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  1. Encounters with medical professionals: a crisis of trust or matter of respect? [REVIEW]Nina Hallowell - 2008 - Medicine, Health Care and Philosophy 11 (4):427-437.
    In this paper I shed light on the connection between respect, trust and patients’ satisfaction with their medical care. Using data collected in interviews with 49 women who had managed, or were in the process of managing, their risk of ovarian cancer using prophylactic surgery or ovarian screening, I examine their reported dissatisfaction with medical encounters. I argue that although many study participants appeared to mistrust their healthcare professionals’ (HCPs) motives or knowledge base, their dissatisfaction arose not from a lack (...)
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  • (1 other version)Genetic technology: A threat to deafness. [REVIEW]Ruth Chadwick & Mairi Levitt - 1998 - Medicine, Health Care and Philosophy 1 (3):209-215.
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  • (1 other version)Genetic technology: A threat to deafness.Ruth Chadwick & Mairi Levitt - 1998 - Medicine, Health Care and Philosophy 1 (3):209-215.
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  • Children as means and ends in large-scale medical research.Garrath Williams - 2011 - Bioethics 26 (8):422-430.
    This paper considers the often-expressed fear that medical research may use children merely as means, and not respect them as ends in themselves – especially insofar as they are deemed less able to consent than adults. The main focus is on large-scale genetic, socio-medical and epidemiological research. The theoretical starting point of the paper is that to be treated as an end in oneself is to be regarded as – and to act as – a participant in cooperative endeavours. This (...)
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  • Public attitudes to participating in UK BioBank: A DNA bank, lifestyle and morbidity database on 500,000 members of the UK public aged 45–69. [REVIEW]Darren Shickle, Rhydian Hapgood, Jane Carlisle, Phil Shackley, Ann Morgan & Chris McCabe - 2003 - In Bartha Maria Knoppers (ed.), Populations and genetics: legal and socio-ethical perspectives. Boston: Martinus Nijhoff.
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  • A well placed trust? Public perceptions of the governance of DNA databases.Mairi Levitt & Sue Weldon - 2005 - .
    Biobanks that are run on an opt-in basis depend on people having the motivation to give and to trust in those who control their samples. Yet in the UK trust in the healthcare system has been in decline and there have been a number of health-related scandals that have received widespread media and public attention. Given this background, and the previous public consultations on UK Biobank, the paper explores the way people express their trust and mistrust in the area of (...)
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