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Informed Consent: Legal Theory and Clinical Practice
Contributor(s): Berg, Jessica W. (Author)
ISBN: 0195126777     ISBN-13: 9780195126778
Publisher: Oxford University Press, USA
OUR PRICE:   $94.05  
Product Type: Hardcover
Published: July 2001
Qty:
Annotation: 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 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 wealth 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.
Additional Information
BISAC Categories:
- Law | Medical Law & Legislation
- Law | Ethics & Professional Responsibility
- Medical | Ethics
Dewey: 344.730
LCCN: 00053069
Physical Information: 1.11" H x 6.44" W x 9.52" (1.44 lbs) 352 pages
 
Descriptions, Reviews, Etc.
Publisher 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 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 wealth 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.