Italian University Sport and Movement, Piazza Lauro de Bosis 6, 00135 Rome, Italy.
Spine J. 2011 Oct;11(10):933-9. doi: 10.1016/j.spinee.2011.08.419.
Few studies have analyzed the results of an interspinous distraction device in patients with lumbar spinal stenosis. It is still unknown whether the outcomes of an interspinous implant are related to the severity of stenosis.
To determine the success rate of the Aperius implant and open decompression with the aim of defining better the indications for the two modalities of treatment.
Comparison of two cohorts of patients with moderate or severe stenosis treated with the Aperius or by open decompression.
The sample comprises 36 patients who had the Aperius implant and 35 who underwent open decompression, both groups followed prospectively. In the two cohorts, central or lateral stenosis was present in similar proportions, and in both, the patients had pure intermittent claudication or symptoms at rest and on walking. In both groups, preoperative diagnosis was made by magnetic resonance imaging (MRI).
Patients of both groups were evaluated with the Zurich Claudication Questionnaire (ZCQ) and Oswestry Disability Index. The results were rated as good or poor based on the ZCQ.
The patients of both cohorts were evaluated at 1 month and 3, 6, and 12 months after operation, the final follow-up being carried out at least 2 years after surgery. Severity of stenosis was determined based on preoperative MRI scans. In 17 patients of the Aperius group, MRI studies were repeated at the 6-month or final follow-up and compared with the preoperative studies.
Of the patients in the Aperius group, six had removal of the implant and open surgical decompression at 2 to 17 months after operation; these patients were considered to have a poor result. At the final follow-up, the result was rated as good in 47% of all patients who had had the Aperius implant. The percentage of good outcomes was 60% in moderate stenosis and 31% in severe stenosis. When considering all not reoperated patients, 57% had good outcomes; however, if only the scores in the patient satisfaction domain of the ZCQ were considered, 67% of these patients were somewhat satisfied with the result of Aperius. No significant relationship was found between patients with pure intermittent claudication and those with leg symptoms also at rest. In 71% of cases in which preoperative and postoperative MRIs were compared, no significant change in size of the spinal canal was found after operation, whereas in the remaining patients a slight increase in size of the canal was detected. In the open decompression cohort, the results were good in 80% of cases and poor in 20%. The outcomes were satisfactory in 69% of moderate stenosis, with no significant difference with the similar subgroup of the Aperius series. In severe stenosis, the 89% rate of good results was significantly higher than in the severe Aperius subgroup (p<.0001).
The Aperius interspinous implant is poorly indicated for severe lumbar stenosis, which is significantly improved only in a small minority of cases, whereas decompression procedures ensure high chances of good results. The implant may be indicated for selected patients with moderate stenosis. The outcomes of the Aperius are not influenced by the type of clinical presentation of lumbar stenosis.
很少有研究分析腰椎管狭窄症患者使用棘突间撑开器的结果。目前尚不清楚棘突间植入物的结果是否与狭窄的严重程度有关。
确定 Aperius 植入物和开放性减压的成功率,旨在更好地确定这两种治疗方式的适应证。
对接受 Aperius 植入物或开放性减压治疗的中度或重度狭窄患者的两组患者进行比较。
共有 36 例接受 Aperius 植入物治疗的患者和 35 例接受开放性减压治疗的患者,两组均前瞻性随访。在两组中,中央或侧方狭窄的比例相似,两组患者均有单纯间歇性跛行或休息和行走时的症状。两组患者的术前诊断均通过磁共振成像(MRI)确定。
两组患者均采用苏黎世间歇性跛行问卷(ZCQ)和 Oswestry 残疾指数进行评估。根据 ZCQ 将结果评为良好或不良。
两组患者在术后 1 个月和 3、6、12 个月进行评估,末次随访时间至少为术后 2 年。术前 MRI 扫描确定狭窄程度。在 Aperius 组的 17 例患者中,在术后 6 个月或末次随访时进行了 MRI 研究,并与术前研究进行了比较。
Aperius 组中有 6 例患者在术后 2 至 17 个月接受了植入物取出和开放性减压手术,这些患者被认为结果较差。在末次随访时,所有接受 Aperius 植入物治疗的患者中,有 47%的结果被评为良好。在中度狭窄患者中,良好结果的比例为 60%,在重度狭窄患者中为 31%。如果仅考虑 ZCQ 中患者满意度的评分,那么在所有未再次手术的患者中,67%的患者对 Aperius 的结果感到满意。在单纯间歇性跛行患者和也有腿部休息时症状的患者之间,未发现显著关系。在比较术前和术后 MRI 的 71%的病例中,术后椎管大小无明显变化,而在其余患者中,发现椎管略有增大。在开放性减压组中,80%的病例结果良好,20%的病例结果较差。在中度狭窄的病例中,69%的结果令人满意,与 Aperius 系列中类似的亚组无显著差异。在重度狭窄患者中,89%的良好结果率明显高于重度 Aperius 亚组(p<.0001)。
Aperius 棘突间植入物对严重腰椎管狭窄症的适应证较差,仅在极少数情况下显著改善,而减压手术可确保获得良好结果的高几率。该植入物可能适用于选择的中度狭窄患者。Aperius 的结果不受腰椎管狭窄症临床表型的影响。