Reflections on palliative sedation.

Palliative Care Pub Date : 2019-01-27 eCollection Date: 2019-01-01 DOI:10.1177/1178224218823511
Robert Twycross
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引用次数: 67

Abstract

'Palliation sedation' is a widely used term to describe the intentional administration of sedatives to reduce a dying person's consciousness to relieve intolerable suffering from refractory symptoms. Research studies generally focus on either 'continuous sedation until death' or 'continuous deep sedation'. It is not always clear whether instances of secondary sedation (i.e. caused by specific symptom management) have been excluded. Continuous deep sedation is controversial because it ends a person's 'biographical life' (the ability to interact meaningfully with other people) and shortens 'biological life'. Ethically, continuous deep sedation is an exceptional last resort measure. Studies suggest that continuous deep sedation has become 'normalized' in some countries and some palliative care services. Of concern is the dissonance between guidelines and practice. At the extreme, there are reports of continuous deep sedation which are best described as non-voluntary (unrequested) euthanasia. Other major concerns relate to its use for solely non-physical (existential) reasons, the under-diagnosis of delirium and its mistreatment, and not appreciating that unresponsiveness is not the same as unconsciousness (unawareness). Ideally, a multiprofessional palliative care team should be involved before proceeding to continuous deep sedation. Good palliative care greatly reduces the need for continuous deep sedation.

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关于姑息性镇静的思考。
“缓和镇静”是一个广泛使用的术语,用于描述故意使用镇静剂来减少垂死之人的意识,以减轻难以忍受的痛苦。研究通常集中在“持续镇静直到死亡”或“持续深度镇静”上。目前尚不清楚是否排除了继发性镇静(即由特定症状管理引起的)。持续的深度镇静是有争议的,因为它会结束一个人的“传记生命”(与他人进行有意义的互动的能力),缩短“生物生命”。从道德上讲,持续深度镇静是一种特殊的最后手段。研究表明,在一些国家和一些姑息治疗服务中,持续深度镇静已成为“常态”。值得关注的是指导方针和实践之间的不协调。在极端情况下,有报道称持续深度镇静最好被描述为非自愿(非请求)安乐死。其他主要的担忧涉及到它的使用仅仅是非身体的(存在的)原因,谵妄的诊断不足及其虐待,以及没有认识到无反应与无意识(无意识)不同。理想情况下,在进行持续深度镇静之前,应该有一个多专业的姑息治疗团队参与。良好的姑息治疗大大减少了对持续深度镇静的需要。
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来源期刊
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0.00%
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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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