Questioning ‘Informed Choice’ in Medical Screening: The Role of Neoliberal Rhetoric, Culture, and Social Context

Author:

Gram Emma12ORCID,Jønsson Alexandra134,Brodersen John124ORCID,Damhus Christina1

Affiliation:

1. Center of General Practice, Department of Public Health, University of Copenhagen, 1353 Copenhagen, Denmark

2. Primary Health Care Research Unit, 4100 Region Zealand, Denmark

3. Department of People and Technology, Roskilde University, 4000 Roskilde, Denmark

4. The Research Unit for General Practice, Department of Social Medicine, University of Tromsø, 9019 Tromsø, Norway

Abstract

Participation in medical screening programs is presented as a voluntary decision that should be based on an informed choice. An informed choice is often emphasized to rely on three assumptions: (1) the decision-maker has available information about the benefits and harms, (2) the decision-maker can understand and interpret this information, and (3) the decision-maker can relate this information to personal values and preferences. In this article, we empirically challenge the concept of informed choice in the context of medical screening. We use document analysis to analyze and build upon findings and interpretations from previously published articles on participation in screening. We find that citizens do not receive neutral or balanced information about benefits and harms, yet are exposed to manipulative framing effects. The citizens have high expectations about the benefits of screening, and therefore experience cognitive strains when informed about the harm. We demonstrate that decisions about screening participation are informed by neoliberal arguments of personal responsibility and cultural healthism, and thus cannot be regarded as decisions based on individual values and preferences independently of context. We argue that the concept of informed choice serves as a power technology for people to govern themselves and can be considered an implicit verification of biopower.

Publisher

MDPI AG

Subject

Health Information Management,Health Informatics,Health Policy,Leadership and Management

Reference75 articles.

1. Det Etiske Råd (1999). Screening—En Redegørelse, Det Etiske Råd.

2. Raffle, A.E., and Gray, J.A.M. (2007). Screening: Evidence and Practice, Oxford University Press.

3. Danish Health Authority (2021, January 27). National Screening Programme. Available online: https://sst.dk/en/English/Responsibilities-and-tasks/Health-promotion/National-screening-programme.

4. Sundhedsstyrelsen (2022, December 15). Anbefalinger Vedrørende Nationale Screeningsprogrammer (Recommendations on National Screening Programmes). Available online: https://www.sst.dk/da/udgivelser/2014//-/media/Udgivelser/2014/Rapport_Sundhedsstyrelsens-anbefalinger-vedr-nationale-screeningsprogrammer.ashx.

5. The Danish Government (2022, November 26). The Danish Health Act 2022, Available online: https://www.retsinformation.dk/eli/lta/2019/903.

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