Hope Lena, Juul-Kristensen Birgit, Løvaas Helene, Løvvik Camilla, Maeland Silje
a Department of Occupational Therapy, Physiotherapy and Radiography, Faculty of Health and Social Sciences , Western Norway University of Applied Sciences , Bergen , Norway.
b Department of Sports Sciences and Clinical Biomechanics , Research Unit of Musculoskeletal Function and Physiotherapy, University of Southern Denmark , Odense , Denmark.
Disabil Rehabil. 2019 Feb;41(3):333-340. doi: 10.1080/09638288.2017.1390695. Epub 2017 Oct 17.
To investigate the prevalence and severity of subjective health complaints and describe illness perception in a population of Joint Hypermobility Syndrome or Ehlers-Danlos Syndrome-Hypermobile Type.
This study was a postal survey with a questionnaire battery on demographic data, subjective health complaints inventory, and illness perception. A total of 110 individuals diagnosed with Joint Hypermobility Syndrome or Ehlers-Danlos Syndrome-Hypermobile Type from two specialized hospitals in Norway were offered participation. Further, 140 gender- and age-matched healthy controls from statistics Norway representing the general population were sent the questionnaire for reference.
Overall response rate was 30.4% (n = 76), with 44.5% (n = 49) in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobile Type and 19.3% (n = 27) in controls. Subjective health complaints were significantly higher in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobile Type - than in the controls (32.06 vs. 11.08; p < 0.001). Further the brief illness perception questionnaire indicated that the adults with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobile Type had low understanding of their illness and symptoms (understanding, mean: 3.93, SD 2.88), and reported to have moderate personal and treatment control over their illness.
Adults with Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobile Type reported higher frequency and severity of subjective health complaints than the matched controls from the general adult population in Norway. Furthermore, Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome-Hypermobile Type reported low understanding of their illness and associated symptoms, and moderate belief that their illness can be kept under control through self-management or treatment. This may indicate one of the reasons why prognosis for these patients is poor. Implications for rehabilitation Awareness of the complexity of the subjective health complaints and inquiry into illness perception could contribute with valuable information about these patients' perceptions of their condition. Such information could in its turn be of value for clinicians as they work towards facilitating a more holistic treatment approach, for example patient education and cognitive behavioural therapy.
调查主观健康问题的患病率和严重程度,并描述关节活动过度综合征或埃勒斯-当洛综合征-高活动型人群的疾病认知情况。
本研究是一项邮寄调查,采用了一系列关于人口统计学数据、主观健康问题清单和疾病认知的问卷。挪威两家专科医院共110名被诊断为关节活动过度综合征或埃勒斯-当洛综合征-高活动型的个体受邀参与。此外,从挪威统计局选取了140名年龄和性别匹配的健康对照者作为一般人群的代表,并向他们发放问卷以供参考。
总体回复率为30.4%(n = 76),其中关节活动过度综合征/埃勒斯-当洛综合征-高活动型组的回复率为44.5%(n = 49),对照组为19.3%(n = 27)。关节活动过度综合征/埃勒斯-当洛综合征-高活动型组的主观健康问题显著高于对照组(32.06对11.08;p < 0.001)。此外,简短疾病认知问卷表明,患有关节活动过度综合征/埃勒斯-当洛综合征-高活动型的成年人对自己的疾病和症状了解程度较低(了解程度,平均值:3.93,标准差2.88),并报告对自己的疾病有中等程度的个人控制和治疗控制。
与挪威一般成年人群中匹配的对照组相比,患有关节活动过度综合征/埃勒斯-当洛综合征-高活动型的成年人报告的主观健康问题频率和严重程度更高。此外,关节活动过度综合征/埃勒斯-当洛综合征-高活动型人群对自己的疾病和相关症状了解程度较低,并且对通过自我管理或治疗控制疾病的信念中等。这可能表明这些患者预后不良的原因之一。对康复的启示了解主观健康问题的复杂性并探究疾病认知情况,可能会提供有关这些患者对自身状况认知的有价值信息。这些信息反过来对临床医生可能有价值,因为他们致力于促进更全面的治疗方法,例如患者教育和认知行为疗法。