Die folgenden Links führen aus den jeweiligen lokalen Bibliotheken zum Volltext:
Alternativ können Sie versuchen, selbst über Ihren lokalen Bibliothekskatalog auf das gewünschte Dokument zuzugreifen.
Bei Zugriffsproblemen kontaktieren Sie uns gern.
150212 Ergebnisse
Sortierung:
Cover -- Title Page -- Copyright Page -- Contents -- Foreword -- About the Authors -- Acknowledgements -- Part 1 Getting Started -- Unit 1.1 Gaining Perspectives -- Part 2 Understanding the Caregiver's Self -- Unit 2.1 Reflecting on Death -- Unit 2.2 Mindfulness -- Unit 2.3 Self-Knowledge -- Unit 2.4 Spiritual Knowledge -- Unit 2.5 The Whole Self: Body-Mind-Spirit -- Unit 2.6 Facing Death -- Part 3 Understanding Ourselves in Service of the Dying Person -- Unit 3.1 Social and Cultural Influences -- Unit 3.2 Spiritual and Religious Influences -- Unit 3.3 The Nature of Loss and Suffering -- Part 4 Ways of Helping the Dying Person -- Unit 4.1 Fundamentals of Communication -- Unit 4.2 Compassionate Presence, Mindful Listening, and Effective Responding -- Unit 4.3 Fears and Assumptions about Death -- Unit 4.4 Narratives of Suffering -- Unit 4.5 Expressive Activities That Aid in Relieving Suffering -- Part 5 Honoring the Caregiver -- Unit 5.1 Nurture and Honor Yourself!
In: The British journal of social work, Band 41, Heft 1, S. 111-130
ISSN: 1468-263X
In: Oxford American Handbooks of Medicine Ser.
Self-awareness and communication -- Sex, gender, sexual orientation, behavior, and health -- Understanding attitudes and access to care -- The history and physical examination -- Shared decision making and family dynamics -- Care planning and coordination -- Ethical and legal issues -- Patient and family education and advocacy -- Psychosocial and spiritual issues -- Ensuring institutional inclusiveness
This practicum report is a summary and reflection upon a Master of Social Work practicum completed at Victoria Hospice, supporting my desire to understand the role of a social worker within an interdisciplinary hospice palliative healthcare team. Several aspects of my practicum experience are explored through a literature review, embracing a biopsychosocial-spiritual model of practice. Included is a brief examination of Medical Assistance in Dying (MAiD) and its legislation in Canada. The knowledge gained from this practicum will guide my hospice palliative social work practice in northern BC, which in turn will provide a learning environment for future social work students wanting to specialize in this area of practice. ; Palliative Care
BASE
This practicum report is a summary and reflection upon a Master of Social Work practicum completed at Victoria Hospice, supporting my desire to understand the role of a social worker within an interdisciplinary hospice palliative healthcare team. Several aspects of my practicum experience are explored through a literature review, embracing a biopsychosocial-spiritual model of practice. Included is a brief examination of Medical Assistance in Dying (MAiD) and its legislation in Canada. The knowledge gained from this practicum will guide my hospice palliative social work practice in northern BC, which in turn will provide a learning environment for future social work students wanting to specialize in this area of practice. ; Palliative Care
BASE
In: Soziologie Bd. 19
In: The International Journal of Knowledge, Culture, and Change Management: Annual Review, Band 6, Heft 5, S. 109-116
ISSN: 1447-9575
This article examines the intersection between masculinity, military culture, and hospice and palliative care (HPC). The authors conducted a narrative literature review, supplemented with clinical annotations, to identify the impact of masculinity and military culture on the following topics salient to end-of-life care with older male veterans: pain management, mental health, coping, communication, autonomy and respect, and family roles. Findings suggest that traits associated with masculinity and military culture have an influence on the end-of-life process and HPC for older male veterans. Specifically, results suggest that older male veterans may deny or minimize physical pain, decline mental health treatment, utilize maladaptive coping strategies, avoid emotional conversations, struggle to manage perceived shifts in autonomy, and experience challenges negotiating changing family roles. The authors provide clinical recommendations for providers across various disciplines to address the aforementioned concerns with older male veterans in HPC. Overall, information presented in this article may be an important contribution to the literature for building cultural competencies with older male veterans and has the potential to improve the delivery of HPC for veterans and their families.
BASE
In: Gender a výzkum, Band 22, Heft 1, S. 202-205
ISSN: 2570-6586
Hospice is the premiere end of life program in the United States, but its requirement that patients forgo disease-directed therapies and that they have a prognosis of 6 months or less means that it serves less than half of dying patients and often for very short periods of time. Palliative care offers careful attention to pain and symptom management, added support for patients and families, and assistance with difficult medical decision making alongside any and all desired medical treatments, but it does not include a comprehensive system of care as is provided by hospice. The practice of pall
In recent years, hospice and palliative care (HPC) has grown, developed, and changed in response to the humanistic and social needs for supporting those with incurable illnesses. As a relatively new discipline, research is needed in HPC, and the priority setting of research is essential to help direct finite resources to support research. To promote creative research in different fields including HPC, the Taiwan government subsidized institutions to conduct research. In this study, we obtained data from the Government Research Bulletin, an open-source online system containing complete information about government subsidized studies since 1993 to investigate the development of research priority in HPC in Taiwan. In total, 552 studies were recorded during 1993–2021, with a continued upward trend. An association was found between research priority and the promulgation of new HPC regulations. The type of diseases in research extended from cancer to all advanced chronic conditions. The increased diversity in out-of-hospital settings of palliative research was also observed. Numerous studies have focused on education, and the theme gradually shifted from "training and education for healthcare professionals" to "public education". Here, the results may serve as a basis to understand the commonalities of research and enhance dialog in HPC research.
BASE