Buyuk Abdul Fettah, Onyekwelu Ikemefuna, Gaffney Christian J, Mehbod Amir A, Dawson John M, Garvey Timothy A, Mueller Benjamin, Schwender James D
Twin Cities Spine Center, Minneapolis, MN, USA.
J Spine Surg. 2020 Dec;6(4):670-680. doi: 10.21037/jss-19-419.
Polyetheretherketone (PEEK) and machined allograft interbody spacers are among devices used as fusion adjuncts in anterior cervical discectomy and fusion (ACDF). Most results are good to excellent but some patients develop pseudarthrosis. We compared the reoperation rates for pseudarthrosis following 1- or 2-level ACDF with PEEK or allograft cages.
This was a retrospective cohort study. We reviewed patients who underwent 1- or 2-level ACDF. The rate of subsequent surgery for pseudarthrosis was calculated for cases confirmed by computerized tomography. Patient-reported outcomes were collected at post-index surgery follow-up and post-revision ACDF follow-up. Radiographic parameters were assessed at a minimum of 1-year post-op on all patients.
Two hundred and nine patients were included: 167 received allograft and 42 received PEEK. Subsidence was demonstrated in 31% of allograft and 29% of PEEK patients. There were no significant differences in clinical outcomes between allograft and PEEK groups. Clinical outcomes were not adversely affected by subsidence. Reoperation for pseudarthrosis was performed in 8% of allograft patients and 14% of PEEK patients (not statistically different). Improvement in patient-reported outcome was significantly better for patients without symptomatic post-operative pseudarthrosis.
Both allograft and PEEK spacers are acceptable options for ACDF surgery. Similar clinical outcomes and rates of radiographic subsidence were found. Subsidence was not a factor in clinical outcomes. Reoperation for pseudarthrosis was associated with poor outcomes. A higher incidence of revision for symptomatic pseudarthrosis occurred in the PEEK group, but this was not statistically significant.
聚醚醚酮(PEEK)和机械加工的同种异体椎间融合器是用于颈椎前路椎间盘切除融合术(ACDF)中作为融合辅助装置的器械。大多数结果良好至优秀,但部分患者会发生假关节形成。我们比较了使用PEEK或同种异体融合器进行单节段或双节段ACDF术后假关节形成的再次手术率。
这是一项回顾性队列研究。我们回顾了接受单节段或双节段ACDF的患者。通过计算机断层扫描确诊的病例计算假关节形成的后续手术率。在初次手术后随访和翻修ACDF术后随访时收集患者报告的结局。对所有患者在术后至少1年评估影像学参数。
纳入209例患者:167例接受同种异体移植物,42例接受PEEK。同种异体移植物组31%和PEEK组29%出现下沉。同种异体移植物组和PEEK组之间的临床结局无显著差异。下沉对临床结局无不利影响。同种异体移植物组8%的患者和PEEK组14%的患者因假关节形成进行了再次手术(无统计学差异)。对于术后无症状性假关节形成的患者,患者报告结局的改善明显更好。
同种异体移植物和PEEK融合器都是ACDF手术的可接受选择。发现了相似的临床结局和影像学下沉率。下沉不是临床结局的影响因素。因假关节形成进行再次手术与不良结局相关。PEEK组有症状性假关节形成的翻修发生率较高,但无统计学意义。