Ethics and Chronic Illness:
This book provides an account of the ethics of chronic illness. Chronic illness differs from other illnesses in that it is often incurable, patients can live with it for many years, and its day-to-day management is typically carried out by the patient or members of their family. These features probl...
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Main Author: | |
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Format: | Electronic eBook |
Language: | English |
Published: |
New York, NY
Routledge
2019
|
Series: | Routledge research in applied ethics
Routledge research in applied ethics |
Subjects: | |
Links: | https://www.taylorfrancis.com/books/9780429264863 |
Summary: | This book provides an account of the ethics of chronic illness. Chronic illness differs from other illnesses in that it is often incurable, patients can live with it for many years, and its day-to-day management is typically carried out by the patient or members of their family. These features problematise key distinctions that underlie much existing work in medical ethics including those between beneficence and autonomy, between treatment and prevention, and between the recipient and provider of treatment. The author carries out a detailed reappraisal of the roles of both autonomy and beneficence across the different stages of treatment for a range of chronic illnesses. A central part of the author's argument is that in the treatment of chronic illness, the patient and/or the patient's family should be seen as acting with healthcare professionals to achieve a common aim. This aspect opens up unexplored questions such as what healthcare professionals should do when patients are managing their illness poorly, the ethical implications of patients being responsible for parts of their treatment, and how to navigate sharing information with those directly involved in patient care without violating privacy or breaching confidentiality. The author addresses these challenges by engaging with philosophical work on shared commitments and joint action, responsibility and justice, and privacy and confidentiality. The Ethics of Chronic Illness provides a new, and much needed, critical reappraisal of healthcare professionals' obligations to their patients. It will be of interests to academics working in bioethics and medical ethics, philosophers interested in the topics of autonomy, responsibility, and consent, and medical practitioners who treat patients with chronic illness |
Physical Description: | 1 online resource (vii, 242 pages) |
ISBN: | 9780429264863 0429264860 9780429559884 0429559887 9780429564352 042956435X 9780429555411 0429555415 |
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520 | |a This book provides an account of the ethics of chronic illness. Chronic illness differs from other illnesses in that it is often incurable, patients can live with it for many years, and its day-to-day management is typically carried out by the patient or members of their family. These features problematise key distinctions that underlie much existing work in medical ethics including those between beneficence and autonomy, between treatment and prevention, and between the recipient and provider of treatment. The author carries out a detailed reappraisal of the roles of both autonomy and beneficence across the different stages of treatment for a range of chronic illnesses. A central part of the author's argument is that in the treatment of chronic illness, the patient and/or the patient's family should be seen as acting with healthcare professionals to achieve a common aim. This aspect opens up unexplored questions such as what healthcare professionals should do when patients are managing their illness poorly, the ethical implications of patients being responsible for parts of their treatment, and how to navigate sharing information with those directly involved in patient care without violating privacy or breaching confidentiality. The author addresses these challenges by engaging with philosophical work on shared commitments and joint action, responsibility and justice, and privacy and confidentiality. The Ethics of Chronic Illness provides a new, and much needed, critical reappraisal of healthcare professionals' obligations to their patients. It will be of interests to academics working in bioethics and medical ethics, philosophers interested in the topics of autonomy, responsibility, and consent, and medical practitioners who treat patients with chronic illness | ||
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any_adam_object | |
author | Walker, Tom 1965- |
author_facet | Walker, Tom 1965- |
author_role | aut |
author_sort | Walker, Tom 1965- |
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dewey-hundreds | 100 - Philosophy & psychology |
dewey-ones | 174 - Occupational ethics |
dewey-raw | 174.2 |
dewey-search | 174.2 |
dewey-sort | 3174.2 |
dewey-tens | 170 - Ethics (Moral philosophy) |
discipline | Philosophie |
format | Electronic eBook |
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isbn | 9780429264863 0429264860 9780429559884 0429559887 9780429564352 042956435X 9780429555411 0429555415 |
language | English |
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physical | 1 online resource (vii, 242 pages) |
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publishDate | 2019 |
publishDateSearch | 2019 |
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publisher | Routledge |
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series2 | Routledge research in applied ethics |
spelling | Walker, Tom 1965- Verfasser aut Ethics and Chronic Illness Tom Walker New York, NY Routledge 2019 1 online resource (vii, 242 pages) txt rdacontent c rdamedia cr rdacarrier Routledge research in applied ethics This book provides an account of the ethics of chronic illness. Chronic illness differs from other illnesses in that it is often incurable, patients can live with it for many years, and its day-to-day management is typically carried out by the patient or members of their family. These features problematise key distinctions that underlie much existing work in medical ethics including those between beneficence and autonomy, between treatment and prevention, and between the recipient and provider of treatment. The author carries out a detailed reappraisal of the roles of both autonomy and beneficence across the different stages of treatment for a range of chronic illnesses. A central part of the author's argument is that in the treatment of chronic illness, the patient and/or the patient's family should be seen as acting with healthcare professionals to achieve a common aim. This aspect opens up unexplored questions such as what healthcare professionals should do when patients are managing their illness poorly, the ethical implications of patients being responsible for parts of their treatment, and how to navigate sharing information with those directly involved in patient care without violating privacy or breaching confidentiality. The author addresses these challenges by engaging with philosophical work on shared commitments and joint action, responsibility and justice, and privacy and confidentiality. The Ethics of Chronic Illness provides a new, and much needed, critical reappraisal of healthcare professionals' obligations to their patients. It will be of interests to academics working in bioethics and medical ethics, philosophers interested in the topics of autonomy, responsibility, and consent, and medical practitioners who treat patients with chronic illness Chronic Disease Ethics, Medical Medical ethics / Case studies Physician and patient https://www.taylorfrancis.com/books/9780429264863 Verlag URL des Erstveroeffentlichers Volltext |
spellingShingle | Walker, Tom 1965- Ethics and Chronic Illness Chronic Disease Ethics, Medical Medical ethics / Case studies Physician and patient |
title | Ethics and Chronic Illness |
title_auth | Ethics and Chronic Illness |
title_exact_search | Ethics and Chronic Illness |
title_full | Ethics and Chronic Illness Tom Walker |
title_fullStr | Ethics and Chronic Illness Tom Walker |
title_full_unstemmed | Ethics and Chronic Illness Tom Walker |
title_short | Ethics and Chronic Illness |
title_sort | ethics and chronic illness |
topic | Chronic Disease Ethics, Medical Medical ethics / Case studies Physician and patient |
topic_facet | Chronic Disease Ethics, Medical Medical ethics / Case studies Physician and patient |
url | https://www.taylorfrancis.com/books/9780429264863 |
work_keys_str_mv | AT walkertom ethicsandchronicillness |