"It Is a Whole Different Life from the Life I Used to Live": Assessing Parents' Support Needs in Paediatric Palliative Care

被引:11
|
作者
Aoun, Samar M. [1 ,2 ,3 ]
Stegmann, Roswitha [3 ]
Deleuil, Renee [4 ]
Momber, Suzanne [4 ]
Cuddeford, Lisa [4 ]
Phillips, Marianne B. [4 ]
Lyon, Maureen E. [5 ,6 ]
Gill, Fenella J. [4 ,7 ]
机构
[1] Univ Western Australia, Crawley, WA 6009, Australia
[2] Perron Inst Neurol & Translat Sci, Nedlands, WA 6009, Australia
[3] La Trobe Univ, Sch Psychol & Publ Hlth, Publ Hlth Palliat Care Unit, Melbourne, Vic 3086, Australia
[4] Perth Childrens Hosp, Child & Adolescent Hlth Serv, Nedlands, WA 6009, Australia
[5] Childrens Natl Hosp, Washington, DC 20010 USA
[6] George Washington Univ, Sch Med & Hlth Sci, Washington, DC 20052 USA
[7] Curtin Univ, Sch Nursing, Perth, WA 6102, Australia
来源
CHILDREN-BASEL | 2022年 / 9卷 / 03期
关键词
palliative care; end-of-life care; equity; public health approach; compassionate communities; caregiving; parents; psychosocial support; END;
D O I
10.3390/children9030322
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aims: This feasibility study aimed to systematically identify and address the support needs of parents of children with life-limiting illnesses and to assess whether the systematic approach was acceptable and relevant to parents. Methods: The CSNAT (Paediatric) intervention consisted of two assessment visits with the paediatric palliative care team, 2-8 weeks apart, comprising conversations about sources for support in a tertiary children hospital in Western Australia (2018-2019). Audio-recorded telephone interviews were conducted with parents, and inductive thematic analysis was undertaken. Results: All 28 parents who were involved in the intervention agreed to be interviewed. Five themes summarised their experience: caregiving challenges, perceived gaps and feelings of isolation; the usefulness and practicality of the systematic assessment; emotional responses to selfreflection; feelings of validation and empowerment; and received supports responsive to their needs. Conclusions: Parents appreciated the value of this systematic approach in engaging them in conversations about their needs and solutions to address them. While clinical service support was affirmed by parents, they were left wanting in other areas of practical, psychosocial, and emotional support. Palliative care services need to build stronger partnerships with supportive community networks through compassionate communities volunteer models of care to address the non-clinical needs of these families.
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收藏
页数:11
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