[Experimental studies on peripheral nerve injuries caused by injection needles].

IF 1.9 Q2 POLITICAL SCIENCE Regional-Anaesthesie Pub Date : 1990-01-01
Y Hirasawa, Y Katsumi, W Küsswetter, G Sprotte
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Abstract

Differences in neural damage due to different injection needles were investigated in vitro on sciatic nerve specimens of adult rabbits. METHODS. Three types of 22-gauge needles were tested: one typical, long-bevelled venous puncture needle; a short bevelled, typical nerve block needle; and a tapered, atraumatic spinal needle. Both sciatic nerves of 50 adult rabbits weighing from 2.5 to 3.0 kg were used for electrophysiological investigations on one side and fluorescence microscopy on the other. ELECTROPHYSIOLOGY. The nerve specimens were placed in an experimental chamber on silver-silver chloride electrodes that were aligned at a distance of 10 mm. Two electrodes at the distal ends of the nerve were used for stimulation by rectangular waves (6-10 v) of 0.01 ms duration. The compound action potential (CAP), its amplitude, and its latency were measured by monopolar recording from four additional electrodes (R1 to R4). Ten nerves were apportioned to each of five groups and the needles were perpendicularly pierced three times in the middle of the nerve trunk at the midpoint between recording sites R2 and R3. THE GROUPS. 1. Long-bevelled needle, the face of the bevel inserted rectangular to the nerve fibers; 2. long-bevelled needle, the face of the bevel parallel to the nerve fibers; 3. short-bevelled needle, the face of the bevel inserted rectangular to the nerve fibers; 4. short-bevelled needle, the face of the bevel parallel to the nerve fibers; 5. tapered, pencil-point needle pierced perpendicularly through the nerve trunk. The amplitude of the CAP was recorded before and after nerve injury from R1 to R4. FLUORESCENCE MICROSCOPY. According to the method described by Steinwall and Olsson, the other five groups of injured nerves were immersed in Evans blue albumin (EBA) and, after washing in saline solution, fixed in 5% formalin. The extent of nerve damage was evaluated by fluorescence microscopy of the glycerol-imbedded frozen sections (longitudinal and transverse). RESULTS. Electrophysiology. After injuring the area between R2 and R3 there was almost no change in the amplitude of the CAP at sites R1 and R2. The amplitude at R3 and R4 was reduced in comparison with the controls. This reduction was most marked in group 1 and very slight in group 5. The percentages of amplitude at R3 after injury compared with control values (mean +/- SD) were 42.2% +/- 22.0% in group 1; 60.9% +/- 18.2% in group 2; 51.0% +/- 22.3% in group 3; 71.0% +/- 18.0% in group 4; and 90.1% +/- 10.9% in group 5. Statistically significant differences were obtained between the tapered, atraumatic needle group and the other four groups (Fig. 3). Fluorescence microscopy. With the tapered injection needle there was the least leakage of EBA, which suggests the least damage to the perineurium, and almost no rupture or tearing of the nerve fibers was observed. In the short- and long-bevelled needles, the damage was reduced when the face of the bevel was inserted parallel to the fibers.

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【注射针致周围神经损伤的实验研究】。
研究了不同注射针对成年兔坐骨神经损伤的差异。方法。测试了三种22号针头:一种典型的长斜角静脉穿刺针;短斜的典型神经阻滞针;还有一根锥形的非创伤性脊髓针。50只体重在2.5 ~ 3.0 kg的成年家兔的坐骨神经一侧电生理检查,另一侧荧光显微镜检查。电生理学。神经标本放置在实验室内的银-氯化银电极上,电极以10毫米的距离排列。在神经远端使用两个电极进行持续0.01 ms的矩形波(6-10 v)刺激。复合动作电位(CAP)、幅值和潜伏期分别在4个电极(R1 ~ R4)上进行单极记录。5组每组10根神经,在记录点R2和R3之间的中点神经干正中垂直刺入针3次。的组。1. 长斜面针,斜面长方形地插入神经纤维;2. 长斜面针,斜面平行于神经纤维;3.短斜面针,斜面长方体插入神经纤维;4. 短斜面针,斜面平行于神经纤维;5. 尖的,铅笔尖的针垂直地穿过神经干。从R1到R4记录神经损伤前后CAP的振幅。荧光显微镜。按照Steinwall和Olsson描述的方法,将其他五组损伤神经浸入埃文斯蓝白蛋白(EBA)中,用生理盐水洗涤后,用5%福尔马林固定。用荧光显微镜观察甘油包埋冷冻切片(纵向和横向)的神经损伤程度。结果。电生理学。在R2和R3之间的区域损伤后,R1和R2位置的CAP振幅几乎没有变化。与对照组相比,R3和R4的振幅减小了。这种减少在第1组最明显,在第5组非常轻微。与对照组相比,1组损伤后R3处振幅百分比(平均+/- SD)为42.2% +/- 22.0%;2组60.9% +/- 18.2%;3组51.0% +/- 22.3%;第4组71.0%±18.0%;第5组90.1%±10.9%。锥形、无外伤针组与其他四组之间的差异有统计学意义(图3)。荧光显微镜。锥形注射针EBA渗漏最少,对神经周围膜损伤最小,几乎未见神经纤维断裂或撕裂。在短斜面针和长斜面针中,当斜面与纤维平行插入时,损伤减少。
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