Postoperative cervical deformity in 215 thoracolumbar patients with adult spinal deformity: prevalence, risk factors, and impact on patient-reported outcome and satisfaction at 2-year follow-up.

dc.contributor.author

Passias, Peter G

dc.contributor.author

Soroceanu, Alex

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Smith, Justin

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Boniello, Anthony

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Yang, Sun

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Scheer, Justin K

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Schwab, Frank

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Shaffrey, Christopher

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Kim, Han Jo

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Protopsaltis, Themistocles

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Mundis, Gregory

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Gupta, Munish

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Klineberg, Eric

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Lafage, Virginie

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Ames, Christopher

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International Spine Study Group

dc.date.accessioned

2023-07-20T19:40:07Z

dc.date.available

2023-07-20T19:40:07Z

dc.date.issued

2015-03

dc.date.updated

2023-07-20T19:39:50Z

dc.description.abstract

Study design

Retrospective review of prospective multicenter database.

Objective

Quantify the incidence of new onset cervical deformity (CD) after adult spinal deformity surgery of the thoracolumbar spine, identify predictors of development, and determine the impact on outcomes.

Summary of background data

High prevalence of residual CD has been identified after surgical treatment of adult spinal deformity. Development of new onset CD is less understood and its clinical impact unclear.

Methods

A total of 215 patients with complete 2-year follow-up and full-length radiographs met inclusion criteria. CD was defined by T1 slope minus Cervical Lordosis (CL) more than 20°, C2-C7 sagittal vertical axis more than 40 mm, or C2-C7 kyphosis more than 10°. Univariate analysis was performed using t tests or tests of proportion. Multivariate logistic regression was used to determine independent predictors of new onset CD. The impact of CD on health-related quality of life and satisfaction was measured using repeated measures mixed models or logistic regression as appropriate, accounting for potential confounders.

Results

The overall rate of CD at 2 years after surgery was 63%. Univariate analysis revealed that patients who developed new onset CD postoperatively had higher incidence of diabetes (7.35% vs. 1.28%, P = 0.05), increased preoperative C2-C7 sagittal vertical axis (P = 0.04) and C2 slope (P = 0.038), and smaller diameter rods used at surgery (P = 0.032). Independent predictors of new onset CD at 2 years included: diabetes (odds ratio, 10.49; P = 0.046) and increased preoperative T1 slope minus cervical lordosis (odds ratio, 1.08/º; P = 0.022). Ending instrumentation below T4 was a negative predictor (odds ratio, 0.31; P = 0.019). Patients with and without CD experienced improvements in 2-year 36-Item Short Form Health Survey (P = 0.0001), Oswestry Disability Index (P = 0.0001), and Scoliosis Research Society (P = 0.0001). Rates and overall improvement were similar. CD was not associated with decreased satisfaction (P = 0.28).

Conclusion

A total of 47.7% of patients without preoperative CD developed new onset postoperative CD after thoracolumbar surgery. Independent predictors of new onset CD at 2 years included diabetes, higher preoperative T1 slope minus cervical lordosis, and ending instrumentation above T4. Significant improvements in health-related quality of life scores occurred despite the development of postoperative CD.

Level of evidence

2.
dc.identifier

00007632-201503010-00004

dc.identifier.issn

0362-2436

dc.identifier.issn

1528-1159

dc.identifier.uri

https://hdl.handle.net/10161/28520

dc.language

eng

dc.publisher

Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Spine

dc.relation.isversionof

10.1097/brs.0000000000000746

dc.subject

International Spine Study Group

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Cervical Vertebrae

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Lumbar Vertebrae

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Thoracic Vertebrae

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Humans

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Scoliosis

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Postoperative Complications

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Radiography

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Treatment Outcome

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Prevalence

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Risk Factors

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Retrospective Studies

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Follow-Up Studies

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Prospective Studies

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Middle Aged

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Patient Satisfaction

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Female

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Male

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Self Report

dc.title

Postoperative cervical deformity in 215 thoracolumbar patients with adult spinal deformity: prevalence, risk factors, and impact on patient-reported outcome and satisfaction at 2-year follow-up.

dc.type

Journal article

duke.contributor.orcid

Passias, Peter G|0000-0002-1479-4070|0000-0003-2635-2226

duke.contributor.orcid

Shaffrey, Christopher|0000-0001-9760-8386

pubs.begin-page

283

pubs.end-page

291

pubs.issue

5

pubs.organisational-group

Duke

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School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Orthopaedic Surgery

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

40

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