Schweitzer R, Kelly B, Foran A, Terry D, Whiting J
Queensland University of Technology, Australia.
Soc Sci Med. 1995 Nov;41(10):1367-72. doi: 10.1016/0277-9536(95)00124-p.
Whilst the debilitating fatigue experienced in patients suffering from Chronic Fatigue Syndrome (CFS) results in a subjective marked impairment in functioning, little research has investigated the impact of this disorder on quality of life. Forty-seven subjects with a confirmed diagnosis of CFS and 30 healthy controls were compared using the Sickness Impact Profile (SIP). A subgroup of subjects were interviewed regarding the impact CFS has had on their social and family relationships, work and recreational activities. Results from both the SIP and the interview revealed that CFS subjects had significantly impaired quality of life, especially in areas of social functioning. These findings highlight the importance of addressing the social isolation and loss of role functioning experienced by CFS sufferers.
虽然慢性疲劳综合征(CFS)患者所经历的使人衰弱的疲劳会导致功能上明显的主观损害,但很少有研究调查这种疾病对生活质量的影响。使用疾病影响量表(SIP)对47名确诊为CFS的受试者和30名健康对照者进行了比较。对一组受试者就CFS对其社交和家庭关系、工作及娱乐活动的影响进行了访谈。SIP和访谈的结果均显示,CFS受试者的生活质量显著受损,尤其是在社会功能方面。这些发现凸显了解决CFS患者所经历的社会孤立和角色功能丧失问题的重要性。