Health care Professionals' Experiences and Needs When Delivering End-of-Life Care to Children: A Qualitative Study.

Palliative Care Pub Date : 2017-08-10 eCollection Date: 2017-01-01 DOI:10.1177/1178224217724770
Eva Bergsträsser, Eva Cignacco, Patricia Luck
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引用次数: 16

Abstract

Pediatric end-of-life care (EOL care) entails challenging tasks for health care professionals (HCPs). Little is known about HCPs' experiences and needs when providing pediatric EOL care in Switzerland. This study aimed to describe the experiences and needs of HCPs in pediatric EOL care in Switzerland and to develop recommendations for the health ministry. The key aspect in EOL care provision was identified as the capacity to establish a relationship with the dying child and the family. Barriers to this interaction were ethical dilemmas, problems in collaboration with the interprofessional team, and structural problems on the level of organizations. A major need was the expansion of vocational training and support by specialized palliative care teams. We recommend the development of a national concept for the provision of EOL care in children, accompanied by training programs and supported by specialized pediatric palliative care teams located in tertiary children's hospitals.

Abstract Image

卫生保健专业人员在为儿童提供临终关怀时的经验和需求:一项定性研究。
儿科临终关怀(EOL)是医疗保健专业人员(HCPs)面临的具有挑战性的任务。在瑞士提供儿科EOL护理时,HCPs的经验和需求知之甚少。本研究旨在描述瑞士HCPs在儿科EOL护理中的经验和需求,并为卫生部提出建议。EOL护理提供的关键方面被确定为与垂死儿童及其家庭建立关系的能力。这种互动的障碍是道德困境,与跨专业团队合作的问题,以及组织层面的结构性问题。一项主要需求是扩大职业培训和专业姑息治疗小组的支持。我们建议制定一个国家概念,为儿童提供EOL护理,并辅以培训计划,并由位于三级儿童医院的专业儿科姑息治疗团队提供支持。
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来源期刊
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊介绍: Palliative Care and Social Practice is an international, peer-reviewed, open access journal that publishes articles on all aspects of palliative care. It welcomes articles from symptom science, clinical practice, and health services research. However, its aim is also to publish cutting-edge research from the realm of social practice - from public health theory and practice, social medicine, and social work, to social sciences related to dying and its care, as well as policy, criticism, and cultural studies. We encourage reports from work with under-represented groups, community development, and studies of civic engagement in end of life issues. Furthermore, we encourage scholarly articles that challenge current thinking about dying, its current care models and practices, and current understandings of grief and bereavement. We want to showcase the next generation of palliative care innovation research and practice - in clinics and in the wider society. Relaunched in July 2019. Partnered with Public Health Palliative Care International (PHPCI) (Title 2008-2018: - Palliative Care: Research and Treatment)
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