Cambridge Law, Medicine and Ethics – serie

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24 produkter

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24 produkter

Del 1 - Cambridge Law, Medicine and Ethics
Genes and Insurance
Ethical, Legal and Economic Issues
AvMarcus Radetzki,Marian Radetzkim. fl.
Häftad, Engelska, 2008
426 kr
Skickas inom 10-15 vardagar
The result of two key social developments in recent years are examined here: the partial dismantling of the welfare state and the progress of genetics. Genetic insights are increasingly valuable for risk assessment, and insurers would like to use these insights to help determine premiums. Combined with the fact that social welfare is being curtailed, this could potentially create an uninsured high-risk population. Along with considerations of autonomy and privacy, this is the basis for an ethical critique of insurer's access to information. The result has often been regulation of such information; but the authors argues that due to adverse selection, regulation will not solve these problems, and this may jeopardize the survival of private personal insurance. Instead, we should look towards the resurrection of social insurance, a key component of the welfare state. This will interest academic researchers as well as professionals involved with genetics and insurance.
Del 12 - Cambridge Law, Medicine and Ethics
Healthcare Decision-Making and the Law
Autonomy, Capacity and the Limits of Liberalism
AvMary Donnelly
Inbunden, Engelska, 2010
1 351 kr
Skickas inom 10-15 vardagar
This analysis of the law's approach to healthcare decision-making critiques its liberal foundations in respect of three categories of people: adults with capacity, adults without capacity and adults who are subject to mental health legislation. Focusing primarily on the law in England and Wales, the analysis also draws on the law in the United States, legal positions in Australia, Canada, Ireland, New Zealand and Scotland and on the human rights protections provided by the ECHR and the Convention on the Rights of Persons with Disabilities. Having identified the limitations of a legal view of autonomy as primarily a principle of non-interference, Mary Donnelly questions the effectiveness of capacity as a gatekeeper for the right of autonomy and advocates both an increased role for human rights in developing the conceptual basis for the law and the grounding of future legal developments in a close empirical interrogation of the law in practice.
Del 7 - Cambridge Law, Medicine and Ethics
Posthumous Interests
Legal and Ethical Perspectives
AvDaniel Sperling
Häftad, Engelska, 2011
698 kr
Skickas inom 10-15 vardagar
Daniel Sperling discusses the legal status of posthumous interests and their possible defeat by actions performed following the death of a person. The author first explores the following questions: Do the dead have interests and/or rights, the defeat of which may constitute harm? What does posthumous harm consist of and when does it occur, if at all? This is followed by a more detailed analysis of three categories of posthumous interests arising in the medico-legal context: the proprietary interest in the body of the deceased, the testamentary interest in determining the disposal of one's body after death and the interest in post-mortem medical confidentiality. Sperling concludes that if we acknowledge the interest in one's symbolic existence and legally protect it, not only do some interests survive a person's death but we should also enjoy a peremptory legal power to shape in advance our symbolic existence after death.
Del 14 - Cambridge Law, Medicine and Ethics
Xenotransplantation and Risk
Regulating a Developing Biotechnology
AvSara Fovargue
Inbunden, Engelska, 2011
883 kr
Skickas inom 10-15 vardagar
Some developing biotechnologies challenge accepted legal and ethical norms because of the risks they pose. Xenotransplantation (cross-species transplantation) may prolong life but may also harm the xeno-recipient and the public due to its potential to transmit infectious diseases. These trans-boundary diseases emphasise the global nature of advances in health care and highlight the difficulties of identifying, monitoring and regulating such risks and thereby protecting individual and public health. Xenotransplantation raises questions about how uncertainty and risk are understood and accepted, and exposes tensions between private benefit and public health. Where public health is at risk, a precautionary approach informed by the harm principle supports prioritising the latter, but the issues raised by genetically engineered solid organ xenotransplants have not, as yet, been sufficiently discussed. This must occur prior to their clinical introduction because of the necessary changes to accepted norms which are needed to appropriately safeguard individual and public health.
Del 13 - Cambridge Law, Medicine and Ethics
Organ Shortage
Ethics, Law and Pragmatism
AvAnne-Maree Farrell,David Pricem. fl.
Inbunden, Engelska, 2011
1 351 kr
Skickas inom 10-15 vardagar
Organ shortage is an ongoing problem in many countries. The needless death and suffering which have resulted necessitate an investigation into potential solutions. This examination of contemporary ethical means, both practical and policy-oriented, of reducing the shortfall in organs draws on the experiences of a range of countries. The authors focus on the resolution and negotiation of ethical conflict, examine systems approaches such as the 'Spanish model' and the US Breakthrough Collaboratives, evaluate policy proposals relating to incentives, presumed consent, and modifications regarding end-of-life care, and evaluate the greatly increased use of (non-heart-beating) donors suffering circulatory death, as well as living donors. The proposed strategies and solutions are not only capable of resolving the UK's own organ-shortage crisis, but also of being implemented in other countries grappling with how to address the growing gap between supply and demand for organs.
Del 9 - Cambridge Law, Medicine and Ethics
The Governance of Genetic Information
Who Decides?
AvTBD,Heather Widdowsm. fl.
Inbunden, Engelska, 2009
809 kr
Skickas inom 10-15 vardagar
This volume maps the areas of ethical concern in the debate regarding the governance of genetic information, and suggests alternative ethical frameworks and models of regulation in order to inform its restructuring. Genetic governance is at the heart of medical and scientific developments, and is connected to global exploitation, issues of commodification, commercialisation and ownership, the concepts of property and intellectual property and concerns about individual and communal identity. Thus the decisions that are made in the next few years about appropriate models of genetic governance will have knock-on effects for other areas of governance. In short the final answer to 'Who Decides?' in the context of genetic governance will fundamentally shape the ethical constructs of individuals and their networks and relationships in the public sphere.
Del 2 - Cambridge Law, Medicine and Ethics
Double Standards in Medical Research in Developing Countries
AvRuth Macklin,Alexander McCall Smith
Häftad, Engelska, 2004
685 kr
Skickas inom 10-15 vardagar
This book examines the ethical controversies that have surrounded the design and conduct of international medical research sponsored by industrialized countries or industry, and carried out in developing countries. The chief concern is that research subjects in developing countries may be exploited because sponsors of research employ double standards. One debate focuses on whether the standard of care provided to subjects of medical research in developing countries should be the same as what research subjects receive in North America and Europe. Other concerns are whether the process of obtaining informed consent in developing countries is adequate, and whether prior ethical review of research meets standards that are well established in the industrialized world. Recent international developments show that essential medications can be made affordable and accessible to developing countries, and that double standards need not prevail.
Del 5 - Cambridge Law, Medicine and Ethics
The Troubled Pregnancy
Legal Wrongs and Rights in Reproduction
AvJ. K. Mason
Häftad, Engelska, 2007
562 kr
Skickas inom 10-15 vardagar
Mason looks at the legal response to those aspects of the troubled pregnancy which require or involve medico-legal intervention. The unwanted pregnancy is considered particularly in the light of the Abortion Act 1967, s.1(1)(d) and the related action for so-called wrongful birth due to faulty ante-natal care. The unexpected or uncovenanted birth of a healthy child resulting from failed sterilisation is approached through an analysis of the seminal case of McFarlane and associated cases involving disability in either the neonate or the mother. The disabled neonate's right to sue for its diminished life is discussed and the legal approach to the management of severe congenital disease is analysed - thus following Baroness Hale in believing that care of the newborn is an integral part of pregnancy. Aspects are considered from historical and comparative perspectives, including coverage of experience in the USA, the Commonwealth and Europe.
Del 6 - Cambridge Law, Medicine and Ethics
Law, Legitimacy and the Rationing of Health Care
A Contextual and Comparative Perspective
AvKeith Syrett
Häftad, Engelska, 2007
611 kr
Skickas inom 10-15 vardagar
Dr Keith Syrett argues for a reappraisal of the role of public law adjudication in questions of healthcare rationing. As governments worldwide turn to explicit rationing strategies to manage the mismatch between demand for and supply of health services and treatments, disappointed patients and the public have sought to contest the moral authority of bodies making rationing decisions. This has led to the growing involvement of law in this field of public policy. The author argues that, rather than bemoaning this development, those working within the health policy community should recognise the points of confluence between the principles and purposes of public law and the proposals which have been made to address rationing's 'legitimacy problem'. Drawing upon jurisprudence from England, Canada and South Africa, the book evaluates the capacity of courts to establish the conditions for a process of public deliberation from which legitimacy for healthcare rationing may be derived.
Del 10 - Cambridge Law, Medicine and Ethics
Human Tissue in Transplantation and Research
A Model Legal and Ethical Donation Framework
AvDavid Price
Häftad, Engelska, 2009
537 kr
Skickas inom 10-15 vardagar
Deficiencies and shortfalls in the supply of human organs for transplantation and human tissue for research generate policy dilemmas across the world and have often given rise to major and deleterious controversies, such as those relating to organ and tissue retention practices following post-mortem examination. They also create an environment in which illegitimate commercial activities flourish. At the same time, patients are denied the therapy they desperately require and researchers are impeded from carrying out vital work into the causes of, and efficacious treatments for, major illnesses and diseases. David Price sets out a clear and integrated legal and policy framework which emanates from the tissue source but protects the interests of donors and relevant professionals through tailored property entitlements, but without presupposing rights to trade in 'original' materials.
Del 11 - Cambridge Law, Medicine and Ethics
Rationality and the Genetic Challenge
Making People Better?
AvMatti Häyry
Häftad, Engelska, 2010
550 kr
Skickas inom 10-15 vardagar
Should we make people healthier, smarter, and longer-lived if genetic and medical advances enable us to do so? Matti Häyry asks this question in the context of genetic testing and selection, cloning and stem cell research, gene therapies and enhancements. The ethical questions explored include parental responsibility, the use of people as means, the role of hope and fear in risk assessment, and the dignity and meaning of life. Taking as a starting point the arguments presented by Jonathan Glover, John Harris, Ronald M. Green, Jürgen Habermas, Michael J. Sandel, and Leon R. Kass, who defend a particular normative view as the only rational or moral answer, Matti Häyry argues that many coherent rationalities and moralities exist in the field, and that to claim otherwise is mistaken.
Del 11 - Cambridge Law, Medicine and Ethics
Rationality and the Genetic Challenge
Making People Better?
AvMatti Häyry
Inbunden, Engelska, 2010
833 kr
Skickas inom 10-15 vardagar
Should we make people healthier, smarter, and longer-lived if genetic and medical advances enable us to do so? Matti Häyry asks this question in the context of genetic testing and selection, cloning and stem cell research, gene therapies and enhancements. The ethical questions explored include parental responsibility, the use of people as means, the role of hope and fear in risk assessment, and the dignity and meaning of life. Taking as a starting point the arguments presented by Jonathan Glover, John Harris, Ronald M. Green, Jürgen Habermas, Michael J. Sandel, and Leon R. Kass, who defend a particular normative view as the only rational or moral answer, Matti Häyry argues that many coherent rationalities and moralities exist in the field, and that to claim otherwise is mistaken.
Del 1 - Cambridge Law, Medicine and Ethics
Genes and Insurance
Ethical, Legal and Economic Issues
AvMarcus Radetzki,Marian Radetzkim. fl.
Inbunden, Engelska, 2003
1 302 kr
Skickas inom 10-15 vardagar
The result of two key social developments in recent years are examined here: the partial dismantling of the welfare state and the progress of genetics. Genetic insights are increasingly valuable for risk assessment, and insurers would like to use these insights to help determine premiums. Combined with the fact that social welfare is being curtailed, this could potentially create an uninsured high-risk population. Along with considerations of autonomy and privacy, this is the basis for an ethical critique of insurer's access to information. The result has often been regulation of such information; but the authors argues that due to adverse selection, regulation will not solve these problems, and this may jeopardize the survival of private personal insurance. Instead, we should look towards the resurrection of social insurance, a key component of the welfare state. This will interest academic researchers as well as professionals involved with genetics and insurance.
Del 2 - Cambridge Law, Medicine and Ethics
Double Standards in Medical Research in Developing Countries
AvRuth Macklin
Inbunden, Engelska, 2004
920 kr
Skickas inom 10-15 vardagar
This book examines the ethical controversies that have surrounded the design and conduct of international medical research sponsored by industrialized countries or industry, and carried out in developing countries. The chief concern is that research subjects in developing countries may be exploited because sponsors of research employ double standards. One debate focuses on whether the standard of care provided to subjects of medical research in developing countries should be the same as what research subjects receive in North America and Europe. Other concerns are whether the process of obtaining informed consent in developing countries is adequate, and whether prior ethical review of research meets standards that are well established in the industrialized world. Recent international developments show that essential medications can be made affordable and accessible to developing countries, and that double standards need not prevail.
Del 5 - Cambridge Law, Medicine and Ethics
The Troubled Pregnancy
Legal Wrongs and Rights in Reproduction
AvJ. K. Mason
Inbunden, Engelska, 2007
1 302 kr
Skickas inom 10-15 vardagar
Mason looks at the legal response to those aspects of the troubled pregnancy which require or involve medico-legal intervention. The unwanted pregnancy is considered particularly in the light of the Abortion Act 1967, s.1(1)(d) and the related action for so-called wrongful birth due to faulty ante-natal care. The unexpected or uncovenanted birth of a healthy child resulting from failed sterilisation is approached through an analysis of the seminal case of McFarlane and associated cases involving disability in either the neonate or the mother. The disabled neonate's right to sue for its diminished life is discussed and the legal approach to the management of severe congenital disease is analysed - thus following Baroness Hale in believing that care of the newborn is an integral part of pregnancy. Aspects are considered from historical and comparative perspectives, including coverage of experience in the USA, the Commonwealth and Europe.
Del 4 - Cambridge Law, Medicine and Ethics
The Ethics and Governance of Human Genetic Databases
European Perspectives
AvMatti Häyry,Ruth Chadwickm. fl.
Inbunden, Engelska, 2007
1 302 kr
Skickas inom 10-15 vardagar
The Medical Biobank of Umeå in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases. The collection, storage and use of this data raise ethical, legal and social issues. In this book, first published in 2007, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.
Del 6 - Cambridge Law, Medicine and Ethics
Law, Legitimacy and the Rationing of Health Care
A Contextual and Comparative Perspective
AvKeith Syrett
Inbunden, Engelska, 2007
1 302 kr
Skickas inom 10-15 vardagar
Dr Keith Syrett argues for a reappraisal of the role of public law adjudication in questions of healthcare rationing. As governments worldwide turn to explicit rationing strategies to manage the mismatch between demand for and supply of health services and treatments, disappointed patients and the public have sought to contest the moral authority of bodies making rationing decisions. This has led to the growing involvement of law in this field of public policy. The author argues that, rather than bemoaning this development, those working within the health policy community should recognise the points of confluence between the principles and purposes of public law and the proposals which have been made to address rationing's 'legitimacy problem'. Drawing upon jurisprudence from England, Canada and South Africa, the book evaluates the capacity of courts to establish the conditions for a process of public deliberation from which legitimacy for healthcare rationing may be derived.
Del 7 - Cambridge Law, Medicine and Ethics
Posthumous Interests
Legal and Ethical Perspectives
AvDaniel Sperling
Inbunden, Engelska, 2008
1 302 kr
Skickas inom 10-15 vardagar
Daniel Sperling discusses the legal status of posthumous interests and their possible defeat by actions performed following the death of a person. The author first explores the following questions: Do the dead have interests and/or rights, the defeat of which may constitute harm? What does posthumous harm consist of and when does it occur, if at all? This is followed by a more detailed analysis of three categories of posthumous interests arising in the medico-legal context: the proprietary interest in the body of the deceased, the testamentary interest in determining the disposal of one's body after death and the interest in post-mortem medical confidentiality. Sperling concludes that if we acknowledge the interest in one's symbolic existence and legally protect it, not only do some interests survive a person's death but we should also enjoy a peremptory legal power to shape in advance our symbolic existence after death.
Del 10 - Cambridge Law, Medicine and Ethics
Human Tissue in Transplantation and Research
A Model Legal and Ethical Donation Framework
AvDavid Price
Inbunden, Engelska, 2009
1 302 kr
Skickas inom 10-15 vardagar
Deficiencies and shortfalls in the supply of human organs for transplantation and human tissue for research generate policy dilemmas across the world and have often given rise to major and deleterious controversies, such as those relating to organ and tissue retention practices following post-mortem examination. They also create an environment in which illegitimate commercial activities flourish. At the same time, patients are denied the therapy they desperately require and researchers are impeded from carrying out vital work into the causes of, and efficacious treatments for, major illnesses and diseases. David Price sets out a clear and integrated legal and policy framework which emanates from the tissue source but protects the interests of donors and relevant professionals through tailored property entitlements, but without presupposing rights to trade in 'original' materials.
Del 8 - Cambridge Law, Medicine and Ethics
Autonomy, Informed Consent and Medical Law
A Relational Challenge
AvAlasdair Maclean
Inbunden, Engelska, 2009
1 351 kr
Skickas inom 10-15 vardagar
Alasdair Maclean analyses the ethical basis for consent to medical treatment, providing both an extensive reconsideration of the ethical issues and a detailed examination of English law. Importantly, the analysis is given a context by situating consent at the centre of the healthcare professional-patient relationship. This allows the development of a relational model that balances the agency of the two parties with their obligations that arise from that relationship. That relational model is then used to critique the current legal regulation of consent. To conclude, Alasdair Maclean considers the future development of the law and contrasts the model of relational consent with Neil Manson and Onora O'Neill's recent proposal for a model of genuine consent.
Del 12 - Cambridge Law, Medicine and Ethics
Healthcare Decision-Making and the Law
Autonomy, Capacity and the Limits of Liberalism
AvMary Donnelly
Häftad, Engelska, 2014
455 kr
Skickas inom 11-20 vardagar
This analysis of the law's approach to healthcare decision-making critiques its liberal foundations in respect of three categories of people: adults with capacity, adults without capacity and adults who are subject to mental health legislation. Focusing primarily on the law in England and Wales, the analysis also draws on the law in the United States, legal positions in Australia, Canada, Ireland, New Zealand and Scotland and on the human rights protections provided by the ECHR and the Convention on the Rights of Persons with Disabilities. Having identified the limitations of a legal view of autonomy as primarily a principle of non-interference, Mary Donnelly questions the effectiveness of capacity as a gatekeeper for the right of autonomy and advocates both an increased role for human rights in developing the conceptual basis for the law and the grounding of future legal developments in a close empirical interrogation of the law in practice.
Del 8 - Cambridge Law, Medicine and Ethics
Autonomy, Informed Consent and Medical Law
A Relational Challenge
AvAlasdair Maclean
Häftad, Engelska, 2013
476 kr
Skickas inom 10-15 vardagar
Alasdair Maclean analyses the ethical basis for consent to medical treatment, providing both an extensive reconsideration of the ethical issues and a detailed examination of English law. Importantly, the analysis is given a context by situating consent at the centre of the healthcare professional-patient relationship. This allows the development of a relational model that balances the agency of the two parties with their obligations that arise from that relationship. That relational model is then used to critique the current legal regulation of consent. To conclude, Alasdair Maclean considers the future development of the law and contrasts the model of relational consent with Neil Manson and Onora O'Neill's recent proposal for a model of genuine consent.
Del 9 - Cambridge Law, Medicine and Ethics
The Governance of Genetic Information
Who Decides?
AvHeather Widdows,Caroline Mullen
Häftad, Engelska, 2013
426 kr
Skickas inom 10-15 vardagar
This volume maps the areas of ethical concern in the debate regarding the governance of genetic information, and suggests alternative ethical frameworks and models of regulation in order to inform its restructuring. Genetic governance is at the heart of medical and scientific developments, and is connected to global exploitation, issues of commodification, commercialisation and ownership, the concepts of property and intellectual property and concerns about individual and communal identity. Thus the decisions that are made in the next few years about appropriate models of genetic governance will have knock-on effects for other areas of governance. In short the final answer to 'Who Decides?' in the context of genetic governance will fundamentally shape the ethical constructs of individuals and their networks and relationships in the public sphere.
The Ethics and Governance of Human Genetic Databases
European Perspectives
AvMatti Häyry,Ruth Chadwickm. fl.
Häftad, Engelska, 2013
438 kr
Skickas inom 10-15 vardagar
The Medical Biobank of Umeå in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases. The collection, storage and use of this data raise ethical, legal and social issues. In this book, first published in 2007, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.

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Cambridge Law, Medicine and Ethics – serie

Genes and Insurance

Healthcare Decision-Making and the Law

Posthumous Interests

Xenotransplantation and Risk

Organ Shortage

The Governance of Genetic Information

Double Standards in Medical Research in Developing Countries

The Troubled Pregnancy

Law, Legitimacy and the Rationing of Health Care

Human Tissue in Transplantation and Research

Rationality and the Genetic Challenge

Rationality and the Genetic Challenge

Genes and Insurance

Double Standards in Medical Research in Developing Countries

The Troubled Pregnancy

The Ethics and Governance of Human Genetic Databases

Law, Legitimacy and the Rationing of Health Care

Posthumous Interests

Human Tissue in Transplantation and Research

Autonomy, Informed Consent and Medical Law

Healthcare Decision-Making and the Law

Autonomy, Informed Consent and Medical Law

The Governance of Genetic Information

The Ethics and Governance of Human Genetic Databases

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