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‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium

BACKGROUND: Delirium is a distressing condition often experienced by hospice in-patients. Increased understanding of current multidisciplinary care of delirium is needed to develop interventions in this setting. AIM(S): To explore hospice staff and volunteers’ practice, its influences and what may n...

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Autores principales: Featherstone, Imogen, Siddiqi, Najma, Jones, Lesley, Coppo, Eleonora, Sheldon, Trevor, Hosie, Annmarie, Wolkowski, Anna, Bush, Shirley H, Taylor, Johanna, Teodorczuk, Andrew, Johnson, Miriam J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320705/
https://www.ncbi.nlm.nih.gov/pubmed/37129262
http://dx.doi.org/10.1177/02692163231170655
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author Featherstone, Imogen
Siddiqi, Najma
Jones, Lesley
Coppo, Eleonora
Sheldon, Trevor
Hosie, Annmarie
Wolkowski, Anna
Bush, Shirley H
Taylor, Johanna
Teodorczuk, Andrew
Johnson, Miriam J
author_facet Featherstone, Imogen
Siddiqi, Najma
Jones, Lesley
Coppo, Eleonora
Sheldon, Trevor
Hosie, Annmarie
Wolkowski, Anna
Bush, Shirley H
Taylor, Johanna
Teodorczuk, Andrew
Johnson, Miriam J
author_sort Featherstone, Imogen
collection PubMed
description BACKGROUND: Delirium is a distressing condition often experienced by hospice in-patients. Increased understanding of current multidisciplinary care of delirium is needed to develop interventions in this setting. AIM(S): To explore hospice staff and volunteers’ practice, its influences and what may need to change to improve hospice delirium care. DESIGN: Qualitative interview study using behaviour change theory from a critical realist stance. SETTING/PARTICIPANTS: Thirty-seven staff, including different professional groups and roles, and volunteers were purposively sampled from two in-patient hospices. RESULTS: We found that participants’ practice focus was on managing hyperactive symptoms of delirium, through medication use and non-pharmacological strategies. Delirium prevention, early recognition and hypoactive delirium received less attention. Our theoretically-informed analysis identified this focus was influenced by staff and volunteers’ emotional responses to the distress associated with hyperactive symptoms of delirium as well as understanding of delirium prevention, recognition and care, which varied between staff groups. Non-pharmacological delirium management was supported by adequate staffing levels, supportive team working and a culture of person-centred and family-centred care, although behaviours that disrupted the calm hospice environment challenged this. CONCLUSIONS: Our findings can inform hospice-tailored behaviour change interventions that develop a shared team understanding and engage staff’s emotional responses to improve delirium care. Reflective learning opportunities are needed that increase understanding of the potential to reduce patient distress through prevention and early recognition of delirium, as well as person-centred management. Organisational support for adequate, flexible staffing levels and supportive team working is required to support person-centred delirium care.
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spelling pubmed-103207052023-07-06 ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium Featherstone, Imogen Siddiqi, Najma Jones, Lesley Coppo, Eleonora Sheldon, Trevor Hosie, Annmarie Wolkowski, Anna Bush, Shirley H Taylor, Johanna Teodorczuk, Andrew Johnson, Miriam J Palliat Med Original Articles BACKGROUND: Delirium is a distressing condition often experienced by hospice in-patients. Increased understanding of current multidisciplinary care of delirium is needed to develop interventions in this setting. AIM(S): To explore hospice staff and volunteers’ practice, its influences and what may need to change to improve hospice delirium care. DESIGN: Qualitative interview study using behaviour change theory from a critical realist stance. SETTING/PARTICIPANTS: Thirty-seven staff, including different professional groups and roles, and volunteers were purposively sampled from two in-patient hospices. RESULTS: We found that participants’ practice focus was on managing hyperactive symptoms of delirium, through medication use and non-pharmacological strategies. Delirium prevention, early recognition and hypoactive delirium received less attention. Our theoretically-informed analysis identified this focus was influenced by staff and volunteers’ emotional responses to the distress associated with hyperactive symptoms of delirium as well as understanding of delirium prevention, recognition and care, which varied between staff groups. Non-pharmacological delirium management was supported by adequate staffing levels, supportive team working and a culture of person-centred and family-centred care, although behaviours that disrupted the calm hospice environment challenged this. CONCLUSIONS: Our findings can inform hospice-tailored behaviour change interventions that develop a shared team understanding and engage staff’s emotional responses to improve delirium care. Reflective learning opportunities are needed that increase understanding of the potential to reduce patient distress through prevention and early recognition of delirium, as well as person-centred management. Organisational support for adequate, flexible staffing levels and supportive team working is required to support person-centred delirium care. SAGE Publications 2023-05-02 2023-07 /pmc/articles/PMC10320705/ /pubmed/37129262 http://dx.doi.org/10.1177/02692163231170655 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any 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 Original Articles
Featherstone, Imogen
Siddiqi, Najma
Jones, Lesley
Coppo, Eleonora
Sheldon, Trevor
Hosie, Annmarie
Wolkowski, Anna
Bush, Shirley H
Taylor, Johanna
Teodorczuk, Andrew
Johnson, Miriam J
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title_full ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title_fullStr ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title_full_unstemmed ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title_short ‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
title_sort ‘it’s tough. it is hard’: a qualitative interview study of staff and volunteers caring for hospice in-patients with delirium
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320705/
https://www.ncbi.nlm.nih.gov/pubmed/37129262
http://dx.doi.org/10.1177/02692163231170655
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