Data driven or data informed? How general practitioners use data to evaluate their own and colleagues’ clinical work in clusters

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

In contemporary policy discourses, data are presented as key assets for improving health-care quality: policymakers want health care to become ‘data driven’. In this article, we focus on a particular example of this ambition, namely a new Danish national quality development program for general practitioners (GPs) where doctors are placed in so-called ‘clusters’. In these clusters, GPs are obliged to assess their own and colleagues’ clinical quality with data derived from their own clinics—using comparisons, averages and benchmarks. Based on semi-structured interviews with Danish GPs and drawing on Science and Technology Studies, we explore how GPs understand these data, and what makes them trust—or question—a data analysis. The GPs describe how they change clinical practices based on these discussions of data. So, when and how do data for quality assurance come to influence their perceptions of quality? By exploring these issues, we carve out a role for a sociological engagement with evidence in everyday medical practices. In conclusion, we suggest a need to move from the aim of being data driven to one of being data informed.
TidsskriftSociology of Health and Illness
Antal sider18
StatusAccepteret/In press - 2024

Bibliografisk note

Funding Information:
We would like to thank the GPs taking their time to share their thoughts and experiences and to exhibiting trust in us. We thank Sara Green for valuable discussions about the concept of relational data. Earlier versions of this article has also benefitted from constructive comments from two anonymous reviewers. This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (Grant Agreement Number 682110).

Publisher Copyright:
© 2023 The Authors. Sociology of Health & Illness published by John Wiley & Sons Ltd on behalf of Foundation for the Sociology of Health & Illness.

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