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《长期抗争:慢性疼痛与边缘化的制度民族志》

Chronic Struggle: An Institutional Ethnography of Chronic Pain and Marginalization.

作者信息

Webster Fiona, Connoy Laura, Sud Abhimanyu, Rice Kathleen, Katz Joel, Pinto Andrew D, Upshur Ross, Dale Craig

机构信息

Arthur Labatt School of Nursing, Faculty of Health Sciences, Western University, London, Ontario, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Arthur Labatt School of Nursing, Faculty of Health Sciences, Western University, London, Ontario, Canada.

出版信息

J Pain. 2023 Mar;24(3):437-448. doi: 10.1016/j.jpain.2022.10.004. Epub 2022 Oct 14.

Abstract

There have been several recent calls to re-think chronic pain in response to the growing awareness of social inequities that impact the prevalence of chronic pain and its management. This in turn has resulted in new explorations of suffering as it relates to pain. While laudable, many of these clinically oriented accounts are abstract and often fail to offer a critical theoretical understanding of social and structural inequities. To truly rethink pain, we must also reconsider suffering, beginning in the everyday expert knowledge of people with chronic pain who can offer insights in relation to their bodies and also the organization of the social circumstances in which they live. Our team undertook a sociological approach known as institutional ethnography (IE) to explicate the work of people in managing lives beset by chronic pain and the inequities that stem from marginalization. In keeping with our critical paradigm, we describe participant accounts as situated, rather than lived, to de-emphasize the individual in favour of the social and relational. Through our analysis, we offer a new concept of chronic struggle to capture how pain, illness, economic deprivation, and suffering constitute a knot of experience that people living with chronic pain are obliged to simplify in order to fit existing logics of medicine. Our goal is to identify the social organization of chronic pain care which underpins experience in order to situate the social as political rather than medical or individual. PERSPECTIVE: This article explicates the health work of people living with chronic pain and marginalization, drawing on their situated experience. We offer the concept of chronic struggle as a conceptualization that allows us to bring into clear view the social organization of chronic pain in which the social is visible as political and structural rather than medical or individual.

摘要

最近,随着人们越来越意识到社会不平等现象对慢性疼痛的患病率及其管理产生影响,有几次呼吁重新思考慢性疼痛问题。这反过来又引发了对与疼痛相关的痛苦的新探索。虽然这些努力值得称赞,但许多以临床为导向的描述都很抽象,往往未能对社会和结构不平等提供批判性的理论理解。要真正重新思考疼痛,我们还必须重新审视痛苦,从慢性疼痛患者的日常专业知识入手,他们能够提供有关自身身体以及他们所生活的社会环境组织的见解。我们的团队采用了一种名为制度民族志(IE)的社会学方法,以阐明人们在管理受慢性疼痛困扰的生活以及因边缘化而产生的不平等方面所做的工作。按照我们的批判范式,我们将参与者的描述视为情境化的,而非生活经历的,以淡化个体因素,强调社会和关系因素。通过我们的分析,我们提出了一个新的“慢性斗争”概念,以捕捉疼痛、疾病、经济匮乏和痛苦如何构成一种经验的纠结,慢性疼痛患者不得不对其进行简化,以适应现有的医学逻辑。我们的目标是确定慢性疼痛护理的社会组织,它支撑着这种经验,以便将社会因素定位为政治因素,而非医学或个体因素。观点:本文借鉴慢性疼痛患者和边缘化人群的情境化经验,阐述了他们的健康工作。我们提出“慢性斗争”这一概念,以便能够清晰地展现慢性疼痛的社会组织,在其中社会因素表现为政治和结构因素,而非医学或个体因素。

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