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首页> 外文期刊>Molecular Genetics and Metabolism Reports >Emotional experience in parents of children with Zellweger spectrum disorders: A qualitative study
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Emotional experience in parents of children with Zellweger spectrum disorders: A qualitative study

机译:Zellweger谱系疾病患儿父母的情感体验:一项定性研究

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Zellweger spectrum disorders (ZSDs) are rare, debilitating genetic diseases of peroxisome biogenesis that require constant management and lifelong care. Nevertheless, the experience of family caregivers for children diagnosed with ZSD is not well understood. In this study, we sought to characterize the emotional experience of ZSD family caregivers. Three 90-min focus groups were conducted with thirty-seven parents (25 mothers and 12 fathers) of children with ZSD during a family advocacy conference. Focus groups were arranged by age of proband (Group 1: 0–4?years, Group 2: 5–10?years, Group 3: 11?years). Audio recordings of focus groups were transcribed and analyzed using software for coding purposes. Analyzed content was validated using peer debriefing, member checking, and method triangulation. Focus group results showed that nearly a third of ZSD caregivers described their overall emotional experience as a “rollercoaster.” Additionally, three interconnected themes were identified: 1) range of emotions, 2) stressors, and 3) coping. Feeling overwhelmed and devastated were the most frequently described emotional responses. Corresponding stressors to these emotions included the burden of caregiver tasks associated with ZSD, and negative interactions with healthcare professionals. The most common coping strategies were acceptance of limitations of the diseases, redefining “normal” in the parenting experience, and advocating on behalf of the child and the patient community. This study underscores the profound emotional impact on parents who are caregivers for children with ZSDs, highlighting the utility of patient community feedback and qualitative approaches to fully characterize the overall family experience. Simple, targeted approaches focusing on improved communication between healthcare professionals and families, as well as offering resources for emotional support may greatly improve the lives of families living with ZSD and other rare pediatric diseases.
机译:Zellweger谱系疾病(ZSD)是罕见的,会破坏过氧化物酶体生物发生的遗传疾病,需要不断进行管理和终生护理。然而,对于被确诊为ZSD的儿童的家庭看护者的经验并没有得到很好的理解。在这项研究中,我们试图刻画ZSD家庭照顾者的情感体验。在家庭倡导会议上,与ZSD儿童的37名父母(25名母亲和12名父亲)进行了三个90分钟的焦点小组讨论。焦点组按先证者的年龄排列(组1:0–4岁,组2:5–10岁,组3:> 11岁)。出于编码目的,使用软件转录并分析了焦点小组的录音。使用对等人员汇报,成员检查和方法三角剖分来验证分析的内容。焦点小组的结果显示,将近三分之一的ZSD护理人员将他们的整体情感体验描述为“过山车”。此外,还确定了三个相互关联的主题:1)情绪范围,2)压力源和3)应对。感觉不知所措和破坏是最经常描述的情绪反应。与这些情绪相对应的压力源包括与ZSD相关的护理人员任务的负担,以及与医疗保健专业人员的负面互动。最常见的应对策略是接受疾病的局限性,在育儿经历中重新定义“正常”,并代表儿童和患者社区进行倡导。这项研究强调了对患有ZSD患儿的父母的深远情感影响,强调了患者社区反馈和定性方法在充分体现整体家庭经历方面的作用。简单,有针对性的方法侧重于改善医疗保健专业人员与家庭之间的沟通,以及提供情感支持资源,可以大大改善患有ZSD和其他罕见儿科疾病的家庭的生活。

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