Literature DB >> 25748112

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

Gavin Daker-White1, Anne Rogers2, Anne Kennedy3, Thomas Blakeman4, Christian Blickem5, Carolyn Chew-Graham6.   

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.
Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  Chronic kidney disease; Diagnosis; Doctor–patient communication; Qualitative study; Self-management; UK

Mesh:

Year:  2015        PMID: 25748112     DOI: 10.1016/j.socscimed.2015.02.035

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  17 in total

1.  Blame the Patient, Blame the Doctor or Blame the System? A Meta-Synthesis of Qualitative Studies of Patient Safety in Primary Care.

Authors:  Gavin Daker-White; Rebecca Hays; Jennifer McSharry; Sally Giles; Sudeh Cheraghi-Sohi; Penny Rhodes; Caroline Sanders
Journal:  PLoS One       Date:  2015-08-05       Impact factor: 3.240

2.  Improving coding and primary care management for patients with chronic kidney disease: an observational controlled study in East London.

Authors:  Sally A Hull; Vian Rajabzadeh; Nicola Thomas; Sec Hoong; Gavin Dreyer; Helen Rainey; Neil Ashman
Journal:  Br J Gen Pract       Date:  2019-06-03       Impact factor: 5.386

3.  RCGP Research Paper of the Year 2015: strong messages for clinical care in all six research categories.

Authors:  Roger Jones
Journal:  Br J Gen Pract       Date:  2016-12       Impact factor: 5.386

4.  The National CKD Audit: a primary care condition that deserves more attention.

Authors:  Sally A Hull; Dorothea Nitsch; Ben Caplin; Kathryn Griffith; David C Wheeler
Journal:  Br J Gen Pract       Date:  2018-08       Impact factor: 5.386

Review 5.  Kidney age, not kidney disease.

Authors:  Richard J Stevens; Julie Evans; Jason Oke; Benjamin Smart; F D Richard Hobbs; Elizabeth Holloway; Jeremy Horwood; Marion Judd; Louise Locock; Julie McLellan; Rafael Perera
Journal:  CMAJ       Date:  2018-04-03       Impact factor: 8.262

6.  Pre-diabetes: opportunity or overdiagnosis?

Authors:  Helen Twohig; Victoria Hodges; Caroline Mitchell
Journal:  Br J Gen Pract       Date:  2018-04       Impact factor: 5.386

7.  Understanding kidney disease in rural central Uganda - Findings from a qualitative study.

Authors:  Janet Seeley; Elizabeth Kabunga; Joseph Ssembatya; Laurie A Tomlinson; June Fabian; Liam Smeeth; Moffat Nyirenda; Robert Newton; Robert Kalyesubula; Dominic Bukenya
Journal:  Glob Public Health       Date:  2020-04-30

8.  Understanding tensions and identifying clinician agreement on improvements to early-stage chronic kidney disease monitoring in primary care: a qualitative study.

Authors:  Rosemary Simmonds; Julie Evans; Gene Feder; Tom Blakeman; Dan Lasserson; Elizabeth Murray; Kristina Bennert; Louise Locock; Jeremy Horwood
Journal:  BMJ Open       Date:  2016-03-17       Impact factor: 2.692

9.  CKD Awareness Among US Adults by Future Risk of Kidney Failure.

Authors:  Chi D Chu; Charles E McCulloch; Tanushree Banerjee; Meda E Pavkov; Nilka R Burrows; Brenda W Gillespie; Rajiv Saran; Michael G Shlipak; Neil R Powe; Delphine S Tuot
Journal:  Am J Kidney Dis       Date:  2020-04-15       Impact factor: 8.860

Review 10.  Chronic kidney disease: identification and management in primary care.

Authors:  Simon Ds Fraser; Tom Blakeman
Journal:  Pragmat Obs Res       Date:  2016-08-17
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