Department of Psychology, DePaul University, Chicago, IL, USA.
Children's Hospital of Orange County, Orange, CA, USA.
J Child Health Care. 2020 Sep;24(3):444-457. doi: 10.1177/1367493519867174. Epub 2019 Aug 1.
Hypermobile Ehlers-Danlos syndrome (hEDS), a genetic connective tissue disorder, involves several body systems which makes symptom management and functioning difficult. The aim of this study was to understand pediatric hEDS patients' symptoms and primary complaints. Additionally, we examined the cumulative impact of symptoms on physical and psychological functioning. Thirty-four youth with hEDS were recruited from a genetics clinic and reported the hardest thing about having hEDS, their pain, fatigue, physical symptoms, functional disability, anxiety, and depression. Physical symptoms (pain and fatigue) and limitations (keeping up with friends) were reported as the most difficult parts of having hEDS. A higher number of somatic symptoms was the strongest predictor of disability, anxiety, and depression. Physical symptoms are subjectively distressing and significantly related to impairments in physical and psychological functioning. Thus, addressing these varied symptoms in treatment may yield better functioning in youth with hEDS.
患有超弹性 Ehlers-Danlos 综合征(hEDS)的儿童,一种遗传性结缔组织疾病,涉及多个身体系统,这使得症状管理和功能变得困难。本研究的目的是了解儿科 hEDS 患者的症状和主要抱怨。此外,我们还检查了症状对身体和心理功能的累积影响。34 名 hEDS 青少年从遗传诊所招募,报告了他们患有 hEDS 的最困难之处,包括疼痛、疲劳、身体症状、功能障碍、焦虑和抑郁。身体症状(疼痛和疲劳)和限制(跟上朋友)被报告为患有 hEDS 最困难的部分。更多的躯体症状是残疾、焦虑和抑郁的最强预测因素。身体症状令人感到痛苦,并与身体和心理功能障碍显著相关。因此,在治疗中解决这些不同的症状可能会改善患有 hEDS 的青少年的功能。