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ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders.

Publication ,  Journal Article
Passias, PG; Horn, SR; Segreto, FA; Bortz, CA; Pierce, KE; Vasquez-Montes, D; Moon, J; Varlotta, CG; Raman, T; Frangella, NJ; Stekas, N ...
Published in: Global Spine J
June 2020

STUDY DESIGN: Retrospective review of single institution. OBJECTIVE: To assess the relationship between Patient-Reported Outcomes Measurement Information System (PROMIS) and Oswestry Disability Index (ODI) scores in thoracolumbar patients. METHODS: Included: Patients ≥18 years with a thoracolumbar spine condition (spinal stenosis, disc herniation, low back pain, disc degeneration, spondylolysis). Bivariate correlations assessed the linear relationships between ODI and PROMIS (Physical Function, Pain Intensity, and Pain Interference). Correlation cutoffs assessed patients with high and low correlation between ODI and PROMIS. Linear regression predicted the relationship of ODI to PROMIS. RESULTS: A total of 206 patients (age 53.7 ± 16.6 years, 49.5% female) were included. ODI correlated with PROMIS Physical Function (r = -0.763, P < .001), Pain Interference (r = 0.800, P < .001), and Pain Intensity (r = 0.706, P < .001). ODI strongly predicted PROMIS for Physical Function (R 2 = 0.58, P < .001), Pain Intensity (R 2 = 0.50, P < .001), and Pain Interference (R 2 = 0.64, P < .001); however, there is variability in PROMIS that ODI cannot account for. ODI questions about sitting and sleeping were weakly correlated across the 3 PROMIS domains. Linear regression showed overall ODI score as accounting for 58.3% (R 2 = 0.583) of the variance in PROMIS Physical Function, 63.9% (R 2 = 0.639) of the variance in Pain Interference score, and 49.9% (R 2 = 0.499) of the variance in Pain Intensity score. CONCLUSIONS: There is a large amount of variability with PROMIS that cannot be accounted for with ODI. ODI questions regarding walking, social life, and lifting ability correlate strongly with PROMIS while sitting, standing, and sleeping do not. These results reinforce the utility of PROMIS as a valid assessment for low back disability, while indicating the need for further evaluation of the factors responsible for variation between PROMIS and ODI.

Duke Scholars

Published In

Global Spine J

DOI

ISSN

2192-5682

Publication Date

June 2020

Volume

10

Issue

4

Start / End Page

399 / 405

Location

England

Related Subject Headings

  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Passias, P. G., Horn, S. R., Segreto, F. A., Bortz, C. A., Pierce, K. E., Vasquez-Montes, D., … Fischer, C. R. (2020). ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders. Global Spine J, 10(4), 399–405. https://doi.org/10.1177/2192568219851478
Passias, Peter G., Samantha R. Horn, Frank A. Segreto, Cole A. Bortz, Katherine E. Pierce, Dennis Vasquez-Montes, John Moon, et al. “ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders.Global Spine J 10, no. 4 (June 2020): 399–405. https://doi.org/10.1177/2192568219851478.
Passias PG, Horn SR, Segreto FA, Bortz CA, Pierce KE, Vasquez-Montes D, et al. ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders. Global Spine J. 2020 Jun;10(4):399–405.
Passias, Peter G., et al. “ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders.Global Spine J, vol. 10, no. 4, June 2020, pp. 399–405. Pubmed, doi:10.1177/2192568219851478.
Passias PG, Horn SR, Segreto FA, Bortz CA, Pierce KE, Vasquez-Montes D, Moon J, Varlotta CG, Raman T, Frangella NJ, Stekas N, Lafage R, Lafage V, Gerling MC, Protopsaltis TS, Buckland AJ, Fischer CR. ODI Cannot Account for All Variation in PROMIS Scores in Patients With Thoracolumbar Disorders. Global Spine J. 2020 Jun;10(4):399–405.
Journal cover image

Published In

Global Spine J

DOI

ISSN

2192-5682

Publication Date

June 2020

Volume

10

Issue

4

Start / End Page

399 / 405

Location

England

Related Subject Headings

  • 3202 Clinical sciences