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  1. Guidelines as governance: Critical reflections from a documentary analysis of guidelines to support user involvement in research.Susanne Stuhlfauth, Ingrid Ruud Knutsen & Ingrid Christina Foss - 2021 - Nursing Inquiry 28 (1):e12378.
    Although guidelines to regulate user involvement in research have been advocated and implemented for several years, literature still describes the process as challenging. In this qualitative study, we take a critical view on guidelines that are developed to regulate and govern the collaboration process of user involvement in research. We adapt a social constructivist view of guidelines and our aim is to explore how guidelines construct the perception of users and researchers and thus the process of involvement. Twenty‐two guidelines published (...)
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  • Health care policy at a crossroads? A discursive study of patient agency in national health quality strategies between 1993 and 2015.Inger Lassen, Aase M. Ottesen & Jeanne Strunck - 2018 - Nursing Inquiry 25 (4):e12252.
    The Danish health care sector currently undergoes changes that imply a gradual transition from an evidence‐based activity model to a value‐based quality model centered on patient involvement and value‐based governance. The patient naturally occupies a central position in health care, and the transition therefore raises important questions about health care quality and how successive national health quality strategies value quality and ascribe roles and agency to patients. To explore the complexity of these quality strategies, we analyze and discuss how political (...)
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  • The reasonable patient – A Swedish discursive construction.Åse Boman, Elisabeth Dahlborg, Henrik Eriksson & Ellinor Tengelin - 2021 - Nursing Inquiry 28 (3):e12401.
    The aim of this study was to analyse how the patient is constructed and socially positioned in Swedish patient information. Corpus‐assisted critical discourse analysis methodology was utilised on a sample of 56 online patient information texts about cancer containing a total of 126,711 words. The findings show an overarching discourse of informed consent guided by specific features to produce a patient norm that we name “the reasonable patient”, who is receptive to arguments, emotionally restrained and makes decisions based on information. (...)
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