
Of all cancers, probably breast cancer is one of the most emotive. Increasingly patients with breast cancer are participating in the surgical and/or medical decisions about their treatment. This involvement raises ethical issues about the rights of patients and their ability to give an informed consent, concerns about the process of communication between the medical staff and the patient, and also issues about the psychology of not only the woman with breast cancer, but also the doctor. This book addresses these issues relating to shared decision making and in particular those areas where a choice of treatment option involves some degree of risk/benefit analysis. It covers the ethical principles and then looks at the evidence that women who are fully informed and who have taken part in the decision making process regarding their treatment, and who have a positive attitude towards their illness, tend to do better in the long run. Appropriate experts have contributed sections on the different treatment options to provide a brief overview of the treatments available and highlight the issues that should be considered by the woman and the doctor in the decision making process. There is also a section on the patients perspective and vignettes throughout to illustrate the importance of communication.
This text investigates the ethical and practical complexities of shared decision-making between patients and medical professionals in the context of breast cancer treatment. The authors, Anna M. Maslin and Trevor J. Powles, utilize their clinical expertise to examine how informed consent, psychological factors, and risk-benefit analysis influence long-term patient outcomes. The book argues that active patient participation in treatment selection, supported by clear communication, correlates with improved patient well-being and recovery trajectories.
What You Will Find
Scope Limits
Medical professionals and patient advocates frequently cite this text as a foundational resource for understanding the nuances of the doctor-patient relationship in cancer care. Experts highlight the book's utility in bridging the gap between clinical necessity and the ethical imperative for patient autonomy.
Page Count:
288
Publication Date:
1999-07-08
Publisher:
Oxford University Press
ISBN-10:
0192629670
ISBN-13:
9780192629678
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