Academic literature on the topic 'Hospice care worker'

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Journal articles on the topic "Hospice care worker"

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Valley, Morgan A., and Lorann Stallones. "Impact of a Mindfulness Intervention on Hospice Care Worker Safety and Well-Being." OBM Integrative and Complementary Medicine 06, no. 03 (2021): 1. http://dx.doi.org/10.21926/obm.icm.2103029.

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Hospice care workers are exposed to the hazards associated with in-home care in uncontrollable environments as well as occupational stress related to caring for terminally ill patients and their families. This study aimed to assess the effectiveness of an abbreviated mindfulness intervention to improve hospice care worker occupational safety performance and well-being. This study used a single-group pre-post design to pilot test an 18-hour mindfulness training as an intervention on self-reported safety performance and well-being among 13 hospice care workers in Colorado. Participants reported
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McMAHON, ROBIN L. "An ethical dilemma in a hospice setting." Palliative and Supportive Care 1, no. 1 (2003): 79–87. http://dx.doi.org/10.1017/s1478951503030013.

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The codes of ethics of the National Hospice and Palliative Care Organization and the National Association of Social Workers support ethical standards of client self-determination and confidentiality. Lack of societal consensus on the parameters of a terminally ill person's right to die continues to confound at times the health care field, including hospice programs. This article explores an actual case where a hospice social worker faced an ethical dilemma related to the sanctity of life versus patient autonomy. While a more seasoned social worker might have chosen a different alternative to t
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GOY, ELIZABETH R., ANN JACKSON, THERESA A. HARVATH, LOIS L. MILLER, MOLLY A. DELORIT, and LINDA GANZINI. "Oregon hospice nurses and social workers' assessment of physician progress in palliative care over the past 5 years." Palliative and Supportive Care 1, no. 3 (2003): 215–19. http://dx.doi.org/10.1017/s1478951503030384.

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Background: The 1997 enactment of the Oregon Death with Dignity Act intensified interest in improving physician education and skills in caring for patients at the end of life.Objective: To obtain hospice nurse and social workers' collateral ratings of efforts made by Oregon physicians to improve their palliative care skills over the previous 5 years.Design: A descriptive survey of nurses and social workers from all 50 Oregon outpatient hospice agencies.Measurement and Results: Oregon hospice nurse (N = 185) and social worker (N = 52) respondents, who had worked in hospice for at least 5 years,
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Noe, Kelly, and Dana A. Forgione. "Charitable contributions and quality in the us hospice care setting." Journal of Public Budgeting, Accounting & Financial Management 26, no. 4 (2014): 539–56. http://dx.doi.org/10.1108/jpbafm-26-04-2014-b001.

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This paper examines the association of charitable donations with quality of care proxies for nonprofit hospice providers in the United States (US). An estimated 1.45 million patients received hospice care in the US in 2008. Medicare hospice spending exceeded $10 billion in 2007 and is expected to more than double over the next 10 years. Using Guidestar and Medicare Hospice Cost Report data, we find donations are positively associated with proxies for nurse and social worker quality of care, but not with our home-health aide quality proxy. This research adds to our understanding of charitable c
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Reese, Dona J., and Ellen L. Csikai. "Social Work Assessment and Outcomes Measurement in Hospice and Palliative Care." American Journal of Hospice and Palliative Medicine® 35, no. 12 (2018): 1553–64. http://dx.doi.org/10.1177/1049909118788342.

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While psychosocial assessment is required in hospice, no requirement exists for documentation of psychosocial outcomes. Social work research has identified the psychosocial and spiritual domains most often and appropriate for social workers to address, and standardized assessment tools have been developed by social workers based on this research. The aims of this study were to document the current use of standardized assessment measures for assessment and documenting outcomes and specifically the use of the Social Work Assessment Tool. A national sample of 203 hospice and palliative care socia
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Ward, Elijah G., and Audrey K. Gordon. "Looming Threats to the Intimate Bond in Hospice Care? Economic and Organizational Pressures in the Case Study of a Hospice." OMEGA - Journal of Death and Dying 54, no. 1 (2007): 1–18. http://dx.doi.org/10.2190/l63m-2623-r1j2-gm8r.

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Hospice organizations are assailed by stiff competition, ever-rising costs, limited funding, and policy changes. Do such pressures stifle the high quality of care these organizations strive to provide? As a case-in-point, we draw from the mid-1990s accounts of caregivers at a nonprofit hospice in a Midwestern city in the United States. We maintain that economic pressures drive organizational restructuring, which then weakens working conditions and, thereby, weakens the staff-client relationship. We discuss effects upon worker behaviors, the worker-client relationship, and client care. This eth
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Empeño, Jessica, Natasha T. J. Raming, Scott A. Irwin, Richard A. Nelesen, and Linda S. Lloyd. "The Impact of Additional Support Services on Caregivers of Hospice Patients and Hospice Social Workers." OMEGA - Journal of Death and Dying 67, no. 1-2 (2013): 53–61. http://dx.doi.org/10.2190/om.67.1-2.f.

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Family caregivers often suffer higher levels of physical and emotional distress when caring for a chronically or terminally ill family member. Providing this kind of care to a loved one at the end of life contributes to increased stress, health problems, and a decreased quality of life. The Hospice Caregiver Support Project provided support services to caregivers identified by the hospice social worker as needing this support and/or assistance. Results from the project show that offering additional services relieved caregiver stress by allowing the caregiver time away from their caregiving rol
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Renzenbrink, Irene. "The Shadow Side of Hospice Care." Illness, Crisis & Loss 15, no. 3 (2007): 245–59. http://dx.doi.org/10.1177/105413730701500306.

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The subject of this article is the dark or “shadow” side of working with dying and bereaved people in hospice and palliative care services, and the interplay of complex personal, professional, and organizational issues that can influence both the quality of patient care and the well-being of staff. Examples of how support needs have been identified and managed are drawn from the author's extensive experience as a social worker, educator, and consultant. It is argued that current understandings of staff stress lack insight into the dark side of hospice care and fail to appreciate the depth of e
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Christian, Thomas, Joan Teno, Kyle Cobb, Sara Galantowicz, Alan Levitt, and Cindy Massuda. "Trends in the Receipt of Consistent Hospice Professional Visits at the End of Life and Ratings of Hospice Care Quality." Innovation in Aging 4, Supplement_1 (2020): 70. http://dx.doi.org/10.1093/geroni/igaa057.228.

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Abstract Caregivers have identified consistent visits by professional hospice staff at the end of life as positively affecting experiences of care quality. Little is known about the prevalence of such visits. Using 100% Medicare hospice claims with discharge dates in Federal Fiscal Year 2018, we identified the rates of providing skilled nurse or social worker visits to hospice beneficiaries in at least two of the last three days of life and compared these rates to percentages of caregivers indicating they would “definitely” recommend the hospice and caregivers rating the hospice a 9 or 10 on a
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&NA;. "Oregon Hospice Social Worker and Author Publishes Spanish Translation of Hospice Guide." Journal of Hospice & Palliative Nursing 11, no. 1 (2009): 7. http://dx.doi.org/10.1097/01.njh.0000319197.18563.d3.

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Dissertations / Theses on the topic "Hospice care worker"

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Jumah, Anne Mukeli. "The nature and extent of palliative care in the Nairobi Hospice." Diss., Pretoria : [s.n.], 2008. http://upetd.up.ac.za/thesis/available/etd-11202008-163831.

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Cain, Cindy L. "Heart Work: Challenges and Adaptations of Hospice Workers." Diss., The University of Arizona, 2013. http://hdl.handle.net/10150/293534.

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This dissertation analyzes the everyday work experiences of hospice, a type of end-of-life care. The following chapters integrate micro-sociological perspectives with meso- and macro- level explanations of organizational behavior to account for workers' performances of emotional labor, care-related identities, constraints on their daily work, and ultimately hospice workers' strong commitment to their jobs and the hospice philosophy. Using a mixed methodological approach, I argue that hospice workers engage in emotional labor, but that instead of feeling dissonance or alienation, hospice work
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Montoya, Ian M. "HISPANICS' UNDER-UTILIZATION OF HOSPICE CARE SERVICES." CSUSB ScholarWorks, 2015. https://scholarworks.lib.csusb.edu/etd/177.

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The purpose of this project was to learn about Hispanics’ utilization of hospice care and to increase knowledge about under-utilization of hospice services by the Hispanic community. Research in hospice services indicates that the Hispanic community underutilizes end-of-life resources when compared to their majority counterparts, European Americans. Research that has controlled for variables such as socio-demographic characteristics, medical history, prognosis, and access to health care demonstrate Hispanics significantly under-utilizing hospice services. This project was conducted within Sout
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Gill, Megumi. "Voices of healthcare workers : experience of being on an interdisciplinary team in hospice palliative care." Thesis, University of British Columbia, 2012. http://hdl.handle.net/2429/42209.

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Having a model of interdisciplinary teamwork is an important part of clinical practice in hospice palliative care. It plays an integral role in providing patient care by multi-disciplines of healthcare professionals who are required to address the intricate needs of patients at the end of life. Yet, the nature of participating in an interdisciplinary patient care team has not been fully understood in theory or clinical work. The purpose of this research was to generate an understanding of the experience of being on an interdisciplinary team in hospice palliative care through healthcare work
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Wong, Lai-cheung. "A study of hospice care : [factors affecting] communication between the health care professionals and the patients /." [Hong Kong : University of Hong Kong], 1992. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13409475.

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Delaney, David C. "Undergraduate social work students' perceptions regarding hospice and end-of-life care." Thesis, California State University, Long Beach, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=1527913.

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<p> End-of-Life (EoL) care is important in social work as this profession plays a vital role on hospice teams. There is a growing need for qualified social workers in hospice, yet not enough social work schools prepare students for this important work, and students often have limited knowledge of these concepts. The purpose of this quantitative study was to describe undergraduate social work students' knowledge and perceptions of hospice and EoL care, their comfort discussing death and dying, and their own end of life advance planning. A total of 58 undergraduate social work students from the
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Stens, Oliver. "Zum Helfen motiviert : eine qualitative Untersuchung zu Motivation und Ressourcen von Mitarbeiterinnen und Mitarbeitern eines Hospizes im Hinblick auf die Bedeutung ihrer Religiosität /." Fribourg : Acad. Press, 2005. http://deposit.ddb.de/cgi-bin/dokserv?id=2675557&prov=M&dok_var=1&dok_ext=htm.

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Lifsey, Gary J. "Hospice and African Americans| Exploring barriers to effective end-of-life care." Thesis, Capella University, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3737465.

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<p> This action research study was undertaken to identify how African Americans perceived and understood the many facets of hospice care, and to identify any barriers they faced in dealing with end-of-life care, any problems they encountered with enrollment in hospice care, and how they utilized hospice services. Qualitative interviews conducted with 10 African American participants resulted in the identification of eight major themes related to end-of-life care. Results indicated that African Americans perceived and understood hospice care through a religious or spiritual lens, and believed
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Wong, Lai-cheung, and 黃麗彰. "A study of hospice care: [factors affecting] communication between the health care professionals and thepatients." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1992. http://hub.hku.hk/bib/B31977182.

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Jimenez, Bernal Maria C. "Hospice Outreach Program for the Latino Community| A Grant Proposal Project." Thesis, California State University, Long Beach, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10784469.

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<p> The purpose of the project was to fund a hospice outreach program for the Latino community. This program will use a culturally sensitive approach to provide education on hospice services. St. Athanasius Church, the hosting agency of this project, is located in Long Beach, California. This Church was selected as the hosting agency since it has a history of conducting effective outreach to Latinos. </p><p> Latinos continue to underutilize hospice services even though it is a covered benefit of Medicare, Medicaid and most private insurances. After conducting a review of the literature, the
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Books on the topic "Hospice care worker"

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Hospice and ministry. Abingdon Press, 1988.

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Hospice social work. Columbia University Press, 2013.

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Ray, M. Catherine. I'm here to help: A guide for caregivers, hospice workers, and volunteers. Bantam Books, 1997.

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M, Saunders Cicely. Cicely Saunders: Founder of the hospice movement : selected letters 1959-1999. Oxford University Press, 2002.

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1953-, Clark David, ed. Cicely Saunders: Founder of the hospice movement : selected letters 1959-1999. Oxford University Press, 2005.

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Cicely Saunders: Selected writings 1958-2004. Oxford University Press, 2006.

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Midwife for souls: Spiritual care for the dying : a guide for hospice care workers and all who live with the terminally ill. St. Paul Books & Media, 1993.

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Resnik, David B. Dying declarations: Notes from a hospice volunteer. Haworth Pastoral Press, 2005.

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Peaceful journey: A hospice chaplain's guide to end of life. Paramount Market Pub., 2005.

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Woods, Deborah. Death Angel: The Journey of a Hospice Chaplin. AuthorHouse, 2007.

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Book chapters on the topic "Hospice care worker"

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Joosten, Dawn. "Palliative and Hospice Care Settings." In Transformative Social Work Practice. SAGE Publications, Inc., 2016. http://dx.doi.org/10.4135/9781506304533.n6.

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Jones, AnneMarie, and Sophia F. Dziegielewski. "The Roles and Services Provided by the Hospice Social Worker." In The Changing Face of Health Care Social Work. Springer Publishing Company, 2013. http://dx.doi.org/10.1891/9780826119438.0011.

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Callahan, Ann M. "Relational Spirituality." In Spirituality and Hospice Social Work. Columbia University Press, 2017. http://dx.doi.org/10.7312/columbia/9780231171731.003.0006.

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Chapter 5 introduces the concept of relational spirituality to suggest how a therapeutic relationship may support a patient’s spiritual experience of enhanced life meaning. Although different types of relationships may inform spirituality, this chapter focuses on the relationship between a hospice social worker and a patient. Research shows that therapeutic engagement involves a balance between technical skills and relational skills relative to caregiver expertise and patient capacity. This chapter suggests that the manner in which the therapeutic process unfolds as part of hospice social work can facilitate enhanced life meaning, called relational spirituality. A relational model for spiritually-sensitive hospice social work is introduced as a means of describing how this spiritual quality of therapeutic engagement can support patient care.
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Goswami, Sourav. "Home Based Palliative Care." In Suggestions for Addressing Clinical and Non-Clinical Issues in Palliative Care. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.98648.

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Palliative care aims at improving the quality of life of a patient who is suffering from a chronic serious ailment like that of advanced cancer. Nobody wants to be away from his/her own family, especially when it’s known, he has limited days to live in this world. A patient gets the best treatment when it’s given in his own home and that too by his close ones. When palliative care is provided at the patient’s home, it provides a sense of safety, privacy, confidentiality and peace of mind for the patient. Specialist home-based palliative care improves symptom control, health-related communication and psychosocial support. It helps in better preparing the patient and the family members to accept death. It is provided by a team of trained members which includes doctor, nurse, social worker, volunteers, physiotherapist etc. They pay regular visits at the home of the patient and provide necessary health care to the patient. Considering the increasing cost of treatment of chronic illnesses, it’s sometimes hard on the part of the family to continue treatment in a hospital or hospice. It’s especially true in scenarios where population are not protected financially, in countries like India. The family members also play a vital role in home-based palliative care. They get trained from the team to learn the basics of palliation. Home based palliative care needs to be integrated into regular home health care services.
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Lookabaugh, Britni, and Charles von Gunten. "Evolution of the Palliative Team." In Palliative and Serious Illness Patient Management for Physician Assistants, edited by Nadya Dimitrov and Kathy Kemle. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190059996.003.0003.

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Hospice and palliative care teams are inherently interdisciplinary to be able to assess and address all the domains of palliative care for patients with chronic, complex, and life-limiting illness. These domains include the physical, psychosocial, spiritual, and practical needs of patients and families, among others. The disciplines include, but are not limited to, physician, advanced practice provider, pharmacist, nurse, social worker, and chaplain, among others. Advanced practice providers are defined in the National Consensus Project Guidelines for Quality Palliative Care as physician assistants and advanced practice nurses utilized to expand the capacity of palliative care interdisciplinary teams to deliver complex care and provide direct care. The term advanced practice provider means either physician assistants or advanced practice nurses. The development of an interdisciplinary team in the midst of team and consult growth is essential to be able to provide high-quality palliative care. Team resilience should be supported and maintained as it is necessary to meet the high demand for specialty palliative care services throughout the care continuum.
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Callahan, Ann M. "Champion of Spiritual Care." In Spirituality and Hospice Social Work. Columbia University Press, 2017. http://dx.doi.org/10.7312/columbia/9780231171731.003.0002.

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Chapter 1 highlights how important it is for hospice social workers to operate as champions of spiritual care with and on behalf of their patients. This begins with exploring why it is important to understand a patient’s experience of spirituality. Spirituality is described as having significant implications for life quality and delivery of hospice care Hospice social workers are essential members on interdisciplinary teams charged with the responsibility of ensuring patient access to quality hospice care, which for some patients necessitates spiritual care. To lay the foundation, hospice social workers need to understand how to engage in spiritually-sensitive hospice social work so they have the capacity to coordinate, if not deliver, spiritual care.
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Callahan, Ann M. "Spiritual Care." In Spirituality and Hospice Social Work. Columbia University Press, 2017. http://dx.doi.org/10.7312/columbia/9780231171731.003.0007.

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Chapter 6 describes the purpose of spiritual care, spiritual care models across disciplines, and utility of the relational model for spiritually-sensitive hospice social work. The relational model for spiritually-sensitive hospice social work is proposed as a means of not only facilitating patient access to spiritual support, but also as a form of spiritual care. This model is believed to help hospice workers maximize opportunities to enhance the spiritual quality of care through mindful intervention, which is particularly important when patients present with spiritual needs that require immediate care. Despite being a promising model for intervention, however, the chapter ends by encouraging caution given the unique dynamics that can emerge in the process of providing spiritual care, some of which may not be controlled through skilled intervention.
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"6. Spiritual Care." In Spirituality and Hospice Social Work. Columbia University Press, 2017. http://dx.doi.org/10.7312/call17172-007.

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Yennurajalingam, Sriram. "Hospice Approach to Palliative Care." In Hospice and Palliative Medicine and Supportive Care Flashcards. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190633066.003.0017.

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For the provision of palliative care in the hospice setting in the United States, Medicare covers any care that is reasonable and necessary to manage palliative and hospice care at end of life. To be eligible for this Medicare hospice benefit, a beneficiary must be entitled to Medicare Part A and be certified by a physician to have a life expectancy of 6 months or less if the illness runs its expected course. Medicare covers medications, nursing care, and medical services including care by a physician, physical therapy, social work. This chapter briefly reviews the various aspects of the Medicare hospice benefit.
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"1. Champion of Spiritual Care." In Spirituality and Hospice Social Work. Columbia University Press, 2017. http://dx.doi.org/10.7312/call17172-002.

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Conference papers on the topic "Hospice care worker"

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White, Jenny. "P-246 Work experience students: embracing change in hospice workforce development." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.271.

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Watson, Sharan, and Alison Hembrow. "P-14 Exploration of support workers’ and volunteers’ initiation of quality of life conversations." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.39.

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Forrow, Helen. "P-90 Wellbeing@Work – reducing hospice staff sickness and turnover rates." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.113.

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Cardwell, Lyndsay, Nancy Preston, and Sean Hughes. "P-84 The experience of home care workers – a hermeneutic review." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.107.

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Penman, Janice. "P-75 Spells of care could work magic in the community…" In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.102.

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Watson, Sharan, and Alison Hembrow. "129 Exploration of volunteers and support workers initiation of quality of life conversations in hospice palliative day care." In The APM’s Supportive & Palliative Care Conference, Accepted Oral and Poster Abstract Submissions, The Harrogate Convention Centre, Harrogate, England, 21–22 March 2019. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-asp.152.

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Mickleburgh, Veronica. "P-231 Creating opportunities to extend patient and carer involvement in hospice work." In Leading, Learning and Innovating, Hospice UK 2017 National Conference, 22–24 November 2017, Liverpool. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/bmjspcare-2017-hospice.256.

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Vaja, Anjana. "P-16 The evolution of cultural link workers in palliative care in the midlands." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.40.

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Wheeler, Rhiannon, and Tara Schrikker. "P-23 The open scrapbook – young volunteers improving practice through project work." In Transforming Palliative Care, Hospice UK 2018 National Conference, 27–28 November 2018, Telford. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-hospiceabs.48.

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Nichols, Rob, and Gemma Purnell. "P-243 Dragonfly – group work with grieving families." In Dying for change: evolution and revolution in palliative care, Hospice UK 2019 National Conference, 20–22 November 2019, Liverpool. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/bmjspcare-2019-huknc.265.

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