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2.
Spine Deform ; 10(6): 1461-1466, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-35776363

RESUMO

PURPOSE: Early-onset scoliosis (EOS) can have harmful effects on pulmonary function. Serial elongation, derotation, and flexion (EDF) casting can cure EOS or delay surgical intervention. Most described casting techniques call for specialized tables, which are not available at many institutions. We describe an innovative technique for EDF casting utilizing a modified Jackson table (MJ) and compare results to a Risser frame (RF). METHODS: All patients who underwent EDF casting at our institution between January 2015 and January 2019 were identified and retrospectively reviewed. Patients were stratified by type of table used and clinical and radiographic outcomes were compared. Standard descriptive statistics were calculated. RESULTS: We identified 25 patients who underwent 77 casting events, 11 on an MJ table and 14 on a RF. Mean follow-up was 32 months (range 11-61 months). 28% of patients had idiopathic scoliosis. There was no significant difference in age at initiation of casting (P = 0.3), initial Cobb angle (equivalence, P = 0.009), or rate of idiopathic scoliosis between the MJ and RF groups. There was no significant difference in initial coronal Cobb angle percent correction (equivalence, P = 0.045) or percent correction at 1-year follow-up (equivalence, P = 0.010) between the two groups. There was no difference in cast related complications. There was a significant difference in surgical time, with the MJ group 11 min shorter than the RF (P = 0.005). CONCLUSION: The MJ table is a safe and effective alternative for applying EDF casts under traction without the need for a specialized table. LEVEL OF EVIDENCE: III.


Assuntos
Escoliose , Humanos , Escoliose/cirurgia , Estudos Retrospectivos , Moldes Cirúrgicos , Duração da Cirurgia
3.
J Neurosurg Pediatr ; 23(1): 16-21, 2018 10 05.
Artigo em Inglês | MEDLINE | ID: mdl-30497201

RESUMO

Pedicle aplasia is an uncommon congenital anomaly most frequently involving the absence of a single pedicle at a single vertebral level. Bilateral pedicle aplasia at multiple levels is exceedingly rare and has only been described once previously in the literature. While single-level pedicle aplasia is often asymptomatic and discovered incidentally, pedicle aplasia of multiple levels may produce severe spinal deformities and neurological deficits. Due to the rarity of this condition, optimal management remains uncertain. In this case report, the authors describe the surgical management of a healthy 9-year-old boy who presented with frequent falls, difficulty running, and severe thoracic kyphotic deformity and was found to have bilateral pedicle aplasia from T3 to T9. A review of the literature regarding pedicle aplasia is also presented.


Assuntos
Cifose/cirurgia , Vértebras Torácicas/anormalidades , Criança , Humanos , Fixadores Internos , Cifose/diagnóstico por imagem , Cifose/etiologia , Masculino , Parafusos Pediculares , Exame Físico , Complicações Pós-Operatórias , Radiografia , Reoperação , Vértebras Torácicas/diagnóstico por imagem , Tomografia Computadorizada por Raios X
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