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首页> 外文期刊>European spine journal: official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society >Clinical effect evaluation of percutaneous vertebroplasty combined with the spinal external fixator for the treatment of osteoporotic compressive fractures with posterior vertebral defect
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Clinical effect evaluation of percutaneous vertebroplasty combined with the spinal external fixator for the treatment of osteoporotic compressive fractures with posterior vertebral defect

机译:经皮椎体成形术联合脊柱外固定架治疗椎体后路骨质疏松性压缩性骨折的临床效果评估

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Purpose: The purpose of this study is to report a new technique and assess clinical outcome of compressive fractures with posterior vertebral defect treated by percutaneous vertebroplasty combined with the spinal external fixator.Method: 80 patients (32 males and 48 females), ranging from 62 to 88 years old with the mean age of 71.5 years, underwent surgery for the compressive fractures with posterior vertebral defect by percutaneous vertebroplasty combined with the spinal external fixator. All patients were diagnosed to have fresh compressive fractures with osteoporosis and posterior vertebral defect shown on roentgenograms, computed tomography scans or magnetic resonance imaging preoperatively. They underwent spinal external fixation firstly to be fixed and restored, then to be carried out percutaneous vertebroplasty. The mean follow-up was 24 months (16–42 months). Spinal canal encroachment, spinal cobb angle and vertebral body height loss were measured to assess clinical outcome before and after surgery, at the final follow-up. The Visual Analogue Scale and Oswestry Disability Index were used for pain and functional assessment. In all cases, preoperative and postoperative radiographs and magnetic resonance imaging were obtained.Results: The average time of surgery was 88 min (75–115 min). The mean blood loss was 10 ml (6–12 ml) during surgery. The anterior height loss of vertebral body decreased significantly from 79.3 ± 11 % before surgery to 8.0 ± 5.2 % after surgery, and 7.6 ± 6.0 % at the final follow-up. The spinal canal encroachment significantly reduced from 19.9 ± 2.6 % preoperatively to 4.0 ± 0.7 % postoperatively, 4.1 ± 0.7 % at the final follow-up. The Cobb angle was corrected from 25.8 ± 7.9° primarily to 8.2 ± 4.1° postoperatively, 7.8 ± 3.1° at the final follow-up. There were significant differences (p < 0.05) among them before and after the surgery. Postoperative VAS and Oswestry scores were both significantly different from the preoperative and follow-up (p < 0.05).Conclusion: The preliminary results are encouraging, showing that the spinal external fixator combined with percutaneous vertebroplasty was a safe and effective method to treat the osteoporotic compressive fractures with posterior vertebral defect.
机译:目的:本研究的目的是报告一种新技术,并评估经皮椎体成形术结合脊柱外固定架治疗后椎骨缺损的压缩性骨折的临床结果。方法:80例患者(男32例,女48例),范围62例。年龄88岁,平均年龄71.5岁,接受经皮椎体成形术结合脊柱外固定架治疗椎体后段缺损的压缩性骨折。所有患者均被诊断出患有新鲜的压缩性骨折,并在术前行放射线照片,计算机断层扫描或磁共振成像中显示出骨质疏松和椎体后部缺损。他们首先进行脊柱外固定,然后进行固定和修复,然后进行经皮椎体成形术。平均随访时间为24个月(16-42个月)。在最后的随访中,测量了椎管侵犯,脊髓柯布角和椎体高度损失,以评估手术前后的临床结局。视觉模拟量表和Oswestry残疾指数用于疼痛和功能评估。在所有情况下,均获得术前和术后X线照片和磁共振成像。结果:平均手术时间为88分钟(75-115分钟)。手术期间平均失血量为10毫升(6-12毫升)。椎体前部高度下降从手术前的79.3±11%显着降低到手术后的8.0±5.2%,在最后的随访中为7.6±6.0%。椎管侵犯率从术前的19.9±2.6%显着降低到术后的4.0±0.7%,在最后的随访中为4.1±0.7%。术后Cobb角从最初的25.8±7.9°校正为8.2±4.1°,最后一次随访为7.8±3.1°。手术前后它们之间存在显着差异(p <0.05)。术后VAS和Oswestry评分与术前和随访均存在显着差异(p <0.05)。结论:初步结果令人鼓舞,表明脊柱外固定架结合经皮椎体成形术是治疗骨质疏松症的安全有效方法压缩性骨折,椎体后部缺损。

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