Rachel Fearnley
Communication and support from health-care professionals to families, with dependent children, following the diagnosis of parental life-limiting illness : a systematic review
Fearnley, Rachel; Boland, Jason W.
Authors
Professor Jason Boland J.Boland@hull.ac.uk
Professor and Honorary Consultant in Palliative Medicine
Abstract
Background: Communication between parents and their children about parental life-limiting illness is stressful. Parents want support from health-care professionals; however, the extent of this support is not known. Awareness of family’s needs would help ensure appropriate support. Aim: To find the current literature exploring (1) how parents with a life-limiting illness, who have dependent children, perceive health-care professionals’ communication with them about the illness, diagnosis and treatments, including how social, practical and emotional support is offered to them and (2) how this contributes to the parents’ feelings of supporting their children. Design: A systematic literature review and narrative synthesis. Data sources: Embase, MEDLINE, PsycINFO, CINAHL and ASSIA ProQuest were searched in November 2015 for studies assessing communication between health-care professionals and parents about how to talk with their children about the parent’s illness. Results: There were 1342 records identified, five qualitative studies met the inclusion criteria (55 ill parents, 11 spouses/carers, 26 children and 16 health-care professionals). Parents wanted information from health-care professionals about how to talk to their children about the illness; this was not routinely offered. Children also want to talk with a health-care professional about their parents’ illness. Health-care professionals are concerned that conversations with parents and their children will be too difficult and time-consuming. Conclusion: Parents with a life-limiting illness want support from their health-care professionals about how to communicate with their children about the illness. Their children look to health-care professionals for information about their parent’s illness. Health-care professionals, have an important role but appear reluctant to address these concerns because of fears of insufficient time and expertise.
Citation
Fearnley, R., & Boland, J. W. (2017). Communication and support from health-care professionals to families, with dependent children, following the diagnosis of parental life-limiting illness : a systematic review. Palliative medicine, 31(3), 212-222. https://doi.org/10.1177/0269216316655736
Journal Article Type | Article |
---|---|
Acceptance Date | May 27, 2016 |
Online Publication Date | Jul 6, 2016 |
Publication Date | 2017-03 |
Deposit Date | Jul 8, 2016 |
Publicly Available Date | Nov 23, 2017 |
Journal | Palliative medicine |
Print ISSN | 0269-2163 |
Publisher | SAGE Publications |
Peer Reviewed | Peer Reviewed |
Volume | 31 |
Issue | 3 |
Pages | 212-222 |
DOI | https://doi.org/10.1177/0269216316655736 |
Keywords | Health-care professionals; Parental life-limiting illness; Children; Communication |
Public URL | https://hull-repository.worktribe.com/output/440786 |
Publisher URL | http://pmj.sagepub.com/content/early/2016/07/06/0269216316655736.abstract |
Additional Information | This is a copy of an open access article published in Palliative medicine, 2017, v.31, issue 3. |
Contract Date | Nov 23, 2017 |
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This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
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