The Patient's Wish to Die

Research, Ethics, and Palliative Care

Edited by Christoph Rehmann-Sutter, Heike Gudat, and Kathrin Ohnsorge

Provides an up-to-date review of the state of knowledge in international end-of-life research and discusses open questions.
Empirical, ethical, and clinical perspectives help readers understand the difficult phenomenon of patients' wishes to die from relevant perspectives, including the patients'.
Offers a cross-disciplinary understanding and collaboration in end-of-life topics.
Dialogues and discussion sections in the book make reading academic chapters easier.
Open and reflective discussions help aid the teaching of this multidimensional topic.

The Patient's Wish to Die

Research, Ethics, and Palliative Care

Edited by Christoph Rehmann-Sutter, Heike Gudat, and Kathrin Ohnsorge

Description

Wish to die statements are becoming a frequent phenomenon in terminally ill patients. Those confronted by these statments need to understand the complexity of such wishes, so they can respond competently and compassionately to the requests. If misunderstood, the statements can be taken at face-value and the practitioner may not recognise that a patient is in fact experiencing ambivalent feelings at the end of life, or they may misinterpret the expressed wish to die as a sign of clinical depression.

Public debate about the morality and ethics of various end-of-life care options has exploded in recent years. However, it has never been sensitive to the finer aspects of clinical reality or the experiences of patients. The Patient's Wish to Die: Research, Ethics, and Palliative Care brings together that reality and the patient's voice, combining them with different research approaches. It presents the best available knowledge and research methodologies about patients' wishes at the end-of-life, together with a series of ethical views and a discussion about the clinical implications for palliative care. The book presents material in an open and unbiased manner whilst remaining sensitive to the spiritual and existential dimensions of dying, and to the different cultural views that provide meaning to the individual.

Written by the best specialists and ethics scholars from around the world, including palliative care practitioners and end-of-life scholars from countries where assisted dying practices are legalized and from those where it isn't, The The Patient's Wish to Die: Research, Ethics, and Palliative Care will prove essential reading for all those working or studying in the field of palliative care.

The Patient's Wish to Die

Research, Ethics, and Palliative Care

Edited by Christoph Rehmann-Sutter, Heike Gudat, and Kathrin Ohnsorge

Section One: Introduction
1. Opening: Why is it important to know about patients' wishes to die, Christoph Rehmann-Sutter, Heike Gudat, Kathrin Ohnsorge
Section Two: Research
2. Illness narratives, meaning making and epistemic injustice in research at the end of life, Yasmin Gunaratnam
3. Expressed desire for hastened death: a phenomenological inquiry, Nessa Coyle and Lois Sculco
4. Commentary: 10 years later - a nursing perspective, Nessa Coyle
5. Euthanasia (requests) after the implementation of the euthanasia law in 2002 in Belgium. Results of empirical studies in Flanders, Belgium, Luc Deliens and Tinne Smets
6. The journey to understanding the wish to hasten death, Tracy A. Schroepfer
7. The desire for hastened death in patients in palliative care, Rinat Nissim, Chris Lo, and Gary Rodin
8. Intentions, motivations and social interactions regarding a wish to die, Kathrin Ohnsorge
9. Acting on a wish to die at the end of life. The Swiss situation, Alexandre Mauron
10. Understanding older people's wish to die, Bregje D. Onwuteaka-Philipsen
11. Dialogue Intermezzo Part I
Section Three: Ethics
12. Caring and killing in the clinic: the argument of self-determination, Lars Johan Materstvedt
13. Towards responsive knowing in matters of life and death, Marian Verkerk
14. Dealing with dilemmas around patients' wishes to die: Moral Case Deliberation in a Dutch hospice, Guy Widdershoven, Margreet Stolper and Bert Molewijk
15. End-of-life ethics from the perspectives of patients' wishes, Christoph Rehmann-Sutter
16. Dialogue Intermezzo Part II
Section Four: Practice
17. Issues of palliative medicine in end-of-life care, H. Christof Muller-Busch
18. Spirituality at the bedside: negotiating the meaning of dying, Settimio Monteverde
19. Communication on wishes to die, Heike Gudat, Christoph Rehmann-Sutter and Kathrin Ohnsorge
20. From understanding to patient centred management: clinical pictures of a wish to die, Heike Gudat
21. What does the wish to hasten death mean for the palliative patient? Clinical implications, Cristina Monforte-Royo, Albert Balaguer and Christian Villavicencio-Chavez
Section Five: Conclusion
22. Concluding Dialogue

The Patient's Wish to Die

Research, Ethics, and Palliative Care

Edited by Christoph Rehmann-Sutter, Heike Gudat, and Kathrin Ohnsorge

Author Information

Christoph Rehmann-Sutter, Professor of Theory and Ethics in the Biosciences, Institute for the History of Medicine and Science Studies, Lubeck, Germany,Heike Gudat, Head of the hospital for palliative care, Hospiz im Park, Hospital for Palliative Care, Arlesheim, Switzerland,Kathrin Ohnsorge, Researcher at the hospital for palliative care, Hospiz im Park, Hospital for Palliative Care, Arlesheim, Switzerland

Christoph Rehmann-Sutter is Professor of Theory and Ethics in the Biosciences at the University of Lubeck in Germany and is also a visiting professor at King's College, London. After a diploma in molecular biology, he studied philosophy and sociology. In 1996 he founded the Unit of Bioethics at the University of Basel, Switzerland, and he was president of the Swiss National Advisory Commission on Biomedical Ethics from 2001 to 2009. Current research interests include the anthropology of genomics, the ethics of transplantation of blood stem cells between siblings, and moral issues in end-of-life care. He has published more than 200 scholarly papers.

Heike Gudat is physician and specialised in palliative care. Since 2000 she has been the medical head of the HOSPIZ IM PARK, an independent hospital for palliative and end of life care in the region of Basel, Switzerland. After medical education at the University of Basel 1988 she specialised in internal medicine, also experiencing the special fields of rehabilitation, gerontology and hematology. From 1992-1994 studies of experimental cytogenetics at the University of Lubeck (Prof. Ch. Fonatsch), supported by the Swiss National Foundation. Since 1996 specialisation in palliative care. Within regular teaching activities Heike Gudat has a teaching assignment for palliative care at the University of Basel. Together with Settimio Monteverde she developed interdisciplinary palliative care training courses for primary care professionals. Current research interests include wishes to die in end of life care situations and implementation of palliative care in family medicine.

Kathrin Ohnsorge is a researcher in bioethics currently working at the HOSPIZ IM PARK, a hospice close to Basel in Switzerland. After her graduation in philosophy, she obtained a European Master in Bioethics from the Universities of Leuven, Nijmengen, Basel and Padua. From 2001 to 2012, she worked at the University of Basel in various research projects regarding ethical issues in end-of-life care. Her current research interests are in ethical issues in end-of-life care and long term care and in narrative and hermeneutic approaches to bioethics. She teaches also bioethics in two postgraduate programs at the University of Padua.

Contributors:

Albert Balaguer, Medicine and Health Sciences School, Centre de Recerca / Estudis Bioètics, Universitat Internacional de Catalunya, Spain
Alexandre Mauron, Institute of Bioethics, University of Geneva, Switzerland
Bregje D. Onwuteaka-Philipsen, EMGO Institute for Health and Care Research, Expertise Center of Palliative Care, VU Medical Center, Amsterdam, The Netherlands
Christian Villavicencio-Chávez, Centre de Recerca i Estudis Bioètics (CREB), Universitat Internacional de Catalunya, Spain; Institut Català d'Oncologia, Spain
Christoph Rehmann-Sutter, Institute for History of Medicine and Science Studies, University of Lübeck, Germany
Cristina Monforte-Royo, Medicine and Health Sciences School, Centre de Recerca I Estudis Bioètics, Universitat Internacional de Catalunya, Spain
Gary Rodin, University of Toronto, Canada and Princess Margaret Cancer Centre, University Health Network Canada
Heike Gudat, Hospiz im Park. Hospital for Palliative Care, Arlesheim, Switzerland
Kathrin Ohnsorge, Hospiz im Park, Hospital for Palliative Care, Arlesheim, Switzerland
Lars Johan Materstvedt, Norwegian University of Science and Technology (NTNU), Trondheim, Norway
Luc Deliens, End-of-life Care Research Group, Ghent University and Vrije Universiteit Brussel, Belgium
Marian Verkerk, University Medical Centre Groningen, Groningen, The Netherlands
Nessa Coyle, Consultant in Pain and Palliative Care and End-of-Life Care, New York, USA
Professor Guy Widdershoven, VU University Medical Center, Amsterdam, The Netherlands
Settimio Monteverde, Institute of Biomedical Ethics, University of Zurich, Switzerland
Tracy A. Schroepfer, School of Social Work, University of Wisconsin-Madison, USA
Yasmin Gunaratnam, Goldsmith College, University of London, UK

The Patient's Wish to Die

Research, Ethics, and Palliative Care

Edited by Christoph Rehmann-Sutter, Heike Gudat, and Kathrin Ohnsorge

Reviews and Awards

"While it may be targeted at medical professionals, this book presents the material in a way that is accessible to those who want to become familiar with the ethical implications and underpinnings of end-of-life care and the thought processes that ultimately lead patients to conclude that their lives are no longer worth living. Weighted Numerical Score: 98 - 5 Stars!" -- Adam Ruggles, Doody's