เปรียบเทียบวิธี
ดูวิธีที่เลือกเทียบกันแบบเคียงข้าง แถวที่ต่างกันจะถูกเน้นไว้
| NMSS× | Multiple Sclerosis Quality of Life-54 (MSQOL-54)× | |
|---|---|---|
| สาขาวิชา | ประสาทวิทยา | ประสาทวิทยา |
| ตระกูล | Process / pipeline | Process / pipeline |
| ปีกำเนิด≠ | 2007 | 1995 |
| ผู้ริเริ่ม≠ | K. Ray Chaudhuri, National Hospital for Neurology and Neurosurgery, London | Barbara G. Vickrey, UCLA |
| ประเภท≠ | Self-report questionnaire and clinician interview | Self-report questionnaire |
| แหล่งต้นตำรับ≠ | Chaudhuri, K. R., Martinez-Martin, P., Brown, R. G., Sethi, K., Stocchi, F., Odin, P., Ondo, W., Whone, A., Rye, D., Bhattacharya, K., Naidu, Y., Schapira, A. H., Brozova, H., Nutt, J., Macphee, G., Carroll, C., Hilten, J. V., Verschuuren, J., & Bonuccelli, U. (2007). The metric properties of a novel non-motor symptoms scale for Parkinson's disease: Results from an international pilot study. Movement Disorders, 22(13), 1901-1911. DOI ↗ | Vickrey, B. G., Hays, R. D., Genovese, B. J., Myers, L. W., & Ellison, G. W. (1995). Outcomes in Multiple Sclerosis: The Multiple Sclerosis Quality of Life-54 Scale. Health Psychology, 14(1), 34-42. DOI ↗ |
| ชื่อเรียกอื่น≠ | Parkinson's Non-Motor Scale, NMSQ, NMS Scale | MS QoL-54 |
| ที่เกี่ยวข้อง | 4 | 4 |
| สรุป≠ | The NMSS is a comprehensive 30-item scale designed to assess the prevalence and impact of non-motor symptoms (NMS) in Parkinson's disease. Developed by Chaudhuri and colleagues in 2007, it addresses the reality that non-motor features—sleep disorders, mood disturbances, autonomic dysfunction, cognitive impairment, and pain—often cause greater disability and suffering than motor symptoms in many PD patients. The scale is essential for comprehensive PD assessment and is increasingly recognized as a critical outcome measure reflecting true patient burden. | The MSQOL-54 is a disease-specific quality-of-life instrument designed to assess the physical and mental burden of multiple sclerosis on patients' daily functioning and well-being. Developed by Vickrey and colleagues in 1995, it combines the widely-used SF-36 generic health questionnaire with 18 MS-specific items to provide comprehensive measurement of QoL in MS populations. This scale is a cornerstone tool in MS clinical research and patient monitoring. |
| ScholarGateชุดข้อมูล ↗ |
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