Department of Orthopaedics, Xinqiao Hospital, Third Military Medical University, Chongqing, Shapingba District, People's Republic of China; Department of Orthopaedics, Fourth Military of Chinese People Liberation Army, Xining, Qinghai, China.
Department of Orthopaedics, Xinqiao Hospital, Third Military Medical University, China.
Pain Physician. 2019 Nov;22(6):E587-E599.
Currently, various retractor systems are widely used for access to the lumbar spine in minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF). Nevertheless, studies concerning the comparison of extensible retractor and inextensible tube systems are quite rare.
This article was to compare perioperative characteristics, clinical outcomes, and multifidus muscle injury of obconic inextensible tube versus extensible retractor system for single-level MIS-TLIF.
A prospective observational study on 91 patients with a mean follow-up of 20.0 ± 4.1 months.
This study was conducted by a university-affiliated hospital in a major Chinese city.
From April 2015 to May 2016, 91 consecutive patients who underwent MIS-TLIF procedure using an obconic inextensible endoscopic tube or extensible retractor system were enrolled in this study. Operation parameters such as incision length, blood loss, postoperative drainage volume, surgical time, analgesic use rate, time to ambulation, and postoperative hospitalization days were evaluated. The concentration of white blood cells, interleukin-6, interleukin-8, tumor necrosis factor alpha, and creatine phosphokinase (CPK)-MM of the enrolled patients were measured for postoperative traumatic stress and muscle injury. Multifidus muscle edema and atrophy were evaluated by T2-weighted magnetic resonance imaging (MRI) at 3 different time points (preoperative, postoperative, and 1-year follow-up). Clinical outcomes such as Visual Analog Scale (VAS) score, Japanese Orthopedic Association (JOA) score, Oswestry Disability Index (ODI) score, fusion rates, and MacNab criteria were assessed for patients' symptoms.
In terms of baseline characteristics, the 2 groups were similar regarding sample size, gender, age, symptoms duration, operation level, body mass index, physical examination, and all the clinical outcomes measures (P > 0.05). Perioperative analysis showed that the inextensible group had comparative incision length, blood loss, operation time, time to ambulation, and postoperative hospitalization (P > 0.05). The inextensible tubular group had less postoperative drainage volume and analgesic use rate (P < 0.05). The concentration level of CPK-MM and c-reactive protein (CRP) was lower in the inextensible tubular group compared with the extensible retractor group.No significant difference was found between the 2 groups regarding MRI T2 signal intensity ratio of multifidus muscle at the immediate postoperative period. The MRI T2 signal intensity ratio of multifidus muscle was lower in the inextensible tubular group than the extensible retractor group at the 1-year follow-up period. The VAS scores for low back pain and leg pain improved significantly in both groups after surgery, as did the JOA and ODI scores. However, there were no significant differences between the 2 groups regarding the preoperative and final follow-up VAS, JOA, and ODI scores, fusion rates, and the distribution of the MacNab criteria.
This was not a randomized controlled trail, which could provide more evidence-based medicine conclusions.
The obconic inextensible endoscopic tube system via the transforaminal approach for lumbar interbody fusion is a safe and sufficient technique. When compared with the extensible retractor system, it has comparable clinical outcomes, with additional significant benefits of less postoperative drainage volume and analgesic use rate, less multifidus muscle injury in terms of lower CPK-MM levels at immediate postoperative period, less change in CRP, and less change in MRI T2 signal intensity ratio of multifidus muscles at 1-year follow-up.
Minimally invasive, endoscopic, lumbar interbody fusion, tubular, multifidus muscle.
目前,各种牵开器系统广泛应用于微创经椎间孔腰椎体间融合术(MIS-TLIF)中。然而,关于可扩展牵开器和不可扩展管系统比较的研究却很少。
比较单节段 MIS-TLIF 中使用锥形不可扩展管与可扩展牵开器系统的围手术期特点、临床结果和多裂肌损伤。
一项前瞻性观察研究,纳入 91 例患者,平均随访 20.0±4.1 个月。
这项研究是在中国一个主要城市的大学附属医院进行的。
从 2015 年 4 月至 2016 年 5 月,91 例连续接受 MIS-TLIF 手术的患者,分别使用锥形不可扩展内镜管或可扩展牵开器系统。评估手术参数,如切口长度、出血量、术后引流体积、手术时间、镇痛药使用率、下床活动时间和术后住院天数。测量患者术后白细胞介素 6(IL-6)、白细胞介素 8(IL-8)、肿瘤坏死因子-α(TNF-α)和肌酸磷酸激酶-MM(CPK-MM)的浓度,以评估术后创伤应激和肌肉损伤。在术前、术后和 1 年随访 3 个不同时间点,采用 T2 加权磁共振成像(MRI)评估多裂肌水肿和萎缩。通过视觉模拟评分(VAS)、日本矫形协会(JOA)评分、Oswestry 残疾指数(ODI)评分、融合率和 MacNab 标准评估患者的症状。
在基线特征方面,2 组在样本量、性别、年龄、症状持续时间、手术水平、体重指数、体格检查和所有临床结果测量方面相似(P>0.05)。围手术期分析显示,不可扩展组的切口长度、出血量、手术时间、下床活动时间和术后住院时间相似(P>0.05)。不可扩展管组的术后引流体积和镇痛药使用率较低(P<0.05)。与可扩展牵开器组相比,不可扩展管组的 CPK-MM 和 C 反应蛋白(CRP)浓度较低。2 组术后即刻 MRI 多裂肌 T2 信号强度比无显著差异。不可扩展管组术后 1 年 MRI 多裂肌 T2 信号强度比低于可扩展牵开器组。术后两组的腰痛和腿痛 VAS 评分均明显改善,JOA 和 ODI 评分也有所改善。然而,两组间术前和最终随访 VAS、JOA 和 ODI 评分、融合率和 MacNab 标准分布无显著差异。
这不是一项随机对照试验,无法提供更具循证医学结论的证据。
经椎间孔入路腰椎体间融合术的锥形不可扩展内镜管系统是一种安全有效的技术。与可扩展牵开器系统相比,它具有相似的临床效果,具有额外的显著优势,即术后引流体积和镇痛药使用率较低,术后即刻 CPK-MM 水平较低,CRP 变化较小,术后 1 年 MRI 多裂肌 T2 信号强度比变化较小。
微创;内镜;腰椎体间融合;管状;多裂肌。