Bøker i Cambridge Bioethics and Law-serien

A collection of bioethical case studies that shows why ethical behaviour matters more than bioethics commentary. Will be of interest to those working and teaching in bioethics, health law, research ethics, public policy, medical technology and pharmaceutical development, governmental affairs, and the history and philosophy of science and medicine.

Personal genetic information is increasingly accessible. Consumers can obtain and share information through DNA tests purchased online. Databases make personal details available for research or criminal investigation. This book examines the right to know or not to know genetic information about yourself and others.

This book provides a comprehensive and approachable overview of Medicare under the Affordable Care Act (ACA). The author illustrates how the ACA addresses the long-term fiscal and demographic challenges facing Medicare, as well as the potential for Medicare to become a single-payer system.

This volume considers historical comparisons and the current laws in jurisdictions such as Canada, the United Kingdom and Norway in order to explore the question of if and when it is appropriate to criminalise the transmission of contagion.

Research in bioethics is becoming increasingly interdisciplinary, and researchers are turning to novel methodologies that combine the benefits of both theoretical and empirical research. Contributions in this volume are written by experts in the field, bringing together the most recent developments in methodological thinking and offering new insights into established approaches.

In times of global economic and political crises, the notion of solidarity is gaining new currency. Exemplified by three case studies from medicine and health, this book shows how solidarity can make a difference in how we frame problems in biomedicine, and help develop innovative solutions.

Continuous sedation is becoming increasingly common in end-of-life care. It raises many concerns, though, especially regarding reducing or removing consciousness, withholding hydration and whether it amounts to 'slow euthanasia'. In this book, ethicists, clinicians and lawyers address these concerns and discuss various justifications and guidelines for the practice.

A comprehensive resource on health information technology and its legal, ethical, and policy implications, focusing on the intersection of law and policy. Combining exhaustive research with accessible writing, it will appeal to readers with diverse levels of expertise, including academics, students, health care providers, attorneys, and policy-makers.

This illuminating study provides a detailed discussion of the role of law and regulation in patient safety and argues that medical professionalism must evolve to embrace a patient-centred perspective. It will appeal to researchers of medical law and ethics, and those working on public health and social policies.