Quality of Life in Multiple Sclerosis: Determinants, Measurement, and Use in Clinical Practice

被引:39
|
作者
Miller, Deborah M. [1 ]
Allen, Rebecca [2 ]
机构
[1] Cleveland Clin, Mellen Ctr Multiple Sclerosis Treatment & Res, Cleveland, OH 44195 USA
[2] Oregon Hlth & Sci Univ, Portland, OR 97239 USA
基金
美国国家卫生研究院;
关键词
Multiple sclerosis; Health-related quality of life; Measurement; Chronic illness; Profiles; Utility assessment; Generic measures; Disease-specific measures; Patient-reported outcomes; Clinical trials; Registries; Clinical care; IMPACT SCALE MSIS-29; OUTCOME MEASURE; SELF-EFFICACY; DISEASE; VALIDATION; DISABILITY; FATIGUE; QUESTIONNAIRE; VALIDITY; MS;
D O I
10.1007/s11910-010-0132-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis (MS) is a complex demyelinating disease with a relatively unpredictable course. It is well established that MS has a significant impact on health-related quality of life (HRQL) for individuals at all stages of the disease. It is argued that clinicians offer treatment to their patients for three reasons: 1) to increase longevity, 2) to prevent future morbidity, and 3) to make patients feel better. To assess how well they are accomplishing the third of these goals, clinicians have come to depend on the direct measurement of patients' HRQL. We review the many physical and emotional symptoms and other consequences of MS that negatively influence HRQL, how HRQL is measured, the unique information these measures provide compared with clinical parameters, the benefit of treatment interventions, and how to include HRQL assessment and data from other sources in clinical encounters and suggest measures to consider for clinical use.
引用
收藏
页码:397 / 406
页数:10
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