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Full-Endoscopic Procedures Versus Traditional Discectomy Surgery for Discectomy: A Systematic Review and Meta-analysis of Current Global Clinical Trials

机译:全内镜手术与传统的椎间盘切除术相比,目前的全球临床试验系统评价和荟萃分析

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Traditional discectomy surgery (TDS) provides good or excellent results in clinical surgical discectomy but may induce neural adhesion, spinal structural damage, instability, and other complications. The potential advantages of full-endoscopic (FE) procedures over standard TDS include less blood loss, less postoperative pain, shorter hospitalization, and an earlier return to work. However, more evidence is needed to support this new technology in clinical applications.OBJECTIVE: The aim of this systematic review and meta-analysis was to compare the safety and efficacy of FE and TDS.STUDY DESIGN: Comprehensive systematic review and meta-analysis of the literature.METHODS: Electronic databases, including PubMed, EMBASE, SinoMed, and Cochrane Library, were searched to identify clinical therapeutic trials comparing FE to TDS for discectomy.RESULTS: Six trials comprising 730 patients were included, and the overall quality of the literature was moderate, including 4 Grade I levels of evidence (4 randomized controlled trials, [RCTs]) and 2 Grade II levels (2 non-RCTs). The pooled data revealed no difference in reoperation rates between FE and TDS (P = 0.94), but the complication rate was significantly lower in the FE group (3.86%) than in the TDS group (11.4%). Perioperative parameters (operation time, blood loss, hospitalization time, and return to work days) were significantly lower in the FE group (P < 0.05 for all groups using either score). Postoperative pain and neurology score assessments were conducted at 4 different time points at 3 months, 6 months, 12 months, and 24 months. Significant differences were detected in the following: lumbar North American Spine Society (NASS) pain at 6 months (P = 0.008); cervical NASS neurology at 6 months (P = 0.03); visual analog scale (VAS) score in leg at 3 months (P < 0.001); VAS score in arm at 24 months (P = 0.002); VAS score in neck at 3 months, 6 months, and 12 months after therapy (P = 0.003, P = 0.004, P = 0.01); and VAS score in neck at 3 months and 6 months (P = 0.01, P = 0.004). Moreover, the pooled data revealed no statistically significant differences in improvements in the Oswestry disability index (ODI), instability (X-ray), and Hilibrand criteria (P > 0.05 for all groups).LIMITATIONS: Only 6 studies were included, 4 of which had the same authors. Between-study heterogeneity due to differences in socioeconomic factors, nutrition, and matching criteria is difficult to avoid.CONCLUSIONS: Based on this meta-analysis of 24 months of clinical results, we conclude that the FE procedure is as effective as TDS but has the additional benefits of lower complication rates and superior perioperative parameters. In addition, patients may experience less pain with FE techniques due to a smaller incision and less operative injury. However, large-volume, well-designed RCTs with extensive follow-up are needed to confirm and update the findings of this analysis.
机译:传统的椎间盘切除术(TDS)在临床外科椎间盘切除术中可提供良好或出色的效果,但可能会引起神经粘连,脊柱结构损伤,不稳定和其他并发症。与标准TDS相比,全内窥镜(FE)手术的潜在优势包括失血量少,术后疼痛少,住院时间短和恢复工作早。然而,需要更多的证据来支持这项新技术的临床应用。目的:本系统评价和荟萃分析的目的是比较FE和TDS的安全性和有效性。研究设计:对FE和TDS的全面系统评价和荟萃分析方法:检索包括PubMed,EMBASE,SinoMed和Cochrane图书馆在内的电子数据库,以鉴定比较FE与TDS进行椎间盘切除术的临床治疗试验。结果:纳入了6项试验,共730名患者,文献的整体质量中度,包括4个I级证据(4个随机对照试验[RCT])和2个II级证据(2个非RCT)。汇总的数据显示FE和TDS之间的再手术率没有差异(P = 0.94),但是FE组的并发症发生率(3.86%)明显低于TDS组(11.4%)。 FE组的围术期参数(手术时间,失血量,住院时间和恢复工作日数)显着降低(使用任一评分的所有组的P <0.05)。分别在3个月,6个月,12个月和24个月的4个不同时间点进行术后疼痛和神经学评分评估。在以下方面检测到显着差异:6个月时腰部北美脊柱学会(NASS)疼痛(P = 0.008); 6个月时的子宫颈NASS神经病学(P = 0.03); 3个月时腿部视觉模拟量表(VAS)评分(P <0.001); 24个月时手臂的VAS评分(P = 0.002);治疗后3个月,6个月和12个月时颈部VAS评分(P = 0.003,P = 0.004,P = 0.01); 3个月和6个月时颈部VAS评分(P = 0.01,P = 0.004)。此外,汇总数据显示Oswestry残疾指数(ODI),不稳定性(X射线)和Hilibrand标准的改善在统计学上无显着差异(所有组P> 0.05)。限制:仅纳入6项研究,其中4项有相同的作者。结论:基于对24个月临床结果的荟萃分析,我们得出结论:有限元程序与TDS一样有效,但是具有有限的研究价值,因此,研究之间的异质性很难避免。降低并发症发生率和改善围手术期参数的其他好处。此外,由于切口较小和手术损伤较小,患者使用有限元技术可减轻疼痛。但是,需要大量的,设计良好的RCT并进行广泛的随访,以确认和更新此分析的结果。

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