Myelopathic Patients Undergoing Severe Pediatric Spinal Deformity Surgery Can Improve Neurologic Function to That of Non-Myelopathic Patients by 1-Year Postoperative.

Journal: Global spine journal

Volume: 13

Issue: 5

Year of Publication: 

Affiliated Institutions:  Department of Orthopaedics, Columbia University Medical Center, The Och Spine Hospital at New York-Presbyterian, New York, NY, USA. Department of Orthopaedics, Washington University, St. Louis, MO, USA. Rady Children's Hospital, San Diego, CA, USA. Johns Hopkins University, Baltimore, MD, USA. Children's Hospital Colorado Aurora, Aurora, CO, USA. Shriners Hospitals for Children, Philadelphia, PA, USA. Children's Hospital of Philadelphia, PA, USA. Department of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Texas Scottish Rite Hospital for Children Dallas, TX, USA. FOCOS Orthopedic Hospital, Accra, Ghana. Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA.

Abstract summary 

Multi-center, prospective, observational cohort.To compare myelopathic vs. non-myelopathic ambulatory patients in short- and long-term neurologic function, operative treatment, and patient-reported outcomes.Pediatric deformity patients from 16 centers were enrolled with the following inclusion criteria: aged 10-21 years-old, a Cobb angle ≥100° in either the coronal or sagittal plane or any sized deformity with a planned 3-column osteotomy, and community ambulators. Patients were dichotomized into 2 groups: myelopathic (abnormal preoperative neurologic exam with signs/symptoms of myelopathy) and non-myelopathic (no clinical signs/symptoms of myelopathy).Of 311 patients with an average age of 14.7 ± 2.8 years, 29 (9.3%) were myelopathic and 282 (90.7%) were non-myelopathic. There was no difference in age ( = 0.18), gender ( = 0.09), and Risser Stage ( = 0.06), while more patients in the non-myelopathic group had previous surgery (16.1% vs. 3.9%; = 0.03). Mean lower extremity motor score (LEMS) in myelopathic patients increased significantly compared to baseline at every postoperative visit: Baseline: 40.7 ± 9.9; Immediate postop: 46.0 ± 7.1, = 0.02; 1-year: 48.2 ± 3.7, < 0.001; 2-year: 48.2 ± 7.7, < 0.001). The non-myelopathic group had significantly higher LEMS immediately postoperative ( = 0.0007), but by 1-year postoperative, there was no difference in LEMS between groups (non-myelopathic: 49.3 ± 3.6, myelopathic: 48.2 ± 3.7, = 0.10) and was maintained at 2-years postoperative (non-myelopathic: 49.2 ± 3.3, myelopathic: 48.2 ± 5.7, = 0.09). Both groups improved significantly in all SRS domains compared to preoperative, with no difference in scores in the domains for pain ( = 0.12), self-image ( = 0.08), and satisfaction ( = 0.83) at latest follow-up.In severe spinal deformity pediatric patients presenting with preoperative myelopathy undergoing spinal reconstructive surgery, myelopathic patients can expect significant improvement in neurologic function postoperatively. At 1-year and 2-year postoperative, neurologic function was no different between groups. While non-myelopathic patients had significantly higher postoperative outcomes in SRS mental-health, function, and total-score, both groups had significantly improved outcomes in every SRS domain compared to preoperative.

Authors & Co-authors:  Cerpa Meghan M Zuckerman Scott L SL Lenke Lawrence G LG Kelly Michael P MP Yaszay Burt B Newton Peter P Sponseller Paul P Erickson Mark M Garg Sumeet S Pahys Joshua J Samdani Amer A Cahill Patrick P McCarthy Richard R Bumpass David D Sucato Daniel D Boachie-Adjei Oheneba O Shah Suken S Gupta Munish M

Study Outcome 

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Statistics
Citations :  Lenke LG, Sides BA, Koester LA, Hensley M, Blanke KM. Vertebral column resection for the treatment of severe spinal deformity. In: Clin Orthop Relat Res. 2010;468(3):687–699. doi:10.1007/s11999-009-1037-x
Authors :  18
Identifiers
Doi : 10.1177/21925682211034837
SSN : 2192-5682
Study Population
Male,Female
Mesh Terms
Other Terms
myelopathy;neurologic deficit;neurologic function;pediatric spine surgery;scoliosis;severe pediatric spinal deformity
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
England