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BMC Musculoskelet Disord ; 18(1): 411, 2017 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-29017495

RESUMO

BACKGROUND: Short-segment pedicle-screw instrumentation is frequently used to stabilize thoracolumbar burst fractures. A recognized disadvantage of this procedure is recurrent kyphosis from intervertebral disc creep into the fractured central endplate. Balloon Assisted Endplate Reduction (BAER) using Tricalcium Phosphate bone cement (TCP) enables elevation of the centrally depressed endplate. Our objective was to evaluate the bone-tissue response to TCP and to analyse whether BAER using TCP can prevent recurrent kyphosis after removal of the instrumentation. METHODS: Fourteen patients with traumatic thoracolumbar burst fractures were operated with BAER using TCP in combination with short-segment instrumentation. Nine months after surgery, instrumentation was removed and transpedicular biopsies were taken for histological and histochemical analysis. Roentgenograms pre- and postoperatively and at latest follow-up after removal of the instrumentation were evaluated. RESULTS: Average follow-up was 2.6 years. Analysis of the biopsies showed a variable degree of bone remodelling with incorporation of TCP into newly formed bone matrix. No extensive foreign body reactions, inflammation, granulomatous responses or tissue necrosis were observed. Wedge-angle, kyphosis-angle and both the anterior-posterior and central-posterior vertebral body height ratios improved significant postoperatively (p < 0.001). After removal of the instrumentation no significant differences in wedge-angle or height ratios were seen (p = 0.12). The kyphosis-angle increased four degrees (p = 0.01). CONCLUSION: TCP showed good histological osseointegration with no adverse events. TCP can therefore be safely used and could be beneficial in treatment of thoracolumbar burst fractures. BAER with TCP in combination with short-segment instrumentation might reduce recurrence of deformity even after removal of the instrumentation in comparison to short-segment instrumentation alone. TRIAL REGISTRATION: This study is registered at the at the Dutch Trial Registry (NTR3498).


Assuntos
Materiais Biocompatíveis/uso terapêutico , Osso e Ossos/efeitos dos fármacos , Fosfatos de Cálcio/uso terapêutico , Fixação de Fratura/métodos , Fraturas da Coluna Vertebral/cirurgia , Adulto , Materiais Biocompatíveis/farmacologia , Cimentos Ósseos/farmacologia , Cimentos Ósseos/uso terapêutico , Fosfatos de Cálcio/farmacologia , Feminino , Humanos , Vértebras Lombares/lesões , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Fraturas da Coluna Vertebral/diagnóstico por imagem , Vértebras Torácicas/lesões , Resultado do Tratamento , Adulto Jovem
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