MSIS-29和SF-36作为继发性进展性MS试验的结局。

Eva Mm Strijbis, Pavle Repovic, Jop Mostert, James D Bowen, Bernard Mj Uitdehaag, Gary Cutter, Marcus W Koch
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引用次数: 3

摘要

背景:患者报告的结果测量(PROMs)常用于临床研究,但很少了解其作为纵向结果的表现。方法:我们使用来自ASCEND(一项大型SPMS试验)的数据(n = 889),在2年的随访中调查简短健康调查36 (SF-36 v2)和多发性硬化症影响量表(MSIS-29)的变化。结果:在2年的随访中,PROM评分变化不大。与身体残疾措施相比,胎膜早破的变化没有一致的趋势:明显恶化的发生与改善的发生一样频繁。使用6个月的确认减少了恶化和改善事件的数量,而不改变它们的相对平衡。基于人群特征的各组恶化事件没有明显差异,使用不同的阈值也没有明显影响临床显著变化。结论:我们发现在SPMS患者的2年随访中MSIS-29和SF-36几乎没有一致的变化。我们的研究结果表明,在这一人群中,残疾恶化与PROM变化之间存在脱节。我们的研究结果对在SPMS试验中使用这些PROMs作为主要结局指标提出了警告,并呼吁对这些指标在SPMS试验中的纵向使用进行批判性的重新评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials.

The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials.

The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials.

The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials.

Background: Patient-reported outcome measures (PROMs) are often used in clinical research, but little is known about their performance as longitudinal outcomes.

Methods: We used data from ASCEND, a large SPMS trial (n = 889), to investigate changes on the Short Form Health Survey 36 (SF-36 v2) and the Multiple Sclerosis Impact Scale (MSIS-29) over 2 years of follow-up.

Results: PROM scores changed little over the 2 years of follow-up. In contrast to physical disability measures, there was no consistent trend in PROM change: significant worsening occurred about as often as improvement. Using a 6-month confirmation reduced the number of both worsening and improvement events without altering their relative balance. There was no clear difference in worsening events in groups based on population characteristics, nor was there a noticeable effect using different thresholds for clinically significant change.

Conclusion: We found little consistent change in MSIS-29 and SF-36 over 2 years of follow-up in people with SPMS. Our findings show a disconnect between disability worsening and PROM change in this population. Our findings raise caution about the use of these PROMs as primary outcome measures in SPMS trials and call for a critical reappraisal of the longitudinal use of these measures in SPMS trials.

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