Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography
Data de publicació
2017ISSN
2044-6055
Resum
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.
Tipus de document
Article
Versió del document
Versió publicada
Llengua
Anglès
Matèries (CDU)
1 - Filosofia i psicologia
61 - Medicina
Paraules clau
Pàgines
13
Publicat per
BMJ Publishing Group
Col·lecció
7;
Publicat a
BMJ Open
Citació
Rodríguez-Prat, Andrea; Balaguer, Albert; Booth, Andrew [et al.]. Understanding patients’ experiences of the wish to hasten death: an updated and expanded systematic review and meta-ethnography. BMJ Open, 2017, 7(9), e016659. Disponible en:<https://bmjopen.bmj.com/content/7/9/e016659>. Fecha de acceso: 29 sep. 2021. DOI: 10.1136/bmjopen-2017-016659
Nota
This study was supported by the Junior Faculty programme grant, cofinanced by L’Obra Social ‘La Caixa’, the Instituto de Salud Carlos III (PI14/00263) and the European Regional Development Fund (FEDER). We are also grateful for the support given by Recercaixa 2015 and WeCare Chair: End-of-life care at the Universitat Internacional de Catalunya and ALTIMA.
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Drets
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/
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