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Evaluation of WOMAC 20 50 70 response criteria in patients treated with hylan G-F 20 for knee osteoarthritis

机译:接受Hylan G-F 20治疗的膝骨关节炎患者中WOMAC 20、50、70反应标准的评估

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摘要

>Objective: A secondary analysis of a previously conducted one year randomised controlled trial to evaluate the capacity of responder criteria based on the WOMAC index to detect between treatment group differences. >Methods: 255 patients with knee osteoarthritis were randomised to "appropriate care with hylan G-F 20" (AC+H) or "appropriate care without hylan G-F 20" (AC). In the original analysis, two definitions of patient response from baseline to month 12 were used: (1) at least a 20% reduction in WOMAC pain score (WOMAC 20P); (2) at least a 20% reduction in WOMAC pain score and at least a 20% reduction in either WOMAC function or stiffness score (WOMAC 20PFS). For this analysis, a responder was identified using 50% and 70% minimum clinically important response levels to investigate how increasing response affects the ability to detect treatment group differences. >Results: The hylan G-F 20 group had numerically more responders using all patient responder criteria. Increasing the response level from 20% to 50% detected similar differences between treatment groups (25% to 29%). Increasing the response level to 70% reduced the differences between treatment groups (11% to 12%) to a point where the differences were not significant after Bonferroni adjustment. >Conclusions: These results provide evidence for incorporating response levels (WOMAC 50) in clinical trials. While differences at the highest threshold (WOMAC 70) were not statistically detectable, an appropriately powered study may be capable of detecting differences even at this very high level of improvement.
机译:>目的:对先前进行的为期一年的随机对照试验的二次分析,以基于WOMAC指数评估治疗者标准来检测治疗组之间的差异。 >方法:将255例膝骨关节炎患者随机分为“使用Hylan G-F 20进行适当护理”(AC + H)或“不使用Hylan G-F 20进行适当护理”(AC)。在最初的分析中,使用了从基线到第12个月患者反应的两种定义:(1)WOMAC疼痛评分(WOMAC 20P)至少降低20%; (2)WOMAC疼痛评分至少降低20%,WOMAC功能或僵硬度评分(WOMAC 20PFS)降低至少20%。对于此分析,使用50%和70%的最低临床重要反应水平来确定反应者,以研究增加的反应如何影响检测治疗组差异的能力。 >结果:根据所有患者反应者标准,hylan G-F 20组的反应者在数字上更多。将反应水平从20%增加到50%,发现治疗组之间的相似差异(从25%增加到29%)。将应答水平提高至70%可以减少治疗组之间的差异(11%至12%),使Bonferroni调整后差异不明显。 >结论:这些结果为在临床试验中纳入反应水平(WOMAC 50)提供了证据。尽管无法通过统计学方法检测出最高阈值(WOMAC 70)上的差异,但即使是在这种非常高的改进水平下,进行适当验证的研究也可能能够检测出差异。

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