Department of Social and Political Sciences (SPS), Università degli Studi di Milano, Milan, Italy.
Department of Cultures, Politics and Society (CPS), Università degli Studi di Torino, Turin, Italy.
Disabil Rehabil. 2020 Dec;42(24):3437-3449. doi: 10.1080/09638288.2019.1597182. Epub 2019 Apr 18.
To identify experiences of persons with multiple sclerosis (MS) in terms of social capital and its components (i.e., social networks, trust, and interpersonal relationships) and social support based on the current scientific knowledge. Systematic literature review was conducted through PubMed, Scopus, Web of Science, ProQuest, and PsycINFO. Included articles were published from 2000 to 2018 and met specific selection criteria. Screening of records determined eligible studies for inclusion to data extraction and synthesis process. A total of 551 abstracts were screened, of which 34 studies met all selection criteria. The themes that emerged referred to the impact of physical and cognitive impairments on social functioning, stigma, psychosocial, emotional and mental challenges, association of quality of life with social capital components and social support, and contribution of social support to improvement of social functioning and health of persons with MS. Persons with MS face a series of issues regarding social support and social capital-related components, primarily facing psychological difficulties, difficulties with making and maintaining interpersonal relationships, and limitations for participating in social and daily activities due to the symptoms of MS, particularly fatigue. It appears that the ability to seek and maintain social relationships and to participate in social and daily activities is important for persons with MS. This has an impact on their quality of life, as well as on their health functioning, however issues around mobility and stigmatization of their condition hinder their social functioning.
为了从当前科学知识的角度,识别多发性硬化症(MS)患者的社会资本及其组成部分(即社交网络、信任和人际关系)和社会支持的相关体验。通过 PubMed、Scopus、Web of Science、ProQuest 和 PsycINFO 进行了系统的文献综述。纳入的文章发表于 2000 年至 2018 年,并符合特定的选择标准。记录筛选确定了符合纳入标准的研究,以进行数据提取和综合。共筛选了 551 篇摘要,其中 34 项研究符合所有选择标准。出现的主题涉及身体和认知障碍对社交功能、污名、心理社会、情感和精神挑战的影响,生活质量与社会资本组成部分和社会支持的关系,以及社会支持对改善多发性硬化症患者的社交功能和健康状况的贡献。多发性硬化症患者面临一系列与社会支持和社会资本相关组成部分有关的问题,主要面临心理困难、建立和维持人际关系的困难,以及由于 MS 症状(尤其是疲劳)导致参与社交和日常活动的受限。似乎寻求和维持社交关系以及参与社交和日常活动的能力对多发性硬化症患者很重要。这对他们的生活质量以及他们的健康功能有影响,但与他们的活动能力和对他们病情的污名化有关的问题阻碍了他们的社交功能。