Guidance of block needle insertion by electrical nerve stimulation

被引:43
作者
Rigaud, Marcel
Filip, Patrick
Lirk, Philipp
Fuchs, Andreas
Gemes, Geza
Hogan, Quinn [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Anesthesiol, MEB, Milwaukee, WI 53226 USA
[2] Zablocki Vet Adm Med Ctr, Dept Anesthesiol, Milwaukee, WI 53295 USA
基金
奥地利科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1097/ALN.0b013e318182af0b
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Little is known regarding the filial needle tip location when various intensities of nerve stimulation are used to guide block needle insertion. Therefore, in control and hyperglycemic dogs, the authors examined whether lower-intensity stimulation results in injection closer to the sciatic nerve than higher-threshold stimulation. Methods: During anesthesia, the sciatic nerve was approached with an insulated nerve block needle emitting either 1 mA (high-current group, n = 9) or 0.5 mA (low-current group, n = 9 in control dogs and n = 6 in hyperglycemic dogs). After positioning to obtain a distal motor response, the lowest current producing a response was identified, and ink (0.5 ml) was injected. Frozen sections of the tissue revealed whether the ink was in con tact with the epineurium of the nerve, distant to it, or within it. Results: In control dog, the patterns of distribution using high-threshold (filial current 0.99 +/- 0.03 mA, mean +/- SD) and low-threshold (final current 0.33 +/- 0.08 mA) stimulation equally showed ink that was in contact with the epineurium or distant to it. One needle placement in the high-threshold group resulted in intraneural injection. In hyperglycemic dogs, all needle insertions used a low-threshold technique (n = 6, final threshold 0.35 +/- 0.08 mA), and all resulted in intraneural injections. Conclusions: in normal dogs, current stimulation levels in the range of 0.33-1.0 mA result in needle placement comparably close to the sciatic nerve but do not correlate with distance from the target nerve. In this experimental design, low-threshold electrical stimulation does not offer satisfactory protection against intraneural injection in the presence of hyperglycemia.
引用
收藏
页码:473 / 478
页数:6
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