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Editor's Note, March 2022 编者按,2022年3月
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-03-01 DOI: 10.1353/ken.2022.0000
S. Harvard, Eric Winsberg, S. Schroeder, Tobias Schönwitz, S. Tresker, D. Howard, A. Omelianchuk
ABSTRACT:Both the distinction between the 'internal' and 'external' phases of science and the concept of 'inductive risk' are core constructs in the values in science literature. However, both constructs have shortcomings, which, we argue, have concealed the unique significance of values in scientific representation. We defend three closely-related proposals to rectify the problem: i) to draw a conceptual distinction between endorsing a 'fact' and making a decision about representation; ii) to employ a conception of inductive risk that aligns with this distinction, not one between internal/external phases in science; iii) to conceptualize 'representational risk' as a unique epistemic risk, no less significant than inductive risk. We outline the implications of each proposal for current debates in the values in science literature.
摘要:科学“内部”和“外部”阶段的区别以及“诱导风险”的概念都是科学文献价值观的核心结构。然而,这两种结构都有缺点,我们认为,这些缺点掩盖了价值观在科学表征中的独特意义。我们为纠正这一问题的三项密切相关的建议辩护:一在概念上区分认可“事实”和就代表权做出决定;ii)采用与这种区别相一致的归纳风险概念,而不是科学内部/外部阶段之间的概念;iii)将“表征风险”概念化为一种独特的认识风险,其重要性不亚于归纳风险。我们概述了每一项提案对当前科学文献价值观辩论的影响。
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引用次数: 0
Values in Science, Biodiversity Research, and the Problem of Particularity 科学价值、生物多样性研究与特殊性问题
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-03-01 DOI: 10.1353/ken.2022.0003
Tobias Schönwitz
ABSTRACT:How to deal with non-epistemic values in science presents a pressing problem for science and society as well as for philosophers of science. In recent years, accounts of democratizing science have been proposed as a possible solution to this. By providing a case study on the establishment of the Intergovernmental Science-Policy comment: Platform on Biodiversity and Ecosystem Services comment: (IPBES), I argue that such accounts run into a problem when values are embedded in the general scientific and societal setup to such an extent that they shape the terrain upon which such a democratization needs to take place. I introduce the notion of particularities as manifestations of values in science and state a problem of particularity, posed by the ways in which the interactive dimension of particularities interferes with democratic procedures for resolving value judgements in science. As a possible remedy, I propose enriching accounts of democratizing science by agonistic theories of democracy.
摘要:如何处理科学中的非认识论价值,是摆在科学和社会以及科学哲学家面前的一个紧迫问题。近年来,人们提出了科学民主化的说法,作为解决这一问题的可能办法。通过提供一个关于建立政府间科学政策评论:生物多样性和生态系统服务评论平台(IPBES)的案例研究,我认为,当价值观被嵌入到一般的科学和社会设置中,以至于它们塑造了这种民主化需要发生的地形时,这些账户就会遇到问题。我介绍了特殊性作为科学价值表现的概念,并阐述了特殊性的问题,这一问题是由特殊性的互动维度干扰解决科学价值判断的民主程序的方式提出的。作为一种可能的补救措施,我建议通过民主的斗争理论来丰富科学民主化的叙述。
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引用次数: 1
Review of Metagnosis: Revelatory Narratives of Health and Identity 形而上学述评:健康与身份的启示性叙述
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-03-01 DOI: 10.1353/ken.2022.0006
D. Howard
Danielle Spencer’s book, “Metagnosis: Revelatory Narratives of Health and Identity,” does many things. It is a work of autotheory, putting Spencer’s own embodied narrative in constant conversation with the testimony of others along with a remarkably diverse set of critical and theoretical approaches. In the book, Spencer coins a new term, “metagnosis”, which occurs when one is newly diagnosed in adulthood with a lifelong condition. The book explores Spencer’s own metagnostic experience involving her eyesight along with chronicling the experiences of others to highlight the ways in which newfound knowledge of a diagnosis can in itself transform us. Born with strabismus—“misaligned eyes,” Spencer is practiced at negotiating the meaning of having a non-normative visual experience and presentation. For the most part, growing up with the condition and frequently subjected to medical attention because of it, Spencer remained largely unconcerned about whether or not she saw differently. But, as the book chronicles, in adulthood, after enduring subpar medical treatment and a series of frustrating surgeries, Spencer is additionally diagnosed with a different visual field condition, homonymous hemianopia, that was likely sustained in infancy, but which up until the diagnosis neither she nor her various doctors had detected. Spencer describes how she discovers in her orthoptist’s office that she can see only half of the visual world of each eye. This discovery leads to a deep ambivalence on Spencer’s part—which includes feelings of physical vulnerability, shame that the condition had gone unnoticed for so long, as well as relief for not having to suffer through the stigma and exclusion that may have come with the additional medical diagnosis in childhood. It also leads to a theoretical examination of the limited narrative and theoretical resources that avail us in trying to make sense of such revelatory experiences and the frustrating inexplicability that such transformative experiences can have for others. This intimate narrative approach democratizes theory. As Spencer says near the end of the book, WEB CONTENT ONLY
丹妮尔·斯宾塞的书《形而上学:健康与身份的启示性叙述》做了很多事情。这是一部自我理论的作品,将斯宾塞自己的具体叙事与他人的证词以及一套非常多样化的批评和理论方法进行了不断的对话。在书中,Spencer创造了一个新的术语,“后生症”,当一个人在成年后被新诊断出患有终身疾病时,就会出现这种情况。这本书探讨了Spencer自己涉及视力的后生经验,并记录了其他人的经验,以强调新发现的诊断知识本身可以改变我们的方式。Spencer天生患有斜视——“错位的眼睛”,擅长协商非规范视觉体验和呈现的含义。在大多数情况下,在这种情况下长大,并经常因此受到医疗护理,斯宾塞基本上不关心自己的看法是否不同。但是,正如书中所记载的那样,成年后,在经历了不理想的医疗和一系列令人沮丧的手术后,Spencer被诊断出患有另一种视野疾病,即同音偏盲,这种疾病可能在婴儿期持续存在,但直到诊断出来,她和她的医生都没有发现。Spencer描述了她是如何在骨科医生的办公室里发现自己每只眼睛只能看到一半的视觉世界的。这一发现导致了Spencer内心深处的矛盾心理,其中包括身体脆弱的感觉,对这种情况被忽视了这么长时间的羞耻感,以及对不必忍受童年时期额外的医学诊断可能带来的耻辱和排斥的宽慰。它还导致了对有限的叙事和理论资源的理论审视,这些叙事和理论来源有助于我们理解这种启示性的经历,以及这种变革性的经历对他人可能产生的令人沮丧的不可解释性。这种亲密的叙述方式使理论民主化。正如Spencer在书的结尾所说,仅限网络内容
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引用次数: 1
Unreliable Threats: Conflicts of Interest Disclosure and the Safeguarding of Biomedical Knowledge 不可靠的威胁:利益冲突披露与生物医学知识的保护
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-03-01 DOI: 10.1353/ken.2022.0004
S. Tresker
ABSTRACT:Medical epistemology lately has seen a strengthening of the view that the construction of evidence should be sensitive to the social context in which it is produced. A poignant illustration of this is the undue influence of the pharmaceutical industry on research results and reporting. I challenge a particular application of this view by examining a common practice in the medical and scientific community: mandatory author disclosure of conflicts of interest (COIs) in published articles. In illustrating problems with COI disclosure policies in biomedical publishing, including unappreciated shortcomings of the scant empirical data supporting mandatory disclosure, I hope to demonstrate that the value given to journal COI disclosure policies as a way to protect the reliability of medical evidence might well be misplaced. Rather than extract away the "messy" details of the real world, the analysis is ultimately more responsive to how medical knowledge is produced and disseminated.
摘要:近年来,医学认识论强化了一种观点,即证据的构建应该对其产生的社会背景敏感。制药行业对研究结果和报告的不当影响就是一个令人心酸的例子。我通过研究医学和科学界的一种常见做法,对这一观点的具体应用提出了质疑:强制作者在发表的文章中披露利益冲突。在阐述生物医学出版中COI披露政策的问题时,包括缺乏支持强制性披露的经验数据的不足,我希望证明期刊COI披露策略作为保护医学证据可靠性的一种方式的价值可能是错误的。该分析最终更能反映医学知识的产生和传播方式,而不是提取现实世界中“混乱”的细节。
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引用次数: 0
Medicalization, Contributory Injustice, and Mad Studies. 医学化、贡献不公正和疯狂研究
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0023
Anne-Marie Gagné-Julien

One recent body of work has concerned medicalization and how it can create epistemic injustice. It focuses on medicalization as a hermeneutical process that shapes the conceptual framework(s) we use to refer to some conditions/experiences. In parallel, some scholars with lived experience of madness have started to explore the epistemic harms suffered by the Mad community. Building on this, I argue that the process of medicalization in psychiatry affects the Mad community in a specific way that has been overlooked in the literature on medicalization and epistemic injustice. That is, medicalization can create what is called "contributory injustice." This form of injustice occurs when marginalized communities have been able to create alternative hermeneutical resources, but these resources are dismissed or discredited by the dominant group. I argue that the emerging field of Mad Studies is a victim of this type of injustice when Mad experiences are unilaterally medicalized.

摘要:最近的一项研究关注的是医学化及其如何造成认知上的不公正。它将医疗化作为一种解释学过程,它塑造了我们用来指代某些条件/经验的概念框架。与此同时,一些有过疯癫经历的学者开始探讨疯癫群体所遭受的认知伤害。在此基础上,我认为精神病学的医学化过程以一种特定的方式影响着疯子群体,而这种方式在关于医学化和认知不公的文献中被忽视了。也就是说,医疗化会造成所谓的“促成性不公正”。这种形式的不公正发生在边缘化群体能够创造替代的解释学资源,但这些资源被主流群体驳回或怀疑的情况下。我认为,当疯狂经历被单方面医学化时,新兴的疯狂研究领域就是这种不公正的受害者。
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引用次数: 0
Editor's Note June 2022. 编者按2022年6月。
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0009
Quill Kukla
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引用次数: 0
Reimagining Commitments to Patients and the Public in Professional Oaths. 重新构想职业誓言对病人和公众的承诺。
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0018
Laura Guidry-Grimes

Robert Veatch argues that physician oaths should not be valued as substantive moral commitments, transformational rituals, or symbolic acts. Further, he insists that oath recitation in medical schools is immoral. I respond to Veatch's criticisms and argue that, with alterations to their content and practice, oaths can have value for articulating moral commitments and building a sense of moral community within the profession. I break down Veatch's multitude of objections to oaths over his career, and I suggest how medical schools can avoid the pitfalls identified by Veatch. A promising and innovative path forward is to integrate a commitment to diversity, equity, and inclusion-though with an understanding that a few lines in an oath are far from sufficient for institutional culture, faculty accountability, or students' education.

罗伯特·韦奇认为,医生的誓言不应被视为实质性的道德承诺、变革仪式或象征性行为。此外,他坚持认为医学院的誓言背诵是不道德的。我对威奇的批评做出了回应,并认为,通过改变誓言的内容和实践,誓言可以在阐明道德承诺和在职业中建立道德共同体意识方面具有价值。我详细分析了韦奇在他的职业生涯中反对宣誓的众多理由,并建议医学院如何避免韦奇指出的陷阱。一条充满希望和创新的前进道路是将对多样性、公平和包容性的承诺整合在一起——尽管要明白,誓言中的几句话远远不足以满足制度文化、教师责任或学生教育的需要。
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引用次数: 0
"White, Fat, and Racist": Racism and Environmental Accounts of Obesity. “白人、肥胖者和种族主义者”:肥胖的种族主义和环境因素
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0024
Megan Dean, Nabina Liebow

This paper offers a novel argument for the claim that "environmental" explanations of obesity meant to help address racial health disparities may actually reinforce racism. While some contend that these explanations reinforce racist and sizeist interracial dynamics, we argue that environmental explanations can bolster intraracial hierarchies of whiteness that reinforce white supremacy. Deployments of environmental accounts in contexts like the U.S. invoke and intertwine two damaging dichotomies: the "good fatty/bad fatty" and the "good white person/bad white person." This supports a cultural system that oppresses people of color and enables thin, white proponents to position themselves as "good white people" against those who deploy racist, moralizing accounts of obesity, and against fat white people, who are implicitly framed as morally inferior. This analysis furthers our understanding of racist and sizeist discourse about fatness and the insidious ways that attempts to address racism can reinforce it.

摘要:有观点认为,肥胖的“环境”解释有助于解决种族健康差异,但实际上可能会加剧种族主义。虽然有些人认为这些解释强化了种族主义和尺寸主义的种族间动态,但我们认为环境解释可以加强种族内部的白人等级制度,从而强化白人至上主义。在美国这样的背景下,环境账户的部署引发并交织了两种破坏性的二分法:“好胖子/坏胖子”和“好白人/坏白人”。这支持了一种压迫有色人种的文化体系,使瘦弱的白人支持者能够将自己定位为“好白人”,而不是那些对肥胖进行种族主义、道德化描述的人,也不是那些被暗中诬陷为道德低下的肥胖白人。这一分析进一步加深了我们对种族主义和体型主义关于肥胖的话语的理解,以及试图解决种族主义的阴险方式可能会强化它。
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引用次数: 0
Suffering in Animal Research: The Need for Limits and the Possibility of Compensation. 动物研究中的痛苦:限制的需要和补偿的可能性。
IF 1.1 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0019
David Wendler

Guidelines and regulations for medical research recognize that the experiences of humans and animals both matter morally. They thus set a presumption against harming research subjects, whether humans or animals, and mandate that the harms subjects experience should be the minimal necessary for achieving the scientific aims of the study. Beyond this, guidelines and regulations place upper limits on the extent to which human, but not animal, subjects may be harmed. They also mandate that human, but not animal, subjects should be compensated for the harms they experience. In this article, I argue that this common approach to regulating medical research is mistaken. In particular, there are upper limits on the extent to which animals may ethically be harmed in order to collect data to benefit others, and there are moral reasons to compensate them for the harms they experience. I conclude that guidelines and regulations for research with animals should be revised accordingly.

医学研究的准则和条例承认,人类和动物的经历在道德上都很重要。因此,他们设定了一个不伤害研究对象(无论是人类还是动物)的假设,并规定受试者所遭受的伤害应该是实现研究科学目标所必需的最低限度。除此之外,指导方针和法规规定了人类(而不是动物)可能受到伤害的程度上限。他们还规定,受试者应该为他们所遭受的伤害获得补偿,而不是动物。在本文中,我认为这种规范医学研究的常见方法是错误的。特别是,为了收集数据以造福他人,动物可能在道德上受到伤害的程度是有上限的,并且有道德上的理由来补偿它们所遭受的伤害。我的结论是,动物研究的指导方针和规定应该相应修改。
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引用次数: 0
Compensation and Limits on Harm in Animal Research. 动物研究中的损害补偿与限制。
IF 1.4 4区 哲学 Q3 ETHICS Pub Date : 2022-01-01 DOI: 10.1353/ken.2022.0020
Jake Earl

Although researchers generally take great care to ensure that human subjects do not suffer very serious harms from their involvement in research, the situation is different for nonhuman animal subjects. Significant progress has been made in reducing unnecessary animal suffering in research, yet researchers still inflict severe pain and distress on tens of thousands of animals every year for scientific purposes. Some bioethicists, scientists, and animal welfare advocates argue for placing an upper limit on the suffering researchers may impose on animal subjects, with rare exceptions for research that promises critical social benefits. In this article, I argue against such an upper limit on harm on the grounds that researchers often can compensate animal subjects for their suffering, even severe and long-lasting suffering. If animal subjects receive adequate compensation for the harms they suffer, then there is no general limit on how much suffering researchers may impose on them for scientific purposes.

虽然研究人员通常会非常小心地确保人类受试者在参与研究时不会受到非常严重的伤害,但对于非人类动物受试者来说,情况就不同了。在减少研究中不必要的动物痛苦方面已经取得了重大进展,然而研究人员为了科学目的,每年仍然对成千上万的动物施加严重的痛苦和痛苦。一些生物伦理学家、科学家和动物福利倡导者主张对研究人员可能施加给动物实验对象的痛苦设定一个上限,除非研究承诺具有关键的社会效益。在这篇文章中,我反对这样的伤害上限,理由是研究人员通常可以补偿动物受试者的痛苦,即使是严重和长期的痛苦。如果动物实验对象受到的伤害得到了足够的补偿,那么研究人员为了科学目的对它们施加多大的痛苦就没有一般的限制。
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引用次数: 1
期刊
Kennedy Institute of Ethics Journal
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