Department of Anesthesiology and Pain Medicine, School of Medicine, Ewha Womans University Mokdong Hospital, Seoul, Republic of Korea.
Department of Anesthesiology and Pain Medicine, Chung-Ang University College of Medicine, Dongjak-gu, Seoul, Republic of Korea.
Pain Physician. 2018 May;21(3):269-278.
The effect of transforaminal epidural steroid injection (TFESI) appears to be influenced by the volume of the injected material because there is a positive correlation between injection volume and extent of pain relief.
The purpose of this study was to examine how many vertebral segments are covered by the subpedicular (SP) approach and the retrodiscal (RD) approach and to compare the clinical outcomes of the 2 approaches in TFESI with high-volume injectates.
A randomized, active control trial.
Medical University centers.
Fifty patients were randomly assigned to either the SP group or the RD group. TFESI was performed with high-volume injectates. A total of 9 mL injectate was divided into 3 injections (0.5 mL, 2.5 mL, and 6 mL) given at 10-second intervals. The primary outcome measure was injectate distribution. The spreading patterns were described as unilateral, bilateral, ventral, or dorsal. Ventral or dorsal flow was also described as being cephalad or caudad, respectively. The secondary outcome measures were pain relief and reduction of functional disability at 4 weeks after the procedure.
The total numbers of vertebral segments and median levels of contrast spread from the injection site were not significantly different between the 2 groups. However, in 3 mL of injectate, the injectate spread showed more extensive bilateral distribution in the RD group. At 4 weeks after treatment, both groups demonstrated statistically significant pain relief and improvement in functional status. No significant differences were observed between the 2 groups.
We enrolled only a small number of patients and did not analyze long-term outcomes. Patients with severe spinal stenosis or herniated nucleus pulposus were included. Slightly different methods were used in the 2 groups to determine the number of levels at which the injectate was spread.
Epidural spreading patterns and clinical outcomes of lumbar TFESI with high-volume injectate were not significantly different between the SP approach and the RD approach.Institutional Review Board (IRB) approval: Institutional Review Board of Ewha Womans University Hospital (EUMC 2015-05-003-003). Clinical trials registration number: Clinical Research Information Service (CRIS, registration number: KCT0002288; RCT URL: https://cris.nih.go.kr/cris/search/search_result_st01.jsp?seq=7309)KEY WORDS: Epidural injections, epidural space, low back pain, radiating pain, disability evaluation, steroids, local anesthetics, intervertebral disc disease, spinal stenosis.
经椎间孔硬膜外类固醇注射(TFESI)的效果似乎受到注射材料体积的影响,因为注射体积与疼痛缓解程度之间存在正相关关系。
本研究旨在检查经皮椎弓根(SP)入路和经椎间盘后路(RD)入路覆盖了多少个椎体节段,并比较两种方法在 TFESI 中使用高容量注射剂的临床效果。
随机、主动对照试验。
医科大学中心。
50 名患者被随机分配到 SP 组或 RD 组。使用高容量注射剂进行 TFESI。总共 9 mL 的注射剂分为 3 次注射(0.5 mL、2.5 mL 和 6 mL),间隔 10 秒。主要结局测量指标为注射剂分布。扩散模式描述为单侧、双侧、腹侧或背侧。腹侧或背侧的流动也分别描述为向头侧或尾侧。次要结局测量指标为治疗后 4 周时的疼痛缓解和功能障碍的减少。
两组之间的总椎体节段数和对比剂从注射部位扩散的中位数水平无显著差异。然而,在 3 mL 的注射剂中,RD 组的注射剂扩散显示出更广泛的双侧分布。治疗后 4 周,两组均表现出统计学显著的疼痛缓解和功能状态改善。两组之间没有观察到显著差异。
我们仅招募了少数患者,并且没有分析长期结果。纳入了严重的椎管狭窄或椎间盘突出症患者。两组使用略有不同的方法来确定注射剂扩散的节段数。
使用高容量注射剂进行腰椎 TFESI 的硬膜外扩散模式和临床结果在 SP 入路和 RD 入路之间没有显著差异。
机构审查委员会(IRB)批准:Ewha Womans 大学医院机构审查委员会(EUMC 2015-05-003-003)。临床试验注册号:临床研究信息服务(CRIS,注册号:KCT0002288;RCT 网址:https://cris.nih.go.kr/cris/search/search_result_st01.jsp?seq=7309)
硬膜外注射、硬膜外腔、下腰痛、放射痛、残疾评估、类固醇、局部麻醉剂、椎间盘疾病、椎管狭窄。