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Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management

Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management
Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management
Early detection of long term conditions is predicated on assumptions that lifestyle changes and medications can be used to reduce or manage the risk of condition progression. However, ambiguity remains about the nature and place of diagnostic disclosure to people in newly recognised or asymptomatic ‘pre’ conditions such as early stage chronic kidney disease (CKD). The disclosure of a diagnosis is relevant to instigating strategies which rely on actively engaging patients as self-managers of their own care. Whilst primary care routinely records a diagnosis of early stage CKD, little is known about how patients learn about the fact that they have CKD or how they respond to this. This study aimed to explore patients' experiences of disclosure of CKD in primary care settings.

A nested qualitative study of participants recruited to a trial of an intervention for CKD patients in Greater Manchester, UK was undertaken. A purposive sample of 26 patients, with a mean age of 72 years (range 59–89, median 71), were interviewed during 2012. Interview transcripts were analysed using constant comparative techniques. Narrative accounts reflected limited or partial disclosure of CKD; often cast in vague terms as “nothing to worry about”. How patients described themselves in terms of participation and their tendencies towards ‘active’ or ‘passive’ involvement in consultations emerged as important components of narratives around disclosure. The findings illuminate the ways in which diagnosis is oriented in a context where it is possible to meet the requirements for remuneration under a pay for performance system of primary care, whilst apparently not disclosing a label or a diagnosis to patients. This challenges the presumptions inherent in wider health policy objectives that are increasingly built on the notion of responsible patients and the ethos of the active support of self-management for pre-conditions.
UK, qualitative study, diagnosis, chronic kidney disease, doctor–patient communication, self-management
0277-9536
31-39
Daker-White, Gavin
9b0569ff-aba1-41d1-a1ca-3852ef7677a6
Rogers, Anne
105eeebc-1899-4850-950e-385a51738eb7
Kennedy, Anne
e059c1c7-d6d0-41c8-95e1-95e5273b07f8
Blakeman, Thomas
c005e534-1e5e-4f74-a3ef-a4f298519399
Blickem, Christian
cc3228ac-f56e-4dca-9aae-cbb6bfac4fb3
Chew-Graham, Carolyn
530beade-2b1c-4eea-846f-1fcef0585ca5
Daker-White, Gavin
9b0569ff-aba1-41d1-a1ca-3852ef7677a6
Rogers, Anne
105eeebc-1899-4850-950e-385a51738eb7
Kennedy, Anne
e059c1c7-d6d0-41c8-95e1-95e5273b07f8
Blakeman, Thomas
c005e534-1e5e-4f74-a3ef-a4f298519399
Blickem, Christian
cc3228ac-f56e-4dca-9aae-cbb6bfac4fb3
Chew-Graham, Carolyn
530beade-2b1c-4eea-846f-1fcef0585ca5

Daker-White, Gavin, Rogers, Anne, Kennedy, Anne, Blakeman, Thomas, Blickem, Christian and Chew-Graham, Carolyn (2015) Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management. Social Science & Medicine, 131, 31-39. (doi:10.1016/j.socscimed.2015.02.035).

Record type: Article

Abstract

Early detection of long term conditions is predicated on assumptions that lifestyle changes and medications can be used to reduce or manage the risk of condition progression. However, ambiguity remains about the nature and place of diagnostic disclosure to people in newly recognised or asymptomatic ‘pre’ conditions such as early stage chronic kidney disease (CKD). The disclosure of a diagnosis is relevant to instigating strategies which rely on actively engaging patients as self-managers of their own care. Whilst primary care routinely records a diagnosis of early stage CKD, little is known about how patients learn about the fact that they have CKD or how they respond to this. This study aimed to explore patients' experiences of disclosure of CKD in primary care settings.

A nested qualitative study of participants recruited to a trial of an intervention for CKD patients in Greater Manchester, UK was undertaken. A purposive sample of 26 patients, with a mean age of 72 years (range 59–89, median 71), were interviewed during 2012. Interview transcripts were analysed using constant comparative techniques. Narrative accounts reflected limited or partial disclosure of CKD; often cast in vague terms as “nothing to worry about”. How patients described themselves in terms of participation and their tendencies towards ‘active’ or ‘passive’ involvement in consultations emerged as important components of narratives around disclosure. The findings illuminate the ways in which diagnosis is oriented in a context where it is possible to meet the requirements for remuneration under a pay for performance system of primary care, whilst apparently not disclosing a label or a diagnosis to patients. This challenges the presumptions inherent in wider health policy objectives that are increasingly built on the notion of responsible patients and the ethos of the active support of self-management for pre-conditions.

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More information

Accepted/In Press date: 24 February 2015
e-pub ahead of print date: 25 February 2015
Published date: April 2015
Keywords: UK, qualitative study, diagnosis, chronic kidney disease, doctor–patient communication, self-management
Organisations: Faculty of Health Sciences

Identifiers

Local EPrints ID: 379923
URI: http://eprints.soton.ac.uk/id/eprint/379923
ISSN: 0277-9536
PURE UUID: 293cee50-08c2-4130-88dd-ac8175c2d186
ORCID for Anne Kennedy: ORCID iD orcid.org/0000-0003-4570-9104

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Date deposited: 11 Aug 2015 13:38
Last modified: 14 Mar 2024 20:51

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Contributors

Author: Gavin Daker-White
Author: Anne Rogers
Author: Anne Kennedy ORCID iD
Author: Thomas Blakeman
Author: Christian Blickem
Author: Carolyn Chew-Graham

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