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Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography
OBJECTIVES: Patients with advanced disease sometimes express a wish to hasten death (WTHD). In 2012, we published a systematic review and meta-ethnography of qualitative studies examining the experience and meaning of this phenomenon. Since then, new studies eligible for inclusion have been reported...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640102/ https://www.ncbi.nlm.nih.gov/pubmed/28965095 http://dx.doi.org/10.1136/bmjopen-2017-016659 |
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author | Rodríguez-Prat, Andrea Balaguer, Albert Booth, Andrew Monforte-Royo, Cristina |
author_facet | Rodríguez-Prat, Andrea Balaguer, Albert Booth, Andrew Monforte-Royo, Cristina |
author_sort | Rodríguez-Prat, Andrea |
collection | PubMed |
description | OBJECTIVES: Patients with advanced disease sometimes express a wish to hasten death (WTHD). In 2012, we published a systematic review and meta-ethnography of qualitative studies examining the experience and meaning of this phenomenon. Since then, new studies eligible for inclusion have been reported, including in Europe, a region not previously featured, and specifically in countries with different legal frameworks for euthanasia and assisted suicide. The aim of the present study was to update our previous review by including new research and to conduct a new analysis of available data on this topic. SETTING: Eligible studies originated from Australia, Canada, China, Germany, The Netherlands, Switzerland, Thailand and USA. PARTICIPANTS: Studies of patients with life-threatening conditions that had expressed the WTHD. DESIGN: The search strategy combined subject terms with free-text searching of PubMed MEDLINE, Web of Science, CINAHL and PsycInfo. The qualitative synthesis followed the methodology described by Noblit and Hare, using the ‘adding to and revising the original’ model for updating a meta-ethnography, proposed by France et al. Quality assessment was done using the Critical Appraisal Skills Programme checklist. RESULTS: 14 studies involving 255 participants with life-threatening illnesses were identified. Five themes emerged from the analysis: suffering (overarching theme), reasons for and meanings and functions of the WTHD and the experience of a timeline towards dying and death. In the context of advanced disease, the WTHD emerges as a reaction to physical, psychological, social and existential suffering, all of which impacts on the patient’s sense of self, of dignity and meaning in life. CONCLUSIONS: The WTHD can hold different meanings for each individual—serving functions other than to communicate a genuine wish to die. Understanding the reasons for, and meanings and functions of, the WTHD is crucial for drawing up and implementing care plans to meet the needs of individual patients. |
format | Online Article Text |
id | pubmed-5640102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56401022017-10-19 Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography Rodríguez-Prat, Andrea Balaguer, Albert Booth, Andrew Monforte-Royo, Cristina BMJ Open Palliative Care OBJECTIVES: Patients with advanced disease sometimes express a wish to hasten death (WTHD). In 2012, we published a systematic review and meta-ethnography of qualitative studies examining the experience and meaning of this phenomenon. Since then, new studies eligible for inclusion have been reported, including in Europe, a region not previously featured, and specifically in countries with different legal frameworks for euthanasia and assisted suicide. The aim of the present study was to update our previous review by including new research and to conduct a new analysis of available data on this topic. SETTING: Eligible studies originated from Australia, Canada, China, Germany, The Netherlands, Switzerland, Thailand and USA. PARTICIPANTS: Studies of patients with life-threatening conditions that had expressed the WTHD. DESIGN: The search strategy combined subject terms with free-text searching of PubMed MEDLINE, Web of Science, CINAHL and PsycInfo. The qualitative synthesis followed the methodology described by Noblit and Hare, using the ‘adding to and revising the original’ model for updating a meta-ethnography, proposed by France et al. Quality assessment was done using the Critical Appraisal Skills Programme checklist. RESULTS: 14 studies involving 255 participants with life-threatening illnesses were identified. Five themes emerged from the analysis: suffering (overarching theme), reasons for and meanings and functions of the WTHD and the experience of a timeline towards dying and death. In the context of advanced disease, the WTHD emerges as a reaction to physical, psychological, social and existential suffering, all of which impacts on the patient’s sense of self, of dignity and meaning in life. CONCLUSIONS: The WTHD can hold different meanings for each individual—serving functions other than to communicate a genuine wish to die. Understanding the reasons for, and meanings and functions of, the WTHD is crucial for drawing up and implementing care plans to meet the needs of individual patients. BMJ Publishing Group 2017-09-29 /pmc/articles/PMC5640102/ /pubmed/28965095 http://dx.doi.org/10.1136/bmjopen-2017-016659 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Palliative Care Rodríguez-Prat, Andrea Balaguer, Albert Booth, Andrew Monforte-Royo, Cristina Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title | Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title_full | Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title_fullStr | Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title_full_unstemmed | Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title_short | Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
title_sort | understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography |
topic | Palliative Care |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640102/ https://www.ncbi.nlm.nih.gov/pubmed/28965095 http://dx.doi.org/10.1136/bmjopen-2017-016659 |
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