Fathers' experiences of living with a child with a progressive life‐limiting condition without curative treatment options: A qualitative systematic review

Author:

Sjuls Marianne1ORCID,Ludvigsen Mette Spliid23ORCID,Robstad Nastasja1ORCID,Fegran Liv1ORCID

Affiliation:

1. Faculty of Health and Sport Sciences, Department of Health and Nursing Science University of Agder Kristiansand Norway

2. Department of Clinical Medicine—Randers Regional Hospital Aarhus University Aarhus Denmark

3. Faculty of Nursing and Health Sciences Nord University Bodø Norway

Abstract

AbstractAimTo systematically review and synthesize findings across qualitative primary studies about fathers' experiences of living with a child with a progressive life‐limiting condition without curative treatment options (C3 conditions).DesignSystematic review and metasynthesis.MethodsSandelowski and Barosso's qualitative research methodology guided this review and metasynthesis. A modification of Ricoeur's interpretation theory, described by Lindseth and Norberg, guided the synthesis of qualitative data. The quality of the studies was evaluated using the Joanna Briggs Institute Checklist for Qualitative Research.Data SourcesA systematic literature search was conducted on 6 May 2022 and updated on 19 July 2023 on MEDLINE, CINAHL Plus with Full Text, APA PsycInfo and Scopus. Inclusion criteria were English‐written qualitative studies from the year 2000, from which we could extract data on fathers' experiences of living with a child from 0 to 18 years with a progressive life‐limiting condition without curative treatment options.ResultsSeven reports from Western countries contributed to the review. Through structural analysis, we developed the following themes: ‘Being shattered in the perception of fatherhood’, ‘Establishing a new normal’ and ‘Striving to be acknowledged as a part of the caring team’.ConclusionFathers had to establish a new normal, and they experienced anticipatory mourning, role conflicts and feeling sidelined in healthcare settings when living with a child with a C3 condition. An important issue for further research on paediatric palliative care (PPC) should be to include fathers in the research sample and report separately on fathers' or mothers' experiences instead of parents' experiences.ImpactThe findings will be of interest to healthcare personnel and multidisciplinary teams working within PPC, as they give insight into fathers' experiences and suggest interventions to increase healthcare personnel's involvement with fathers, such as telemedicine.Reporting MethodFollowing EQUATOR guidelines, the study was reported according to the enhancing transparency in reporting the synthesis of qualitative research (ENTREQ) framework.Patient or Public ContributionNo patient or Public Contribution.

Publisher

Wiley

Subject

General Nursing

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