Basic Science
Psychometric 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

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Background

The Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function Computerized Adaptive Test (PF CAT) is a newly developed patient-reported outcome instrument designed by the National Institutes of Health to measure generalized physical function. However, the measurement properties of the PF CAT have not been compared with established shoulder-specific patient-reported outcomes.

Methods

Patients with clinical diagnosis of rotator cuff disease completed the American Shoulder and Elbow Surgeons (ASES) score, Simple Shoulder Test (SST), and PF CAT. Responses to each of the 3 instruments were statistically analyzed with a Rasch partial credit model. Associations between instruments, convergent validity, item and person reliability, ceiling and floor effects, dimensionality, and survey length were determined.

Results

Responses from 187 patients were analyzed. The PF CAT required fewer questions than the ASES or SST (PF CAT, 4.3; ASES, 11; SST, 12). Correlation between all instruments was moderately high. Item reliability was excellent for all instruments, but person reliability of the PF CAT was superior (0.93, excellent) to the SST (0.71, moderate) and ASES (0.48, fair). Ceiling effects were similar among all instruments (PF CAT, 0.53%; SST, 6.1%; ASES, 2.3%). Floor effects were found in 21% of respondents to the SST but in only 3.2% of PF CAT and 2.3% of ASES respondents.

Conclusion

The measurement properties of the PROMIS PF CAT compared favorably with the ASES and SST despite requiring fewer questions to complete. The PROMIS PF CAT had improved person reliability compared with the ASES score and fewer floor effects compared with the SST.

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.

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