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End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families

End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families
End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families
The aims of this qualitative study were to identify patients’ and family members’ experiences of acute stroke and their preferences for end-of-life care. Twenty-eight purposely sampled patients with an acute stroke who had high (n = 13) and low (n = 15) disability were selected from 191 sequential cases admitted to two general hospitals in north-east England. In addition, 25 family members of other stroke patients were recruited. Views about current stroke services and preferences for end-of-life care were elicited in semi-structured interviews.

Communication between patients and family members and healthcare professionals was consistently highlighted as central to a positive experience of stroke care. Honesty and clarity of information was required, even where prognoses were bleak or uncertain. Patients and family members appeared to attach as much importance to the style of communication as to the substance of the transfer of information. Where decisions had been made to shift the focus of care from active to more passive support, families, and where possible patients, still wished to be included in ongoing dialogue with professionals. Where patients were thought to be dying, family members were keen to ensure that the death was peaceful and dignified.

Families reported few opportunities for engagement in any form of choice over place or style of end-of-life care. No family member reported being offered the possibility of the patient dying at home. Uncertainty about prognosis is inevitable in clinical practice, and this can be difficult for patients and families. Our findings demonstrate the importance of improving communication between patient, family and health professionals for seriously ill patients with stroke in UK hospitals.
communication, end-of-life care, family support. palliative care, stroke
0269-2163
146-153
Payne, Sheila
d7c97f41-ec69-4157-9339-ca07c521fbcc
Burton, Christopher
c8e0ea0c-9df7-4760-8e6b-159762b95ead
Addington-Hall, Julia
87560cc4-7562-4f9b-b908-81f3b603fdd8
Jones, Amanda
b252e3a1-7e42-4b77-9ef0-f8930435368a
Payne, Sheila
d7c97f41-ec69-4157-9339-ca07c521fbcc
Burton, Christopher
c8e0ea0c-9df7-4760-8e6b-159762b95ead
Addington-Hall, Julia
87560cc4-7562-4f9b-b908-81f3b603fdd8
Jones, Amanda
b252e3a1-7e42-4b77-9ef0-f8930435368a

Payne, Sheila, Burton, Christopher, Addington-Hall, Julia and Jones, Amanda (2010) End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families. Palliative Medicine, 24 (2), 146-153. (doi:10.1177/0269216309350252).

Record type: Article

Abstract

The aims of this qualitative study were to identify patients’ and family members’ experiences of acute stroke and their preferences for end-of-life care. Twenty-eight purposely sampled patients with an acute stroke who had high (n = 13) and low (n = 15) disability were selected from 191 sequential cases admitted to two general hospitals in north-east England. In addition, 25 family members of other stroke patients were recruited. Views about current stroke services and preferences for end-of-life care were elicited in semi-structured interviews.

Communication between patients and family members and healthcare professionals was consistently highlighted as central to a positive experience of stroke care. Honesty and clarity of information was required, even where prognoses were bleak or uncertain. Patients and family members appeared to attach as much importance to the style of communication as to the substance of the transfer of information. Where decisions had been made to shift the focus of care from active to more passive support, families, and where possible patients, still wished to be included in ongoing dialogue with professionals. Where patients were thought to be dying, family members were keen to ensure that the death was peaceful and dignified.

Families reported few opportunities for engagement in any form of choice over place or style of end-of-life care. No family member reported being offered the possibility of the patient dying at home. Uncertainty about prognosis is inevitable in clinical practice, and this can be difficult for patients and families. Our findings demonstrate the importance of improving communication between patient, family and health professionals for seriously ill patients with stroke in UK hospitals.

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More information

Published date: March 2010
Keywords: communication, end-of-life care, family support. palliative care, stroke

Identifiers

Local EPrints ID: 162815
URI: http://eprints.soton.ac.uk/id/eprint/162815
ISSN: 0269-2163
PURE UUID: 46950d86-915f-4ba0-ab16-b2874534207d

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Date deposited: 31 Aug 2010 08:58
Last modified: 14 Mar 2024 02:03

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Contributors

Author: Sheila Payne
Author: Christopher Burton
Author: Amanda Jones

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