Europainclinics, Prague, Czech Republic.
Europainclinics, Nové Mesto, Slovak Republic.
Pain Med. 2018 Jul 1;19(7):1436-1444. doi: 10.1093/pm/pnx328.
Epiduroscopy is a proven method of diagnosis and treatment for chronic radicular pain after spinal surgery, which is known as failed back surgery syndrome (FBSS). The aim of the study was to compare the efficacy of drugs (the enzyme hyaluronidase and corticosteroid DEPO-Medrol) administrated into the epidural space during epiduroscopy, performed within the ventral and ventro-lateral epidural space with a focus on releasing foraminal adhesions.
Forty-eight patients with diagnosed FBBS were randomized into two groups before epiduroscopy. Group A received the standard treatment-mechanical lysis of fibrotic tissue in the epidural space. Group B received hyaluronidase and corticosteroid methylprednisolone acetate during the procedure. Subjects were followed for six and 12 months via scheduled double-blinded examinations by pain physicians. Leg and back pain intensity was assessed by an 11-point numerical rating scale, and patients' functional disability was assessed by the Oswestry Disability Index (ODI).
Study subjects showed a significant decrease in ODI score in both groups (P < 0.05). Significantly lower pain scores for leg pain (P < 0.05) and back pain (P < 0.05) were also recorded after the six-month follow-up. However, the one-year follow-up showed a return to the baseline ODI values of most monitored pain scores in both groups (P > 0.05). Improvement was only noted on the NRS for back pain at one-year follow-up (P < 0.05).
A significant improvement of leg and back pain was found in both groups after six months. ODI was significantly improved only in group B in both the six- and 12-month intervals. Back pain at one-year follow-up was only improved in group B.
椎管内视镜检查是一种已被证实的诊断和治疗方法,可用于治疗脊柱手术后的慢性神经根痛,即所谓的失败性脊柱手术综合征(FBSS)。本研究的目的是比较在椎管内视镜检查期间将药物(酶透明质酸酶和皮质类固醇地塞米松)注入硬膜外腔的疗效,重点是释放椎间孔粘连。
48 例确诊为 FBSS 的患者在椎管内视镜检查前随机分为两组。A 组接受标准治疗-硬膜外空间内纤维组织的机械松解。B 组在手术过程中接受透明质酸酶和皮质类固醇甲泼尼龙醋酸酯。通过疼痛医师进行计划的双盲检查,对受试者进行 6 个月和 12 个月的随访。通过 11 点数字评分量表评估腿部和背部疼痛强度,通过 Oswestry 残疾指数(ODI)评估患者的功能障碍。
两组患者的 ODI 评分均显著下降(P<0.05)。两组患者腿部疼痛(P<0.05)和背部疼痛(P<0.05)的评分在 6 个月的随访中也显著降低。然而,在 1 年的随访中,两组大多数监测的疼痛评分的 ODI 值均恢复到基线(P>0.05)。仅在 1 年的随访中观察到背部疼痛的 NRS 有所改善(P<0.05)。
两组患者在 6 个月后腿部和背部疼痛均显著改善。ODI 在 6 个月和 12 个月时仅在 B 组显著改善。仅在 B 组在 1 年的随访中观察到背部疼痛有所改善。