Udo Schüklenk

Societies around the world are becoming increasingly multicultural, while the range of new or controversial medical procedures that are available to patients also grows. This has led to an increase in claims from healthcare professionals regarding their right to abide by their own moral or religious views and refuse a long list medical interventions or drugs. This list includes abortions, euthanasia, access to contraceptives, sterilizations, cosmetic surgery, and many others. Depending on circumstances, these interventions might or might not be consistent with professional standards; however, when deciding whether to provide them, many doctors would rely on their own conscientious views about the morality of each case instead of professional standards. As societies become more pluralistic and the range of medical options continues to grow, it is inevitable that the problem of conscientious objection in healthcare will as well. Rethinking Conscientious Objection in Health Care presents the case against the right of healthcare professionals to refuse delivery of certain healthcare services based on their moral views. It provides philosophical analyses of conscience and freedom of conscience, as well as the arguments and principles typically utilized when arguing in favor of allowing healthcare professionals conscientious objection. The authors criticize those arguments and offer a philosophical and historical analysis of the concept of professionalism, as well as an appeal to the nature of professional obligations, to build their case against the right to conscientious objection in healthcare. They explain why arguments for pluralism, tolerance, and diversity which support a right to freedom of conscience in society at large do not necessarily support the same right within the healthcare profession, or indeed any profession that is governed by internal norms of professionalism which an individual freely decides to enter.

Should editing the human genome be allowed? What are the ethical implications of social restrictions during a pandemic? Is it ethical to use animals in clinical research? Is prioritizing COVID-19 treatment increasing deaths from other causes? Bioethics is a dynamic field of inquiry that draws on interdisciplinary expertise and methodology to address normative issues in healthcare, medicine, biomedical research, biotechnology, public health, and the environment. This Is Bioethics is an ideal introductory textbook for students new to the field, exploring the fundamental questions, concepts, and issues within this rapidly evolving area of study. Assuming no prior knowledge of the subject, this accessible volume helps students consider both traditional and cutting-edge questions, develop informed and defensible answers, and evaluate the strengths and weaknesses of a diverse range of ethical positions in medicine. The authors avoid complex technical terms and jargon in favor of an easy-to-follow, informal writing style with engaging chapters designed to stimulate student interest and encourage class discussion. The book also features a deep dive into the realm of global public health ethics, including the response to the COVID-19 pandemic. It considers topics like triage decision-making, the proportionality of society's response to COVID-19, whether doctors have a professional obligation to treat COVID-19 patients, and whether vaccines for this virus should be mandatory. A timely addition to the acclaimed This Is Philosophy series, This Is Bioethics is the ideal primary textbook for undergraduate bioethics and practical ethics courses, and is a must-have reference for students in philosophy, biology, biochemistry, and medicine.

This volume features a collection of the most important articles on the social, ethical and legal implications of a variety of problems caused by AIDS. The wide range of articles selected for inclusion were chosen on the basis of three criteria: their theoretical depth and coherence, their impact on the subsequent debate and on the social and ethical relevance of the problems addressed. Sections in the book include: physicians and patients, AIDS and the law, HIV testing, clinical research in developed countries, clinical research in developing countries and dying with dignity