
Informed Consent
Legal Theory and Clinical Practice
Oxford University Press
2nd Edition
Published on 16. August 2001
Book
Hardback
352 pages
978-0-19-512677-8 (ISBN)
Description
Informed consent - as an ethical ideal and legal doctrine - has been the source of much concern to clinicians. Drawing on a diverse set of backgrounds and two decades of research in clinical settings, the authors - a lawyer, a physician, a social scientist, and a philosopher - help clinicians understand and cope with their legal obligations and show how the proper handling of informed consent can improve , rather than impede, patient care. Following a concise review of the ethical and legal foundations of informed consent, they provide detailed, practical suggestions for incorporating informed consent into clinical practice. This completely revised and updated edition discusses how to handle informed consent in all phases of the updated edition discusses how to handle informed consent in all phases of the doctor-patient relationship, use of consent forms, patients' refusals of treatment, and consent to research. It comments on recent laws and national policy, and addresses cutting edge issues such as fulfilling physician obligations under managed care.
This clear and succinct book contains a weath of information that will not only help clinicians meet the legal requirements of informed consent and understand its ethical underpinnings, but also enhance their ability to deal with their patients more effectively. It will be of value to all those working in areas where issues of informed consent are likely to arise, including medicine, biomedical research, mental health care, nursing, dentistry, biomedical ethics, and law.
This clear and succinct book contains a weath of information that will not only help clinicians meet the legal requirements of informed consent and understand its ethical underpinnings, but also enhance their ability to deal with their patients more effectively. It will be of value to all those working in areas where issues of informed consent are likely to arise, including medicine, biomedical research, mental health care, nursing, dentistry, biomedical ethics, and law.
Reviews / Votes
"This remarkable book would be an excellent core text for every medical school curriculum." -- American Journal of Opthalmology "...an interesting and well researched book...demonstrates extensive knowledge over a range of disciplines...useful and stimulating." -- Bioethics "It is appropriate reading for all physicians who seek to improve their skills in establishing an effective therapeutic relationship." -- American Journal of Psychiatry "Because it integrates theory and practice this book represents an advance in the informed-consent literature and should be read by medical students, house staff, attending physicians, nurses and all other who care for and about patients. Those who view informed consent as a bureaucratic nuissance or who believe consent is something to "get" will be forced to question their assumptions. Lawyers who read this book will discover that adversarial legal proceedings may not promote quality patient care. Finally, this book should be read by lay people. They will become even better partners in the process of medical decision-making." -- Canadian Medical Association Journal "Who should read this book? Ideally, every health care professional; realistically, those charged with the education of students and the continuing education of those now in practice." -- Journal of the American Medical AssociationMore details
Edition
2nd Revised edition
Language
English
Place of publication
Oxford
United Kingdom
Target group
College/higher education
Professional and scholarly
Edition type
Revised edition
Dimensions
Height: 240 mm
Width: 161 mm
Thickness: 24 mm
Weight
699 gr
ISBN-13
978-0-19-512677-8 (9780195126778)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

Jessica W. Berg | Paul S. Appelbaum | Charles W. Lidz
Informed Consent
Legal Theory and Clinical Practice
E-Book
07/2001
2nd Edition
OUP eBook
€60.49
Available for download
Persons
Author
Assistant Professor of Law and BioethicsAssistant Professor of Law and Bioethics, Case Western Reserve Unviersity, Schools of Law and Medicine
A. F. Zelenik Distinguished Professor of Psychiatry and ChairA. F. Zelenik Distinguished Professor of Psychiatry and Chair
Research Professor of PsychiatryResearch Professor of Psychiatry, both at the University of Massachusetts Medical School
Associate Professor and Director of Graduate EducationAssociate Professor and Director of Graduate Education, University of Pittsburgh
Content
1. Informed Consent: Framing the Questions ; 2. The Concept and Ethical Justification of Informed Consent ; 3. The Legal Requirements for Disclosure and Consent: History and Current Status ; 4. Exceptions to the Legal Requirements: Emergency, Waiver, Therapeutic Privilege and Compulsory Treatment ; 5. Exceptions to the Legal Requirements: Incompetence ; 6. Legal Rules for Recovery ; 7. Critical Approaches to the Law of Informed Consent ; 8. The Role of Informed Consent in Medical Decision-making ; 9. Consent Forms: Documentation and Guidance ; 10. Managed Care and Informed Consent ; 11. Patients Who Refuse Treatment ; 12. The Independent Evolution of Informed Consent to Research ; 13. Fulfilling the Underlying Purpose of Informed Consent to Research ; 14. The Limits of Informed Consent ; 15. An Agenda for the Future