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Author: Sylvie Fainzang
Publisher: PUF
ISBN: 2130739245
Category : Social Science
Languages : fr
Pages : 205
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Book Description
De nos jours, il semble acquis que le patient est un individu doté d'un véritable pouvoir de décision fondé sur une information complète de la part du corps médical. Il semble, au terme de cette étude, qu'il faille réinterroger ce qui paraît être une évidence acquise : on assiste davantage à des affirmations sur l'évidente nécessité de cette information que sur une réalité. Le but de cet ouvrage est donc d'analyser la réalité de cette information dans la relation médecins-malades. Quelle est la nature de l'information, comment est-elle donnée, comment le malade la comprend-il, quelle est la possibilité de la part du malade d'accéder à une information complète et accessible, comment cette information peut-elle induire des choix thérapeutiques ? Une analyse passionnante qui nous concerne tous.
Author: Sylvie Fainzang
Publisher: PUF
ISBN: 2130739245
Category : Social Science
Languages : fr
Pages : 205
Get Book Here
Book Description
De nos jours, il semble acquis que le patient est un individu doté d'un véritable pouvoir de décision fondé sur une information complète de la part du corps médical. Il semble, au terme de cette étude, qu'il faille réinterroger ce qui paraît être une évidence acquise : on assiste davantage à des affirmations sur l'évidente nécessité de cette information que sur une réalité. Le but de cet ouvrage est donc d'analyser la réalité de cette information dans la relation médecins-malades. Quelle est la nature de l'information, comment est-elle donnée, comment le malade la comprend-il, quelle est la possibilité de la part du malade d'accéder à une information complète et accessible, comment cette information peut-elle induire des choix thérapeutiques ? Une analyse passionnante qui nous concerne tous.
Author: Justine Perret
Publisher:
ISBN:
Category :
Languages : fr
Pages : 46
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Book Description
Contexte. La relation médecin-patient a longtemps été empreinte d'un mensonge admis dans l'intérêt du malade. Au milieu du 20e siècle, les droits des patients à l'information et le modèle autonomiste ont proscrit le mensonge de la relation médecin-patient. Objectif. L'objectif de ce travail était de décrire la place laissée au mensonge dans ce modèle de relation par les patients. Méthode. Après avoir réfléchi à leur posture, les chercheurs ont mené une étude qualitative par théorisation ancrée. Des entretiens individuels semi-directifs ont été menés entre octobre 2014 et février 2016. L'échantillonnage était théorique. Le guide d'entretien utilisé a cherché à décrire les concepts de relation et de mensonge sans les aborder trop directement. Le nombre d'entretiens a été conditionné par la recherche de la saturation des données. La validité interne a été établie par une double analyse indépendante des données issues de la retranscription. Résultats. Les quinze patients interrogés pensaient le mensonge en dehors de la relation médecin-patient. Sa connotation était très négative. Tout dire au médecin était important pour leur santé et pour la relation de confiance. Ce mensonge impossible serait détecté par le médecin comme par le patient. Les médecins ne pouvaient mentir puisqu'ils avaient l'obligation d'informer. Le non-dit se différenciait du mensonge par l'intention, et tenait une place importante dans la relation. La proximité, la peur du diagnostic, du jugement, et la volonté de se protéger conduisaient les patients aux non-dits. Les non-dits des médecins étaient justifiés par l'incertitude et la protection du patient. Conclusion. Les patients ont clairement fait apparaître une différence entre un mensonge impossible et des non-dits usuels. Ils pensaient que le médecin pouvait adapter l'information au patient et aux circonstances.
Author: Céline Deldon
Publisher:
ISBN:
Category :
Languages : fr
Pages : 58
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Book Description
Jusqu'au 20em; siècle, la relation médecin-patient reposait sur une attitude paternaliste où le mensonge était admis dans l'intérêt des patients. L'émergence d'un modèle autonomiste pouvait faire envisager une évolution du rapport au mensonge. Ce travail met en lumière un débat ancien et de grandes divergences d'opinions et de pratiques des médecins autour du mensonge. Malgré une mauvaise image, le mensonge s'immisçait dans la relation dans un but protecteur pour le patient et pour le médecin. Les médecins pensaient que les patients mentaient. Les mensonges menaçaient la confiance indispensable à la relation de soins. Une interrogation demeure sur la posture sociale du médecin ressentie ou non par lui comme catalysante du mensonge.
Author: Sylvie Fainzang
Publisher: Routledge
ISBN: 1317182073
Category : Medical
Languages : en
Pages : 233
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Book Description
In the era of health democracy, where a patient’s right to be informed is not only widely advocated but also guaranteed by law, what is the real situation regarding patient information? Do patients receive the information that they request with regard to their diagnosis, prognosis or treatments? And what information do patients themselves give to their doctors? Drawing on observational research in hospitals and covering the exchanges between doctors and patients on the subject of cancer treatment and that of other pathologies, this book reveals that the practice of telling lies is widespread amongst parties on both sides of the medical relationship. With attention to the manner in which information of various types is withheld and the truth concealed on either side of the doctor-patient relationship, the author explores the boundaries between what is said and what is left unsaid, and between those who are given information and those who are lied to. Considering the misunderstandings that occur in the course of medical exchanges and the differences between the lies told by doctors and patients, An Anthropology of Lying: Information in the Doctor-Patient Relationship analyses the role of mendacity in the exercise of, and resistance to power. A fascinating study of the mechanisms at work and social conditions surrounding the accomplishment of lying in medical settings, this book casts fresh light on a subject that has so far been overlooked. As such, it will appeal not only to sociologists and anthropologists of health and medicine, but also to medical professionals.
Author: Jérôme Béranger
Publisher: John Wiley & Sons
ISBN: 1119178266
Category : Computers
Languages : en
Pages : 300
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Book Description
The exponential digitization of medical data has led to a transformation of the practice of medicine. This change notably raises a new complexity of issues surrounding health IT. The proper use of these communication tools, such as telemedicine, e-health, m-health the big medical data, should improve the quality of monitoring and care of patients for an information system to "human face". Faced with these challenges, the author analyses in an ethical angle the patient-physician relationship, sharing, transmission and storage of medical information, setting pins to an ethic for the digitization of medical information. Drawing on good practice recommendations closely associated with values, this model is developing tools for reflection and present the keys to understanding the decision-making issues that reflect both the technological constraints and the complex nature of human reality in medicine .
Author: Daniel Barredo-Ibáñez
Publisher: Springer Nature
ISBN: 2494069254
Category : Education
Languages : en
Pages : 361
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Book Description
This is an open access book. CISOC’2022 – The 2022 International Conference on International Studies in Social Sciences and Humanities, invites the entire scientific, academic and professional community to present their contributions, which can be written in French, English, Spanish or Portuguese. All papers (full articles) will be submitted to a “double-blind review” by at least two members of the Scientific Committee, based on relevance, originality, importance and clarity. The papers presented must bring discussions on actual theoretical, or methodological, or empirical workshop proposals around Social Sciences and Humanities. The topics proposed for the Conference are related to: Psychology, Education, History, Linguistics and language, Political science, Religious studies, Philosophy, Globalization, Humanities, Archaeology, Anthropology, Inter-cultural studies, Development, Geography, Library and Information Sciences.
Author: Sylvie Fainzang
Publisher: Aarhus Universitetsforlag
ISBN: 8779344410
Category : Medical
Languages : en
Pages : 258
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Book Description
The Taste for Knowledge: Medical Anthropology Facing Medical Realities demonstrates how medical anthropology is becoming increasingly important in the fields of medical research and public health. The authors examine some of the major issues in medical anthropology today. In this volume, a group of international researchers reflect, for example, on: the way anthropology faces and deals with interdisciplinarity in its encounter with medicine and doctors; the new medical realities and patient strategies that exist in changing medical systems; and the interactions between practice, power and science. The book will appeal to clinicians/practitioners, anthropologists in general, and all those engaged in the interface between medicine and anthropology, but will also be a valuable tool for students of medicine and anthropology who have a special interest in the social realities and interdisciplinarity of health and illness.
Author: Nathan Emmerich
Publisher: Springer Nature
ISBN: 3030400336
Category : Philosophy
Languages : en
Pages : 393
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Book Description
This book examines the ethics of end of life care, focusing on the kinds of decisions that are commonly made in clinical practice. Specific attention is paid to the intensification of treatment for terminal symptoms, particularly pain relief, and the withdrawal and withholding of care, particularly life-saving or life-prolonging medical care. The book is structured into three sections. The first section contains essays examining end of life care from the perspective of moral theory and theology. The second sets out various conceptual terms and distinctions relevant to decision-making at the end of life. The third section contains chapters that focus on substantive ethical issues. This format not only provides for a comprehensive analysis of the ethical issues that arise in the context of end of life care but allows readers to effectively trace the philosophical, theological and conceptual underpinnings that inform their specific interests. This work will be of interest to scholars working in the area as well as clinicians, specialists and healthcare professionals who encounter these issues in the course of their practice.
Author: Catherine Myser
Publisher: Oxford University Press
ISBN: 0199749825
Category : Medical
Languages : en
Pages : 329
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Book Description
Contemporary bioethics, now roughly 40 years old as a discipline, originated in the United States with a primarily Anglo-American cultural ethos. It continues to be professionalized and institutionalized as a maturing discipline at the intersections of philosophy, medicine, law, social sciences, and humanities. Increasingly bioethics - along with its foundational values, concepts and principals - has been exported to other countries, not only in the developed West, but also in developing and/or Eastern countries. Bioethics thus continues to undergo intriguing transformations as it is globalized and adapted to local cultures. These processes have occurred rapidly in the last two decades, with relatively little reflection and examination. This volume brings together contributors from a wide variety of disciplines to take a critical, empirical look at bioethics around the globe, examining how it is being transformed - at both local and global levels - in this process of cross-cultural exporting and importing. One concern is to identify sociocultural forces and consequences which may positively or negatively affect ethics and social justice goals. This book thereby offers the first comparative anthropology and sociology of globalizing bioethics in the field, exploring the global dissemination, local adaptations, cultural meanings and social functions of bioethics theories, practices and institutions and comparing developed and developing countries. The volume considers a full range of countries on every inhabited continent, including: Africa, Asia, Australia, Central and South America, Europe, the Middle East, and North America. Topics include government agendas such as nationalism and nation building; agendas of powerful, associated professions (e.g., medicine, law); theological and political agendas such as 'culture wars'; agendas of entrepreneurial economies of profit; and other cultural and ideological agendas consciously or unconsciously advanced or contested by bioethics work in particular countries based on their unique history, politics and culture. This cross-cultural exploration of globalizing bioethics will be of great interest to a field that is increasingly introspective about its underlying sociocultural assumptions and biases. "At last-an unabashedly sociological and anthropological look at the globalization of bioethics, a really fresh approach to a maturing discipline. The chapters speak from the perspective of sophisticated Western-developed exporters of the bioethical paradigm [and equally sophisticated] Eastern-developing and third-world and interdisciplinary critics suspicious of the canonical view. Trained in the dominant school of American, mainstream philosophy, Myser draws on her long-standing commitment to a social and cultural approach to bioethics to take a fresh look at bioethics globally. She grasps the globalization of bioethics and the skepticism about analytical philosophy's Americanized consensus. The book sets the stage for a new era in bioethics theory and practice {debating] whether a universal common morality underlies the rich variation in national and cultural bioethics traditions." - Robert Veatch, Georgetown University "This path-breaking volume is the first to explore the global export of Western bioethics to a variety of non-Western settings. Explicitly critical, the book also points to the liberating potential of bioethics to achieve social justice and improve the lives of patients around the world. The book is a must-read for all medical anthropologists interested in bioethics." - Marcia Inhorn, Yale University "Bioethics Around the Globe should change the way bioethics is conceived and practiced in the U.S. and elsewhere. Its rich and wide-ranging comparative examination opens new possibilities for bioethical reflection. I enthusiastically recommend this wonderful book." - James F. Childress, University of Virginia "The past 40 years have seen a remarkable spread of bioethics to every part of the world. Dr. Myser's collection is a wonderful and rich exploration of its international impact, revealing important similarities and differences from country to country. It will have an important impact." - Daniel Callahan, The Hastings Center
Author: Laurence Corroy
Publisher: John Wiley & Sons
ISBN: 1786308932
Category : Health & Fitness
Languages : en
Pages : 260
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Book Description
This book studies the way chronic and long-term illnesses are represented in media, and the issues and structures associated with them. It also examines the way in which patients define themselves, the relationships they form with their carers and the experiences of these carers themselves. The way in which the figure of the caregiver can be portrayed as a necessary support for the patient is also discussed. Testimonies from digital platforms, fictional universes, examples from everyday life and from public and private organizations provide insight into the relationships between patients, caregivers and carers.
