Agerskov Hanne, Thiesson Helle C, Pedersen Birthe D
Department of Nephrology, Odense University Hospital and Department of Clinical Institute, University of Southern Denmark, Odense, Denmark.
RN Department of Clinical Institute, University of Southern Denmark, Odense, Denmark.
J Ren Care. 2019 Dec;45(4):205-211. doi: 10.1111/jorc.12297. Epub 2019 Aug 27.
Chronic kidney disease in children is a complex medical and psychosocial disease with factors that differ from the adult disease in significant ways. Among parents, there is uncertainty about disease progression and lack of confidence in caring for the child. The disease has an impact on the emotional and social well-being of the whole family.
To investigate everyday life experiences from the perspectives of members of a family that includes a child with end stage renal disease.
The study took a phenomenological-hermeneutical approach. Semi-structured individual interviews were conducted with seven fathers, seven mothers, five children with kidney disease and five siblings. The data were analysed using Ricoeur's theory of narrative and interpretation, on three levels: naïve reading, structural analysis, critical interpretation and discussion.
It was significant that everyday life and caring for the child were structured around parents' energy reserves. The disease left its mark and changes to daily life caused anxiety, especially for siblings. The search for normalcy was significant and, although the families coped with conditions around the disease, it could be a challenge.
Family members feel vulnerable and concerned and need attention, support and care. Limitations in everyday life cause a dilemma, and the well-being of one family member has an impact on the well-being of the family as a whole.
Health care professionals should focus on the impact of the family's experiences and needs, and the parents' role in family relationships, to support the entire family unit.
儿童慢性肾脏病是一种复杂的医学和社会心理疾病,其相关因素在很大程度上与成人疾病不同。在家长中,对于疾病进展存在不确定性,并且在照顾孩子方面缺乏信心。该疾病对整个家庭的情感和社会福祉都有影响。
从一个有终末期肾病患儿的家庭中成员的角度,调查日常生活经历。
本研究采用现象学-诠释学方法。对七位父亲、七位母亲、五位肾病患儿和五位兄弟姐妹进行了半结构化的个人访谈。运用利科的叙事与诠释理论,在三个层面分析数据:朴素阅读、结构分析、批判性诠释与讨论。
日常生活及对孩子的照料围绕着父母的精力储备展开,这一点很重要。疾病留下了印记,日常生活的改变引发了焦虑,尤其是对兄弟姐妹而言。对正常生活的追寻很重要,尽管家庭应对着与疾病相关的状况,但这可能是一项挑战。
家庭成员感到脆弱和担忧,需要关注、支持和照料。日常生活中的限制造成了一种困境,而且一名家庭成员的福祉会对整个家庭的福祉产生影响。
医疗保健专业人员应关注家庭经历和需求的影响,以及父母在家庭关系中的角色,以支持整个家庭单元。