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Raymond Fitzpatrick [11]Ray Fitzpatrick [11]
  1. Jill Rutter, Raymond Fitzpatrick & Paul Rutter (2015). What Effect Does Medicine Advice Provided by UK Medicines Information Pharmacists Have on Prescriber Practice and Patient Care: A Qualitative Primary Care Study. Journal of Evaluation in Clinical Practice 21 (2):307-312.
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  2. Jantina de Vries, Thomas N. Williams, Kalifa Bojang, Dominic P. Kwiatkowski, Raymond Fitzpatrick & Michael Parker (2014). Knowing Who to Trust: Exploring the Role of 'Ethical Metadata' in Mediating Risk of Harm in Collaborative Genomics Research in Africa. BMC Medical Ethics 15 (1):62.
    The practice of making datasets publicly available for use by the wider scientific community has become firmly integrated in genomic science. One significant gap in literature around data sharing concerns how it impacts on scientists’ ability to preserve values and ethical standards that form an essential component of scientific collaborations. We conducted a qualitative sociological study examining the potential for harm to ethnic groups, and implications of such ethical concerns for data sharing. We focused our empirical work on the MalariaGEN (...)
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  3. Vicki Marsh, Francis Kombe, Raymond Fitzpatrick, Thomas N. Williams, Michael Parker & Sassy Molyneux (2013). Consulting Communities on Feedback of Genetic Findings in International Health Research: Sharing Sickle Cell Disease and Carrier Information in Coastal Kenya. [REVIEW] BMC Medical Ethics 14 (1):41.
    International health research in malaria-endemic settings may include screening for sickle cell disease, given the relationship between this important genetic condition and resistance to malaria, generating questions about whether and how findings should be disclosed. The literature on disclosing genetic findings in the context of research highlights the role of community consultation in understanding and balancing ethically important issues from participants’ perspectives, including social forms of benefit and harm, and the influence of access to care. To inform research practice locally, (...)
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  4. Geoffrey Lairumbi, Michael Parker, Raymond Fitzpatrick & Michael English (2012). Forms of Benefit Sharing in Global Health Research Undertaken in Resource Poor Settings: A Qualitative Study of Stakeholders' Views in Kenya. Philosophy, Ethics, and Humanities in Medicine 7 (1):1-8.
    BackgroundIncrease in global health research undertaken in resource poor settings in the last decade though a positive development has raised ethical concerns relating to potential for exploitation. Some of the suggested strategies to address these concerns include calls for providing universal standards of care, reasonable availability of proven interventions and more recently, promoting the overall social value of research especially in clinical research. Promoting the social value of research has been closely associated with providing fair benefits to various stakeholders involved (...)
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  5. Tony Hope, Jacinta Tan, Anne Stewart & Ray Fitzpatrick (2011). Anorexia Nervosa and the Language of Authenticity. Hastings Center Report 41 (6):19-29.
    It feels like there’s two of you inside—like there’s another half of you, which is my anorexia, and then there’s the real K [own name], the real me, the logic part of me, and it’s a constant battle between the two. The anorexia almost does become part of you, and so in order to get it out of you I think you do have to kind of hurt you in the process. I think it’s almost inevitable. We came to the (...)
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  6. Geoffrey M. Lairumbi, Parker Michael, Raymond Fitzpatrick & Michael C. English (2011). Ethics in Practice: The State of the Debate on Promoting the Social Value of Global Health Research in Resource Poor Settings Particularly Africa. BMC Medical Ethics 12 (1):22.
    BackgroundPromoting the social value of global health research undertaken in resource poor settings has become a key concern in global research ethics. The consideration for benefit sharing, which concerns the elucidation of what if anything, is owed to participants, their communities and host nations that take part in such research, and the obligations of researchers involved, is one of the main strategies used for promoting social value of research. In the last decade however, there has been intense debate within academic (...)
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  7. Geoffrey M. Lairumbi, Michael Parker, Raymond Fitzpatrick & Michael C. English, Ethics in Practice: The State of the Debate on Promoting the Social Value of Global Health Research in Resource Poor Settings Particularly Africa.
    Background: Promoting the social value of global health research undertaken in resource poor settings has become a key concern in global research ethics. The consideration for benefit sharing, which concerns the elucidation of what if anything, is owed to participants, their communities and host nations that take part in such research, and the obligations of researchers involved, is one of the main strategies used for promoting social value of research. In the last decade however, there has been intense debate within (...)
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  8. Geoffrey M. Lairumbi, Michael Parker, Raymond Fitzpatrick & Mike C. English, Stakeholders Understanding of the Concept of Benefit Sharing in Health Research in Kenya: A Qualitative Study.
    Background: The concept of benefit sharing to enhance the social value of global health research in resource poor settings is now a key strategy for addressing moral issues of relevance to individuals, communities and host countries in resource poor settings when they participate in international collaborative health research. The influence of benefit sharing framework on the conduct of collaborative health research is for instance evidenced by the number of publications and research ethics guidelines that require prior engagement between stakeholders to (...)
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  9. Geoffrey M. Lairumbi, Michael Parker, Raymond Fitzpatrick & English C. Mike (2011). Stakeholders Understanding of the Concept of Benefit Sharing in Health Research in Kenya: A Qualitative Study. BMC Medical Ethics 12 (1):20.
    BackgroundThe concept of benefit sharing to enhance the social value of global health research in resource poor settings is now a key strategy for addressing moral issues of relevance to individuals, communities and host countries in resource poor settings when they participate in international collaborative health research.The influence of benefit sharing framework on the conduct of collaborative health research is for instance evidenced by the number of publications and research ethics guidelines that require prior engagement between stakeholders to determine the (...)
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  10. Jacinta Tan, Anne Stewart, Ray Fitzpatrick & R. A. Hope (2007). Competence to Make Treatment Decisions in Anorexia Nervosa: Thinking Processes and Values. Philosophy, Psychiatry, and Psychology 13 (4):267-282.
  11. Jacinta Tan, Anne Stewart, Ray Fitzpatrick & R. A. Hope (2007). Studying Penguins to Understand Birds. Philosophy, Psychiatry, and Psychology 13 (4):299-301.
  12. Susan Marshall, Kirstie Haywood & Ray Fitzpatrick (2006). Impact of Patient‐Reported Outcome Measures on Routine Practice: A Structured Review. Journal of Evaluation in Clinical Practice 12 (5):559-568.
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  13. Jacinta Oa Tan, Tony Hope, Anne Stewart & Raymond Fitzpatrick (2006). Competence to Make Treatment Decisions in Anorexia Nervosa: Thinking Processes and Values. Philosophy, Psychiatry, and Psychology: Ppp 13 (4):267.
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  14. Kirstie L. Haywood, Andrew M. Garratt & Raymond Fitzpatrick (2005). Older People Specific Health Status and Quality of Life: A Structured Review of Self‐Assessed Instruments. Journal of Evaluation in Clinical Practice 11 (4):315-327.
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  15. Ray Fitzpatrick, Josephine M. Norquist, Barnaby C. Reeves, Richard W. Morris, David W. Murray & Paul J. Gregg (2004). Equity and Need When Waiting for Total Hip Replacement Surgery. Journal of Evaluation in Clinical Practice 10 (1):3-9.
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  16. Mary Dixon‐Woods, Ray Fitzpatrick & Karen Roberts (2001). Including Qualitative Research in Systematic Reviews: Opportunities and Problems. Journal of Evaluation in Clinical Practice 7 (2):125-133.
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  17. Ray Fitzpatrick (1999). Principles and Problems in the Assessment of Quality of Life in Health Care. Ethical Theory and Moral Practice 2 (1):37-46.
    A remarkable surge in efforts to assess the quality of life of patients has occurred in recent years in medical research. Philosophical discussions of these developments have focused, on the one hand, on epistemological reservations about the plausibility of measuring quality of life and, on the other hand, on moral and ethical qualms about the meaning of life conveyed in such assessments. Whilst providing an important note of caution, such critiques fail to recognise two basic principles of quality of life (...)
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  18. Mary Boulton, Ray Fitzpatrick & Clare Swinburn (1996). Qualitative Research in Health Care: II. A Structured Review and Evaluation of Studies. Journal of Evaluation in Clinical Practice 2 (3):171-179.
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  19. Ray Fitzpatrick (1996). A Pragmatic Defence of Health Status Measures. Health Care Analysis 4 (4):265-272.
    A family of instruments has been developed over the last twenty five years in order to measure the individual's subjective view of his health. The instruments vary in how broadly they define health. A wide range of critiques have challenged both the validity of these measures and their uses. This paper argues that disproportionate attention has been given to one form of health status measure—the so-called utility-based measures. The ensuing controversies have distracted from the substantial progress achieved in the application (...)
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  20. Ray Fitzpatrick & Mary Boulton (1996). Qualitative Research in Health Care: I. The Scope and Validity of Methods. Journal of Evaluation in Clinical Practice 2 (2):123-130.
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  21. Rhona Panton & Raymond Fitzpatrick (1996). The Involvement of Pharmacists in Professional and Clinical Audit in the UK: A Review and Assessment of Their Potential Role. Journal of Evaluation in Clinical Practice 2 (3):193-198.
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  22. Charlotte Turner, Peter Anderson, Ray Fitzpatrick, Godfrey Fowler & Richard Mayon-White (1988). Sexual Behaviour, Contraceptive Practice and Knowledge of AIDS of Oxford University Students. Journal of Biosocial Science 20 (4):445-451.
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