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全内镜与微创腰椎椎间融合术治疗腰椎退行性疾病:系统评价与Meta分析

Full-Endoscopic versus Minimally Invasive Lumbar Interbody Fusion for Lumbar Degenerative Diseases : A Systematic Review and Meta-Analysis.

作者信息

Son Seong, Yoo Byung Rhae, Lee Sang Gu, Kim Woo Kyung, Jung Jong Myung

机构信息

Department of Neurosurgery, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.

出版信息

J Korean Neurosurg Soc. 2022 Jul;65(4):539-548. doi: 10.3340/jkns.2021.0168. Epub 2022 Jun 29.

Abstract

OBJECTIVE

Although full-endoscopic lumbar interbody fusion (Endo-LIF) has been tried as the latest alternative technique to minimally invasive transforaminal lumbar interobody fusion (MIS-TLIF) since mid-2010, the evidence is still lacking. We compared the clinical outcome and safety of Endo-LIF to MIS-TLIF for lumbar degenerative disease.

METHODS

We systematically searched electronic databases, including PubMed, EMBASE, and Cochrane Library to find literature comparing Endo-LIF to MIS-TLIF. The results retrieved were last updated on December 11, 2020. The perioperative outcome included the operation time, blood loss, complication, and hospital stay. The clinical outcomes included Visual analog scale (VAS) of low back pain and leg pain and Oswestry disability index (ODI), and the radiological outcome included pseudoarthosis rate with 12-month minimum follow-up.

RESULTS

Four retrospective observational studies and one prospective observational study comprising 423 patients (183 Endo-LIF and 241 MIS-TLIF) were included, and the pooled data analysis revealed low heterogeneity between studies in our review. Baseline characteristics including age and sex were not different between the two groups. Operation time was significantly longer in Endo- LIF (mean difference [MD], 23.220 minutes; 95% confidence interval [CI], 10.669-35.771; p=0.001). However, Endo-LIF resulted in less perioperative blood loss (MD, -144.710 mL; 95% CI, 247.941-41.478; p=0.023). Although VAS back pain at final (MD, -0.120; p=0.586), leg pain within 2 weeks (MD, 0.005; p=0.293), VAS leg pain at final (MD, 0.099; p=0.099), ODI at final (MD, 0.141; p=0.093) were not different, VAS back pain within 2 weeks was more favorable in the Endo-LIF (MD, -1.538; 95% CI, -2.044 to -1.032; p<0.001). On the other hand, no statistically significant group difference in complication rate (relative risk [RR], 0.709; p=0.774), hospital stay (MD, -2.399; p=0.151), and pseudoarthrosis rate (RR, 1.284; p=0.736) were found.

CONCLUSION

Relative to MIS-TLIF, immediate outcomes were favorable in Endo-LIF in terms of blood loss and immediate VAS back pain, although complication rate, mid-term clinical outcomes, and fusion rate were not different. However, the challenges for Endo-LIF include longer operation time which means a difficult learning curve and limited surgical indication which means patient selection bias. Larger-scale, well-designed study with long-term follow-up and randomized controlled trials are needed to confirm and update the results of this systematic review.

摘要

目的

自2010年年中以来,全内镜下腰椎椎间融合术(Endo-LIF)已被尝试作为微创经椎间孔腰椎椎间融合术(MIS-TLIF)的最新替代技术,但仍缺乏相关证据。我们比较了Endo-LIF与MIS-TLIF治疗腰椎退行性疾病的临床疗效和安全性。

方法

我们系统检索了电子数据库,包括PubMed、EMBASE和Cochrane图书馆,以查找比较Endo-LIF与MIS-TLIF的文献。检索结果的最后更新时间为2020年12月11日。围手术期结果包括手术时间、失血量、并发症和住院时间。临床结果包括腰痛和腿痛的视觉模拟量表(VAS)以及Oswestry功能障碍指数(ODI),影像学结果包括至少随访12个月的假关节形成率。

结果

纳入了四项回顾性观察性研究和一项前瞻性观察性研究,共423例患者(183例Endo-LIF和241例MIS-TLIF),汇总数据分析显示我们的综述中各研究之间异质性较低。两组患者的年龄和性别等基线特征无差异。Endo-LIF组的手术时间明显更长(平均差[MD],23.220分钟;95%置信区间[CI],10.669 - 35.771;p = 0.001)。然而,Endo-LIF导致围手术期失血量更少(MD,-144.710 mL;95% CI,-247.941 - 41.478;p = 0.023)。虽然最终腰痛的VAS评分(MD,-0.120;p = 0.586)、术后2周内腿痛的VAS评分(MD,0.005;p = 0.293)、最终腿痛的VAS评分(MD,0.099;p = 0.099)、最终ODI评分(MD,0.141;p = 0.093)无差异,但Endo-LIF组术后2周内的腰痛VAS评分更优(MD,-1.538;95% CI,-2.044至-1.032;p < 0.001)。另一方面,在并发症发生率(相对危险度[RR],0.709;p = 0.774)、住院时间(MD,-2.399;p = 0.151)和假关节形成率(RR,1.284;p = 0.736)方面,两组之间无统计学显著差异。

结论

相对于MIS-TLIF,Endo-LIF在失血量和术后早期腰痛VAS评分方面的近期疗效较好,尽管并发症发生率、中期临床疗效和融合率无差异。然而,Endo-LIF面临的挑战包括手术时间更长,这意味着学习曲线较难,以及手术适应证有限,这意味着存在患者选择偏倚。需要更大规模、设计良好的长期随访研究和随机对照试验来证实和更新本系统评价的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae02/9271818/90fdab397f59/jkns-2021-0168f1.jpg

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