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Measuring Outcomes in Adult Spinal Deformity

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Abstract

Several multicenter prospective registries have been created to evaluate quality and value of delivered spine care in population of patients with adult spinal deformity (ASD). Despite these efforts, global surveillance of patients with ASD and comparative effectiveness of treatment has been hindered by lack of a standardized systematic approach towards outcome measurement and reporting. Although meaningful and valuable for their own local purposes at the originating site, data elements that are not completely consistent between registries may not be used for comparison or aggregate analysis as different outcomes, measurement instruments, and risk stratification variables are used. This inconsistency limits the application of research findings into clinical practice, and prevents clinician investigators from informing policy makers about efficacy of various treatment strategies.

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Faraj, S.S.A., Haanstra, T.M., Wright, A.K., De Kleuver, M., Van Hooff, M.L. (2020). Measuring Outcomes in Adult Spinal Deformity. In: Sethi, R., Wright, A., Vitale, M. (eds) Value-Based Approaches to Spine Care . Springer, Cham. https://doi.org/10.1007/978-3-030-31946-5_8

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  • DOI: https://doi.org/10.1007/978-3-030-31946-5_8

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