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使用超声和双神经刺激法,比较2%利多卡因与0.5%布比卡因混合液和单纯0.5%布比卡因用于终末期肾病患者动静脉内瘘造瘘术时锁骨下臂丛神经麻醉的起效时间

Onset Time of 2% Lidocaine and 0.5% Bupivacaine Mixture versus 0.5% Bupivacaine Alone using Ultrasound and Double Nerve Stimulation for Infraclavicular Brachial Plexus Anesthesia in ESRD Patients Undergoing Arteriovenous Fistula Creation.

作者信息

Pongraweewan Orawan, Inchua Nipa, Kitsiripant Chanatthee, Kongmuang Benchawan, Tiwirach Wannapa

出版信息

J Med Assoc Thai. 2016 May;99(5):589-95.

Abstract

OBJECTIVE

To reduce the onset of 0.5% bupivacaine by adding 2% lidocaine with 0.5% bupivacaine for ultrasound-guided and double stimulation technique at musculocutaneous and radial nerve for infraclavicular brachial plexus block.

DESIGN

Prospective randomized double-blinded, controlled trial study.

MATERIAL AND METHOD

90 patients undergoing creation of arteriovenous fistula under ultrasound-guided infraclavicular brachial plexus block were randomized into 2 groups. Gr B (46 patients) received 0.5% bupivacaine 30 mL and Gr BL (44 patients) received mixture of 0.5% bupivacaine 20 mL and 2% lidocaine 10 mL. The onset of sensory block were assessed by response to pinprick (grading: 0 = no sensation, 1 = hypoesthesia, and 2 = normal sensation). Rescue analgesia during the operation, duration of sensory and motor blockade were recorded. Surgeon and patient satisfactions are also evaluated using 6-point scale (0 = dissatisfied to 5 = very satisfied).

RESULTS

There were no significant difference in the onset time of either group. Duration of sensory and motor block was not different. Surgeons' and patients' satisfaction were also not significantly different between the groups.

CONCLUSION

Mixing 2% lidocaine with 0.5% bupivacaine to the final concentration of 0.67%for lidocaine and 0.33% for bupivacaine does not reduce the onset of ultrasound-guided infraclavicular brachial plexus block.

摘要

目的

在超声引导下采用双重刺激技术,于肌皮神经和桡神经处行锁骨下臂丛神经阻滞时,将2%利多卡因与0.5%布比卡因混合,以减少0.5%布比卡因的起效时间。

设计

前瞻性随机双盲对照试验研究。

材料与方法

90例行超声引导下锁骨下臂丛神经阻滞以建立动静脉内瘘的患者被随机分为两组。B组(46例患者)接受30 mL 0.5%布比卡因,BL组(44例患者)接受20 mL 0.5%布比卡因与10 mL 2%利多卡因的混合液。通过对针刺的反应评估感觉阻滞的起效情况(分级:0 = 无感觉,1 = 感觉减退,2 = 感觉正常)。记录术中的补救镇痛情况、感觉和运动阻滞的持续时间。还采用6分制量表(0 = 不满意至5 = 非常满意)评估外科医生和患者的满意度。

结果

两组的起效时间无显著差异。感觉和运动阻滞的持续时间无差异。两组之间外科医生和患者的满意度也无显著差异。

结论

将2%利多卡因与0.5%布比卡因混合,使利多卡因最终浓度达到0.67%、布比卡因最终浓度达到0.33%,并不会缩短超声引导下锁骨下臂丛神经阻滞的起效时间。

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