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Validation of PROMIS® Physical Function Computerized Adaptive Tests for Orthopaedic Foot and Ankle Outcome Research

  • Symposium: ABJS Carl T. Brighton Workshop on Outcome Measures
  • Published:
Clinical Orthopaedics and Related Research®

Abstract

Background

In 2012, the American Orthopaedic Foot & Ankle Society® established a national network for collecting and sharing data on treatment outcomes and improving patient care. One of the network’s initiatives is to explore the use of computerized adaptive tests (CATs) for patient-level outcome reporting.

Questions/purposes

We determined whether the CAT from the NIH Patient Reported Outcome Measurement Information System® (PROMIS®) Physical Function (PF) item bank provides efficient, reliable, valid, precise, and adequately covered point estimates of patients’ physical function.

Methods

After informed consent, 288 patients with a mean age of 51 years (range, 18–81 years) undergoing surgery for common foot and ankle problems completed a web-based questionnaire. Efficiency was determined by time for test administration. Reliability was assessed with person and item reliability estimates. Validity evaluation included content validity from expert review and construct validity measured against the PROMIS® Pain CAT and patient responses based on tradeoff perceptions. Precision was assessed by standard error of measurement (SEM) across patients’ physical function levels. Instrument coverage was based on a person-item map.

Results

Average time of test administration was 47 seconds. Reliability was 0.96 for person and 0.99 for item. Construct validity against the Pain CAT had an r value of −0.657 (p < 0.001). Precision had an SEM of less than 3.3 (equivalent to a Cronbach’s alpha of ≥ 0.90) across a broad range of function. Concerning coverage, the ceiling effect was 0.32% and there was no floor effect.

Conclusions

The PROMIS® PF CAT appears to be an excellent method for measuring outcomes for patients with foot and ankle surgery. Further validation of the PROMIS® item banks may ultimately provide a valid and reliable tool for measuring patient-reported outcomes after injuries and treatment.

Level of Evidence

Level III, diagnostic study. See Instructions for Authors for a complete description of levels of evidence.

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Acknowledgments

The authors thank Ian Alexander MD (Cleveland Clinic–Medina Hospital, Medina, OH, USA) for his extensive contributions to the AOFAS OFAR Network and this project. We acknowledge the contributing investigators of the OFAR Network, including Timothy R. Daniels MD (University of Toronto, Toronto, ON, Canada), James Brodsky MD (Baylor University, Houston, TX, USA), Jon Deland MD (Hospital for Special Surgery, New York, NY, USA), Scott Ellis MD (Hospital for Special Surgery, New York, NY, USA), Phinit Phisitkul MD (University of Iowa, Iowa City, IA, USA), W. Hodges Davis MD (OrthoCarolina Research Institute, Charlotte, NC, USA), Susan Ishikawa MD (The University of Tennessee–Campbell Clinic, Memphis, TN, USA), Loretta B. Chou MD (Stanford University, Redwood City, CA, USA), John Ketz MD (University of Rochester, Rochester, NY, USA), Margaret Chilvers MD (University of Arizona, Tucson, AZ, USA), Sam Flemister MD (University of Rochester, Rochester, NY, USA), Florian Nickisch MD (University of Utah, Salt Lake City, UT, USA), and Timothy Beals MD (University of Utah, Salt Lake City, UT, USA). We are thankful for the contributions of each of the 10 clinical testing sites in the OFAR Network. We also thank Lousanne Lofgren BS (AOFAS, Rosemont, IL, USA) and Rose Olea BS (AOFAS, Rosemont, IL, USA) for their tireless work on this project. Special thanks go to Christine Cheng BS (University of Utah, Salt Lake City, UT, USA) and Shirley D. Hon BS (University of Utah, Salt Lake City, UT, USA) for their tremendous support in data collection, analysis, manuscript preparation, and review. Finally, the study design, statistical and psychometric support, and computing resources provided by the Center for Outcomes Research and Assessment at the University of Utah Department of Orthopaedics are gratefully acknowledged.

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Correspondence to Man Hung PhD, MSTAT, MED.

Additional information

Each author certifies that he or she has no commercial associations (eg, consultancies, stock ownership, equity interest, patent/licensing arrangements, etc) that might pose a conflict of interest in connection with the submitted article.

All ICMJE Conflict of Interest Forms for authors and Clinical Orthopaedics and Related Research editors and board members are on file with the publication and can be viewed on request.

Each author certifies that his or her institution approved the human protocol for this investigation, that all investigations were conducted in conformity with ethical principles of research, and that informed consent for participation in the study was obtained.

Subjects were enrolled through a distributed consortium of foot and ankle clinics participating in the National Orthopaedic Foot & Ankle Outcomes Research Network, sponsored by the American Orthopaedic Foot & Ankle Society®. Institutions participating in this network include Baylor University (Houston, TX, USA), The University of Tennessee–Campbell Clinic (Memphis, TN, USA), Hospital for Special Surgery (New York, NY, USA), OrthoCarolina Research Institute (Charlotte, NC, USA), Stanford University (Redwood City, CA, USA), University of Arizona (Tucson, AZ, USA), University of California Los Angeles (Los Angeles, CA, USA), University of Iowa (Iowa City, IA, USA), University of Rochester (Rochester, NY, USA), and University of Utah (Salt Lake City, UT, USA).

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Appendix 1

Appendix 1

National Orthopaedic Foot & Ankle Outcomes Research Network Sites and Principal Investigators

Site

Principal investigator

The University of Tennessee–Campbell Clinic (Memphis, TN, USA)

Sue Ishikawa MD, G. Andrew Murphy MD, David Richardson MD

Stanford University (Redwood City, CA, USA)

Kenneth J. Hunt MD

University of Arizona (Tucson, AZ, USA)

L. Daniel Latt MD

University of Utah (Salt Lake City, UT, USA)

Charles L. Saltzman MD, Man Hung PhD

University of Iowa (Iowa City, IA, USA)

Phinit Phisitkul MD

University of Rochester (Rochester, NY, USA)

Judith F. Baumhauer MD

Hospital for Special Surgery (New York, NY, USA)

Jonathan T. Deland MD, Scott Ellis MD

University of California Los Angeles (Los Angeles, CA, USA)

Nelson Soohoo MD

OrthoCarolina Research Institute (Charlotte, NC, USA)

W. Hodges Davis MD

Baylor University (Houston, TX, USA)

James W. Brodsky MD

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Hung, M., Baumhauer, J.F., Latt, L.D. et al. Validation of PROMIS® Physical Function Computerized Adaptive Tests for Orthopaedic Foot and Ankle Outcome Research. Clin Orthop Relat Res 471, 3466–3474 (2013). https://doi.org/10.1007/s11999-013-3097-1

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