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A Retrospective Review of Radiographic and Clinical Findings from the M6 Cervical Prosthesis

机译:M6宫颈假体的放射学和临床发现的回顾性回顾

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Study Design Retrospective clinical study. Purpose To evaluate clinical results of the M6 cervical prosthesis. Overview of Literature Cervical disk prostheses have been developed to preserve motion and reduce degeneration in adjacent segments in degenerative disk diseases. Methods A retrospective evaluation was performed on 43 patients who received the M6 cervical disk prosthesis between 2012 and 2016. Standard and dynamic radiographs, computed tomography, and magnetic resonance imaging were used to evaluate all the patients preoperatively and postoperatively. The Neck Disability Index (NDI) and Visual Analog Scale (VAS) scores were examined in evaluating the clinical and functional results of patients with collapsed disk herniation who had received the M6 cervical prosthesis and to evaluate whether the core structure of the prosthesis protects motion. Results The mean follow-up period was 34.12±6.70 months. Radiologically, the preoperative cervical segment ROM was measured as a mean of 5.77°±2.19° preoperatively and 8.49°±2.37° at the inal postoperative follow-up examination. In the patients with a preoperative disk height of 4 mm, the cervical segment ROM increased from 6.4°±1.45° preoperatively to 8.6°±2.02° at the inal postoperative follow-up examination. The NDI scores reduced from 53.86±9.77 preoperatively to 22.69±7.26 postoperatively and the VAS scores reduced from 8.74±0.58 to 1.88±1.14. During follow-up in any patient, no collapse of the levels at which surgery was performed was observed. No heterotopic ossiication or implant failure was recorded in any patient during the follow-up period. Conclusions The M6 new-generation cervical disk prosthesis had few complications. No heterotopic ossiication was observed in any patient, and lexion-extension ROM was maintained in all the patients, indicating the M6 prosthesis as a promising alternative.
机译:研究设计回顾性临床研究。目的评估M6颈部假体的临床结果。文献综述颈椎间盘假体已经被开发出来,以保持运动并减少变性椎间盘疾病中相邻节段的退化。方法对2012年至2016年间接受M6颈椎盘假体治疗的43例患者进行回顾性评估。术前和术后均采用标准和动态X光片,计算机体层摄影和磁共振成像对所有患者进行评估。检查颈部残疾指数(NDI)和视觉模拟量表(VAS)评分,以评估接受M6颈部假体的椎间盘突出症患者的临床和功能结果,并评估假体的核心结构是否能保护运动。结果平均随访时间为34.12±6.70个月。放射学上,术前颈段ROM的平均测量值是术前5.77°±2.19°,术后随访检查的平均值为8.49°±2.37°。术前椎间盘高度为4 mm的患者,在术后随访中,颈段ROM从术前的6.4°±1.45°增加到8.6°±2.02°。 NDI评分从术前的53.86±9.77降低到术后的22.69±7.26,VAS评分从术前的8.74±0.58降低到1.88±1.14。在任何患者的随访期间,均未观察到手术水平的降低。在随访期间,任何患者均未记录到异位骨化或植入失败。结论M6新一代颈椎盘假体并发症少。在所有患者中均未观察到异位骨化,并且所有患者均保留了lexion-extension ROM,这表明M6假体是一种有前途的选择。

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