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Global statistical tests for comparing multiple outcomes in rheumatoid arthritis trials

✍ Scribed by Barbara C. Tilley; Stanley R. Pillemer; Stephen P. Heyse; Shuhui Li; Daniel O. Clegg; Graciela S. Alarćon


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
145 KB
Volume
42
Category
Article
ISSN
0004-3591

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✦ Synopsis


Objective:

To evaluate global statistical tests (gsts) of treatment effectiveness for rheumatoid arthritis (ra) trials measuring multiple outcomes.

Methods:

Using outcome measures from american college of rheumatology (acr) core set variables available in 3 ra trials, gsts were calculated using the o'brien ranking procedure and a procedure for binary data. gsts take correlations among outcomes into account. power calculations using 1 trial data set provide comparisons of gsts and acr criteria for improvement.

Results:

Spearman correlations among outcomes ranged from 0.21 to 0.73. erythrocyte sedimentation rate had the lowest correlation with other outcomes in all 3 trials. within a trial, joint swelling and joint tenderness or patient and physician assessment had the highest correlations, depending on the trial. results were consistent with results using the acr criteria, although the gst was more powerful.

Conclusion:

Gsts are a useful tool for comparing treatment effects across multiple clinically meaningful outcome measures. the gst allows easy inclusion of validated, reliable new measures that are not a part of acr criteria, such as quality of life, and can be computed with or without selecting a cutoff point defining patient improvement. gsts should be considered for rheumatic disease treatment trials.


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✍ van der Kooij, S. M. ;de Vries-Bouwstra, J. K. ;Goekoop-Ruiterman, Y. P. M. ;Ewa 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 204 KB

## Abstract ## Objective To investigate the effectiveness of 4 different treatment strategies for recent‐onset rheumatoid arthritis (RA) on 2‐year patient‐reported outcomes, including functioning and quality of life. ## Methods A total of 508 patients with recent‐onset RA were randomly assigned