Böcker i Issues in Biomedical Ethics-serien

Investigates a theoretical question that is at the centre of practical and professional ethics: what are the criteria for having moral status? This work argues that no single property will do as a sole criterion, and puts forward seven basic principles which establish moral status.

This is the first book that explains how you actually go about doing good bioethics. John McMillan develops an account of the nature of bioethics; he reveals how a number of methodological spectres have obstructed bioethics; and then he shows how moral reason can be brought to bear upon practical issues via an 'empirical, Socratic' approach.

Embryonic stem cell research holds great promise for biomedical research, but involves the destruction of human embryos. Katrien Devolder explores the tension between the view that embryos should never be deliberately harmed, and the view that such research must go forward. She provides an in-depth analysis of major attempts to resolve the problem.

Transplantation is a medically successful and cost-effective way to treat people whose organs have failed-but not enough organs are available to meet demand. T. M. Wilkinson explores the major ethical problems raised by policies for acquiring organs. Key topics include the rights of the dead, the role of the family, and the sale of organs.

The ethics of medical care and biomedical research are rapidly becoming global. This volume gathers leading bioethicists to explore many new questions raised by the internationalization of medical care and biomedical research. Topics covered include, amongst others, the impact of globalization and the relation of religion to global bioethics.

In these twelve papers notable ethicists use the resources of ethical theory to illuminate important theoretical and practical topics, including the nature of public health, notions of community, population bioethics, the legitimate role of law, the use of cost-effectiveness as a methodology, vaccinations, and the nature of infectious disease.

Examines the moral principles that guide parents in making health care decisions for their children, and the role of children in the decision-making process. This book argues against the movement to increase child autonomy, in favor of respect for family autonomy. It is meant for health care providers, ethicists, and public policy analysts.

What role should the law play in regulating risks? What limits do we wish to place upon public health activities? Addressing such questions, this book explores various issues in public health ethics using the resources of moral theory, political philosophy, philosophy of science, applied ethics, law, and economics.

Giordano presents the first full philosophical study of ethical issues in the treatment of anorexia and bulimia nervosa. She analyses these conditions, explores their complex causes, then addresses legal and ethical dilemmas such as a patient's refusal of life-saving treatment. Essential for anyone working on these much misunderstood conditions.

Lainie Ross presents a rigorous critical investigation of the development of policy governing the involvement of children in medical research. She examines the shift in focus from protection of medical research subjects, enshrined in post-World War II legislation, to the current era in which access is assuming greater precedence.

In bioethics, discussions of justice have tended to focus on questions of fairness in access to health care: is there a right to medical treatment, and how should priorities be set when medical resources are scarce. But health care is only one of many factors that determine the extent to which people live healthy lives, and fairness is not the only consideration in determining whether a health policy is just. In this pathbreaking book, senior bioethicists Powers andFaden confront foundational issues about health and justice. How much inequality in health can a just society tolerate. The audience for the book is scholars and students of bioethics and moral and political philosophy, as well as anyone interested in public health and health policy.

An international team of eighteen doctors, philosophers, and lawyers present a fresh and thorough discussion of the ethical, legal, and social issues raised by testing and screening for HIV and AIDS. They aim to point the way to practical advances but also to give an accessible guide for those new to the debate.

An international team of eighteen doctors, philosophers, and lawyers present a fresh and thorough discussion of the ethical, legal, and social issues raised by testing and screening for HIV and AIDS. They aim to point the way to practical advances but also to give an accessible guide for those new to the debate.

Explains ethics, law, and human rights to healthcare providers and administrators, and reproductive health to lawyers and women's health advocates. This book explores and illustrates limitations and dysfunctions of the health systems and their legal regulation, but also propose opportunities for reform.

A team of experts explore the ethics of making families through adoption or technologically assisted reproduction. They examine the moral choices involved, and the social norms that can distort decision-making, such as the norm in favour of having biologically related children, or the privileging of a traditional understanding of family.

A team of experts explore the ethics of making families through adoption or technologically assisted reproduction. They examine the moral choices involved, and the social norms that can distort decision-making, such as the norm in favour of having biologically related children, or the privileging of a traditional understanding of family.

What is health policy for? Alan Cribb addresses this question in a way that cuts across disciplinary boundaries. His core argument is that biomedical ethics should draw upon public health values and ethics. He argues that everybody has some share of responsibility for health, including a responsibility for promoting greater health equality.

Brings together work, by a group of contributors from various fields and perspectives, on ethical, social, and legal issues raised by advances in reproductive technology. This title discusses topics that include gender and race selection, genetic engineering, fertility treatment, ovarian tissue transfer, and post-menopausal pregnancy.

Features fourteen essays that provide an overview of the key moral, legal, and social themes raised by new ways of making babies. This book offers perspectives on these topics from a variety of disciplines and professions as well as from a range of national and cultural perspectives.

To what extent should parents be allowed to use reproductive technologies to determine the characteristics of their future children? Is there something morally wrong with choosing what their sex will be, or with trying to 'screen out' as much disease and disability as possible before birth? Stephen Wilkinson offers answers to such questions.