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

被引:2
作者
Sjuls, Marianne [1 ]
Ludvigsen, Mette Spliid [2 ,3 ]
Robstad, Nastasja [1 ]
Fegran, Liv [1 ]
机构
[1] Univ Agder, Fac Hlth & Sport Sci, Dept Hlth & Nursing Sci, Kristiansand, Norway
[2] Aarhus Univ, Randers Reg Hosp, Dept Clin Med, Aarhus, Denmark
[3] Nord Univ, Fac Nursing & Hlth Sci, Bodo, Norway
关键词
child; family-centred care; fathers; hospice and palliative nursing; life-limiting conditions; male; paediatric palliative care; palliative care; parents; qualitative research; UNCHARTED TERRITORY; PALLIATIVE CARE; FAMILIES; PARENTS;
D O I
10.1111/jan.15884
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
AimTo 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.
引用
收藏
页码:1670 / 1685
页数:16
相关论文
共 67 条
[1]   A Metasynthesis: Uncovering What Is Known About the Experiences of Families With Children Who Have Life-limiting and Life-threatening Illnesses [J].
Bally, Jill M. G. ;
Smith, Nicole R. ;
Holtslander, Lorraine ;
Duncan, Vicky ;
Hodgson-Viden, Heather ;
Mpofu, Christopher ;
Zimmer, Marcelline .
JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2018, 38 :88-98
[2]   Alone in a Crowd? Parents of Children with Rare Diseases' Experiences of Navigating the Healthcare System [J].
Baumbusch, Jennifer ;
Mayer, Samara ;
Sloan-Yip, Isabel .
JOURNAL OF GENETIC COUNSELING, 2019, 28 (01) :80-90
[3]   International Standards for Pediatric Palliative Care: From IMPaCCT to GO-PPaCS [J].
Benini, Franca ;
Papadatou, Danai ;
Bernada, Mercedes ;
Craig, Finella ;
De Zen, Lucia ;
Downing, Julia ;
Drake, Ross ;
Friedrichsdorf, Stefan ;
Garros, Daniel ;
Giacomelli, Luca ;
Lacerda, Ana ;
Lazzarin, Pierina ;
Marceglia, Sara ;
Marston, Joan ;
Muckaden, Mary Ann ;
Papa, Simonetta ;
Parravicini, Elvira ;
Pellegatta, Federico ;
Wolfe, Joanne .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2022, 63 (05) :E529-E543
[4]   Emotional experience in parents of children with Zellweger spectrum disorders: A qualitative study [J].
Bose, Mousumi ;
Mahadevan, Meena ;
Schules, Dana R. ;
Coleman, Rory K. ;
Gawron, Kelly M. ;
Gamble, Melissa B. ;
Roullet, Jean-Baptiste ;
Gibson, K. Michael ;
Rizzo, William B. .
MOLECULAR GENETICS AND METABOLISM REPORTS, 2019, 19
[5]   Parents as informal caregivers of children and adolescents with spinal muscular atrophy: a systematic review of quantitative and qualitative data on the psychosocial situation, caregiver burden, and family needs [J].
Brandt, Maja ;
Johannsen, Lene ;
Inhestern, Laura ;
Bergelt, Corinna .
ORPHANET JOURNAL OF RARE DISEASES, 2022, 17 (01)
[6]   Fathers Are Parents, Too! Widening the Lens on Parenting for Children's Development [J].
Cabrera, Natasha J. ;
Volling, Brenda L. ;
Barr, Rachel .
CHILD DEVELOPMENT PERSPECTIVES, 2018, 12 (03) :152-157
[7]   Fatherhood in the twenty-first century [J].
Cabrera, NJ ;
Tamisk-LeMonda, CS ;
Bradley, RH ;
Hofferth, S ;
Lamb, ME .
CHILD DEVELOPMENT, 2000, 71 (01) :127-136
[8]   Fathers' experiences of their transition to fatherhood: a metasynthesis [J].
Chin, Rachel ;
Hall, Pauline ;
Daiches, Anna .
JOURNAL OF REPRODUCTIVE AND INFANT PSYCHOLOGY, 2011, 29 (01) :4-18
[9]   Describing the psychosocial profile and unmet support needs of parents caring for a child with a life-limiting condition: A cross-sectional study of caregiver-reported outcomes [J].
Collins, Anna ;
Burchell, Jodie ;
Remedios, Cheryl ;
Thomas, Kristina .
PALLIATIVE MEDICINE, 2020, 34 (03) :358-366
[10]  
Corbin J., 2008, BASICS QUALITATIVE R, DOI 10.4135/9781452230153