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

Author:

Cerpa Meghan1ORCID,Zuckerman Scott L.1,Lenke Lawrence G.1,Kelly Michael P.2ORCID,Yaszay Burt3,Newton Peter3,Sponseller Paul4,Erickson Mark5,Garg Sumeet5,Pahys Joshua6,Samdani Amer6,Cahill Patrick7,McCarthy Richard8,Bumpass David8,Sucato Daniel9,Boachie-Adjei Oheneba10,Shah Suken11,Gupta Munish2ORCID

Affiliation:

1. Department of Orthopaedics, Columbia University Medical Center, The Och Spine Hospital at New York-Presbyterian, New York, NY, USA

2. Department of Orthopaedics, Washington University, St. Louis, MO, USA

3. Rady Children’s Hospital, San Diego, CA, USA

4. Johns Hopkins University, Baltimore, MD, USA

5. Children’s Hospital Colorado Aurora, Aurora, CO, USA

6. Shriners Hospitals for Children, Philadelphia, PA, USA

7. Children’s Hospital of Philadelphia, PA, USA

8. Department of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA

9. Texas Scottish Rite Hospital for Children Dallas, TX, USA

10. FOCOS Orthopedic Hospital, Accra, Ghana

11. Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA

Abstract

Study Design: Multi-center, prospective, observational cohort. Objective: To compare myelopathic vs. non-myelopathic ambulatory patients in short- and long-term neurologic function, operative treatment, and patient-reported outcomes. Methods: 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). Results: 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 ( P = 0.18), gender ( P = 0.09), and Risser Stage ( P = 0.06), while more patients in the non-myelopathic group had previous surgery (16.1% vs. 3.9%; P = 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, P = 0.02; 1-year: 48.2 ± 3.7, P < 0.001; 2-year: 48.2 ± 7.7, P < 0.001). The non-myelopathic group had significantly higher LEMS immediately postoperative ( P = 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, P = 0.10) and was maintained at 2-years postoperative (non-myelopathic: 49.2 ± 3.3, myelopathic: 48.2 ± 5.7, P = 0.09). Both groups improved significantly in all SRS domains compared to preoperative, with no difference in scores in the domains for pain ( P = 0.12), self-image ( P = 0.08), and satisfaction ( P = 0.83) at latest follow-up. Conclusion: 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.

Publisher

SAGE Publications

Subject

Neurology (clinical),Orthopedics and Sports Medicine,Surgery

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