Kim David D, Asif Asma, Kataria Sandeep
Department of Anesthesiology, Henry Ford Hospital, Detroit, MI, USA.
Korean J Pain. 2016 Jul;29(3):158-63. doi: 10.3344/kjp.2016.29.3.158. Epub 2016 Jul 1.
Phenol and alcohol have been used to ablate nerves to treat pain but are not specific for nerves and can damage surrounding soft tissue. Lidocaine at concentrations > 8% injected intrathecal in the animal model has been shown to be neurotoxic. Tests the hypothesis that 10% lidocaine is neurolytic after a peri-neural blockade in an ex vivo experiment on the canine sciatic nerve.
Under ultrasound, one canine sciatic nerve was injected peri-neurally with 10 cc saline and another with 10 cc of 10% lidocaine. After 20 minutes, the sciatic nerve was dissected with gross inspection. A 3 cm segment was excised and preserved in 10% buffered formalin fixative solution. Both samples underwent progressive dehydration and infusion of paraffin after which they were placed on paraffin blocks. The sections were cut at 4 µm and stained with hemoxylin and eosin. Microscopic review was performed by a pathologist from Henry Ford Hospital who was blinded to which experimental group each sample was in.
The lidocaine injected nerve demonstrated loss of gross architecture on visual inspection while the saline injected nerve did not. No gross changes were seen in the surrounding soft tissue seen in either group. The lidocaine injected sample showed basophilic degeneration with marked cytoplasmic vacuolation in the nerve fibers with separation of individual fibers and endoneurial edema. The saline injected sample showed normal neural tissue.
Ten percent lidocaine causes rapid neurolytic changes with ultrasound guided peri-neural injection. The study was limited by only a single nerve being tested with acute exposure.
苯酚和酒精已被用于神经消融以治疗疼痛,但它们对神经不具有特异性,且会损伤周围软组织。在动物模型中,鞘内注射浓度>8%的利多卡因已被证明具有神经毒性。在犬坐骨神经的体外实验中,测试了在神经周围阻滞术后10%利多卡因具有神经溶解作用的假设。
在超声引导下,一条犬坐骨神经周围注射10 cc生理盐水,另一条注射10 cc 10%利多卡因。20分钟后,解剖坐骨神经并进行大体检查。切下3 cm长的一段神经,保存在10%缓冲福尔马林固定液中。两个样本均进行逐步脱水和石蜡灌注,然后置于石蜡块上。切片厚度为4 µm,用苏木精和伊红染色。由亨利·福特医院的一名病理学家进行显微镜检查,该病理学家对每个样本所属的实验组不知情。
肉眼观察发现,注射利多卡因的神经组织结构丧失,而注射生理盐水的神经则没有。两组周围软组织均未观察到明显变化。注射利多卡因的样本显示嗜碱性变性,神经纤维中出现明显的细胞质空泡化,单个纤维分离,神经内膜水肿。注射生理盐水的样本显示神经组织正常。
超声引导下神经周围注射10%利多卡因会导致快速的神经溶解变化。该研究仅对一条神经进行急性暴露测试,存在局限性。