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Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries

BACKGROUND: Spiritual distress is prevalent in advanced disease, but often neglected, resulting in unnecessary suffering. Evidence to inform spiritual care practices in palliative care is limited. AIM: To explore spiritual care needs, experiences, preferences and research priorities in an internatio...

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Autores principales: Selman, Lucy Ellen, Brighton, Lisa Jane, Sinclair, Shane, Karvinen, Ikali, Egan, Richard, Speck, Peter, Powell, Richard A, Deskur-Smielecka, Ewa, Glajchen, Myra, Adler, Shelly, Puchalski, Christina, Hunter, Joy, Gikaara, Nancy, Hope, Jonathon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758929/
https://www.ncbi.nlm.nih.gov/pubmed/29020846
http://dx.doi.org/10.1177/0269216317734954
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author Selman, Lucy Ellen
Brighton, Lisa Jane
Sinclair, Shane
Karvinen, Ikali
Egan, Richard
Speck, Peter
Powell, Richard A
Deskur-Smielecka, Ewa
Glajchen, Myra
Adler, Shelly
Puchalski, Christina
Hunter, Joy
Gikaara, Nancy
Hope, Jonathon
author_facet Selman, Lucy Ellen
Brighton, Lisa Jane
Sinclair, Shane
Karvinen, Ikali
Egan, Richard
Speck, Peter
Powell, Richard A
Deskur-Smielecka, Ewa
Glajchen, Myra
Adler, Shelly
Puchalski, Christina
Hunter, Joy
Gikaara, Nancy
Hope, Jonathon
author_sort Selman, Lucy Ellen
collection PubMed
description BACKGROUND: Spiritual distress is prevalent in advanced disease, but often neglected, resulting in unnecessary suffering. Evidence to inform spiritual care practices in palliative care is limited. AIM: To explore spiritual care needs, experiences, preferences and research priorities in an international sample of patients with life-limiting disease and family caregivers. DESIGN: Focus group study. SETTING/PARTICIPANTS: Separate patient and caregiver focus groups were conducted at 11 sites in South Africa, Kenya, South Korea, the United States, Canada, the United Kingdom, Belgium, Finland and Poland. Discussions were transcribed, translated into English and analysed thematically. RESULTS: A total of 74 patients participated: median age 62 years; 53 had cancer; 48 were women. In total, 71 caregivers participated: median age 61 years; 56 were women. Two-thirds of participants were Christian. Five themes are described: patients’ and caregivers’ spiritual concerns, understanding of spirituality and its role in illness, views and experiences of spiritual care, preferences regarding spiritual care, and research priorities. Participants reported wide-ranging spiritual concerns spanning existential, psychological, religious and social domains. Spirituality supported coping, but could also result in framing illness as punishment. Participants emphasised the need for staff competence in spiritual care. Spiritual care was reportedly lacking, primarily due to staff members’ de-prioritisation and lack of time. Patients’ research priorities included understanding the qualities of human connectedness and fostering these skills in staff. Caregivers’ priorities included staff training, assessment, studying impact, and caregiver’s spiritual care needs. CONCLUSION: To meet patient and caregiver preferences, healthcare providers should be able to address their spiritual concerns. Findings should inform patient- and caregiver-centred spiritual care provision, education and research.
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spelling pubmed-57589292018-01-29 Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries Selman, Lucy Ellen Brighton, Lisa Jane Sinclair, Shane Karvinen, Ikali Egan, Richard Speck, Peter Powell, Richard A Deskur-Smielecka, Ewa Glajchen, Myra Adler, Shelly Puchalski, Christina Hunter, Joy Gikaara, Nancy Hope, Jonathon Palliat Med Psychosocial Care and Quality of Life BACKGROUND: Spiritual distress is prevalent in advanced disease, but often neglected, resulting in unnecessary suffering. Evidence to inform spiritual care practices in palliative care is limited. AIM: To explore spiritual care needs, experiences, preferences and research priorities in an international sample of patients with life-limiting disease and family caregivers. DESIGN: Focus group study. SETTING/PARTICIPANTS: Separate patient and caregiver focus groups were conducted at 11 sites in South Africa, Kenya, South Korea, the United States, Canada, the United Kingdom, Belgium, Finland and Poland. Discussions were transcribed, translated into English and analysed thematically. RESULTS: A total of 74 patients participated: median age 62 years; 53 had cancer; 48 were women. In total, 71 caregivers participated: median age 61 years; 56 were women. Two-thirds of participants were Christian. Five themes are described: patients’ and caregivers’ spiritual concerns, understanding of spirituality and its role in illness, views and experiences of spiritual care, preferences regarding spiritual care, and research priorities. Participants reported wide-ranging spiritual concerns spanning existential, psychological, religious and social domains. Spirituality supported coping, but could also result in framing illness as punishment. Participants emphasised the need for staff competence in spiritual care. Spiritual care was reportedly lacking, primarily due to staff members’ de-prioritisation and lack of time. Patients’ research priorities included understanding the qualities of human connectedness and fostering these skills in staff. Caregivers’ priorities included staff training, assessment, studying impact, and caregiver’s spiritual care needs. CONCLUSION: To meet patient and caregiver preferences, healthcare providers should be able to address their spiritual concerns. Findings should inform patient- and caregiver-centred spiritual care provision, education and research. SAGE Publications 2017-10-12 2018-01 /pmc/articles/PMC5758929/ /pubmed/29020846 http://dx.doi.org/10.1177/0269216317734954 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Psychosocial Care and Quality of Life
Selman, Lucy Ellen
Brighton, Lisa Jane
Sinclair, Shane
Karvinen, Ikali
Egan, Richard
Speck, Peter
Powell, Richard A
Deskur-Smielecka, Ewa
Glajchen, Myra
Adler, Shelly
Puchalski, Christina
Hunter, Joy
Gikaara, Nancy
Hope, Jonathon
Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title_full Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title_fullStr Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title_full_unstemmed Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title_short Patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: A focus group study across nine countries
title_sort patients’ and caregivers’ needs, experiences, preferences and research priorities in spiritual care: a focus group study across nine countries
topic Psychosocial Care and Quality of Life
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758929/
https://www.ncbi.nlm.nih.gov/pubmed/29020846
http://dx.doi.org/10.1177/0269216317734954
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