“…Six empirical studies, four qualitative studies and two quantitative studies, also contribute to the demand for developing knowledge about the meanings and implications of autonomy. The two quantitative studies (Välimäki, 1998 ; Vernooij-Dassen, Osse, Schadé, & Grol, 2005 ) may contribute to a general operationalisation of the concept of patient autonomy, emphasising in particular factors such as dependency, loss of control, limitations of activities, and informational support offered by health care professionals on patients’ informed decision making. The four qualitative studies (Dickert & Kass, 2009 ; Ellefsen, 2002 ; Lomborg, Bjørn, Dahl, & Kirkevold, 2005 ; Luoma & Hakamies-Blomqvist, 2004 ), however, point to specific experiences that report patients’ attempts to preserve their dignity by various adaptive manoeuvres and compensatory acts.…”