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Final Acts: The End of Life: Hospice and Palliative Care [Kietas viršelis]

  • Formatas: Hardback, 258 pages, aukštis x plotis: 229x152 mm, weight: 640 g
  • Serija: Death, Value and Meaning Series
  • Išleidimo metai: 30-Nov-2013
  • Leidėjas: Baywood Publishing Company Inc
  • ISBN-10: 089503865X
  • ISBN-13: 9780895038654
Kitos knygos pagal šią temą:
  • Formatas: Hardback, 258 pages, aukštis x plotis: 229x152 mm, weight: 640 g
  • Serija: Death, Value and Meaning Series
  • Išleidimo metai: 30-Nov-2013
  • Leidėjas: Baywood Publishing Company Inc
  • ISBN-10: 089503865X
  • ISBN-13: 9780895038654
Kitos knygos pagal šią temą:
The editors undertook this project to promote the International Conference on Death, Grief, and Bereavement in La Crosse, Wisconsin. Throughout its history, the conference has attracted internationally known speakers. This book illustrates the quality of their presentations. Section One, "Professional Applications in End of Life Care," begins with Currier, Hammer, and Neimeyer's examination of the importance of the social network, including both religion and family, not just the individual, in working with those at the end of their lives. The authors analyze the impact of social support and its health implications. In Chapter 2, Parkes looks at the influence of child development on adult life and bereavement. Rather than simply showing how insecure child development affects loss as adults, he examines how insecure attachments in childhood can lead to extreme attachments to God, homes, territories, political leaders, and symbols and discusses interventions for these extreme attachments. Papadatou (Chapter 3) develops a model for professionals and caregivers who work with the dying. She suggests that those who give care to the dying also have multiple needs and also face suffering, examines the private world of professionals and what is healthy and what is unavoidable, and describes both functional and dysfunctional coping patterns used by professionals. Kobler (Chapter 4) uses case studies to explain how to develop and maintain relationships with children and their families in pediatric palliative care. She offers strategies for using rituals and ways to initiate and maintain relationships with children and their families. Thompson (Chapter 5) focuses on the effects of working in situations involving high levels of emotion and the stress that may result. He makes a strong case that such stress can do harm to individuals, groups, and whole organizations and offers a model for a more holistic approach that incorporates social and organizational strategies and practical ways to prevent and manage stress. Eves-Baine and colleagues (Chapter 6) examine the application of pediatric and adult-based principles to the newborn period. They discuss how to create the best situations for families when life-sustaining medical therapy has been withdrawn, how to support the family, and the ethical challenges that perinatal palliative care presents. The authors offer models for care through the journey of palliative and bereavement care. Section Two, "Facing End of Life and Its Care," begins with Gilbert's chapter presenting a strong argument that caregivers need to honor the multiple tracks that come with dying while maintaining a focus on the wishes of the dying person. He offers ways for the team to better meet the needs of the dying person. Koppleman (Chapter 8) follows the journey of a friend who faced death. It is a powerful story, told from the point of view of the dying in a scholarly fashion. Smith and Potter (Chapter 9) suggest that palliative care for the dying can be defined as offering “comfort care,” both for those who are dying and for their loved ones. The authors present a model of the psycho-spiritual side of palliative care as a way of offering comfort to all those involved. Adams (Chapter 10) examines different methods of working with patients and families. It looks at the ways in which such work can be complicated by factors of geographic distance, differences in family reactions, differences in treatment plan concepts, and in meaning making. All of these factors may become stumbling blocks and may prevent the delivery of positive support. Pizzini (Chapter 11) looks at the experience of dying in prison from the perspective of inmates who are terminally ill, prison medical staff, and prison security staff. She discusses how to maintain dignity of the dying and a “good death” while in prison. McCord (Chapter 12) discusses attempts by hospice patients and others diagnosed with terminal illnesses to die either by their own hand or with physician assistance. She presents common risk factors, strategies to assess the degree of risk and possible plans for suicide and suicide postvention in the context of hospice.Section Three, "Cultural Considerations in End-of-Life Care" begins with The End of Life: Two Perspectives in which Robert G. Stevenson looks at two perspectives on the end of life that are not often examined in terms of their impact on the individual and his/her attitude toward this time. The two perspectives are that of adolescents, and that are shown in a military ceremony used in the 18th and 19th centuries, the Feu de Joie or Fire of Joy. In Chapter Fourteen, Janet McCord discusses suicide attempts by hospice patients and others diagnosed with terminal illnesses to die either by their own hand or with physician assistance. Connor's description of the need for hospice and palliative care around the world and the challenges of developing palliative care globally, and offers models that can be used around the world. Cox and Cox (Chapter 15) suggest ways to offer end-of-life care to Roman Catholics who do not fit the traditional model of hospice care and examine special needs, theology, and rituals. Cox and Sullivan (Chapter 16) offer suggestions on end-of-life care for American Indians, explaining cultural differences among American Indians and suggesting ways to improve care to a group that is generally neglected in hospice care. Smith (Chapter 17) looks at the cultural differences and understandings of Fundamentalist Christian views of a “good death” and the afterlife, ways to negotiate faith understandings that complicate end-of-life care, and ways to comfort individuals who may be marginalized because they do not share the theological views of the dying individual or key family members. Intended Audience: Caregivers, hospice workers, educators, physicians, nurses, families, palliative caregivers, social workers, counselors, case managers, funeral service directors, individuals dealing with personal losses, general public.

This book examines a change that has taken place in how people respond to the end of life. After coping through avoidance or denial, people have begun to address this time directly and seek to improve its quality. This book explores the roles of hospice and palliative care. These give quality to the end of life's story…its Final Acts.

This guide is intended for healthcare professionals, caregivers, social workers, counselors, case managers, and funeral service directors. Emphasizing that palliative care is a human right, contributors in counseling, social work, palliative care, and nursing offer perspectives, experiences, and guidelines on professional applications and cultural considerations in end-of-life care. Some areas addressed include dealing with stress, best practices for infant death, death in prison, spiritual healing, and understanding suicide in the context of end-of-life care. There is also material on understanding the needs of patients from specific religious backgrounds, including Catholicism, fundamental Christianity, and Native American spirituality. Annotation ©2014 Book News, Inc., Portland, OR (booknews.com)
Foreword ix
Preface xiii
Acknowledgments xvii
SECTION 1 Professional Applications in End-of-Life Care
1(90)
Chapter 1 Existential Empathy: Caregiver Understanding of Patients' Religious Beliefs at the End-of-Life
1(14)
Joseph M. Currier
Miyoung Yoon Hammer
Robert A. Neimeyer
Chapter 2 Attachments and Losses: Individual and Global Perspectives
15(10)
Colin Murray Parkes
Chapter 3 The Private Worlds of Professionals, Teams, and Organizations in Palliative Care
25(20)
Danai Papadatou
Chapter 4 Honoring Relationship in Pediatric Palliative Care
45(20)
Kathie Kobler
Chapter 5 Meeting the Stress Challenge
65(12)
Neil Thompson
Denise Bevan
Chapter 6 When Birth and Death Collide: Best Practices in End-of-Life at the Beginning
77(14)
Lori Ives-Baine
Jessica Faust
Jessica Drewry
Jatinder Kalra
Michael Marshall
Roop Johal
Alyson Mayne
SECTION 2 Facing End-of-Life and Its Care
91(92)
Chapter 7 To Be is To Be, and the Do-ing Should Follow
91(12)
Richard B. Gilbert
Chapter 8 Stepping Through the Looking Glass into "Cancer World"
103(12)
Kent Koppelman
Chapter 9 The Psycho-Spiritual Side of Palliative Care: Two Stories and Ten Transformations Toward Healing
115(14)
Douglas C. Smith
Conley M. Potter
Chapter 10 "And the Sun Refused to Shine"
129(16)
Susan Adams
Chapter 11 The Experience of Dying in Prison
145(10)
Nicole Pizzini
Chapter 12 The "Other" Kind of Pain: Understanding Suicide in the Context of End-of-Life Care
155(20)
Janet S. McCord
Chapter 13 The End of Life: Two Perspectives
175(8)
Robert G. Stevenson
SECTION 3 Cultural Considerations
183(44)
Chapter 14 Palliative Care is a Human Right
183(8)
Stephen R. Connor
Chapter 15 Spirituality in End-of-Life Care: A Roman Catholic Perspective
191(8)
Gerry R. Cox
Christopher W. Cox
Chapter 16 Grief and the American Indian
199(6)
Gerry R. Cox
Andrea R. Sullivan
Chapter 17 "It Will Do When I Am Dying": Navigating the Nuances of Fundamentalist Christianity's Understandings of Death and Dying
205(22)
Harold Ivan Smith
Contributors 227(6)
Index 233
Gerry R. Cox (Author) ,  Robert G. Stevenson (Author)