姑息治疗伦理:医学的帮助责任

Palliative Care Pub Date : 2019-04-06 DOI:10.5772/INTECHOPEN.85160

Ş. Keleş

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引用次数: 1

摘要

在姑息治疗中，死亡是人性的一部分，被认为是一个正常的过程。这种类型的护理关心的是生活质量而不是寿命。在这种情况下，基本目标是以一种不会引起任何伦理怀疑的方式来执行减轻患者的做法。在这个框架内，姑息治疗可以说是医学帮助义务的要求。本章的目的是提请注意伦理价值的重要性，在配置姑息治疗服务的病人谁是在他们的生命的最后一段时间或谁有绝症。在姑息治疗中，必须以一种不会引起任何道德上怀疑的方式安排护理服务，以增加对处于生命最后几天的病人及其亲属的福利。在本研究中，将从伦理角度对土耳其卫生部于2015年制定的“姑息治疗服务实施程序指令”进行评估。

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Palliative Care Ethics: Medicine’s Duty to Help

In palliative care, death, which is a part of human nature, is considered as a normal process. This type of care is concerned with the quality of life rather than its duration. In this context, the basic aim is to perform practices to relieve the patient in a way that does not raise any ethical suspicion. Within this framework, it can be said that palliative care is a requirement of medicine’s duty to help. The aim of this chapter is to draw attention to the importance of ethical values in the configuration of palliative care services for patients who are in the last period of their life or the ones who have terminal illnesses. In palliative care, it is essential to arrange care services in a manner that does not raise any ethical doubt about the measures taken to increase beneficence both to the patients who are in the last days of their life and to their relatives. In this study, “The Directive for Implementing Procedures of Palliative Care Services” prepared by the Ministry of Health in Turkey in 2015 will be evaluated in terms of ethics.

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来源期刊

Palliative Care

自引率

0.00%

发文量

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)