Scoliosis Research Society QoL - Revised (SRS-22r)

22-item quality of life survey across function, pain, self-image, mental health, & treatment satisfaction for scoliosis

Audience: PATIENT

Published by EVAL Foundation

Revision 1 · Published April 22, 2026

Citation

Scoliosis Research Society https://www.srs.org/Research/Patient-Outcome-Questionnaires?

Haher, Thomas R., et al. “Results of the Scoliosis Research Society instrument for evaluation of surgical outcome in adolescent idiopathic scoliosis: a multicenter study of 244 patients.” Spine 24.14 (1999): 1435.

Summary

The SRS-22r is a validated, condition-specific quality of life instrument for scoliosis patients. It comprises 22 items organized into five domains:

Each item uses a 5-point ordinal scale (1–5), with higher scores indicating better outcomes. Domain scores and a total score are calculated as averages, ranging from 1 to 5.

The instrument is sensitive to clinical change and appropriate for tracking longitudinal outcomes in patients managed conservatively (observation, bracing) or surgically.

Clinically meaningful minimally detectable change is approximately 0.5 points on the 5-point scale.

The SRS-22r is widely used in research and clinical practice for preoperative assessment, postoperative follow-up, and comparative effectiveness studies.

Original Literature:

Additional References

For a complete list of references, go to https://www.srs.org/Files/Research/SRS22_bibliography.pdf

For more information on the SRS-22r, to include scoring, go to https://www.srs.org/Research/Patient-Outcome-Questionnaires

Instructions

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Literature

Revisions

Current: Revision 1

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