Radiographical spinopelvic parameters and disability in the setting of adult spinal deformity: a prospective multicenter analysis.

dc.contributor.author

Schwab, Frank J

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Blondel, Benjamin

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Bess, Shay

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Hostin, Richard

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Shaffrey, Christopher I

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Smith, Justin S

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Boachie-Adjei, Oheneba

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Burton, Douglas C

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Akbarnia, Behrooz A

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Mundis, Gregory M

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Ames, Christopher P

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Kebaish, Khaled

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Hart, Robert A

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Farcy, Jean-Pierre

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Lafage, Virginie

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International Spine Study Group (ISSG)

dc.date.accessioned

2023-08-29T23:44:37Z

dc.date.available

2023-08-29T23:44:37Z

dc.date.issued

2013-06

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2023-08-29T23:44:36Z

dc.description.abstract

Study design

Prospective multicenter study evaluating operative (OP) versus nonoperative (NONOP) treatment for adult spinal deformity (ASD).

Objective

Evaluate correlations between spinopelvic parameters and health-related quality of life (HRQOL) scores in patients with ASD.

Summary of background data

Sagittal spinal deformity is commonly defined by an increased sagittal vertical axis (SVA); however, SVA alone may underestimate the severity of the deformity. Spinopelvic parameters provide a more complete assessment of the sagittal plane but only limited data are available that correlate spinopelvic parameters with disability. METHODS.: Baseline demographic, radiographical, and HRQOL data were obtained for all patients enrolled in a multicenter consecutive database. Inclusion criteria were: age more than 18 years and radiographical diagnosis of ASD. Radiographical evaluation was conducted on the frontal and lateral planes and HRQOL questionnaires (Oswestry Disability Index [ODI], Scoliosis Research Society-22r and Short Form [SF]-12) were completed. Radiographical parameters demonstrating highest correlation with HRQOL values were evaluated to determine thresholds predictive of ODI more than 40.

Results

Four hundred ninety-two consecutive patients with ASD (mean age, 51.9 yr) were enrolled. Patients from the OP group (n = 178) were older (55 vs. 50.1 yr, P < 0.05), had greater SVA (5.5 vs. 1.7 cm, P < 0.05), greater pelvic tilt (PT; 22° vs. 11°, P < 0.05), and greater pelvic incidence/lumbar lordosis PI/LL mismatch (PI-LL; 12.2 vs. 4.3; P < 0.05) than NONOP group (n = 314). OP group demonstrated greater disability on all HRQOL measures compared with NONOP group (ODI = 41.4 vs. 23.9, P < 0.05; Scoliosis Research Society score total = 2.9 vs. 3.5, P < 0.05). Pearson analysis demonstrated that among all parameters, PT, SVA, and PI-LL correlated most strongly with disability for both OP and NONOP groups (P < 0.001). Linear regression models demonstrated threshold radiographical spinopelvic parameters for ODI more than 40 to be: PT 22° or more (r = 0.38), SVA 47 mm or more (r = 0.47), PI - LL 11° or more (r = 0.45).

Conclusion

ASD is a disabling condition. Prospective analysis of consecutively enrolled patients with ASD demonstrated that PT and PI-LL combined with SVA can predict patient disability and provide a guide for patient assessment for appropriate therapeutic decision making. Threshold values for severe disability (ODI > 40) included: PT 22° or more, SVA 47 mm or more, and PI - LL 11° or more.
dc.identifier

00007632-201306010-00014

dc.identifier.issn

0362-2436

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1528-1159

dc.identifier.uri

https://hdl.handle.net/10161/28830

dc.language

eng

dc.publisher

Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Spine

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10.1097/brs.0b013e318292b7b9

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International Spine Study Group (ISSG)

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Pelvis

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Spine

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Humans

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Scoliosis

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Radiography

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Disability Evaluation

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Prognosis

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Linear Models

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Sensitivity and Specificity

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Prospective Studies

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Reproducibility of Results

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Quality of Life

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Adolescent

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Adult

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Aged

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Aged, 80 and over

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Middle Aged

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Female

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Male

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Young Adult

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Surveys and Questionnaires

dc.title

Radiographical spinopelvic parameters and disability in the setting of adult spinal deformity: a prospective multicenter analysis.

dc.type

Journal article

duke.contributor.orcid

Shaffrey, Christopher I|0000-0001-9760-8386

pubs.begin-page

E803

pubs.end-page

E812

pubs.issue

13

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Duke

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School of Medicine

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Clinical Science Departments

pubs.organisational-group

Orthopaedic Surgery

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

38

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