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End of life choices for cancer patients : an international perspective / editors: Dr Ruth E. Board, Professor Michael I. Bennett, Professor Penny Lewis, Professor John Wagstaff, Professor Peter Selby.

Contributor(s): Board, Ruth E [editor] | Association of Cancer PhysiciansPublisher: Oxford, UK : EBN Health, 2020Description: 67 pages : illustrations, maps ; 25 cmISBN: 9780995595446 (paperback)Subject(s): Cancer -- Patients -- Care | Terminal care | Assisted suicide | Euthanasia | Patient refusal of treatmentSummary: There have been impressive improvements in the diagnosis and treatment of cancer in recent decades. In economically advantaged countries with well-developed healthcare systems over 50% of all cancer patients achieve long term survival and are probably cured. Not only has survival improved radically for cancer patients but also there has been an increasing focus on the quality of patient's lives, on improving the patient experience of care and on developing effective support for the very many cancer survivors. Despite the progress in cancer treatment, unfortunately a substantial number of cancer patients will still ultimately die of their disease. For many this will follow periods of successful treatment which results in good remissions and good quality of life. Helping patients to make the right choices about their care towards the end of their lives is one of the greatest and most challenging responsibilities of all healthcare professionals. Legal change on the provision of assisted dying by healthcare professionals has occurred in a substantial number of jurisdictions. This work brings together contributions on end of life choices from experienced professionals from oncology disciplines, palliative care, law, nurses and professions allied to medicine. The goals are: to better inform cancer care professionals and the wider community about developments in choices in end of life care for cancer patients internationally. To better answer questions from patients and respond to requests from patients, including questions about and requests for assisted dying in countries where it is legal to do so. To have a balanced and well informed dialogue about choices available to patients without developing a formal policy position on change in law. To provide a basis of information for future educational activities.
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Item type Current library Collection Call number Status Date due Barcode
Book Book Mercy University Hospital Psycho-oncology Adult EL 48 (Browse shelf(Opens below)) Available 39117000000307

Includes bibliographical references.

There have been impressive improvements in the diagnosis and treatment of cancer in recent decades. In economically advantaged countries with well-developed healthcare systems over 50% of all cancer patients achieve long term survival and are probably cured. Not only has survival improved radically for cancer patients but also there has been an increasing focus on the quality of patient's lives, on improving the patient experience of care and on developing effective support for the very many cancer survivors. Despite the progress in cancer treatment, unfortunately a substantial number of cancer patients will still ultimately die of their disease. For many this will follow periods of successful treatment which results in good remissions and good quality of life. Helping patients to make the right choices about their care towards the end of their lives is one of the greatest and most challenging responsibilities of all healthcare professionals. Legal change on the provision of assisted dying by healthcare professionals has occurred in a substantial number of jurisdictions. This work brings together contributions on end of life choices from experienced professionals from oncology disciplines, palliative care, law, nurses and professions allied to medicine. The goals are: to better inform cancer care professionals and the wider community about developments in choices in end of life care for cancer patients internationally. To better answer questions from patients and respond to requests from patients, including questions about and requests for assisted dying in countries where it is legal to do so. To have a balanced and well informed dialogue about choices available to patients without developing a formal policy position on change in law. To provide a basis of information for future educational activities.

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