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  1. “I don’t need my patients’ opinion to withdraw treatment”: patient preferences at the end-of-life and physician attitudes towards advance directives in England and France.Ruth Horn - 2014 - Medicine, Health Care and Philosophy 17 (3):425-435.
    This paper presents the results of a qualitative interview study exploring English and French physicians’ moral perspectives and attitudes towards end-of-life decisions when patients lack capacity to make decisions for themselves. The paper aims to examine the importance physicians from different contexts accord to patient preferences and to explore the role of advance directives in each context. The interviews focus on problems that emerge when deciding to withdraw/-hold life-sustaining treatment from both conscious and unconscious patients; decision-making procedures and the participation (...)
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  • Barriers in implementing the dying patient law: the Israeli experience - a qualitative study.Avi Zigdon & Rachel Nissanholtz-Gannot - 2020 - BMC Medical Ethics 21 (1):1-11.
    Background Coping with end-of-life issues is a major challenge for governments and health systems. Despite progress in legislation, many barriers exist to its full implementation. This study is aimed at identifying these end-of-life barriers in relation to Israel. Methods Qualitative in-depth interviews using professionals and decision makers in the health-care and related systems were carried out, along with two focus groups based on brainstorming techniques consisting of nurses and social workers. Data was managed and analyzed using Naralyzer software. Results Qualitative (...)
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  • The Concept of Dignity and Its Use in End-of-Life Debates in England and France.Ruth Horn & Angeliki Kerasidou - 2016 - Cambridge Quarterly of Healthcare Ethics 25 (3):404-413.
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  • Solidarity and autonomy: two conflicting values in English and French health care and bioethics debates?Marie Gaille & Ruth Horn - 2016 - Theoretical Medicine and Bioethics 37 (6):441-446.
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