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埃勒斯-当洛综合征患者对残疾的接受程度和连贯感

Acceptance of disability and sense of coherence in individuals with Ehlers-Danlos syndrome.

作者信息

Berglund Britta, Mattiasson Anne-Cathrine, Nordström Gun

机构信息

Department of Nursing, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Clin Nurs. 2003 Sep;12(5):770-7. doi: 10.1046/j.1365-2702.2003.00776.x.

Abstract

Ehlers-Danlos syndrome (EDS) is a relatively rare, inherited connective tissue disorder and skin hyperextensibility, joint hypermobility, chronic joint and limb pain, blood vessel and tissue fragility are frequent symptoms. The aims of this study were to describe the degree to which individuals with EDS accept and cope with perceived limitations related to the syndrome, and to determine the relationships between acceptance of disability (AD), sense of coherence (SOC), functional health status and background data. Four questionnaires were mailed: the AD scale Modified (ADM), the SOC Scale, the Sickness Impact Profile (SIP) and a background form. The respondents with EDS were recruited through the EDS National Association in Sweden and the response rate was 74% (69 females and eight males). The Ethical Committee at Huddinge University Hospital (ref. no. 152/95) approved the study. This study has shown that the level of AD and SOC in individuals with EDS is similar to other patient groups, e.g. individuals with ostomy and with diabetes. Further, the SOC was in concordance with that of the general population. Those working full-time accepted their disability to a greater degree than those on sick leave or disability pension. A multiple regression analysis showed that a greater AD was associated with a higher level of SOC and a better functional health status. The SOC and SIP together accounted for 50% of the variance in the ADM. For health promotion in nursing practice it is important to have insight into the problem areas which may influence the overall life situation for an individual with EDS. A key issue for nurses is to identify individuals with low acceptance of their disease and/or low SOC in order to support these persons' adaptation process. Future research on EDS may be directed towards projects focusing on the development and implementation of models to strengthen the level of AD and SOC in this group.

摘要

埃勒斯-当洛综合征(EDS)是一种相对罕见的遗传性结缔组织疾病,皮肤过度伸展、关节活动过度、慢性关节和肢体疼痛以及血管和组织脆弱是其常见症状。本研究的目的是描述EDS患者接受和应对与该综合征相关的感知限制的程度,并确定残疾接受度(AD)、连贯感(SOC)、功能健康状况和背景数据之间的关系。我们邮寄了四份问卷:修订后的AD量表(ADM)、SOC量表、疾病影响概况量表(SIP)和一份背景表格。通过瑞典的EDS全国协会招募了EDS患者,回复率为74%(69名女性和8名男性)。胡丁厄大学医院伦理委员会(参考编号152/95)批准了该研究。本研究表明,EDS患者的AD和SOC水平与其他患者群体相似,例如造口术患者和糖尿病患者。此外,SOC与普通人群的情况一致。全职工作的人比休病假或领取残疾抚恤金的人对自己的残疾接受程度更高。多元回归分析表明,更高的AD与更高水平的SOC和更好的功能健康状况相关。SOC和SIP共同解释了ADM中50%的变异。在护理实践中促进健康,了解可能影响EDS患者整体生活状况的问题领域很重要。护士的一个关键问题是识别那些对自己疾病接受度低和/或SOC低的人,以便支持这些人的适应过程。未来关于EDS的研究可能会针对侧重于开发和实施模型以提高该群体AD和SOC水平的项目。

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