van Hooff Miranda L, Heesterbeek Petra J C, Spruit Maarten
Sint Maartenskliniek, Nijmegen, the Netherlands.
Radboud University Medical Center, Nijmegen, the Netherlands.
Global Spine J. 2020 May;10(3):294-302. doi: 10.1177/2192568219850763. Epub 2019 May 23.
Prospective cohort study.
To investigate the primary stability of the Prodisc-C Vivo cervical disc arthroplasty with regard to the adjacent cervical vertebrae using radiostereometric analysis (RSA), and to monitor its clinical performance.
Sixteen patients with degenerative cervical disc disease were included. RSA radiographs were obtained at the first postoperative day, at 6 weeks, 3 months, and 6 months postoperatively. Migration (translation [mm]) of the superior and inferior implant components were measured with model-based RSA, expressed along the 3 orthogonal axes, and calculated as total translation. Clinical outcomes were Neck Disability Index, numeric rating scales for neck and arm pain, Likert-type scales for satisfaction, and adverse events. Range of motion was reported as C2-C7 flexion-extension mobility (ROM).
At final follow-up, no significant increase over time in median total translation was found. One inferior and 3 superior components subsided but were asymptomatic. ROM remained stable and clinical outcomes improved over time. Although 3 patients were unsatisfied and 3 adverse events occurred, this was not related to translation of the components.
On a group level, both components of the Prodisc-C Vivo cervical disc arthroplasty remained stable over time and below the clinical threshold of 1 mm. Individual outliers for translation were not clinically relevant and probably related to settling of the components into the vertebral endplates. RSA allowed us to perform a preliminary but accurate study on the micromotion of a new cervical disc replacement in a small sample size, without putting large numbers of patients at risk.
前瞻性队列研究。
使用放射立体测量分析(RSA)研究Prodisc-C Vivo颈椎间盘置换术相对于相邻颈椎的初始稳定性,并监测其临床性能。
纳入16例退行性颈椎间盘疾病患者。在术后第1天、术后6周、3个月和6个月获取RSA X光片。使用基于模型的RSA测量植入物上下组件的移位(平移[mm]),沿3个正交轴表示,并计算为总平移。临床结果包括颈部残疾指数、颈部和手臂疼痛的数字评分量表、满意度的李克特式量表以及不良事件。活动范围报告为C2-C7屈伸活动度(ROM)。
在最终随访时,未发现总平移中位数随时间有显著增加。1个下组件和3个上组件下沉,但无症状。ROM保持稳定,临床结果随时间改善。尽管有3例患者不满意且发生了3起不良事件,但这与组件的平移无关。
在组水平上,Prodisc-C Vivo颈椎间盘置换术的两个组件随时间保持稳定,且低于1 mm的临床阈值。个别平移异常值在临床上不相关,可能与组件在椎体终板中的沉降有关。RSA使我们能够在小样本量的情况下对一种新型颈椎间盘置换物的微动进行初步但准确的研究,而不会使大量患者面临风险。