A two-institution pilot study on the psychological burden and distress of parents caring for children with shunted hydrocephalus.

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY Journal of neurosurgery. Pediatrics Pub Date : 2024-10-18 DOI:10.3171/2024.8.PEDS2443
Friederike Knerlich-Lukoschus, Gesa Cohrs, H Maximilian Mehdorn, Michael Synowitz, Martina Messing-Jünger, Simone Goebel
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Abstract

Objective: Little is known about the emotional health of parents caring for children with shunted hydrocephalus. The aim of this pilot study was to find out whether parents caring for shunt-treated hydrocephalic children experience serious psychological problems and psychosocial distress and whether these problems are related to the sociodemographic background of the caregivers, the clinical characteristics of their children, and parents' illness-related concerns and perceived burden of their children's illness.

Methods: This pilot study was performed in an outpatient setting at two German hospitals. The following questionnaires were handed out to parents of children with shunted hydrocephalus (< 21 years of age): the Patient Health Questionnaire (PHQ-9) for depression, the Generalized Anxiety Disorder Scale (GAD-7) for anxiety, the Distress Thermometer (DT) for psychosocial distress, the Hydrocephalus Concerns Questionnaire (HCQ) for assessment of parents' illness-related concerns, and the Hydrocephalus Outcome Questionnaire (HOQ) for assessment of perceived children's disease burden. Clinical data of the respective children were collected from electronic charts. Parents' demographic data were evaluated via questionnaires. Parents' psychological variables were correlated with demographic and clinical data and HCQ and HOQ scores. Regression analyses of HCQ and HOQ scores with psychological items were performed.

Results: Sixty-three parents were included in this study. Of these, 60% reported clinically relevant levels of either depression (11%), anxiety (10%), and/or psychosocial distress (57%). There were no associations between parental sociodemographic or children's clinical characteristics with parents' psychosocial well-being or psychosocial distress. Depression, anxiety, and DT scores were highly intercorrelated and significantly correlated with HCQ scores (r = 0.508, r = 0.516, r = 0.442; p < 0.01). Thereby, worries about shunt-related complications were the most reported concern in the HCQ. Depression and anxiety correlated with the scores of some HOQ subcategories. In preliminary regression analyses, higher illness-related concerns predicted occurrence of parents' anxiety.

Conclusions: The authors' results support the notion that there is a need for psychosocial support for a proportion of parents who care for shunted hydrocephalic children. Perceived child symptom burden and parental illness concerns were identified as relevant correlates of parental psychological well-being. Thus, concerns specific to shunt-related problems could be a first starting point for the development of individual support measures.

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由两家机构共同开展的试点研究:照顾分流脑积水患儿的父母的心理负担和痛苦。
目的:人们对照顾分流脑积水患儿的父母的情绪健康状况知之甚少。本试验性研究旨在了解照顾分流治疗脑积水患儿的父母是否会遇到严重的心理问题和社会心理困扰,以及这些问题是否与照顾者的社会人口背景、患儿的临床特征、父母对疾病的担忧和对患儿疾病负担的感知有关:这项试点研究在两家德国医院的门诊环境中进行。研究人员向分流脑积水患儿(年龄小于 21 岁)的家长发放了以下调查问卷:患者健康问卷 (PHQ-9)(抑郁)、广泛焦虑症量表 (GAD-7)(焦虑)、压力温度计 (DT)(心理社会压力)、脑积水相关问题问卷 (HCQ) (评估家长对疾病的担忧)以及脑积水结果问卷 (HOQ)(评估家长对子女疾病负担的认知)。相关儿童的临床数据来自电子病历。家长的人口统计学数据通过问卷进行评估。家长的心理变量与人口统计学和临床数据以及 HCQ 和 HOQ 分数相关。对HCQ和HOQ得分与心理项目进行回归分析:本研究共纳入 63 名家长。其中,60%的家长报告了临床相关程度的抑郁(11%)、焦虑(10%)和/或心理社会困扰(57%)。父母的社会人口学特征或儿童的临床特征与父母的社会心理健康或社会心理困扰之间没有关联。抑郁、焦虑和 DT 分数高度相互关联,并与 HCQ 分数显著相关(r = 0.508、r = 0.516、r = 0.442;p < 0.01)。因此,在 HCQ 中,对与回避有关的并发症的担忧是报告最多的担忧。抑郁和焦虑与 HOQ 的某些子类别得分相关。在初步回归分析中,与疾病相关的担忧越多,父母的焦虑程度就越高:作者的研究结果支持这样一种观点,即照顾分流型脑积水患儿的部分家长需要社会心理支持。感知到的儿童症状负担和父母对疾病的担忧被认为是父母心理健康的相关因素。因此,对分流相关问题的关注可以作为制定个人支持措施的首要出发点。
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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
期刊最新文献
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