Informed Consent

Legal Theory and Clinical Practice
 
 
Oxford University Press Inc
  • erschienen am 21. Mai 1987
 
  • Buch
  • |
  • Hardcover
  • |
  • 320 Seiten
978-0-19-503841-5 (ISBN)
 
Few issues affecting the therapeutic professions are as much discussed and as little understood as informed consent. Although most physicians and other professionals who are affected by the legal requirements for informed consent recognize that there is some legal obligation to talk with patients and obtain their agreement to proposed treatment, often their knowledge of the details are a mixture of myth and misunderstanding. Written by a psychiatrist, a social scientist, and an attorney, this book provides the first comprehensive introduction to the theory and practice of informed consent. Beginning with an overview of the issues raised by the development of the idea of informed consent and the ethical theories on which informed consent rests, the book then details the legal requirements for practitioners, paying particular attention to areas of legal ambiguity with which practitioners must cope in formulating their approaches to informed consent. The book next considers the problems faced by health professional in applying informed consent theory in the clinical setting and proposes a model for simplifying that task.
  • Englisch
  • New York
  • |
  • USA
  • Für höhere Schule und Studium
  • |
  • Für Beruf und Forschung
  • Höhe: 220 mm
  • |
  • Breite: 140 mm
  • 536 gr
978-0-19-503841-5 (9780195038415)

PART I: AN INTRODUCTION TO INFORMED CONSENT; Informed consent: framing the questions; ethical principles underlying informed consent; PART II: THE LEGAL THEORY OF INFORMED CONSENT; The law of informed consent: requirements for disclosure and consent; exceptions to the requirements for disclosure and consent: emergency, waiver, and therapeutic privilege; exceptions to the requirements for disclosure and consent: incompetency; rules governing patients' redress in the courts for failure to obtain informed consent; critical approaches to the law of informed consent; PART III: INFORMED CONSENT IN THE CLINICAL SETTING; the role of informed consent in medical decisionmaking; consent forms; patients who refuse treatment; PART IV: INFORMED CONSENT IN THE RESEARCH SETTING; the law of consent to research; informed consent and decisionmaking about research; advancing informed consent: an agenda for the future.

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