Relevant bibliographies by topics / Medical ethics – Great Britain

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Medical ethics – Great Britain'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Medical ethics – Great Britain"

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Logarajah, Sri, and Sue Roff. "Structured learning for clinical ethics in anaesthesia." Clinical Ethics 11, no. 4 (August 19, 2016): 200–209. http://dx.doi.org/10.1177/1477750916660831.

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The ‘SLICE’ model for Structured Learning in Clinical Ethics provides a template to help medical professionals identify their own “moral compass” to provide guidance in complex ethical areas. The model has five domains – Conscience, Compliance, Concurrence, Conversation and Conversion. The use of ‘SLICE’ model as a tool for ethics education has been described in various undergraduate and postgraduate settings. These include teaching ethical aspects of transplantation; legislation for undergraduates and consent in paediatric anaesthesia. Its use as tool for teaching reflective ethical practice has been recently described demonstrating the potential of the SLICE model for supporting appraisal and professional development. In this article, we explore the suitability of the SLICE model to provide a general framework encompassing all the requirements for Ethical Clinical practice in anaesthesia. Good Medical Practice guidance produced by the General Medical Council and guidance provided jointly by the Royal College of Anaesthetists and Association of Anaesthetists of Great Britain and Ireland is used as the foundation for developing this framework. The Good Practice Guide for anaesthetic departments provides a solid ethical frame work for interpreting and applying Good Medical Practice guidance by the General Medical Council. Tools such as the SLICE model complement the guides produced by the professional organisations by providing a choice of different methods to facilitate education, decision making and reflective practice.
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Schulkin, Jay. "Hormone Therapy, Dilemmas, Medical Decisions." Journal of Law, Medicine & Ethics 36, no. 1 (2008): 73–88. http://dx.doi.org/10.1111/j.1748-720x.2008.00239.x.

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The question of why women, in consultation with their physicians, should choose hormone therapy (HT) in response to menopause represents a renewed controversy at the beginning of the new century. Conflicting messages regarding the health risks and benefits of HT have been conveyed in the mainstream media, especially information in the media regarding the results of large-scale studies of the health impact of hormone therapy. Women who have been on one or another of the hormone replacement regimes have been forced to reconsider continuing on HT. Doctors who suggest these hormones to their patients are somewhat confused, as are perimenopausal women who are considering HT. Pharmaceutical companies that produce these compounds are worried, and public health officials are on the defensive.Media coverage of HT research has been extensive. In particular, two large-scale studies, one here in the U.S. (the Women's Health Initiative, or WHI) and the other in Great Britain, have recently cast a negative light on the use of hormone therapy, after years of routine prescription of HT for menopausal women.
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Petrashko, L. P., and O. V. Martyniuk. "Ethical compass for medical solutions in the COVID-19 pandemic." Ukrainian Society 77, no. 2 (July 15, 2021): 9–25. http://dx.doi.org/10.15407/socium2021.02.009.

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The article actualizes and structures significant problems of the medical sphere that arise in the context of the COVID-19 pandemic, in terms of the relations vectors: global world – state – person, state – clinic – society, clinic – doctor (medical staff), clinic – patient, doctor (medical staff) – the patient. The authors presented the evolutionary context of the norming process of medical resources and emphasized the hierarchical scheme of the regulation process of scarce resources norming in the health care system under the pandemic crisis conditions. The paper substantiates approaches to making medical decisions on “sorting” and applying a number of its forms depending on various regional, national, religious, and local models of the ethical values system formation. Emphasis is placed on American and European models of bioethics. The authors consider the utilitarian approach to preparing medical solutions of “clinical sorting” to level ethical catastrophes in a pandemic based on Catholic ethics. The issues of regulated norming of scarce medical resources and the “clinical triage” of patients during the COVID-19 pandemic in Ukraine have been investigated. The main bioethical dilemma of the COVID-19 pandemic is outlined. The authors actualize criteria and models of ethical medical solutions for equitable allocation of scarce medical resources in the context of the COVID-19 pandemic. These criteria and models are defined in the Ethical Guidelines for Responding to COVID-19 of the Bioethics Committee at the Council of Europe, the US Department of Health and Human Services; in normative documents in the field of ethics of medical decisions during the COVID-19 pandemic of the National Medical Associations, chambers, centres of bioethics of Italy, Hungary, USA, Great Britain; in the guidelines of national, religious and local institutions for the preparation of medical decisions for the levelling ethical catastrophes during the pandemic and the studies of international bioethics experts. The paper identified the need to formalize the fair distribution of scarce resources during the COVID-19 pandemic in Ukraine. The authors suggested recommendations for the implementation of ethical values and priorities for their application in critical conditions of shortage of medical resources and personnel in the COVID-19 pandemic in the health care system of Ukraine.
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Price, David P. T. "Contemporary Transplantation Initiatives: Where's the Harm in Them?" Journal of Law, Medicine & Ethics 24, no. 2 (1996): 139–49. http://dx.doi.org/10.1111/j.1748-720x.1996.tb01846.x.

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Two contemporary strategies in cadaver organ transplantation, both with the potential to affect significantly expanding organ transplant waiting list sizes, have evolved: elective ventilation (EV) and use of nonheart-beating donors (NHBDs). Both are undergoing a period of critical review. It is not clear how widely EV is practiced around the world. In Great Britain, the Royal Devon and Exeter Hospital was the first hospital to develop an EV protocol (the Exeter Protocol), in 1988, after which other British hospitals followed suit. In the 1980s, new NHBD protocols of two distinct types were implemented worldwide, although both rely on death confirmed by traditional cardiopulmonary criteria. The first type involves the removal of organs immediately after death, the preeminent example being the University of Pittsburgh Medical Center Protocol (the Pittsburgh Protocol). The second involves the perfusion and cooling of kidneys immediately following death and subsequent organ removal. Protocols of this type have sprung up in Holland, Great Britain (for example, at Leicester General Hospital), Italy, France, Spain, Japan, and the United States (for example, the Regional Organ Bank of Illinois).
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Gupta, Suresh. "Ethical and legal issues in aesthetic surgery." Indian Journal of Plastic Surgery 45, no. 03 (September 2012): 547–49. http://dx.doi.org/10.4103/0970-0358.105973.

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ABSTRACTRapid growth and expansion of plastic surgery in general and aesthetic surgery in particular in the past decade has brought in its wake some confusions particularly raising questions for the surgeons conduct towards his colleagues and the patients in the light of ethical requirements. Some thoughts from eminent thinkers form a backdrop to consideration of theories of medical ethics. In this article raging and continuous debates on these subjects have been avoided to maintain the momentum. Apart from the western thoughts, directions from our old scriptures on ethical conduct have been included to accommodate prevelant Indian practices. The confusion created by specialists advertising their abilities directly to the lay public following removal of ethical bars by the American Courts as also latitudes allowed by the General Medical Council of Great Britain have been discussed. The medical fraternity however has its reservations. Unnecessary skirmishes with the law arose in cosmetic surgery from the freedom exercised by the police to file criminal proceedings against attending doctors in the event of a patient′s death with or without any evidence of wrong doing. This has now been curtailed in the judgement of the Supreme Court of India[1] where norms have been laid down for such prosecution. This has helped doctors to function without fear of harassment. An effort has been made to state a simple day-to-day routine for an ethical doctor-patient relationship.
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Balls, Michael. "Chimpanzee Medical Experiments: Moral, Legal and Scientific Concerns." Alternatives to Laboratory Animals 23, no. 5 (September 1995): 607–14. http://dx.doi.org/10.1177/026119299502300510.

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FRAME'S role in drawing attention to the special scientific and ethical concerns raised by the use of non-human primates as laboratory animals is reviewed, with special emphasis on the FRAME/CRAE proposals to the British Government (1987) and the RSPCA/FRAME survey of research on non-human primates conducted in Great Britain between 1984 and 1988. Attention is then focused on the moral case and the scientific case against using chimpanzees as laboratory animals, with particular emphasis on research on AIDS. Finally, a call is made for universal agreement that no more laboratory experiments should ever be performed on chimpanzees.
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Schmidt, Ulf. "Creating a ‘FatherConfessor’: the origins of research ethics committees in UK military medical research, 1950–1970. Part II, origins and organisation." Journal of the Royal Army Medical Corps 165, no. 4 (June 4, 2019): 291–97. http://dx.doi.org/10.1136/jramc-2019-001207.

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Using a major ethics crisis as a methodological approach to study secret science environments, part II examines the origins and organisation of the Applied Biology Committee (ABC), the first independent research ethics committee (REC) at Porton Down, Britain’s biological and chemical warfare establishment since the First World War. Although working in great secrecy, the UK military, and Porton in particular, did not operate in a social, political and legal vacuum. Paradigm shifts in civilian medical ethics, or public controversy about atomic, chemical and biological weapons, could thus influence Porton’s self-perception and the conduct of its research. The paper argues that the creation of the first REC at Porton in 1965, that is, the ABC, as the ‘fatherconfessor’ inside the UK’s military research establishment reflected a broader paradigm shift in the field of human research ethics in the mid-1960s.
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Norfolk, J. C. Gallagher, and I. M. Jessiman. "Submission to the Committee on the Ethics of Gene Therapy by the Joint Ethico-Medical Committee of the Catholic Union of Great Britain and the Guild of Catholic Doctors." Linacre Quarterly 57, no. 4 (November 1990): 14–18. http://dx.doi.org/10.1080/00243639.1990.11878077.

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Hampson, Judith, Jacqueline Southee, David Howell, and Michael Balls. "An RSPCA/FRAME Survey of the Use of Non-human Primates as Laboratory Animals in Great Britain, 1984–1988." Alternatives to Laboratory Animals 17, no. 4 (June 1990): 335–99. http://dx.doi.org/10.1177/026119299001700407.

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A literature-based survey of the use of non-human primates as laboratory animals in Great Britain in 1984–1988 was carried out as a background to extending debate about the ethical and practical issues involved. The 289 publications considered were grouped in 15 subject areas and reviewed in terms of scientific purpose, methods employed, numbers and species of animals used, and their source, care and ultimate fate. In addition, the Association of the British Pharmaceutical Industry provided a comment on the use of non-human primates by pharmaceutical companies. Specific causes for concern were identified, and future prospects considered.
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Gillon, Raanan. "Medical ethics in Britain." Theoretical Medicine 9, no. 3 (October 1988): 251–69. http://dx.doi.org/10.1007/bf00489701.

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Dissertations / Theses on the topic "Medical ethics – Great Britain"

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Ferguson, Angus H. "Should a doctor tell? : medical confidentiality in interwar England and Scotland." Thesis, University of Glasgow, 2005. http://theses.gla.ac.uk/3150/.

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Medical confidentiality is integral to the doctor - patient relationship and an important element in efficient and effective medical practice. However, it is generally acknowledged that medical confidentiality can not be absolute. At times it must be broken in order to serve a ‘higher’ interest - be it public health or the legal justice system. Yet, very little is known about the historical evolution of the boundaries of medical confidentiality in Britain. The absence of detailed historical research on the subject has meant that contemporary writers have tended to use citations of the Hippocratic Oath or short quotations from key legal cases to place their work into longer term context. The current thesis provides a more detailed examination of the delineation of the boundaries of medical confidentiality during a period of intense debate - the interwar years of the twentieth century. The increase in state interest in the health of the population, the growth in divorce after the First World War and the prominence of the medical issues of venereal disease and abortion, all brought unprecedented challenges to the traditional concept of medical confidentiality. Having examined the, oft-cited, benchmark precedent for medical confidentiality from the late eighteenth century, the thesis proceeds to examine the ways in which medicine had changed by the interwar years. The high-point of the debate in the early 1920s is examined from the perspective of the three key interest groups - the Ministry of Health, the British Medical Association and the Lord Chancellor. Overall, the work provides insight into the historical delineation of medical confidentiality in Britain, both in statute and common law. As such it lends a longer-term context to current debates over the boundaries of medical confidentiality in the twenty-first century.
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Murphy, Richard. "Health professionals and ethnic Pakistanis in Britain : risk, thalassaemia and audit culture." Thesis, University of St Andrews, 2005. http://hdl.handle.net/10023/2802.

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The central theme or 'red-thread' that I consider in this thesis is the concept of risk as it is perceived by and affects the two sides of the medical encounter -in this instance ethnic Pakistanis and Health Professionals- in Britain. Each side very often perceives risk quite distinctively, relating to the balance between the spiritual and temporal realms. This is particularly germane in matters to do with possible congenital defects within the prenatal realm for the ethnic Pakistani, and predominantly Muslim, side of this encounter. Thus one of the factors considered in this thesis is how senses of Islam impact upon the two sides. By ethnic Pakistanis Islam is seen as central to all life decisions, whilst Health Professionals view Islam with some considerable trepidation, little understanding it or its centrality to the former's decision-making processes. This is particularly significant with regard to attitudes to health and health care. In the initial stages of the project I had thought first cousin marriage (FCM), seen by ethnic Pakistanis as desirable and by Health Professionals as putting ethnic Pakistanis at-risk to be central to the argument, but concluded that concerns around FCM were a 'red herring', merely a trope for the tensions between the two sides -at once both British and at-risk from audit culture. Although no longer central, FCM remains a viable touchstone in consideration of the two sides' perceptions of genetic risk. In this thesis the medical encounter between ethnic Pakistanis and Health Professionals is performed within the realm of the so called New Genetics. Here the respective understandings of the New Genetics are informed by the enculturation processes that shape the two sides' world view. Furthermore, I will agree with Lord Robert Winston's and others' concern that any attempt to eradicate an adaptive genetic mutation, in this instance, thalassaemia, from the gene pool is not only undesirable in the short term, but also that such eradications may have an adverse, and far reaching, effect on whole population groups in the future. The main thrust of my argument is that audit culture not only compounds risk for both sides, but also perpetuates institutional racism within the National Health Service (NHS), by promulgating what I have called the language myth. That is to say that much institutional racism is the unwanted by-product of the NHS's attempts to become more patient centred and its continuing efforts to develop systems of best practice. This professionalisation process within the NHS can be seen to impact most strongly in relation to communication -particularly the claimed language barrier between the two sides. This 'barrier' has worrying policy implications for any meaningful communication between the two sides, notably relating to obtaining informed consent from ethnic Pakistani patients -with a resultant increase in risk for the two sides and clear economic consequences for the NHS.
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Liu, Lixun. "Exploring ethnic inequalities in cardiovascular disease using Hospital Episode Statistics." Thesis, St Andrews, 2009. http://hdl.handle.net/10023/819.

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de, Andrade Marisa. "Pharmaffiliation : a model of intra-elite communication in pharmaceutical regulation." Thesis, University of Stirling, 2011. http://hdl.handle.net/1893/6500.

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In 2005, the House of Commons (HoC) Health Committee produced a report on The Influence of the Pharmaceutical Industry – the first of its kind since 1914. The inquiry concluded that there were ‘over-riding concerns about the volume, extent and intensity of the industry’s influence, not only on clinical medicine and research but also on patients, regulators, the media, civil servants and politicians’, and stressed the need ‘to examine critically the industry’s impact on health to guard against excessive and damaging dependencies’ (HoC 2005, p. 97). It also noted that it is important to comprehensively analyse pharmaceutical regulation in order to ascertain whether there are systemic problems: In some circumstances, one particular item of influence may be of relatively little importance. Only when it is viewed as part of a larger package of influences is the true effect of the company’s activity recognised and the potential for distortion seen. The possibility that certain components of any such campaign are covert and their source undeclared is particularly worrying. (HoC 2005, p. 97) This study addresses this recommendation and was primarily conducted to examine whether recognised concerns are merely ad hoc or as a result of systemic flaws in the current system of pharmaceutical regulation. The work addresses a gap in the academic literature by drawing on the fragmented criticisms of the pharmaceutical industry in order to produce a model to illustrate how various stakeholders collaborate with drug companies to promote licensed products, and to explore the nature of the relationships between these elite stakeholders. The thesis begins with a literature review which determines who is involved in pharmaceutical regulation; how the regulatory system works; and explores the key role of communication in this process (Chapters 1 to 3). The recurrent theme is the neglect or exclusion of the patient/consumer, which leads to the development a model of intra-elite communication in drug regulation called Pharmaffiliation (Chapter 3). The thesis then looks for evidence to support or refute this model, using multiple methods (Chapter 4). Four case studies (with specific selection criteria) are chosen to test the model’s constructs and indicators (Chapters 5 to 8). The research uncovers systemic problems in the current system of pharmaceutical regulation which can ultimately harm the patient/consumer, and the implications of these findings are discussed (Chapter 9). Solutions on a micro-level include consumer involvement in decision making processes, which can be enhanced through public education and awareness campaigns and the instigation of public inquiries whenever drugs are withdrawn from the market (HoC 2005, p. 105). On a macro-level, however, this will involve critically exploring neoliberal capitalism and the empowerment of the citizenry (Street 2001).
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Archer, Patricia Margaret Alice. "A history of the Medical Artists' Association of Great Britain 1949-1997." Thesis, University College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311981.

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Grubb, Penelope Ann. "The impact of information technology upon primary health care in Great Britain." Thesis, University of Hull, 1991. http://hydra.hull.ac.uk/resources/hull:4567.

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This is a study of the impact of information technology on health care in Great Britain. Its major aim is to identify means by which information technology may improve the quality of health care in specific areas within the health services.The study concentrated upon general practice and was split into three stages. The first was a survey of general practice computing, conducted to give an overview of the use of computers in general practice. Following this, was a more detailed study of general practice miniclinics. The final stage was an in-depth investigation into the use of computers in the care and treatment of diabetes.
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Beniuk, Kathleen. "Integrating evidence-based medicine and service design : a study of emergency department crowding." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610514.

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McCormack, Brendan. "An exploration of the theoretical framework underpinning the autonomy of older people in hospital and its relationship to professional nursing practice." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670229.

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Humphris, Rachel Grace. "New migrants' home encounters : an ethnography of 'Romanian Roma' and the local state in Luton." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:3af69cfa-2cd7-4972-afb2-14d92238d25a.

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This ethnographic study explores how 'Romanian Roma' migrants in the UK, without previous relationships to their place of arrival, negotiate their identity to make place in a diverse urban area. The thesis argues that state forms are (re)produced through embedded social relations. The restructuring of the UK welfare state, coupled with processes of labelling, means that the notion of public and private space is changing. Migrants' encounters with state actors in the home are increasingly important. I lived with three families between January 2013 and March 2014, during a period of shifting labour market regulations and the end of European Union transitional controls in January 2014. Through mapping families' relationships and connections, I identify encounters in the home with state actors regarding children as a defining feature of place-making. The thesis introduces the term 'home encounter' to trace the interplay of discourses and performances between state actors and those they identified as 'Romanian Roma'. Due to the restructuring of UK welfare, various roles assume different 'faces of the state'. These include education officers, health visitors, sub-contracted NGO workers, charismatic pastors and volunteers. The home encounter is presented as a public 'state act' (Bourdieu 2012) where negotiations of values take place in private space determining access to membership and welfare resources. In addition, blurring boundaries between welfare regulations and immigration control mean that these actors' seemingly small decisions have far-reaching consequences. The analysis raises questions of how to understand practices of government in diverse urban areas; the affect of labelling, place and performance on material power inequalities; and processes of discrimination and othering.
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White, Christopher P. "NHS resource allocation 1997 to 2003 with particular reference to the impact on rural areas." Thesis, St Andrews, 2009. http://hdl.handle.net/10023/825.

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Books on the topic "Medical ethics – Great Britain"

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Medical law and ethics. 4th ed. Oxford, U.K: Oxford University Press, 2012.

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Medical law and ethics. 3rd ed. Oxford: Oxford University Press, 2010.

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Bell, Leanne. Medical law and ethics. Harlow, England: Pearson, 2012.

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Medical law and ethics. Oxford: Oxford University Press, 2006.

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Medical law and ethics. 2nd ed. Oxford: Oxford University Press, 2008.

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Julian, Savulescu, and Hendrick Judith, eds. Medical ethics and law: The core curriculum. Edinburgh: Churchill Livingstone, 2003.

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A, McCall Smith R., ed. Law and medical ethics. 2nd ed. London: Butterworths, 1987.

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Mason, J. K. Law and medical ethics. 2nd ed. London: Butterworths, 1987.

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1948-, McCall Smith Alexander, and Laurie G. T, eds. Law and medical ethics. 6th ed. London: LexisNexis UK, 2002.

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1948-, McCall Smith Alexander, ed. Law and medical ethics. 3rd ed. London: Butterworths, 1991.

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Book chapters on the topic "Medical ethics – Great Britain"

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Cohen-Almagor, Raphael. "The Work of the Press Councils in Great Britain, Canada, and Israel: a Comparative Appraisal." In Speech, Media and Ethics, 124–51. London: Palgrave Macmillan UK, 2001. http://dx.doi.org/10.1057/9780230501829_7.

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Goold, Imogen, and Jonathan Herring. "Medical Negligence." In Great Debates in Medical Law and Ethics, 71–108. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_4.

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Crowther, M. Anne. "Forensic medicine and medical ethics in nineteenth-century Britain." In The Codification of Medical Morality, 173–90. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-0-585-27444-7_9.

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Goold, Imogen, and Jonathan Herring. "General Ethical Theories." In Great Debates in Medical Law and Ethics, 1–26. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_1.

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Goold, Imogen, and Jonathan Herring. "Ending Life." In Great Debates in Medical Law and Ethics, 232–49. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_10.

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Goold, Imogen, and Jonathan Herring. "Consent." In Great Debates in Medical Law and Ethics, 27–49. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_2.

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Goold, Imogen, and Jonathan Herring. "Capacity." In Great Debates in Medical Law and Ethics, 50–70. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_3.

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Goold, Imogen, and Jonathan Herring. "Reproduction." In Great Debates in Medical Law and Ethics, 109–37. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_5.

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Goold, Imogen, and Jonathan Herring. "Abortion." In Great Debates in Medical Law and Ethics, 138–58. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_6.

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Goold, Imogen, and Jonathan Herring. "Organ Donation." In Great Debates in Medical Law and Ethics, 159–83. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-32747-5_7.

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Conference papers on the topic "Medical ethics – Great Britain"

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Vinnikova, Liliia, and Maria Prokopchuk. "HISTORICAL PHASES OF HIGHER MEDICAL EDUCATION DEVELOPMENT IN GREAT BRITAIN." In Relevant Issues of the Development of Science in Central and Eastern European Countries. Publishing House “Baltija Publishing”, 2019. http://dx.doi.org/10.30525/978-9934-588-11-2_49.

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Wang, Wen-Li. "On the Medical Ethics Thought of the “Great Medical Doctor”." In Proceedings of the 5th Annual International Conference on Management, Economics and Social Development (ICMESD 2019). Paris, France: Atlantis Press, 2019. http://dx.doi.org/10.2991/icmesd-19.2019.74.

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Vickers, Z., H. Avula, and CR Fertleman. "G444(P) Medical students embracing change: how do we learn from lessons of the past to be great doctors of the future?" In Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 13–15 March 2018, SEC, Glasgow, Children First – Ethics, Morality and Advocacy in Childhood, The Journal of the Royal College of Paediatrics and Child Health. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2018. http://dx.doi.org/10.1136/archdischild-2018-rcpch.433.

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