Searight Ethical Challenges in Multi-Cultural Patient Care

Cross Cultural Issues at the End of Life
1. Auflage 2019
ISBN: 978-3-030-23544-4
Verlag: Springer International Publishing
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 107 Seiten, eBook

Reihe: SpringerBriefs in Ethics

This book provides an up-to-date description of cross-cultural aspects of end-of-life decision-making. The work places this discussion in the context of developments in the United States such as the emphasis on patient informed consent, “right to die” legal cases, and the federal Patient Self-Determination Act. With the globalization of health care and increased immigration from developing to developed countries, health care professionals are experiencing unique challenges in communicating with seriously ill patients and their families about treatment options as well as counselling all patients about advance medical care planning. While many Western countries emphasize individual autonomy and patient-centered decision-making, cultures with a greater collectivist orientation have, historically, often protected patients from negative health information and emphasized family-centered decision-making. In order to place these issues in context, the history of informed consent in medicineis reviewed. Additionally, cross-cultural issues in health care decision-making are analysed from the perspective of multiple philosophical theories including deontology, utilitarianism, virtues, principlism, and communitarian ethics.  This book is a valuable addition to courses on end-of-life care, death and dying, cross-cultural health, medical anthropology, and medical ethics and an indispensable guide for healthcare workers dealing with patients coming from various cultural backgrounds.

Zielgruppe

Research

Autoren/Hrsg.

Searight, H. Russell

Inhaltsverzeichnis

Chapter 1. Introduction to the Topic.- Chapter 2. Ethical Theories Influencing Health Care Decisions.- Chapter 3. Social Factors Influencing End-of-Life Decision-Making.- Chapter 4. Physician Communication.- Chapter 5. Representing the Seriously Ill Patient’s Interests.- Chapter 6. Legal and Policy Issues Influencing End-of-Life Decisions.- Chapter 7. Conclusion—Future Directions.

Über Autor(innen)

H. Russell Searight. Ph.D., MPH is currently Professor of Psychology in the School of Health Services at Lake Superior State University. He has held previous academic positions at Saint Louis University School of Medicine and Southern Illinois University-Edwardsville. Dr. Searight has conducted original research and published widely on cultural diversity, mental health and ethical issues in primary health care, and family dynamics.