A retrospective descriptive preliminary study on early experience using all pedicle screw correction Pedicle screw fixation enables enhanced correction of spinal deformities. However, the technique is still in early development in our clinic. Tends of the scoliosis patient to come in late ages make maximum correction failed. A total 16 patients are subjected to pedicle screw fixation for spinal deformities were analyzed descriptively as an early follow-up in the last two-year. 14 patients are girl and 2 are boys. The age range between 12 to 18 year. 8 are Kings type II and 8 are Kings type III, 212 screws were inserted between Th3 – L2 (14-18 screws per-patient), all concave pedicles were inserted with screws but in convex side every two or three pedicles were inserted. The position of screws was analyzed using the post-operative plain X ray film. Before surgery the mean deformity measurement are 52.56° (range, 42-72°, correction achieved was 18° (range 10-34%, it was correlated to 68% achievement (range, 53-80%). All patients are happy with their image improvement. In total 212 screws inserted, 28 screws are malpositions (13.2%), but no clinical complication recorded. In this early experience using all pedicle screw scoliosis surgery, all patients are happy with the results although the correction only 53-80(. More patients are needed to improve this achievement.
Bone morphogenic protein (BMP-2) is used in spinal arthrodesis to induce bone growth. Studies have demonstrated that it achieves similar fusion rates compared to iliac crest bone graft when used in instrumented fusions. Our study aims at evaluating the requirement for instrumentation in one and two-level spinal arthrodeses when BMP-2 is used in conjunction with local bone to achieve fusion. 50 patients were recruited and randomized to instrumented versus non-instrumented spinal arthrodesis. BMP-2 with local autologous bone was used in all patients. Patients are evaluated at 3-months, 6-months, 12-months, and 24-months postoperatively with questionnaires to assess clinical outcome (ODI, VAS and SF-36), and PA and lateral x-rays of the spine to assess radiographic fusion (Lenke score). At 24 months, a thin-cut (1mm) CT scan was performed.Purpose
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