Robert M. Veatch

The Basics of Bioethics

This brief summary of the issues of biomedical ethics provides a balanced, systematic, unbiased framework designed to help health professionals an lay people understand and analyze a wide range of topics that are currently controversial in medicine–or that are likely to arise in the future. Broad in scope, it considers ethical systems from various religious and secular traditions, including those of non-western cultures such as Asian religious and secular traditions. Topics include the history of codes of ethics; the definition of death, abortion, animal rights and welfare; problems in deciding what will benefit patients; confidentiality, truth-telling, informed consent; the care of the terminally ill; genetics, birth technologies; and problems of social ethics, including resource allocation, organ transplant, and human subjects research. For use in allied health fields.

Values and Life-extending Technologies

Life Span

Lainie F. Ross

Although the history of organ transplant has its roots in ancient Christian mythology, it is only in the past fifty years that body parts from a dead person have successfully been procured and transplanted into a living person. After fourteen years, the three main issues that Robert Veatch first outlined in his seminal study Transplantation Ethics still remain: deciding when human beings are dead; deciding when it is ethical to procure organs; and deciding how to allocate organs, once procured. However, much has changed. Enormous strides have been made in immunosuppression. Alternatives to the donation model are debated much more openly—living donors are used more widely and hand and face transplants have become more common, raising issues of personal identity. In this second edition of Transplantation Ethics, coauthored by Lainie Friedman Ross, transplant professionals and advocates will find a comprehensive update of this critical work on transplantation policies.

Transplantation Ethics, Second Edition

Amy Marie Haddad

Dan C. English

The most comprehensive and up-to-date collection of its kind, Case Studies in Biomedical Ethics: Decision-Making, Principles, and Cases, Second Edition, explores fundamental ethical questions arising from real situations faced by health professionals, patients, and others. Featuring a wide range of more than 100 case studies drawn from current events, court cases, and physicians' experiences, the book is divided into three parts. Part 1 presents a basic framework for ethical decision-making in healthcare, while Part 2 explains the relevant ethical principles: beneficence and nonmaleficence, justice, respect for autonomy, veracity, fidelity, and avoidance of killing. Parts 1 and 2 provide students with the background to analyze the ethical dilemmas presented in Part 3, which features cases on a broad spectrum of issues including abortion, mental health, experimentation on humans, the right to refuse treatment, and much more. The volume is enhanced by opening text boxes in each chapter that cross-reference relevant cases in other chapters, an appendix of important ethical codes, and a glossary of key terms.

Decision-making, Principles, and Cases

Case Studies in Biomedical Ethics

Hans-Martin Sass

Rihito Kimura

"The objective of this transnational, transdisciplinary study was not to predict the future. Much less was it to determine which culture has the best legal, public policy, and ethical systems. Rather, it was to understand the systems--their similarities and differences--and their implications for shaping the public policies that will shape the legal and medical world to come."--from the introduction Advance directives to determine the care of terminally ill patients have revolutionized health care decision making. But writing a directive that accomplishes exactly what a patient wants can be a difficult process and can be ethically controversial. While Americans, deeply immersed in Western liberal political philosophy, have an intuitive attraction to advance directives, other cultures do not. In this volume, an international team of experts examines the controversy surrounding advance directives in three countries: the United States, Germany, and Japan. Within each section, the subjects are addressed from the points of view of clinicians, legal experts, and bioethicists. The authors find that the United States and Japan are at opposite ends of a spectrum of opinion regarding patient autonomy, whereas Germany falls somewhere between.

United States, Germany, and Japan

Advance Directives and Surrogate Decision Making in Health Care

"The change is in how we think about medical decision-making. Whereas modern medicine's core idea was that medical decisions should be based on the cold, hard facts of science-the province of the doctor-the "new medicine" reflects the notion that all medical decisions must impose value judgments. Since physicians can claim no expertise on making those value judgments, the pendulum has swung greatly toward the patient in evaluating alternatives and making decisions about their treatment." "Veatch uses a range of fascinating contemporary and historical examples to reveal how values underlie almost all medical procedures, and illustrate his case that this change is inevitable and a positive trend for patients."--BOOK JACKET.

How the New Medicine Puts the Patient in Charge

Patient, Heal Thyself

A collection of readings on topics such as abortion, organ transplantation, and HIV. Valuable for practitioners, and students of medical ethics.

Medical Ethics

E. J. Last

Pharmacists constantly face ethical choices -- sometimes dramatic matters of life-and-death decisions, but more often subtle, less conspicuous choices that are nonetheless important. Case Studies in Pharmacy Ethics identifies and discusses the broad range of ethics issues pharmacists confront in practice. Ranging from situations faced in direct patient care to broader issues, this book uses cases to explore topics and the ethical framework within which practitioners make decisions about such issues as assisted suicide, conscientious refusal, pain management, and confidentiality as well as the equitable distribution of drug resources within institutions or managed care organizations and clinical studies on vulnerable populations. As the scope of the pharmacist's role expands, pharmacists find themselves facing new ethical challenges. This third edition accounts for some of the many changes in pharmacy practice and in the delivery of health care since the second edition. It includes an entirely new chapter on health insurance and health system planning, and a discussion of the impact of the Affordable Care Act and cases that are updated to reflect current pharmacy practice models. It serves as a valuable resource regarding topics that are both specific to pharmacy practice and those that involve the health care system more generally.

Case Studies in Pharmacy Ethics

Tom L. Beauchamp

This anthology of major classical and contemporary views on key ethical aspects of death and dying is the only philosophically sophisticated, interdisciplinary, and up-to-date introduction to the subject available. Pairs pro and con arguments to give a balanced perspective. Covers a range of topics that reflect the latest developments at the frontier of the field. Provides clearly and carefully written section introductions that define the issues to be discussed. Introduces each selection with a brief editorial essay. Features up-to-date and solid analyses of all issues. Offers an excellent introduction to ethical theory.

Ethical Issues in Death and Dying

Cross- Cultural Perspectives in Medical Ethics, Second Edition, is an anthology of the latest and best readings on the medical ethics of as many of the major religious, philosophical, and medical traditions that are available today.

Cross-cultural Perspectives in Medical Ethics

Our Last Quest for Responsibility

Death, Dying, and the Biological Revolution

Albert R. Jonsen

LeRoy Walters

Government agencies and commissions, courts, and legislatures have during the past several decades produced reports, rendered decisions, and passed laws that have both defined the fundamental issues in the field of bioethics and established ways of managing them in our society. Providing a history of these key bioethical decisions, this Source Book in Bioethics is the first and only comprehensive collection of the critical public documents in biomedical ethics, including many hard-to-find or out-of-print materials. Covering the period from 1947 to 1995, this volume brings together core legislative documents, court briefs, and reports by professional organizations, public bodies, and governments around the world. Sections on human experimentation, care of the terminally ill, genetics, human reproduction, and emerging areas in bioethics include such pivotal works as "The Nuremberg Code," "The Tuskegee Report," and "In the Matter of Baby M," as well less readily available documents as "The Declaration of Inuyama," the Council for International Organizations of Medical Sciences statement on genetic engineering, and "The Warnock Committee Report" on reproductive technologies from the United Kingdom. Three eminent scholars in the field provide brief introductions to each document explaining the significance of these classic sources. This historical volume will be a standard text for courses in bioethics, health policy, and death and dying, and a primary reference for anyone interested in this increasingly relevant field.

A Documentary History

Source Book in Bioethics

For most of human history there was little question about whether someone was dead or alive--a heartbeat or a pulse, or a foggy mirror under the nostrils, provided sufficient evidence. But in the mid-20th century, with new technologies and medical interventions that prolonged the dying process, the questions around the precise moment of death became much more complicated. Today the global medical community recognizes three general definitions of death: whole-brain, circulatory or somatic, and higher-brain. But even in the United States alone no single concept of death has the support of the majority of its citizens. Despite attempts to create and establish a uniform definition of death, physicians and policymakers continue to disagree on criteria and standards--resulting in confusion and acrimony in medicine, law, and insurance, not to mention families gathered around the bedside of a dying loved one. In this brief introduction Veatch and Ross lay out the history of this contentious issue and describe the three major definitions of death in detail. They contend that choosing a particular definition of death reflects an individual's basic religious and philosophical beliefs about what is essential to human existence. So while they propose higher-brain death as a default policy, they argue for some degree of personal choice.

The Case for Choice

Defining Death

Sara T. Fry

Rev. ed. of: Case studies in nursing ethics / Robert M. Veach, Sara T. Fry. 1987.

Case Studies in Nursing Ethics

Carol R. Taylor

Important Notice: The digital edition of this book is missing some of the images or content found in the physical edition. As the healthcare professional in closest contact with both the patient and the physician, nurses face biomedical ethical problems in unique ways. Accordingly, Case Studies in Nursing Ethics presents basic ethical principles and specific guidance for applying these principles in nursing practice, through analysis of over 150 actual case study conflicts that have occurred in nursing practice. Each case study allows readers to develop their own approaches to the resolution of ethical conflict and to reflect on how the traditions of ethical thought and professional guidelines apply to the situation. The Fourth Edition has been completely revised and updated. It includes two new chapters, one on Moral Integrity and Moral Distress which contains AACN model of moral distress and work and one on Respect which addresses several aspects of the general problem of showing r

Robert M. Veatch

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