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Informed Consent - Jessica W. Berg, Paul S. Appelbaum, Charles W. Lidz, Lisa S. Parker

Informed Consent

Legal Theory and Clinical Practice
Buch | Hardcover
352 Seiten
2001 | 2nd Revised edition
Oxford University Press (Verlag)
978-0-19-512677-8 (ISBN)
CHF 115,10 inkl. MwSt
Informed consent - as an ethical and legal doctrine - has been the source of much concern to physicians. This much expanded and updated edition provides information to help clinicians meeting their legal and ethical obligations. It offers practical suggestions for incorporating informed consent into clinical practice.
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.

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

Erscheint lt. Verlag 16.8.2001
Verlagsort Oxford
Sprache englisch
Maße 164 x 242 mm
Gewicht 653 g
Themenwelt Medizin / Pharmazie Gesundheitswesen
Medizin / Pharmazie Medizinische Fachgebiete Medizinethik
Studium Querschnittsbereiche Geschichte / Ethik der Medizin
ISBN-10 0-19-512677-7 / 0195126777
ISBN-13 978-0-19-512677-8 / 9780195126778
Zustand Neuware
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