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Psychological impact of working with patients with cystic fibrosis at end-of-life, pre-transplant stage

Published online by Cambridge University Press:  13 December 2012

Nicola Clisby ,
Samantha Shaw  and
Maggie Cormack
Nicola Clisby*
Affiliation:
Avon & Wiltshire Mental Health Trust, Wickham Unit, Blackberry Hill Hospital, Bristol, United Kingdom
Samantha Shaw
Affiliation:
Paediatric Unit, Bristol Royal Hospital for Children, Bristol, United Kingdom
Maggie Cormack
Affiliation:
Bristol Doctorate in Clinical Psychology, Bristol, United Kingdom
*
Address correspondence and reprint requests to: Nicola Clisby, Avon & Wiltshire Mental Health Trust, Bristol, United Kingdom. E-mail: nichol.clisby@awp.nhs.uk
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Abstract

Objective:

Multidisciplinary staff who work with end-of-life, pre-transplant patients with cystic fibrosis (CF) have to juggle two seemingly opposing care approaches; active care to maintain their patients’ health and condition in anticipation of a transplant, and sensitive palliative care that takes their end-of-life wishes into consideration should they not receive a transplant. Little is known about the psychological impact on staff working within this care dichotomy. The aim of this study is to explore staff's experiences and understand more about the psychological impact of this work on them professionally and personally, and how this affects their ability to provide appropriate care for their patients.

Method:

A qualitative explorative research design was used. Ten semistructured interviews with multidisciplinary staff working in cystic fibrosis centers and units across the United Kingdom were analyzed using interpretative phenomenological analysis (IPA).

Results:

Two superordinate themes emerged from the analysis: factors contributing to the “juggle” of active and palliative care, and extent of emotional impact on staff.

Significance of results:

The study indicates that there is an emotional impact on staff working with patients with CF at end-of-life, pre-transplant stages. Specifically, it reveals the extent of the unpredictability that staff work with, and the range of emotions that staff experience, including uncertainty about professional identity and anxiety about working practices. The depth and intimacy of professional–patient relationships is highlighted, particularly for staff in close contact with and similar in age to their patients. Additionally, the strength of staff's commitment and desire to care for patients within broader humanistic terms that mesh with their own personal values is brought to light. Despite the difficulties with their work, the majority of staff adopted numerous coping strategies to manage their emotions, many of which emphasized the link between their professional and personal values in undertaking their roles.

Keywords

United KingdomCFQualitative researchIPAStaff experiences
Type
Original Articles
Information
Palliative & Supportive Care , Volume 11 , Issue 2 , April 2013 , pp. 111 - 121
Copyright
Copyright © Cambridge University Press 2012

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