Department of Orthopaedic Surgery, The Third Hospital of Hebei Medical University, Shijiazhuang, 050051, People's Republic of China.
The Key Laboratory of Orthopedic Biomechanics of Hebei Province, The Third Hospital of Hebei Medical University, Shijiazhuang, 050051, People's Republic of China.
J Orthop Surg Res. 2020 Aug 14;15(1):326. doi: 10.1186/s13018-020-01837-w.
We determined the incidence and risk factors of low back pain (LBP) in patients with lumbar degenerative disease after single-level oblique lateral interbody fusion (OLIF).
We retrospectively reviewed 120 lumbar degenerative disease patients who underwent single-level OLIF. We compared preoperative and postoperative radiographic parameters, including segmental lordosis (SL), lumbar lordosis (LL), disk height (DH), pelvic incidence (PI), pelvic tilt (PT), sacral slope (SS), thoracic kyphosis (TK), and C7-sagittal vertical axis (SVA). Clinical outcomes were evaluated using the Oswestry Disability Index (ODI) scores and visual analog scale (VAS) scores for back and leg pain. All patients were followed up for at least 2 years.
Thirty-eight patients had postoperative LBP (VAS score for back pain ≥3; LBP group); the remaining 82 patients were in the non-LBP group. Age (P = 0.082), gender (P = 0.425), body mass index (P = 0.138), diagnosis (degenerative spondylolisthesis vs. lumbar spinal stenosis; P = 0.529), surgical level (P = 0.651), blood loss (P = 0.889), and operative time (P = 0.731) did not differ between the groups. In both groups, the ODI and VAS scores for back pain and leg pain significantly improved at the final follow-up compared with the preoperative scores (P = 0.003). Except for the VAS score for back pain (P = 0.000), none of the scores significantly differed between the two groups at the final follow-up (P > 0.05). In the non-LBP group, LL, SL, DH, TK, and SS significantly improved, while PT and C7-SVA significantly decreased at the final follow-up as compared with the preoperative values. In both groups, DH significantly improved postoperatively, with no significant between-group difference (P = 0.325). At the final follow-up, LL, PI-LL mismatch, PT, and C7-SVA showed significantly greater improvement in the non-LBP group than in the LBP group (P < 0.05). Multivariate analysis identified PT, PI-LL mismatch, and C7-SVA as significant risk factors for LBP after OLIF.
OLIF for single-level lumbar degenerative disease had satisfactory clinical outcomes. PT, PI-LL mismatch, and C7-SVA were significant risk factors for postoperative LBP. Patients with appropriately decreased PT, improved C7-SVA, and PI-LL match experienced less LBP.
我们确定了单节段斜外侧腰椎间融合术(OLIF)后腰椎退行性疾病患者腰痛(LBP)的发生率和危险因素。
我们回顾性分析了 120 例接受单节段 OLIF 的腰椎退行性疾病患者。我们比较了术前和术后的影像学参数,包括节段前凸角(SL)、腰椎前凸角(LL)、椎间盘高度(DH)、骨盆入射角(PI)、骨盆倾斜角(PT)、骶骨倾斜角(SS)、胸椎后凸角(TK)和 C7 矢状垂直轴(C7-SVA)。使用 Oswestry 功能障碍指数(ODI)评分和背部及腿部疼痛视觉模拟评分(VAS)评估临床结果。所有患者均随访至少 2 年。
38 例患者术后出现腰痛(背部 VAS 评分≥3;LBP 组);其余 82 例患者为非 LBP 组。两组间年龄(P=0.082)、性别(P=0.425)、体重指数(P=0.138)、诊断(退行性滑脱与腰椎管狭窄;P=0.529)、手术节段(P=0.651)、出血量(P=0.889)和手术时间(P=0.731)均无差异。两组患者末次随访时 ODI 和 VAS 评分均较术前显著改善(P=0.003)。末次随访时,除 VAS 评分(P=0.000)外,两组间无其他评分差异(P>0.05)。在非 LBP 组中,末次随访时 LL、SL、DH、TK 和 SS 均显著改善,而 PT 和 C7-SVA 较术前显著降低。两组患者术后 DH 均显著改善,组间无显著差异(P=0.325)。末次随访时,LL、PI-LL 不匹配、PT 和 C7-SVA 在非 LBP 组的改善程度明显大于 LBP 组(P<0.05)。多变量分析显示,PT、PI-LL 不匹配和 C7-SVA 是 OLIF 后 LBP 的显著危险因素。
OLIF 治疗单节段腰椎退行性疾病具有满意的临床效果。PT、PI-LL 不匹配和 C7-SVA 是术后 LBP 的显著危险因素。PT 适当降低、C7-SVA 改善、PI-LL 匹配良好的患者腰痛程度较轻。