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Topic:
Issue:
Spine
Category:
Congenital
Title:
Functional Outcomes of Congenital Scoliosis at a Mean 35-Year Follow-up Post In Situ Fusion. Revisiting Patients From the 2002 Goldberg et al Study
Author:
Kelly, Martin J. MCh, FRCS; Alberghina, Flavia FEBOT; McCabe, Patrick MSc, FRCS; Goldberg, Caroline J. MD; Fogarty, Esmond E. FRACS, FRCS; Dowling, Frank E. BSc, FRCS; O’Toole, Patrick MCh, FRCS; Noël, Jacques MCh, FEBOT, FRCS; Kiely, Patrick J. FRCS; Moore, David P. MCh, FRCS; Kennedy, James F. MCh, FRCS
Journal:
Journal of Pediatric Orthopaedics
Date:
May/June 2024
Reference:
44(5):p e381-e388, DOI: 10.1097/BPO.0000000000002649
Level Of Evidence:
# of Patients:
43
Study Type:
Retrospective review with long-term follow-up
Location:
Single institution scoliosis database (1976–2002)
Summary:
Evaluated the long-term clinical and functional outcomes of spinal fusion for congenital scoliosis, revisiting a cohort from a prior study. Investigated demographic, radiographic, surgical, and functional data at an average 35-year follow-up.
Methods:
Retrospective analysis of patient records and radiographs. Functional outcomes assessed via SRS 22, EQ5D–5L, and Oswestry Disability Index (ODI).
Exclusions:
Patients lost to follow-up or who declined participation.
Results:
Mean age at diagnosis: 3.4 years. Mean age at surgery: 5.8 years. Mean follow-up: 35 years. 12 patients (54%) underwent unplanned return to the operating room (UPROR). Thoracic fusions constituted 77% of surgeries. Functional outcomes: SRS 22: Mean score 4.5/5. EQ5D-5L: Mean score 7.2/15. ODI: Mean score 8% (range 2%-30%). Educational attainment: 45% completed university, 2 with doctorates. Employment: 77% of patients in paid employment.
Conclusions:
This study represents the largest long-term follow-up of congenital scoliosis treated with in situ fusion. Thoracic growth continued post-fusion, and patient-reported outcomes indicate satisfactory quality of life. Superior educational and employment outcomes were observed, and unplanned surgeries in adulthood were rare.
Relevance:
Limitations:
Perspective: