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Health Professionals and Trust

Health Professionals and Trust Author Mark Henaghan
ISBN-10 9781136621062
Release 2012-03-12
Pages 160
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"Over the past twenty years there has been a shift in medical law and practise to increasingly distrust the judgement of health professionals. An increasing number of codes of conduct, disciplinary bodies, ethics committees and bureaucratic policies now prescribe how health professional and health researchers should act and relate to their patients. The result of this, Mark Henaghan argues, has been to undermine trust and professional judgement in health professionals, while simultaneously failing to trust the patient to make decisions about their care. This book will look at the issue of health professionals and trust comparatively in a number of countries including the USA, Canada, Australia, New Zealand and the UK. The book will show by historical analysis of legislation, case law, disciplinary proceedings reports, articles in medical and law journals and protocols produced by management teams in hospitals, how the shift from trust to lack of trust has happened. Drawing comparisons between situations where trust is respected such as in emergency situations, and where it is not for example routine decisions such as obtaining consent for an anaesthetic procedure, the book shows how this erosion of trust has the potential to dehumanise the special nature of the relationship between healthcare professionals and patients. The effect of this is that the practice of health care is turned into a mechanistic enterprise controlled by "management processes" rather than governed by trust and individual care and judgement. This book will be an invaluable resource for students and scholars of medical law and medical sociology, public policy-makers and a range of associated professionals, from health service managers to medical science and clinical researchers"--Provided by publisher.



Pioneering Healthcare Law

Pioneering Healthcare Law Author Catherine Stanton
ISBN-10 9781317506003
Release 2015-10-16
Pages 308
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This book celebrates Professor Margaret Brazier’s outstanding contribution to the field of healthcare law and bioethics. It examines key aspects developed in Professor Brazier’s agenda-setting body of work, with contributions being provided by leading experts in the field from the UK, Australia, the US and continental Europe. They examine a range of current and future challenges for healthcare law and bioethics, representing state-of-the-art scholarship in the field. The book is organised into five parts. Part I discusses key principles and themes in healthcare law and bioethics. Part II examines the dynamics of the patient–doctor relationship, in particular the role of patients. Part III explores legal and ethical issues relating to the human body. Part IV discusses the regulation of reproduction, and Part V examines the relationship between the criminal law and the healthcare process. Offering a collaborative review of key and innovative themes in the field, the book will be of great interest and use to academics and students working in healthcare law and bioethics, and those working in health policy, law and regulation at both national and international levels. Chapter 10 of this book is freely available as a downloadable Open Access PDF at www.tandfebooks.com/openaccess. It has been made available under a Creative Commons Attribution-Non Commercial-No Derivatives 3.0 license.



Big Data Health Law and Bioethics

Big Data  Health Law  and Bioethics Author I. Glenn Cohen
ISBN-10 9781108153645
Release 2018-03-08
Pages
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When data from all aspects of our lives can be relevant to our health - from our habits at the grocery store and our Google searches to our FitBit data and our medical records - can we really differentiate between big data and health big data? Will health big data be used for good, such as to improve drug safety, or ill, as in insurance discrimination? Will it disrupt health care (and the health care system) as we know it? Will it be possible to protect our health privacy? What barriers will there be to collecting and utilizing health big data? What role should law play, and what ethical concerns may arise? This timely, groundbreaking volume explores these questions and more from a variety of perspectives, examining how law promotes or discourages the use of big data in the health care sphere, and also what we can learn from other sectors.



Legal and Ethical Regulation of Biomedical Research in Developing Countries

Legal and Ethical Regulation of Biomedical Research in Developing Countries Author Dr Remigius N Nwabueze
ISBN-10 9781409466123
Release 2013-05-28
Pages 336
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There has been a rapid increase in the pace and scope of international collaborative research in developing countries in recent years. This study argues that whilst ethical regulation of biomedical research in Africa and other developing countries has attracted global attention, legal liability issues, such as the application of common law rules and the development of legally enforceable regulations, have been neglected. It examines some of the major research scandals in Africa and suggests a new ethical framework against which clinical trials could be conducted. The development of research guidelines in Uganda, Tanzania, Malawi and Nigeria are also examined as well as the role of ethics committees. Providing a detailed analysis of the law of negligence and its application to research ethics committees and their members, common law and constitutional forms of action and potential negligence claims, the book concludes by suggesting new protocols and frameworks, improved regulation and litigation. This book will be a valuable guide for students, researchers, and policy-makers with an interest in medical law and ethics, bioethics, customary law in Africa and regulation in developing countries.



Society s Choices

Society s Choices Author Committee on the Social and Ethical Impacts of Developments in Biomedicine
ISBN-10 9780309051323
Release 1995-02-27
Pages 560
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Breakthroughs in biomedicine often lead to new life-giving treatments but may also raise troubling, even life-and-death, quandaries. Society's Choices discusses ways for people to handle today's bioethics issues in the context of America's unique history and culture--and from the perspectives of various interest groups. The book explores how Americans have grappled with specific aspects of bioethics through commission deliberations, programs by organizations, and other mechanisms and identifies criteria for evaluating the outcomes of these efforts. The committee offers recommendations on the role of government and professional societies, the function of commissions and institutional review boards, and bioethics in health professional education and research. The volume includes a series of 12 superb background papers on public moral discourse, mechanisms for handling social and ethical dilemmas, and other specific areas of controversy by well-known experts Ronald Bayer, Martin Benjamin, Dan W. Brock, Baruch A. Brody, H. Alta Charo, Lawrence Gostin, Bradford H. Gray, Kathi E. Hanna, Elizabeth Heitman, Thomas Nagel, Steven Shapin, and Charles M. Swezey.



Ethics and Law for the Health Professions

Ethics and Law for the Health Professions Author Ian Kerridge
ISBN-10 1862879095
Release 2013
Pages 1208
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Ethics and Law for the Health Professions is a cross-disciplinary medico-legal book whose previous editions have been widely used by students, teachers and practitioners in the health professions and in law. This new 4th edition has been extensively revised and updated to take account of developments in law, biomedical science, healthcare delivery and bioethics. Sections dealing with critical reasoning, problem solving, professionalism, negligence, standards of care, public health and the emerging biosciences have been considerably expanded and entirely new chapters have been added dealing with sexuality, culture, rural health, evidence and global health.As with previous editions, the 4th edition of Ethics and Law for the Health Professions focuses on issues that are relevant both to clinicians and to health-policy-makers. It combines insights from philosophy, bioethics and the health social sciences, biomedical research data and case law. Importantly, this book recognises that health professionals must understand both the ethical and legal implications of their practice but is careful to distinguish between the two.This book provides an invaluable resource for those who are responsible for the design and delivery of health care and for those who have an interest in how health care can best meet the needs and reflect the values of the community.



Public Health Ethics Cases Spanning the Globe

Public Health Ethics  Cases Spanning the Globe Author Drue H. Barrett
ISBN-10 9783319238470
Release 2016-04-12
Pages 329
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This Open Access book highlights the ethical issues and dilemmas that arise in the practice of public health. It is also a tool to support instruction, debate, and dialogue regarding public health ethics. Although the practice of public health has always included consideration of ethical issues, the field of public health ethics as a discipline is a relatively new and emerging area. There are few practical training resources for public health practitioners, especially resources which include discussion of realistic cases which are likely to arise in the practice of public health. This work discusses these issues on a case to case basis and helps create awareness and understanding of the ethics of public health care. The main audience for the casebook is public health practitioners, including front-line workers, field epidemiology trainers and trainees, managers, planners, and decision makers who have an interest in learning about how to integrate ethical analysis into their day to day public health practice. The casebook is also useful to schools of public health and public health students as well as to academic ethicists who can use the book to teach public health ethics and distinguish it from clinical and research ethics.



Canadian Health Law and Policy

Canadian Health Law and Policy Author Joanna N. Erdman
ISBN-10 0433490314
Release 2017
Pages 560
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Much more than the study of laws relevant to the area of medicine, Canadian Health Law and Policy draws together the legal and policy issues that are relevant to human health, and sheds new light on emerging and continuing trends. Written by Canada's leading health law scholars, the fifth edition of this unique work provides expert commentary and analysis on a wide range of emerging health law related issues. It is a vital resource for anyone seeking to understand the developing and critical issues in health law and policy.



A History and Theory of Informed Consent

A History and Theory of Informed Consent Author Ruth R. Faden
ISBN-10 9780195036862
Release 1986
Pages 392
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Patient / Einwirkung.



Ethics Medicine and Information Technology

Ethics  Medicine  and Information Technology Author
ISBN-10 9781107624733
Release
Pages
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Ethics Medicine and Information Technology has been writing in one form or another for most of life. You can find so many inspiration from Ethics Medicine and Information Technology also informative, and entertaining. Click DOWNLOAD or Read Online button to get full Ethics Medicine and Information Technology book for free.



Autonomy Paternalism

Autonomy   Paternalism Author Thomas Nys
ISBN-10 9042918802
Release 2007
Pages 183
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In recent years, the triumph of autonomy has made paternalist interventions increasingly problematic. The value of a patient's right to self-determination and the practice of informed consent are considered supremely important in present-day health care ethics. In general, the idea of 'doctor knows best' has become more and more suspicious. This has left us with a situation in which paternalist medicine seems difficult to reconcile with respect for patient autonomy. This book offers a thorough reflection on the relationship between autonomy and paternalism, and argues that, from both theoretical and practical angles, the tension between these concepts is not as acute as it might seem. In long-term care, psychiatry, and care for the severely handicapped, the principle of respect for autonomy is particularly ill-suited. This, however, does not mean that such respect is totally irrelevant, but that it should take a different shape. Good care in those cases requires us to transcend the sharp dichotomy between autonomy and paternalism. In Autonomy and Paternalism: Reflections on the Theory and Practice of Health Care various acclaimed authors present their views on this interesting and extremely relevant debate.



Where Science and Ethics Meet Dilemmas at the Frontiers of Medicine and Biology

Where Science and Ethics Meet  Dilemmas at the Frontiers of Medicine and Biology Author Chris Willmott
ISBN-10 9781440851353
Release 2016-06-13
Pages 180
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Through engaging case studies and clear explanations of the underlying science, this book makes the social impacts and ethical consequences of recent advances in biomedicine understandable for general readers. • Provides clear, easily understandable information for nonspecialist readers with sufficient detail to enable an understanding of the science behind the discoveries and the range of ethical problems they generate • Presents a dynamic mix of present or near-future case studies (fictional), scientific explanations, and discussions of ethics • Addresses topics that are frequently in the media, such as cloning, organ transplantation, and genetic modification, and clarifies concepts that people have heard about but may not fully understand • Summarizes arguments in favor and against to allow readers to form their own opinions on important ethical debates



Oxford Handbook of Neuroethics

Oxford Handbook of Neuroethics Author Judy Illes
ISBN-10 9780191620911
Release 2011-04-07
Pages 976
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The past two decades have seen unparalleled developments in our knowledge of the brain and mind. However, these advances have forced us to confront head-on some significant ethical issues regarding our application of this information in the real world- whether using brain images to establish guilt within a court of law, or developing drugs to enhance cognition. Historically, any consideration of the ethical, legal, and social implications of emerging technologies in science and medicine has lagged behind the discovery of the technology itself. These delays have caused problems in the acceptability and potential applications of biomedical advances and posed significant problems for the scientific community and the public alike - for example in the case of genetic screening and human cloning. The field of Neuroethics aims to proactively anticipate ethical, legal and social issues at the intersection of neuroscience and ethics, raising questions about what the brain tells us about ourselves, whether the information is what people want or ought to know, and how best to communicate it. A landmark in the academic literature, the Oxford Handbook of Neuroethics presents a pioneering review of a topic central to the sciences and humanities. It presents a range of chapters considering key issues, discussion, and debate at the intersection of brain and ethics. The handbook contains more than 50 chapters by leaders from around the world and a broad range of sectors of academia and clinical practice spanning the neurosciences, medical sciences and humanities and law. The book focuses on and provides a platform for dialogue of what neuroscience can do, what we might expect neuroscience will do, and what neuroscience ought to do. The major themes include: consciousness and intention; responsibility and determinism; mind and body; neurotechnology; ageing and dementia; law and public policy; and science, society and international perspectives. Tackling some of the most significant ethical issues that face us now and will continue to do so over the coming decades, The Oxford Handbook of Neuroethics will be an essential resource for the field of neuroethics for graduate students and postdoctoral fellows, basic scientists in the neurosciences and psychology, scholars in humanities and law, as well as physicians practising in the areas of primary care in neurological medicine.



National Library of Medicine Current Catalog

National Library of Medicine Current Catalog Author National Library of Medicine (U.S.).
ISBN-10 MINN:31951D010928702
Release 1993
Pages
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National Library of Medicine Current Catalog has been writing in one form or another for most of life. You can find so many inspiration from National Library of Medicine Current Catalog also informative, and entertaining. Click DOWNLOAD or Read Online button to get full National Library of Medicine Current Catalog book for free.



Ethical Legal and Social Issues in Medical Informatics

Ethical  Legal and Social Issues in Medical Informatics Author Duquenoy, Penny
ISBN-10 9781599047829
Release 2008-06-30
Pages 320
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The utilization of information and communication technologies in almost all spheres of modern society has changed the social picture in significant ways while simultaneously leading to tensions with regard to traditional ethical and legal practices—particularly given the global context of its application. Where these technologies impact on the practice and implementation of healthcare, it is vital to recognize the extent and nature of the ethical and social impact both at the level of professional practice and the patient. Ethical, Legal and Social Issues in Medical Informatics presents a fundamental compendium of research on the ethical, social, and legal issues facing the healthcare industry as it adopts information technologies to provide fast, efficient, and cost effective healthcare. An essential resource for every reference library, this comprehensive book offers a multidisciplinary perspective, drawing from the expertise of a wide variety of global industries including law, ethics, medicine, philosophy, and computer science.



Solidarity and Justice in Health and Social Care

Solidarity and Justice in Health and Social Care Author Ruud ter Meulen
ISBN-10 9781107069800
Release 2017-08-31
Pages 228
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This book presents a new view on the concept of solidarity and explains how it complements justice in health and social care.



The Fetus as a Patient

The Fetus as a Patient Author Dagmar Schmitz
ISBN-10 9781351692779
Release 2018-04-17
Pages 214
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Due to new developments in prenatal testing and therapy the fetus is increasingly visible, examinable and treatable in prenatal care. Accordingly, physicians tend to perceive the fetus as a patient and understand themselves as having certain professional duties towards it. However, it is far from clear what it means to speak of a patient in this connection. This volume explores the usefulness and limitations of the concept of ‘fetal patient’ against the background of the recent seminal developments in prenatal or fetal medicine. It does so from an interdisciplinary and international perspective. Featuring internationally recognized experts in the field, the book discusses the normative implications of the concept of ‘fetal patient’ from a philosophical-theoretical as well as from a legal perspective. This includes its implications for the autonomy of the pregnant woman as well as its consequences for physician-patient-interactions in prenatal medicine.