Ruth Chadwick

This comprehensive and thought-provoking textbook offers both an essential introduction to key aspects of nursing ethics, including the role of professional codes of conduct and challenges to be encountered in the 21st century, and an in-depth exploration of ethical issues in relation to specific patient groups, such as the unborn, those with mental health difficulties, and the dying. In addition, the book provides a stimulating discussion of ethics relating to public health issues, such as smoking and obesity, as well as the fundamental matter of ethics in nursing research.With ethics at the core of nursing practice, this fully updated textbook is a must-read for students on nursing undergraduate programmes and qualified practitioners wanting to ensure their skills are update and they’re delivering the best care possible.New to this Edition:- Fully updated new edition- Illustrated by a wealth of case studies relating to real-life conflicts to aid understanding and application of knowledge and encourage students to think about practical rather than abstract issues

The Medical Biobank of Umeå in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases. The collection, storage and use of this data raise ethical, legal and social issues. In this book, first published in 2007, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.

The Medical Biobank of Umeå in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases. The collection, storage and use of this data raise ethical, legal and social issues. In this book, first published in 2007, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.