Literature DB >> 24850420

The challenge to health professionals when carers resist truth telling at the end of life: a qualitative secondary analysis.

Helen Noble1, Jayne E Price, Sam Porter.   

Abstract

AIMS AND
OBJECTIVES: To draw out the similar complexities faced by staff around truth-telling in a children's and adult population and to interrogate the dilemmas faced by staff when informal carers act to block truth-telling.
BACKGROUND: Policy encourages normalisation of death, but carers may act to protect or prevent the patient from being told the truth. Little is known about the impact on staff.
DESIGN: Secondary analysis of data using a supra-analysis design to identify commonality of experiences.
METHODS: Secondary 'supra-analysis' was used to transcend the focus of two primary studies in the UK, which examined staff perspectives in a palliative children's and a palliative adult setting, respectively. The analysis examined new theoretical questions relating to the commonality of issues independently derived in each primary study. Both primary studies used focus groups. Existing empirical data were analysed thematically and compared across the studies.
RESULTS: Staff reported a hiding of the truth by carers and sustained use of activities aimed at prolonging life. Carers frequently ignored the advance of end of life, and divergence between staff and carer approaches to truth-telling challenged professionals. Not being truthful with patients had a deleterious effect on staff, causing anger and feelings of incompetence.
CONCLUSIONS: Both children's and adult specialist palliative care staff found themselves caught in a dilemma, subject to policies that promoted openness in planning for death and informal carers who often prevented them from being truthful with patients about terminal prognosis. This dilemma had adverse psychological effects upon many staff. RELEVANCE TO CLINICAL PRACTICE: There remains a powerful death-denying culture in many societies, and carers of dying patients may prevent staff from being truthful with their patients. The current situation is not ideal, and open discussion of this problem is the essential first step in finding a solution.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  end of life; informal carer; paediatric; palliative; qualitative; renal; staff challenges; truth telling

Mesh:

Year:  2014        PMID: 24850420     DOI: 10.1111/jocn.12634

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  6 in total

1.  End-of-Life Decision Making in Palliative Care and Recommendations of the Council of Europe: Qualitative Secondary Analysis of Interviews and Observation Field Notes.

Authors:  Sandra Martins Pereira; Emília Fradique; Pablo Hernández-Marrero
Journal:  J Palliat Med       Date:  2018-01-03       Impact factor: 2.947

2.  Urban-Dwelling Community Members' Views on Biomedical Research Engagement.

Authors:  Yamnia I Cortés; Adriana Arcia; Joan Kearney; Jose Luchsinger; Robert J Lucero
Journal:  Qual Health Res       Date:  2016-01-29

3.  Establishing a clinical phenotype for cachexia in end stage kidney disease - study protocol.

Authors:  Joanne Reid; Helen R Noble; Gary Adamson; Andrew Davenport; Ken Farrington; Denis Fouque; Kamyar Kalantar-Zadeh; John Mallett; C McKeaveney; S Porter; David S Seres; Joanne Shields; Adrian Slee; Miles D Witham; Alexander P Maxwell
Journal:  BMC Nephrol       Date:  2018-02-13       Impact factor: 2.388

4.  Lack of Truth-Telling in Palliative Care and Its Effects among Nurses and Nursing Students.

Authors:  Ines Testoni; Michael Alexander Wieser; Dafni Kapelis; Sara Pompele; Marino Bonaventura; Robert Crupi
Journal:  Behav Sci (Basel)       Date:  2020-05-11

5.  Support received by family members before, at and after an ill person's death.

Authors:  Anna O'Sullivan; Anette Alvariza; Joakim Öhlén; Cecilia Larsdotter
Journal:  BMC Palliat Care       Date:  2021-06-24       Impact factor: 3.234

6.  Perceptions of patients with end-stage kidney disease (ESKD) and their informal caregivers on palliative care as a treatment option: a qualitative study.

Authors:  Catherine Sarfo-Walters; Edward Appiah Boateng
Journal:  BMC Palliat Care       Date:  2020-08-20       Impact factor: 3.234

  6 in total

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