追踪矛盾心理:在慢性疼痛背景下对数据化的存在主义批判。

IF 2.3 2区 哲学 Q1 ETHICS
Michelle Charette
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引用次数: 0

摘要

近年来,以数据为驱动的慢性疼痛护理方法急剧增加。然而,慢性疼痛患者对数据化的做法感到矛盾。通过对慢性疼痛患者的深入访谈,我对这种矛盾心理进行了讨论和分析。一方面,参与者接受了数据化的承诺,认为数据化可以组织和控制疼痛中的身体。另一方面,他们又对所收集的数据类型提出质疑和批评。这种对疼痛追踪体验的微观分析揭示了数据化与慢性疼痛之间的紧张关系。数据化要求病人传递有关其身体的信息,而这些信息是不明确的。然而,慢性疼痛是模棱两可、充满矛盾的。本文揭示了数据化热衷者与追踪疼痛的慢性疼痛患者之间的情感鸿沟,并指出这种热情可能会导致恶意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tracking ambivalence: an existential critique of datafication in the context of chronic pain.

In recent years, data-driven approaches to chronic pain care have increased dramatically. However, people living with chronic pain are ambivalent about datafication practices. Drawing on in-depth interviews with individuals living with chronic pain, I discuss and analyze this ambivalence. On the one hand, participants imbibe the promissory rhetoric of data as that which may organize and control the body in pain. On the other hand, they dismiss and critique the type of data collected. This micro-level analysis of the pain tracking experience illuminates a tension between datafication and chronic pain. Datafication demands that the patient relay information about their body that is free of ambiguity. However, chronic pain is ambiguous and full of paradox. This article illuminates the emotional chasm between datafication enthusiasts and chronic pain patients who track their pain and suggests that such enthusiasm may lead to bad faith.

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来源期刊
CiteScore
4.30
自引率
4.80%
发文量
64
期刊介绍: Medicine, Health Care and Philosophy: A European Journal is the official journal of the European Society for Philosophy of Medicine and Health Care. It provides a forum for international exchange of research data, theories, reports and opinions in bioethics and philosophy of medicine. The journal promotes interdisciplinary studies, and stimulates philosophical analysis centered on a common object of reflection: health care, the human effort to deal with disease, illness, death as well as health, well-being and life. Particular attention is paid to developing contributions from all European countries, and to making accessible scientific work and reports on the practice of health care ethics, from all nations, cultures and language areas in Europe.
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