Jack N T M, Liem E B, Vonhögen L H
St Maartenskliniek, Nijmegen, The Netherlands.
Br J Anaesth. 2005 Aug;95(2):250-4. doi: 10.1093/bja/aei161. Epub 2005 May 27.
There is continuing debate as to whether the use of electrical stimulation that aids in localizing nerves is also beneficial for optimizing placement of nerve catheters and lead to improved clinical outcomes, such as reductions in pain scores and opioid consumption.
We undertook a retrospective, non-randomized comparison of stimulating and non-stimulating nerve catheters in 419 patients undergoing total knee replacement between December 2002 and July 2004. Before surgery, patients received sciatic and femoral nerve blocks with a catheter for the femoral nerve. In 159 patients a stimulating catheter system (Stimucath; Arrow International, Reading, PA, USA) and in 260 patients a non-stimulating catheter system (Contiplex; B. Braun, Melsungen, Germany) was used. After surgery, pain scores and morphine consumption were recorded at 4-h intervals until the first postoperative morning. In a subset of 85 patients, the postoperative evaluation period was lengthened to 3 days.
Postoperative visual analogue scores (VAS) for pain were similar in the two groups during the first 24 h (P=0.305). In patients followed for 3 days, VAS scores did not differ on any of the days (P=0.427). Total morphine consumption did not differ on the first postoperative day (mean [95% CI]: stimulating, 12.4 [10.1-14.7] mg; non-stimulating 10.4 [8.9-11.8] mg; P=0.140) or on subsequent days.
The practical advantages of the stimulating catheter, as reported by previous investigators, were not obvious in this clinical situation. In terms of outcome measures such as pain scores and morphine consumption, we found no significant differences between stimulating and non-stimulating catheters.
关于辅助神经定位的电刺激的使用是否也有利于优化神经导管的放置并带来改善的临床结果,如降低疼痛评分和阿片类药物消耗量,一直存在争议。
我们对2002年12月至2004年7月期间接受全膝关节置换术的419例患者的刺激型和非刺激型神经导管进行了回顾性、非随机比较。手术前,患者接受坐骨神经和股神经阻滞,并在股神经处放置导管。159例患者使用了刺激型导管系统(Stimucath;美国宾夕法尼亚州雷丁市箭牌国际公司),260例患者使用了非刺激型导管系统(Contiplex;德国梅尔松根市贝朗公司)。术后,每4小时记录一次疼痛评分和吗啡消耗量,直至术后第一个早晨。在85例患者的子集中,术后评估期延长至3天。
两组患者术后第1个24小时的视觉模拟疼痛评分(VAS)相似(P = 0.305)。在随访3天的患者中,任何一天的VAS评分均无差异(P = 0.427)。术后第一天的吗啡总消耗量无差异(均值[95%CI]:刺激型,12.4[10.1 - 14.7]mg;非刺激型,10.4[8.9 - 11.8]mg;P = 0.140),随后几天也无差异。
先前研究者报道的刺激型导管的实际优势在这种临床情况下并不明显。在疼痛评分和吗啡消耗量等结局指标方面,我们发现刺激型和非刺激型导管之间没有显著差异。