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使用不可吸收聚醚醚酮与可吸收聚-L-丙交酯-共-D,L-丙交酯融合装置进行腰椎后路椎间融合术:一项评估融合及临床结果的前瞻性随机研究

Posterior lumbar interbody fusion using nonresorbable poly-ether-ether-ketone versus resorbable poly-L-lactide-co-D,L-lactide fusion devices: a prospective, randomized study to assess fusion and clinical outcome.

作者信息

Jiya Timothy, Smit Theo, Deddens James, Mullender Margriet

机构信息

Department of Orthopaedic Surgery VU University medical centre, Amsterdam, Netherlands.

出版信息

Spine (Phila Pa 1976). 2009 Feb 1;34(3):233-7. doi: 10.1097/BRS.0b013e318194ed00.

Abstract

STUDY DESIGN

A prospective randomized clinical study. OBJECTIVE.: To assess fusion, clinical outcome, and complications.

SUMMARY OF BACKGROUND DATA

Resorbable poly-L- lactide-co-D,L-lactide (PLDLLA) cages intended to aid spinal interbody fusion have been introduced into clinical practice within the last decade. Although early case series show promising results with respect to fusion rate, worries persist with regards to efficacy and potential risks of early failure of these implants. Despite widespread clinical application this is the first randomized prospective study to assess clinical and radiologic outcomes of PLDLLA cage compared with a traditionally applicable counterpart.

METHODS

Twenty-six patients were randomly assigned to undergo instrumented posterior lumbar interbody fusion whereby either a nonresorbable poly-ether-ether-ketone (PEEK) cage or a resorbable PLDLLA cage was implanted to aid fusion. Fusion rate, subsidence, and clinical outcome based on visual analog scale scores for leg pain and back pain, as well as Oswestry Disability Index and SF-36 questionnaires were documented and analyzed. Complications and adverse events were recorded.

RESULTS

Fusion rate was significantly higher with the PEEK cage compared with PLDLLA cage (Fisher exact test, P = 0.0302). Rate of subsidence was significantly higher with the PLDLLA cage compared to PEEK cage (Fisher exact test, P = 0.0414). The PEEK group demonstrated greater improvement in the Oswestry Disability Index compared with the PLDLLA group (Fisher exact test, P = 0.1414). Two cases of mild to moderate osteolysis were seen in the PLDLLA group.

CONCLUSION

Our results strongly suggest that PLDLLA cage proffers a lower rate of fusion compared with PEEK cage, and also confirms that the efficacy of PLDLLA cage in enhancing interbody spinal fusion is yet to be established. The higher rate of subsidence and occurrence of osteolysis seen in association with PLDLLA cages in this study remain worrisome.

摘要

研究设计

一项前瞻性随机临床研究。目的:评估融合情况、临床结果及并发症。

背景数据总结

可吸收聚-L-丙交酯-共-D,L-丙交酯(PLDLLA)椎间融合器旨在辅助脊柱椎间融合,在过去十年已引入临床实践。尽管早期病例系列显示融合率有良好前景,但这些植入物的疗效及早期失败的潜在风险仍令人担忧。尽管已广泛临床应用,但这是第一项将PLDLLA椎间融合器与传统适用的同类产品进行比较,评估其临床和放射学结果的随机前瞻性研究。

方法

26例患者被随机分配接受后路腰椎椎间融合内固定术,术中植入不可吸收聚醚醚酮(PEEK)椎间融合器或可吸收PLDLLA椎间融合器以辅助融合。记录并分析基于腿痛和背痛视觉模拟量表评分、Oswestry功能障碍指数及SF-36问卷的融合率、下沉情况及临床结果。记录并发症和不良事件。

结果

与PLDLLA椎间融合器相比,PEEK椎间融合器的融合率显著更高(Fisher精确检验,P = 0.0302)。与PEEK椎间融合器相比,PLDLLA椎间融合器的下沉率显著更高(Fisher精确检验,P = 0.0414)。与PLDLLA组相比,PEEK组在Oswestry功能障碍指数方面改善更大(Fisher精确检验,P = 0.1414)。PLDLLA组出现2例轻度至中度骨质溶解。

结论

我们的结果强烈表明,与PEEK椎间融合器相比,PLDLLA椎间融合器的融合率较低,也证实了PLDLLA椎间融合器在增强脊柱椎间融合方面的疗效尚未确立。本研究中PLDLLA椎间融合器出现的较高下沉率及骨质溶解情况仍令人担忧。

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