Towards collaborative tinkering in contraceptive consultations: Negotiating side-effects in contraceptive care.

IF 1.9 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Health Pub Date : 2025-02-18 DOI:10.1177/13634593251319920
Ellen Algera
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引用次数: 0

Abstract

Patients' online information-seeking and sharing has sparked worries about medical misinformation and declining trust in biomedical professionals. At the same time, scholars advocate for including patients as knowers in the clinical encounter. Yet we lack empirical insights into the differing ways care providers and patients substantiate health-related knowledge. This article thus examines (1) how both groups substantiate claims about contraceptive side-effects, (2) the ways their substantiation processes differ and (3) how we can navigate this epistemic tension in contraceptive care. I draw on data from nine interviews with Dutch contraceptive care providers (one nurse practitioner, one gynaecologist and seven general practitioners) and 17 contraceptive users, observations of 11 contraceptive consultations in the Netherlands and analysis of Dutch clinical guidelines. Results reveal that patients substantiate their claims through combining embodied modes of knowing with self-experimentation as well as validation through social media exchanges. Care providers switch between two complementary approaches: demarcating biomedical knowledge from non-scientific claims and clinical tinkering. I show that epistemic tensions between provider and patient may arise because the two groups have differing definitions of what a side-effect is and differing evaluations of information shared online. Based on these findings, I argue that care providers invalidating information shared online may contribute to patients' growing distrust in biomedical authority while collaborative tinkering may provide a common ground for care providers and patients to co-create knowledge.

在避孕咨询中走向协作修补:协商避孕护理中的副作用。
患者在网上寻找和分享信息引发了对医疗错误信息和对生物医学专业人员信任度下降的担忧。同时,学者们主张将患者作为知者纳入临床相遇。然而,我们缺乏对护理提供者和患者证实健康相关知识的不同方式的经验见解。因此,本文探讨(1)两组如何证实关于避孕副作用的主张,(2)他们的证实过程不同的方式,以及(3)我们如何在避孕护理中导航这种认知紧张。我利用了对荷兰避孕护理提供者(一名执业护士、一名妇科医生和七名全科医生)和17名避孕药具使用者的9次访谈的数据,对荷兰11次避孕咨询的观察和对荷兰临床指南的分析。结果表明,患者通过将认知的具身模式与自我实验相结合以及通过社交媒体交流进行验证来证实其主张。医疗服务提供者在两种互补的方法之间切换:区分生物医学知识与非科学主张和临床修补。我表明,提供者和患者之间的认知紧张可能会出现,因为这两个群体对副作用有不同的定义,对在线共享的信息有不同的评估。基于这些发现,我认为护理提供者使在线共享的信息无效可能会导致患者对生物医学权威的不信任,而协作修补可能为护理提供者和患者共同创造知识提供共同基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health
Health Multiple-
CiteScore
4.90
自引率
0.00%
发文量
0
期刊介绍: Health: is published four times per year and attempts in each number to offer a mix of articles that inform or that provoke debate. The readership of the journal is wide and drawn from different disciplines and from workers both inside and outside the health care professions. Widely abstracted, Health: ensures authors an extensive and informed readership for their work. It also seeks to offer authors as short a delay as possible between submission and publication. Most articles are reviewed within 4-6 weeks of submission and those accepted are published within a year of that decision.
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