Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare by Klaus Hoeyer (review)

IF 0.9 2区 哲学 Q4 HEALTH CARE SCIENCES & SERVICES
Kim Gallon
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Hoeyer uses Denmark as a case study for exploring what he calls “intensified data sourcing,” the stated drive for more data in health care and the lack of consensus on how the data will be utilized. This is the central paradox <strong>[End Page 332]</strong> of data in Denmark’s health care system. Hoeyer makes the case for a hyperlocal analysis of Denmark, beyond the obvious explanation that he is a researcher at the University of Copenhagen, because it has established a sophisticated digital health system that runs on an integrated data infrastructure. However, Hoeyer’s focus on Denmark precludes it from being solely a local study. Indeed, he argues that Denmark’s stated drive to be at the forefront of digital health care reflects the larger value other nations ascribe to data. In what he describes as an “ethno-graphic engagement” and anthropological discourse on data, Hoeyer explores the interconnections among policy, practice, and experience in Denmark’s health care system (p. 27).</p> <p>The book is organized thematically to introduce readers to a series of paradoxes about data that people produce through their belief that it promises new knowledge and the potential to do good. Drawing on interviews with researchers, reports, and strategy papers, Hoeyer argues that promises lie at the heart of the politics of data. These promises produce “data living,” a state of being where people’s well-being and health are inextricably linked to data that stands in as a representative of that person.</p> <p>Some of the most enlightening discussions in the book occur when Hoeyer explores “data work” and illuminates the multifaceted nature of data work in Denmark’s health system and the relatively large number of people who are involved in creating data infrastructure. 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Their relationship with data originates in emotionality and a drive for meaning-making. The paradox of data experiences is that crises like the pandemic produced intensified data sourcing, which is conveyed in broadly distributed data visualizations. However, this data simultaneously engenders and closes off political contestation, depending on one’s data experiences.</p> <p>Hoeyer also explores data wisdom, the ability to produce and apply “robust knowledge” to data to investigate the relationship between data and wise decision-making (p. 151). Those with data wisdom, according to Hoeyer, believe they know when and how to use data in such a way that it reflects one’s ability to acquire more knowledge and make sound decisions. The paradox of this view is that although people readily acknowledge that data is not neutral or objective, they still want more and feel that data creates knowledge that will be useful in the process of <strong>[End Page 333]</strong> making decisions. 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引用次数: 0

Abstract

Reviewed by:

  • Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare by Klaus Hoeyer
  • Kim Gallon
Klaus Hoeyer. Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare. Infrastructures Series. Cambridge, Mass.: MIT Press, 2023. 314 pp Ill. $50.00 (978-0-262-54541-9).

It is virtually impossible to discuss health care in the twenty-first century without referencing data-driven decision-making. This is the basis for the major arguments of Klaus Hoeyer’s book, Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare. Hoeyer uses Denmark as a case study for exploring what he calls “intensified data sourcing,” the stated drive for more data in health care and the lack of consensus on how the data will be utilized. This is the central paradox [End Page 332] of data in Denmark’s health care system. Hoeyer makes the case for a hyperlocal analysis of Denmark, beyond the obvious explanation that he is a researcher at the University of Copenhagen, because it has established a sophisticated digital health system that runs on an integrated data infrastructure. However, Hoeyer’s focus on Denmark precludes it from being solely a local study. Indeed, he argues that Denmark’s stated drive to be at the forefront of digital health care reflects the larger value other nations ascribe to data. In what he describes as an “ethno-graphic engagement” and anthropological discourse on data, Hoeyer explores the interconnections among policy, practice, and experience in Denmark’s health care system (p. 27).

The book is organized thematically to introduce readers to a series of paradoxes about data that people produce through their belief that it promises new knowledge and the potential to do good. Drawing on interviews with researchers, reports, and strategy papers, Hoeyer argues that promises lie at the heart of the politics of data. These promises produce “data living,” a state of being where people’s well-being and health are inextricably linked to data that stands in as a representative of that person.

Some of the most enlightening discussions in the book occur when Hoeyer explores “data work” and illuminates the multifaceted nature of data work in Denmark’s health system and the relatively large number of people who are involved in creating data infrastructure. The paradox in data, Hoeyer persuasively argues, is that data makes less work and more work at the same time.

In a surprising but ultimately useful turn, Hoeyer uses an autoethnographic method to disclose his own data experiences, to disclose broader meaning about how people interact with data infrastructures in their everyday lives. However, these data infrastructures are often invisible to most people. In other words, they do not manifest themselves in people’s lives. Instead, encounters with data are sensory experiences that are mediated through wires, hardware, and software. For Hoeyer, this raises a dematerialization and rematerialization data process that is paradoxical.

Hoeyer also explores the different responses and engagements people have with data and creates a language for discussing what is often unspoken in these relationships with data. According to Hoeyer, people do not simply communicate or interact with data. Their relationship with data originates in emotionality and a drive for meaning-making. The paradox of data experiences is that crises like the pandemic produced intensified data sourcing, which is conveyed in broadly distributed data visualizations. However, this data simultaneously engenders and closes off political contestation, depending on one’s data experiences.

Hoeyer also explores data wisdom, the ability to produce and apply “robust knowledge” to data to investigate the relationship between data and wise decision-making (p. 151). Those with data wisdom, according to Hoeyer, believe they know when and how to use data in such a way that it reflects one’s ability to acquire more knowledge and make sound decisions. The paradox of this view is that although people readily acknowledge that data is not neutral or objective, they still want more and feel that data creates knowledge that will be useful in the process of [End Page 333] making decisions. An important point Hoeyer makes is that people would rather take the risk of having bad data than no data at all. To make...

数据悖论:克劳斯-霍耶尔(Klaus Hoeyer)所著的《当代医疗保健中强化数据源的政治学》(评论
评论者: 数据悖论:Klaus Hoeyer Kim Gallon Klaus Hoeyer 著,《数据悖论:当代医疗保健中强化数据源的政治学》(Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare)。数据悖论:数据悖论:当代医疗保健领域强化数据挖掘的政治学》(Data Paradoxes: The Politics of Intensified Data Sourcing in Contemporary Healthcare)。基础设施丛书。马萨诸塞州剑桥:麻省理工学院出版社,2023 年。314 pp Ill. 50.00 美元 (978-0-262-54541-9)。在讨论 21 世纪的医疗保健时,几乎不可能不提到数据驱动决策。这是克劳斯-霍耶尔(Klaus Hoeyer)的著作《数据悖论》(Data Paradoxes:数据悖论:当代医疗保健中强化数据源的政治学》一书的主要论点。Hoeyer 以丹麦为案例,探讨了他所谓的 "强化数据采购",即在医疗保健领域公开推动更多数据,但对如何利用这些数据却缺乏共识。这就是丹麦医疗保健系统中数据的核心悖论 [尾页 332]。除了他是哥本哈根大学的研究人员这一显而易见的解释外,Hoeyer 还提出了对丹麦进行超本地化分析的理由,因为丹麦已经建立了一个基于综合数据基础设施运行的先进数字医疗系统。然而,Hoeyer 对丹麦的关注并不意味着这仅仅是一项本地研究。事实上,他认为丹麦宣称要走在数字医疗的前沿,这反映了其他国家对数据的重视。在他所描述的 "民族地理参与 "和数据人类学论述中,Hoeyer 探索了丹麦医疗保健系统中政策、实践和经验之间的相互联系(第 27 页)。本书按主题编排,向读者介绍了一系列与数据有关的悖论,人们相信数据会带来新的知识,并有可能带来好的结果。通过对研究人员的访谈、报告和战略文件,霍耶尔认为,承诺是数据政治的核心。这些承诺造就了 "数据生活",在这种生活状态中,人们的福祉和健康与作为个人代表的数据密不可分。书中一些最有启发性的讨论发生在霍耶探讨 "数据工作 "时,他揭示了丹麦卫生系统中数据工作的多面性,以及参与创建数据基础设施的人数相对较多。霍耶尔令人信服地指出,数据的悖论在于,数据在减少工作的同时也增加了工作。令人惊讶但最终有益的是,霍耶尔采用了一种自述式的方法来披露自己的数据经验,从而揭示了人们在日常生活中如何与数据基础设施互动的更广泛意义。然而,大多数人往往看不到这些数据基础设施。换句话说,它们并没有在人们的生活中显现出来。相反,与数据的接触是通过电线、硬件和软件进行中介的感官体验。对霍耶尔来说,这就产生了一种矛盾的非物质化和再物质化数据过程。霍耶尔还探讨了人们对数据的不同反应和参与,并创造了一种语言,用于讨论在这些与数据的关系中通常无法言说的东西。根据霍耶尔的观点,人们并不只是简单地与数据交流或互动。他们与数据的关系源于情感和创造意义的动力。数据体验的悖论在于,像大流行病这样的危机产生了强化的数据来源,并通过广泛传播的数据可视化得到传达。然而,根据个人的数据经验,这些数据同时也会引发和阻止政治争论。Hoeyer 还探讨了数据智慧,即对数据产生和应用 "强大知识 "的能力,以研究数据与明智决策之间的关系(第 151 页)。霍耶尔认为,那些拥有数据智慧的人相信,他们知道何时以及如何使用数据,从而反映出一个人获取更多知识和做出正确决策的能力。这种观点的悖论在于,尽管人们很乐意承认数据不是中立或客观的,但他们仍然想要更多的数据,并认为数据创造的知识在 [End Page 333] 决策过程中是有用的。霍耶尔提出的一个重要观点是,人们宁可冒拥有糟糕数据的风险,也不愿没有数据。为了使...
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来源期刊
Bulletin of the History of Medicine
Bulletin of the History of Medicine 医学-科学史与科学哲学
CiteScore
0.90
自引率
0.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: A leading journal in its field for more than three quarters of a century, the Bulletin spans the social, cultural, and scientific aspects of the history of medicine worldwide. Every issue includes reviews of recent books on medical history. Recurring sections include Digital Humanities & Public History and Pedagogy. Bulletin of the History of Medicine is the official publication of the American Association for the History of Medicine (AAHM) and the Johns Hopkins Institute of the History of Medicine.
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