儿童先天代谢异常的影响:父母对限制、歧视、计划生育和应急管理的看法。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY Orphanet Journal of Rare Diseases Pub Date : 2024-08-26 DOI:10.1186/s13023-024-03315-6
Tanjana Harings, Martina P Neininger, Simone Eisenhofer, Alena G Thiele, Wieland Kiess, Astrid Bertsche, Thilo Bertsche, Skadi Beblo
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引用次数: 0

摘要

背景:从父母的角度调查儿童先天性代谢异常(IEMs)对儿童及其父母生活的影响。方法:我们对 108 名先天性代谢异常患儿的父母进行了问卷调查:我们对在代谢门诊就诊的 119 名 IEM 患儿的 108 名家长进行了问卷调查。根据疾病严重程度的增加将患儿分为 4 组(第 1 组:严重程度最低的 IEM 患儿,第 4 组:严重程度最高的 IEM 患儿),并通过 Tobit 回归进行比较:结果:儿童 IEM 的严重程度与父母认为自己和孩子在生活各个方面受到的限制强度增加有关:在一般情况下、与朋友接触、追求爱好、照顾孩子/上学/工作以及情绪压力。在所有组群中,父母自己在与朋友接触时受到的限制强度最高(与第一组群相比:第二组群:c. 3.556,p = 0.002;第三组群:c. 4.159,p = 0.003;第四组群:c. 7.224,p 结论:在所有组群中,父母自己在与朋友接触时受到的限制强度最高:从家长的角度来看,限制的强度随着儿童 IEM 的严重程度而增加。这项研究表明,羊膜腔积液对羊膜腔积液患儿家长的影响很大,他们每天都要面对各种挑战。这些发现强调了为患儿家长提供全面支持的重要性。
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The impact of a child's inborn error of metabolism: the parents' perspectives on restrictions, discrimination, family planning, and emergency management.

Background: To investigate the impact of children's inborn error of metabolism (IEMs) on the children's and their parents' lives from the parents' perspective. We focused on disease-related restrictions in various issues of daily life, experienced discrimination, parental family planning, and management of metabolic emergencies.

Methods: We conducted a questionnaire-based survey with 108 parents of 119 children with IEM who attended a metabolic outpatient clinic. The children were categorized into 4 cohorts, based on increasing disease severity (cohort 1: IEMs with lowest severity, cohort 4: IEMs with highest severity), and compared by using Tobit regressions.

Results: The severity of the child's IEM was associated with an increase in the intensity of perceived restrictions from the parents' perspective for themselves and their children in all aspects of life: in general, in contact with friends, in the pursuit of hobbies, in childcare/school/occupation, and due to emotional stress. The highest intensity of restrictions in all cohorts was found for the parents themselves in contact with friends (compared to cohort 1: cohort 2: c. 3.556, p = 0.002; cohort 3: c. 4.159, p = 0.003; cohort 4: c. 7.224, p < 0.001). Parents of 8% of children reported that their children were discriminated against because of IEM, with the highest proportion of affected children (43%) in cohort 4. Parental family planning decisions were influenced in 34% of parents, with fear of recurrence being a predominant aspect. Of the parents of children diagnosed with IEMs associated with metabolic emergencies, 68% stated that they felt well or very well prepared for the occurrence of a metabolic emergency, and 100% of parents were able to name the necessary action steps from memory. Nevertheless, 58% stated that they experienced an occurring emergency as rather or very stressful.

Conclusions: From the parents' perspective, the intensity of restrictions increased with the severity of the child's IEM. The study shows the high impact of IEM on parents of children with IEM and the daily challenges they face. These findings emphasize the importance of comprehensive support for parents of children with IEM.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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