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Responsiveness of pain, disability, and physical impairment outcomes in patients with low back pain.

机译:下腰痛患者的疼痛,残疾和身体损伤结果的反应性。

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STUDY DESIGN: Cohort study. OBJECTIVE: To conduct a head-to-head comparison of the responsiveness of pain, disability, and physical impairment measures in patients with low back pain. SUMMARY OF BACKGROUND DATA: Pain, disability, and physical impairment measures are routinely measured in clinical practice and clinical research. However, to date, a head-to-head comparison has not been performed. METHODS: A numerical pain scale (0-10), the 24-item and 2 modified 18-item versions of the Roland Morris questionnaire, the patient specific functional scale, and physical impairment measures were completed by 155 patients with low back pain at baseline and then again after 6 weeks together with an 11-point global perceived effect scale. Responsiveness was evaluated by using effect sizes and t tests, correlating the change scores for each outcome with the global perceived effect score and by calculating the Guyatt responsiveness index. RESULTS: The most responsive outcome proved to be the patient specific functional scale (effect size = 1.6), followed by the numerical pain scale (effect size = 1.3) and 24-item Roland Morris questionnaire (effect size = 0.8). The responsiveness of the two 18-item Roland Morris versions was equal to the 24-item version. However, the physical impairment measures were not very responsive (effect size 0.1-0.6). The ranking of the responsiveness indices was consistent across all statistical analyses. CONCLUSIONS: Physical impairments are routinely measured in clinical practice and clinical research, but the lower responsiveness indicates that this approach is not optimal. Our findings suggest that more emphasis should be placed on change in pain and disability scores than on change in physical impairments.
机译:研究设计:队列研究。目的:对腰背痛患者的疼痛,残疾和身体损伤措施的反应性进行正面对比。背景数据摘要:在临床实践和临床研究中常规测量疼痛,残疾和身体损伤的措施。但是,迄今为止,还没有进行直接的比较。方法:由155名基线腰背痛的患者完成了数字疼痛量表(0-10),Roland Morris问卷的24项和2项修改的18项版本,患者特定的功能量表以及身体障碍的测量然后在6周后再加上11点整体感知效果量表。通过使用效应大小和t检验,将每个结果的变化得分与总体感知效应得分相关联并通过计算Guyatt响应指数来评估响应能力。结果:最有效的结果被证明是患者特定的功能量表(效应量= 1.6),其次是数字疼痛量表(效应量= 1.3)和24项Roland Morris问卷(效应量= 0.8)。两个18个项目的Roland Morris版本的响应速度等于24个版本。但是,身体损伤的措施反应不太快(效应大小为0.1-0.6)。在所有统计分析中,反应性指数的排名均保持一致。结论:在临床实践和临床研究中常规测量身体损伤,但较低的反应性表明该方法不是最佳方法。我们的发现表明,应更多地关注疼痛和残疾评分的变化,而不是身体上的障碍的变化。

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