Choi E, Nahm F S, Lee P-B
Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, #166, Gumi-ro, Bundang-gu, Seongnam 463-707, Korea.
Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, #166, Gumi-ro, Bundang-gu, Seongnam 463-707, Korea
Br J Anaesth. 2015 Nov;115(5):768-74. doi: 10.1093/bja/aev342.
The different methods of cervical epidural injection include the median or paramedian interlaminar (PI) approach and the transforaminal (TF) approach. We hypothesized that the modified PI (mPI) approach could deliver drugs suitably and safely into the anterior epidural space compared with the TF approach.
A total of 62 patients were randomized into either the mPI group (n=31) or the TF group (n=31). Contrast to the anterior epidural space (primary outcome, grade 1-3), vascular uptake and discomfort were assessed. Furthermore, pain intensity in the arm and neck [numeric rating scale (NRS)] and the degree of symptoms (5-point Likert scale) before the procedure and 2 weeks, 1 and 3 months following the procedure were compared between two groups. Effectiveness (a secondary outcome) was defined as a ≥50% reduction on the NRS for arm and neck pain and a result of 3 or 4 on the Likert scale at 3 months following the procedure.
Contrast to the anterior epidural space in the mPI group was significantly greater than that in the TF group (P=0.036). Vascular uptake and discomfort in the mPI group were significantly lower than those in the TF group (P<0.001, respectively). Of the patients in whom the procedure was effective, 24 (77.4%) were from the mPI group and 20 (64.5%) were from the TF group (P=0.263).
This result suggests that the mPI approach allows for suitable and safe delivery of drugs into the anterior epidural space.
Institutional Review Board of Seoul National University Bundang Hospital (B-1206/159-004) and Clinical Research Information Service (KCT0000626).
颈椎硬膜外注射的不同方法包括正中或旁正中椎间孔(PI)入路和经椎间孔(TF)入路。我们假设改良的PI(mPI)入路与TF入路相比,能够将药物合适且安全地注入硬膜前间隙。
总共62例患者被随机分为mPI组(n = 31)或TF组(n = 31)。评估硬膜前间隙造影(主要结局,1 - 3级)、血管摄取情况和不适感。此外,比较两组患者术前以及术后2周、1个月和3个月时手臂和颈部的疼痛强度[数字评分量表(NRS)]和症状程度(5级李克特量表)。有效性(次要结局)定义为术后3个月时手臂和颈部疼痛的NRS降低≥50%,且李克特量表评分为3或4。
mPI组硬膜前间隙造影明显大于TF组(P = 0.036)。mPI组的血管摄取和不适感明显低于TF组(P分别<0.001)。在手术有效的患者中,24例(77.4%)来自mPI组,20例(64.5%)来自TF组(P = 0.263)。
该结果表明mPI入路能够将药物合适且安全地注入硬膜前间隙。
首尔国立大学盆唐医院机构审查委员会(B - 1206/159 - 004)和临床研究信息服务中心(KCT0000626)。