchi
3M ago
Journal of Palliative Care, Ahead of Print. As space exploration becomes increasingly common, palliative care for astronauts will require greater consideration. All aspects of palliative care need to be specifically adapted for astronauts. For example, addressing additional circumstances such as inability to see loved ones from Earth will be an important part of meeting their psychological and spiritual needs. A different approach to pharmacological management of end-of-life symptoms is also warranted due to changes in human physiology and pharmacokinetics in space ..read more
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Chinese Diaspora Communities’ Knowledge of and Engagement with Advance Care Planning: A Systematic Integrative Review
SAGE Journals » Journal of Palliative Care
by Zhuangshuang Li, Esther Ruth Beck, Sonja McIlfatrick, Felicity Hasson
3M ago
Journal of Palliative Care, Ahead of Print. ObjectivesTo synthesize evidence regarding Chinese diasporas’ understanding, experience, and factors influencing engagement with advance care planning. Methods: A systematic integrative review using content analysis. Seven electronic databases (Embase, CINAHL, SCOPUS, Web of Science, Medline (OVID), PsycINFo, and The Cochrane Library) and gray resources were searched for studies from January 1990 to March 2022. Study quality appraisal was undertaken. Results: 27 articles were identified and rated as moderate to good. Two overarching and interrelated ..read more
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Deathbed Etiquette – The Guide: A Qualitative Study Exploring the Views of Practitioners on its Introduction into End-of-Life Care Settings
SAGE Journals » Journal of Palliative Care
by Mette Kragh-Furbo, Maddy French, Lesley Dunleavy, Sophie Hancock, Karen Sanders, Margaret Doherty, Amy Gadoud
3M ago
Journal of Palliative Care, Ahead of Print. Objectives: It is common for relatives to feel uncertain about what to expect at the bedside of a dying loved one. The Centre for the Art of Dying Well together with clinical, academic and communications experts created a ‘Deathbed Etiquette’ guide offering information and reassurance to relatives. This study explores the views of practitioners with experience in end-of-life care on the guide and how it might be used. Methods: Three online focus groups and nine individual interviews were conducted with a purposive sample of 21 participants involved i ..read more
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