焦虑与未确诊罕见疾病患儿父母的生活质量:一项多地点定量调查研究

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Ria Patel, Bettina Friedrich, Saskia C. Sanderson, Holly Ellard, Celine Lewis
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引用次数: 0

摘要

养育患有罕见的未确诊遗传疾病的孩子会影响心理健康,包括焦虑和与健康相关的生活质量。我们对父母进行了多地点的定量调查,以了解哪些父母和孩子的特征可以预测较差的心理结果。1366份调查在英格兰的七个NHS信托基金中进行;383例返回并纳入分析(应答率27%)。我们使用GAD-7来测量父母的广泛性焦虑,使用PedsQL家庭影响模块(FIM)来测量自我报告的身体、情感、社会和认知功能(健康相关生活质量[HRQOL]总结得分)、沟通、担忧、日常活动和家庭关系(家庭功能[FF]总结得分)。参与者特征包括:测量父母弹性的6项简短弹性量表,评估父母对不确定性的容忍度的定制单题,测量儿童健康相关生活质量的EQ-5D-Y-3L,评估儿童病情的严重性/后果的两个定制问题,以及标准特征问题(例如,年龄,种族,教育程度,收入)。总体而言,父母焦虑较低(平均= 5.31;SD = 5.82,范围0-21),但21.9%患有中度(11.4%)或重度(10.5%)焦虑。多变量分析显示,较高的焦虑得分与父母年龄较小(p = 0.010)、受教育程度较低(0.004)、适应能力较低(p = 0.049)和对不确定性的容忍度较低(p = 0.021)显著相关。FIM总分0 ~ 100分,平均53.68分,标准差20.45分。父母在日常活动(43.68分)、担忧(47.29分)、沟通(51.31分)和身体功能(52.45分)单项得分最低。与其他情况相比,发育障碍儿童父母的家庭功能总结得分明显较低(p = 0.016)。多变量分析发现,较低的分数(反映较差的结果)与较低的父母适应能力和较低的不确定性耐受性显著相关(p < 0.001)。我们的研究结果强调了养育一个患有罕见未确诊疾病的孩子会给一些父母带来巨大的心理负担,以及制定量身定制的支持策略的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anxiety and quality-of-life for parents of children with undiagnosed rare conditions: A multi-site quantitative survey study

Anxiety and quality-of-life for parents of children with undiagnosed rare conditions: A multi-site quantitative survey study

Parenting a child with a rare undiagnosed genetic condition can impact psychological well-being, including anxiety and health-related quality-of-life. We conducted a multi-site quantitative survey with parents to understand which parent and child characteristics are predictive of poorer psychological outcomes. 1366 surveys were sent out across seven NHS Trusts in England; 383 were returned and included in analysis (27% response rate). We used the GAD-7 to measure parents' generalized anxiety and the PedsQL Family Impact Module (FIM) to measure self-reported physical, emotional, social, and cognitive functioning (the health-related quality-of-life [HRQOL] summary score), communication, worry, daily activities, and family relationships (the family functioning [FF] summary score). Participant characteristics included: the 6-item Brief Resilience Scale to measure parental resilience, a bespoke single question to assess parents' tolerance for uncertainty, the EQ-5D-Y-3L to measure child health-related quality-of-life, two bespoke questions to assess the perceived seriousness/consequences of the child's condition, and standard characteristics questions (e.g., age, ethnicity, education, income). Overall, parental anxiety was low (mean = 5.31; SD = 5.82, range 0–21), although 21.9% had moderate (11.4%) or severe (10.5%) anxiety. A multivariable analysis indicated that higher anxiety scores were significantly associated with younger parental age (p = 0.010), lower education attainment (0.004), lower resilience (p = 0.049), and lower tolerance for uncertainty (p = 0.021). FIM total scores ranged from 0 to 100 (mean = 53.68, SD 20.45). Parents scored lowest on the subscale daily activities (43.68), worry (47.29), communication (51.31), and physical functioning (52.45). Family functioning summary scores were significantly lower for parents of children with developmental disorders compared to other conditions (p = 0.016). Multivariable analysis identified that lower scores (reflecting poorer outcomes) were significantly associated with lower parental resilience and lower tolerance for uncertainty (p < 0.001, respectively). Our findings highlight the significant psychological burden parenting a child with a rare undiagnosed condition can have on some parents and the importance of developing tailored support strategies.

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来源期刊
Journal of Genetic Counseling
Journal of Genetic Counseling GENETICS & HEREDITY-
CiteScore
3.80
自引率
26.30%
发文量
113
审稿时长
6 months
期刊介绍: The Journal of Genetic Counseling (JOGC), published for the National Society of Genetic Counselors, is a timely, international forum addressing all aspects of the discipline and practice of genetic counseling. The journal focuses on the critical questions and problems that arise at the interface between rapidly advancing technological developments and the concerns of individuals and communities at genetic risk. The publication provides genetic counselors, other clinicians and health educators, laboratory geneticists, bioethicists, legal scholars, social scientists, and other researchers with a premier resource on genetic counseling topics in national, international, and cross-national contexts.
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