Department of Orthopedics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Int J Surg. 2017 Jun;42:128-137. doi: 10.1016/j.ijsu.2017.04.066. Epub 2017 May 3.
To compare the clinical outcomes and complications and radiographic outcomes of the two different surgical strategies (arthrodesis in situ and arthrodesis following reduction) for the surgical management of spondylolisthesis.
After systematic search the PubMed, Ovid MEDLINE, Cochrane, and Embase databases, comparative studies were selected according to eligibility criteria. Checklists by Furlan and by The Newcastle-Ottawa quality assessment scale (NOS scale) were used to evaluate the risk of bias of the included randomized clinical trials (RCTs) and nonrandomized controlled studies, respectively. The final strength of evidence was expressed as different levels recommended by the GRADE Working Group.
Three RCTs. and nine comparative observational studies were identified. Low-quality evidence indicated that reduction group (RG) was not more effective than fusion in situ group for clinical satisfaction (OR 0.77, 95% CI 0.39-1.54, P = 0.46). and neurologic complication rate (OR 0.89, 95 CI 0.38-2.03, P = 0.78). In secondary outcomes, Low-quality evidence indicated that RG improved fusion rate (OR 2.66, 95% CI 1.15-6.14, P = 0.02). There was no significant difference in the other complication rate (OR 0.89, 95% CI 0.44-1.79, P = 0.63) and blood loss (WMD 14.22, 95% CI -9.53-37.79, P = 0.24) between two groups. Statistical difference was found between the two groups with regard to slipping angle (WMD -6.33, 95% CI -12.60 to -0.06, P = 0.05).
There was no definite benefit of reduction over fusion in situ in clinical satisfaction rate and neurologic complication rate. The fusion rate significantly improved while the slipping angle considerably decreased postoperation in reduction group.
比较两种不同手术策略(原位融合和复位后融合)治疗腰椎滑脱的临床结果和并发症以及影像学结果。
通过系统检索 PubMed、Ovid MEDLINE、Cochrane 和 Embase 数据库,根据纳入标准选择了对照研究。使用 Furlan 清单和纽卡斯尔-渥太华质量评估量表(NOS 量表)分别评估纳入的随机临床试验(RCT)和非随机对照研究的偏倚风险。最终证据强度表示为 GRADE 工作组推荐的不同级别。
共纳入 3 项 RCT 和 9 项对照观察性研究。低质量证据表明,复位组(RG)在临床满意度(OR 0.77,95%CI 0.39-1.54,P=0.46)和神经并发症发生率(OR 0.89,95%CI 0.38-2.03,P=0.78)方面并不优于原位融合组。在次要结局方面,低质量证据表明 RG 提高了融合率(OR 2.66,95%CI 1.15-6.14,P=0.02)。两组之间其他并发症发生率(OR 0.89,95%CI 0.44-1.79,P=0.63)和出血量(WMD 14.22,95%CI -9.53-37.79,P=0.24)无显著差异。两组在滑脱角度方面存在统计学差异(WMD -6.33,95%CI -12.60 至 -0.06,P=0.05)。
在临床满意度和神经并发症发生率方面,复位并不优于原位融合。复位组术后融合率显著提高,滑脱角度明显减小。