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Developing a New Clinical Ethics Framework for Rehab: A Pre-Implementation Evaluation from the Perspective of Future Users 构建康复临床伦理新框架:基于未来使用者视角的实施前评价
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098555ar
L. Leblanc, S. Ménard, C. Maïano, Louis Perron, Catherine Baril, Nicole Ouellette-Hughes
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引用次数: 0
Frameworks and Practices in Bioethics 生物伦理学的框架和实践
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098562ar
J. Dwyer
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引用次数: 0
Where Do I Go to Wait? Ethical Considerations During the 90 Day Reflection Period for MAiD 我该去哪里等?女佣90天反思期的道德考量
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098559ar
Kesi Disha, Andria Bianchi, R. Shanker, Nikolija Lukich
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引用次数: 0
An Ethics Journey: From Kant to Assisted Suicide 伦理之旅:从康德到协助自杀
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098567ar
Michael S. Gordon
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引用次数: 0
Respect for Patient Confidentiality Must Not Be Dependent Upon a Fee: The Case of Adolescents’ Access to Contraceptives in Ontario 对病人保密的尊重不能依赖于费用:青少年在安大略省获得避孕药具的情况
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098569ar
J. Brisson
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引用次数: 0
Operationalizing Equity in Surgical Prioritization 手术优先顺序的操作公平性
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1101124ar
Kayla Wiebe, Simon Kelley, Annie Fecteau, Mark Levine, Iram Blajchman, Randi Zlotnik Shaul, Roxanne Kirsch
The allocation of critical care resources and triaging patients garnered a great deal of attention during the COVID-19 pandemic, but there is a paucity of guidance regarding the ethical aspects of resource allocation and patient prioritization in ‘normal’ circumstances for Canadian healthcare systems. One context where allocation and prioritization decisions are required are surgical waitlists, which have been globally exacerbated due to the COVID-19 pandemic. In this paper, we detail the process used to develop an ethics framework to support prioritization for elective surgery at The Hospital for Sick Children, Toronto, a tertiary pediatric hospital. Our goal was to provide guidance for the more value-laden aspects of prioritization, particularly when clinical urgency alone is insufficient to dictate priority. With this goal in mind, we worked to capture familial, relational, and equity considerations. As part of our institution’s concerted efforts to ethically and effectively address our surgical backlog, an ethics working group was formed comprising clinicians from surgery, anesthesiology, intensive care, a hospital bioethicist, a parent advisor, and an academic bioethics researcher. A reflective equilibrium process was used to develop an ethics framework. To this end, the same methodology was used to create a support for patient prioritization that identifies clinically and morally relevant factors for prioritization among medically similar surgical cases, with a substantive goal being to identify and redress health inequities in surgical prioritization, inasmuch as this is possible. While further steps are needed to validate several aspects of the framework, our research suggests that an ethics framework grounded in the practical realities of hospital operations provides consistency, transparency, and needed support for decisions that are often left to individual clinicians, as well as an opportunity to reflect upon the presence of health inequities in all domains of healthcare delivery.
在COVID-19大流行期间,重症监护资源的分配和患者分诊引起了极大的关注,但加拿大医疗保健系统在“正常”情况下缺乏关于资源分配和患者优先级的道德方面的指导。需要做出分配和优先排序决定的一个情况是手术等候名单,由于COVID-19大流行,这一情况在全球范围内加剧了。在本文中,我们详细介绍了用于制定道德框架的过程,以支持多伦多儿童医院(一家三级儿科医院)择期手术的优先顺序。我们的目标是为优先次序的更有价值的方面提供指导,特别是当临床紧迫性本身不足以决定优先次序时。有了这个目标,我们努力捕捉家庭、关系和公平的考虑。为了从伦理上有效地解决手术积压问题,我们组织了一个伦理工作组,成员包括来自外科、麻醉科、重症监护室的临床医生、一名医院生物伦理学家、一名家长顾问和一名学术生物伦理学研究员。一个反思的平衡过程被用来发展一个伦理框架。为此目的,采用同样的方法为患者优先排序提供支持,在医学上类似的手术病例中确定临床和道德上相关的优先因素,其实质性目标是尽可能确定和纠正手术优先排序方面的卫生不公平现象。虽然需要进一步的步骤来验证该框架的几个方面,但我们的研究表明,基于医院运营实际情况的伦理框架为通常留给临床医生个人的决策提供了一致性、透明度和所需的支持,同时也为反思医疗保健服务所有领域中存在的卫生不平等提供了机会。
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引用次数: 1
La collégialité dans la mise en place d’une sédation profonde et continue dans un centre de cancérologie en France 在法国的一个癌症中心实施深度和持续镇静的合作
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1101131ar
Bettina Couderc, Alfonsina Faya Robles, Nathalie Caunes-Hilary, Laurie Galiby, Emmanuelle Rial Sebbag
Une procédure collégiale désigne le fait de recueillir, avant de prendre une décision médicale délicate, l’avis de l’ensemble de l’équipe de soins responsable du patient, incluant le personnel infirmier et aide-soignant, entre autres. La loi Claeys-Leonetti relative à la fin de vie (2016) l’inscrit dans le droit français comme étant obligatoire lors de la mise en place d’une sédation profonde et continue maintenue jusqu’au décès (SPCMD). L’objectif de l’étude est de faire un état des lieux de la connaissance de cet aspect de loi par le personnel soignant d’un institut de cancérologie et d’identifier comment la collégialité se met en place pour une décision de SPCMD selon les services. Nous avons proposé un questionnaire en ligne et anonyme à l’ensemble des acteurs du soin (connaissance de la loi Claeys-Leonetti) puis nous avons rencontré les soignants des différents services en groupes de discussion (cadres, personnel infirmier et aides-soignants) ou en entretiens individuels (médecins). Les résultats montrent que la loi est mieux connue, toutes professions confondues, des jeunes soignants (moins de 5 ans d’expérience) et surtout mieux revendiquée par les infirmières et aides-soignantes que par les médecins. Nous rapportons la diversité de la mise en oeuvre de la collégialité pour une décision de sédation, en termes de formalisation, de standardisation et d’inter professionnalisation. Nous concluons que la mise en place de la collégialité de façon anticipée pour une décision élargit les modes de communication pluri/inter professionnelle et permet d’apaiser la souffrance des patients, des médecins et des soignants.
集体程序是指在做出敏感的医疗决定之前,征求负责病人的整个护理团队的意见,包括护士和护理助理等。《克莱-列奥内蒂生命终结法》(2016年)在法国法律中规定,在实施持续深度镇静直至死亡(SPCMD)时,这是强制性的。这项研究的目的是评估癌症研究所护理人员对法律这方面的知识,并确定如何根据服务部门为SPCMD的决定建立合作关系。我们向所有护理人员(了解claey - leonetti法律)提出了一份在线匿名问卷,然后我们以焦点小组(管理人员、护士和护理助理)或个人访谈(医生)的形式与不同服务的护理人员会面。结果表明,在所有职业中,年轻护理人员(工作经验少于5年)对该法案的了解程度更高,最重要的是,护士和护理助理比医生更了解该法案。我们报告了在正规化、标准化和内部专业化方面实施镇静决策的集体合作的多样性。我们的结论是,在决策的早期阶段引入共同合作,扩大了多/跨专业沟通的范围,并减轻了患者、医生和护理人员的痛苦。
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引用次数: 1
Collecting Race-Based Data in Health Research: A Critical Analysis of the Ongoing Challenges and Next Steps for Canada 在卫生研究中收集基于种族的数据:对加拿大目前面临的挑战和今后步骤的批判性分析
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098560ar
F. Sheikh, A. Fox-Robichaud, Lisa Schwartz
The COVID-19 pandemic has had a global effect. The disproportionate impact on Indigenous peoples and racialized groups has brought ethical challenges to the forefront in research and clinical practice. In Canada, the Tri-Council Policy Statement (TCPS2), and specifically the principle of justice, emphasizes additional care for individuals "whose circumstances make them vulnerable", including Indigenous and racialized communities. In the absence of race-based data to measure and inform health research and clinical practice, we run the risk of causing more harm and contributing to ongoing injustices. However, without an accepted framework for collecting, maintaining, and reporting race-based data in Canada, more guidance is needed on how to do this well. Importantly, a framework for collecting race-based data should build on existing guidance from Indigenous and other structurally marginalized communities, the TCPS2, recommendations from the World Health Organization, and involve relevant stakeholders. In this paper, we describe historical examples of unethical studies on Indigenous and racialized groups, discuss the challenges and potential benefits of collecting race-based data, and conclude with objectives for a pan-Canadian framework to inform how race-based data is collected, stored, and accessed in health research.
2019冠状病毒病大流行已产生全球影响。对土著人民和种族化群体的不成比例的影响在研究和临床实践中带来了伦理挑战。在加拿大,《三理事会政策声明》(TCPS2),特别是正义原则,强调对“处境使其脆弱”的个人,包括土著和种族化社区,给予额外照顾。在缺乏基于种族的数据来衡量卫生研究和临床实践并为其提供信息的情况下,我们面临造成更多伤害和助长持续不公正的风险。然而,在加拿大,没有一个公认的框架来收集、维护和报告基于种族的数据,需要更多的指导来做好这一点。重要的是,收集基于种族的数据的框架应建立在土著和其他结构上被边缘化社区的现有指导意见、第二阶段方案、世界卫生组织的建议的基础上,并让相关利益攸关方参与进来。在本文中,我们描述了关于土著和种族化群体的不道德研究的历史例子,讨论了收集基于种族的数据的挑战和潜在好处,并总结了一个泛加拿大框架的目标,以告知如何在健康研究中收集、存储和访问基于种族的数据。
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引用次数: 0
The Invisibility of the Asian American Identity in North American Bioethics 北美生命伦理学中亚裔美国人身份的隐蔽性
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098568ar
Katherine Huerne
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引用次数: 0
The Blessings of Books 书籍的祝福
Q4 MEDICAL ETHICS Pub Date : 2023-01-01 DOI: 10.7202/1098566ar
M. Gordon
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引用次数: 0
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Canadian Journal of Bioethics
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