Caring for a Child with Phenylketonuria: Parental Experiences from a Eurasian Country.

P. Zengin Akkus, Berrak Bilginer Gurbuz, Kısmet Çıkı, E. İLTER BAHADUR, S. Karahan, E. Ozmert, T. Coşkun, S. Sivri
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引用次数: 2

Abstract

OBJECTIVES Phenylketonuria (PKU) and mild hyperphenylalaninemia (HPA) are characterized by increased blood phenylalanine concentrations varying from mild to severe. Management of PKU was reported to be time consuming and burdensome for caregivers. This study intended to explore the experiences of families caring for a child with PKU/HPA in a country with a high PKU rate. The aim of this study was to compare parental well-being between parents of children with and without dietary restrictions and to explore the factors associated with parental psychological well-being. METHODS Participants were interviewed about their experiences, concerns, and challenges related to the disease by using a semistructured questionnaire. After the interview, parents filled out the Beck Depression Inventory and State-Trait Anxiety Inventory-Trait. RESULTS This study highlighted the adverse psychological, financial, and social effects of the diagnosis and management of the disease regarding the lives of the families of children with PKU/HPA. Although parental anxiety scores of children with and without dietary restrictions were similar, depressive symptom scores were higher in parents of children with dietary restrictions. However, in multiple regression analysis, lower household income and absence of perceived social support were found to be independent factors associated with higher depressive symptom scores. Having a daughter diagnosed with PKU/HPA and lower household income were found to be factors associated with higher anxiety scores. CONCLUSION This study revealed that income level, perceived social support, and gender of the child were factors associated with psychological well-being of parents caring for children with PKU/HPA. Health care professionals should identify the challenges faced by families and should be aware of risk factors associated with lower parental well-being to achieve better family adjustment and better health outcomes.
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照顾一个患有苯丙酮尿症的孩子:来自欧亚国家的父母经验。
目的苯丙酮尿症(PKU)和轻度高苯丙氨酸血症(HPA)的特点是血液中苯丙氨酸浓度升高,从轻度到重度不等。据报道,对护理人员来说,PKU的管理既耗时又繁重。本研究旨在探讨在一个PKU发生率较高的国家,家庭对PKU/HPA患儿的照顾经验。本研究的目的是比较有和没有饮食限制的孩子的父母之间的父母幸福感,并探讨与父母心理健康相关的因素。方法采用半结构化问卷对参与者进行访谈,了解他们与疾病相关的经历、担忧和挑战。访谈结束后,家长填写了贝克抑郁量表和状态-特质焦虑量表。结果本研究强调了PKU/HPA患儿的诊断和治疗对其家庭生活的不良心理、经济和社会影响。虽然有和没有饮食限制的孩子的父母焦虑得分相似,但有饮食限制的孩子的父母抑郁症状得分更高。然而,在多元回归分析中,较低的家庭收入和缺乏感知的社会支持被发现是高抑郁症状得分的独立因素。发现女儿被诊断为PKU/HPA和家庭收入较低是高焦虑得分的相关因素。结论收入水平、儿童感知社会支持、儿童性别是影响PKU/HPA患儿父母心理健康的因素。卫生保健专业人员应确定家庭面临的挑战,并应意识到与较低的父母幸福感相关的风险因素,以实现更好的家庭调整和更好的健康结果。
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