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颈椎全椎间盘置换术后 M6-C™人工椎间盘的异位骨化、骨溶解和假体失败。

Heterotopic ossification, osteolysis and implant failure following cervical total disc replacement with the M6-C™ artificial disc.

机构信息

Neurospine Institute, Murdoch, Australia.

Department of Orthopaedic Surgery and Traumatology, Inselspital, University Hospital Bern, University Bern, Bern, Switzerland.

出版信息

Eur Spine J. 2024 Mar;33(3):1292-1299. doi: 10.1007/s00586-024-08129-5. Epub 2024 Feb 16.

Abstract

INTRODUCTION

A recent study reported a 34% mid-term revision rate after M6-C™ cervical total disc replacement (CTDR) for wear-related osteolysis. Here, we aim to investigate the prevalence, risk factors, and radiographic characteristics of periprosthetic bony changes and implant failure of the M6-C™ artificial disc.

METHODS

We retrospectively analysed radiographic (conventional X-ray, CT scan) and clinical outcomes (EQ-5D-5L, Neck Disability Index (NDI), and Visual Analog Scale (VAS) for neck and arm pain) data collected during routine follow-up of patients who underwent CTDR with the M6-C™ between 2011 and 2015.

RESULTS

In total, 85 patients underwent CTDR with the M6-C™. Follow-up data were available for 43 patients (54% female, mean age 44 years) with 50 implants and a mean follow-up of 8.1 years (6.5-11 years). Implant failure with the presence of severe osteolysis was identified in 5 (12%) patients who were all male (p = 0.016) and implanted at the C5/6 level (p = 0.11). All failed implants required revision surgery. The overall prevalence of osteolysis was 44% (22/50 implants) and 34% (17/50 implants) for significant heterotopic ossification. Patients with high-grade osteolysis showed higher VAS arm pain (p = 0.05) and lower EQ-5D-VAS health VAS (p = 0.03).

CONCLUSION

We report a lower reoperation rate for failed M6-C™ implants than previously published, but confirmed that osteolysis and heterotopic ossification are common following CTDR with the M6-C™ and may be asymptomatic. Therefore, we strongly recommend ongoing clinical and radiographic monitoring after CTDR with the M6-C™, particularly for male patients implanted at the C5/6 level.

摘要

介绍

最近的一项研究报告称,在 M6-C™颈椎间盘置换术后(CTDR),因磨损相关的骨溶解,中期翻修率为 34%。在此,我们旨在研究 M6-C™人工椎间盘的假体周围骨变化和植入物失败的发生率、危险因素和影像学特征。

方法

我们回顾性分析了 2011 年至 2015 年间接受 M6-C™ CTDR 的患者在常规随访中收集的影像学(常规 X 线、CT 扫描)和临床结果(EQ-5D-5L、颈残障指数(NDI)和颈部、手臂疼痛视觉模拟量表(VAS))数据。

结果

共 85 例患者接受了 M6-C™ CTDR。43 例(54%为女性,平均年龄 44 岁)50 枚植入物的随访数据可用,平均随访时间为 8.1 年(6.5-11 年)。5 例(12%)男性(p=0.016)和 C5/6 节段植入的患者出现植入物失败和严重骨溶解(p=0.11)。所有失败的植入物都需要进行翻修手术。总体骨溶解发生率为 44%(22/50 个植入物),显著异位骨化发生率为 34%(17/50 个植入物)。高分级骨溶解患者的 VAS 手臂疼痛评分更高(p=0.05),EQ-5D-VAS 健康 VAS 评分更低(p=0.03)。

结论

与先前发表的研究相比,我们报告 M6-C™植入物失败的再次手术率较低,但证实 M6-C™ CTDR 后骨溶解和异位骨化很常见,可能无症状。因此,我们强烈建议 M6-C™ CTDR 后进行持续的临床和影像学监测,特别是对于 C5/6 节段植入的男性患者。

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