Evidence map›Paper›PMID 40359340›Full record

ArticleSociology of health & illness2025

Health-Related Stigma: The Affordances of Electronic Health Management Systems in the Production of Structural Stigma.

Emily Lenton, Kate Seear, Adrian Farrugia, Chris Lemoh, Elena Cama, Gemma Nourse, Carla Treloar

Abstract read
In one paragraph

Article in Sociology of health & illness, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Emily LentonAustralian Research Centre in Sex, Health and Society, La Trobe University, Bundoora, Australia.ORCID 0000-0002-4465-2604
Kate SeearAustralian Research Centre in Sex, Health and Society, La Trobe University, Bundoora, Australia.ORCID 0000-0002-0886-7069
Adrian FarrugiaAustralian Research Centre in Sex, Health and Society, La Trobe University, Bundoora, Australia.ORCID 0000-0003-3751-9060
Chris LemohWestern Health, Footscray, Australia.ORCID 0000-0002-8383-9471
Elena CamaCentre for Social Policy Research, University of New South Wales, Social Policy Research Centre, UNSW Sydney, Sydney, Australia.ORCID 0000-0002-3080-2472
Gemma NourseAustralian Research Centre in Sex, Health and Society, La Trobe University, Bundoora, Australia.ORCID 0000-0003-0678-2122
Carla TreloarCentre for Social Policy Research, University of New South Wales, Social Policy Research Centre, UNSW Sydney, Sydney, Australia.ORCID 0000-0002-8230-0386

Funding

Australian Commonwealth Department of Health 4-H1NUV9Z
6 · The paper itself

Abstract

Encounters with stigma in healthcare settings are well-documented. In recent years, significant attention has begun to be paid to how we can reduce these stigmas, including through the identification and reformation of structural forces that shape and sustain them. This article analyses 30 interviews conducted with clinical and nonclinical healthcare workers, as part of a larger project that aims to reduce health-related stigma for all. A major theme running through the interviews was the constitutive role of medical records in the production of stigma. Interview participants expressed several concerns about the ways such records can produce and reproduce stigma associated with numerous health conditions, identities, and practices. We examine how the very process of producing medical records can be implicated in stigma. We ask, how do systems shape data production, reproduction, access and dissemination? To what extent might processes and systems help to generate, maintain or exacerbate stigma through the demands of medical record keeping, and are reforms needed at these levels too? In addressing these questions, we work with Latour's notion of affordances to examine medical records as a technology that can reflect and reproduce social and political arrangements, including stigma. We argue that institutions and structures responsible for the governance of these systems need to contend with the important entanglements between medical record systems and stigma. We conclude with recommendations for how policymakers, health service leaders and researchers might intervene in the production of stigma afforded by these forms of communication.

Indexed as

Attitude of Health PersonnelElectronic Health RecordsHealth PersonnelSocial StigmaFemaleHumansInterviews as TopicMaleQualitative Researchmedical recordsquality carestigma

Identifiers

PMID40359340
PMCPMC12074563

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.