Basic SciencePsychometric evaluation of the PROMIS Physical Function Computerized Adaptive Test in comparison to the American Shoulder and Elbow Surgeons score and Simple Shoulder Test in patients with rotator cuff disease
Section snippets
Participants and data collection
A total of 609 consecutive patients who were seen by a single shoulder and elbow surgeon at a single academic institution completed the ASES, SST, and PF CAT (Appendices A-C) between April 2013 and February 2014 at their initial patient encounter. We obtained Institutional Review Board approval to analyze the data as part of our institution's musculoskeletal outcomes registry before conducting this observational cross-sectional study. Patients were included in the analysis if a clinical
Results
We included 187 patients in the final analysis. There were 106 men and 81 women. Average age of the patients was 60 years. Demographic data are summarized in Table I.
The distribution of responses was evaluated for normalcy by computing the skewness statistic for each instrument: PF CAT (skewness, −0.28; 95% CI, −0.59 to 0.09); ASES (skewness, −0.92; 95% CI, −1.89 to 0.33); and SST (skewness, 0.06; 95% CI, −0.21 to 0.31). Results indicated that all 3 scales have nonsignificant skewness. After
Discussion
The psychometric properties of the PROMIS PF CAT compared favorably with the ASES and SST in this population of patients with rotator cuff disease. The PF CAT required approximately one third of the questions that are used in the ASES and SST yet showed excellent person and item reliability, with few ceiling or floor effects. Relative weaknesses of the ASES in this study included its comparatively lower person reliability; relative weaknesses of the SST in this study included a large floor
Conclusion
The psychometric properties of the PROMIS PF CAT compared favorably with the ASES and SST in this population of patients with rotator cuff disease. The PF CAT required fewer questions than the ASES and SST, and it showed excellent reliability and unidimensionality with fewer ceiling and floor effects.
Acknowledgment
This investigation was supported by the University of Utah Department of Orthopaedics and the Center for Outcomes Research and Assessment, with funding in part from the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health under Award Number U01AR067138. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Study data were collected and managed using
Disclaimer
The authors, their immediate families, and any research foundation with which they are affiliated have not received any financial payments or other benefits from any commercial entity related to the subject of this article.
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Institutional Review Board approval was obtained from the University of Utah School of Medicine before initiation of this study: No. 00071740.