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日间手术中利多卡因用于静脉区域麻醉的处置

Disposition of lignocaine for intravenous regional anaesthesia during day-case surgery.

作者信息

Simon M A, Gielen M J, Vree T B, Booij L H

机构信息

Department of Anaesthesiology, Medisch Spectrum Twente, Enschede, The Netherlands.

出版信息

Eur J Anaesthesiol. 1998 Jan;15(1):32-7. doi: 10.1046/j.1365-2346.1998.00217.x.

Abstract

Lignocaine is a suitable and safe agent for intravenous regional anaesthesia (IVRA) with rapid onset of good surgical anaesthesia. The onset time of the local anaesthetic action of lignocaine was 11.2 +/- 5.1 min. Satisfactory surgical conditions, evidenced by good sensory blockade were achieved within 20 min, and no additional analgesics were required. There was no trend towards a fixed sequence, radial, median and ulnar in the development of sensory blockade. No patient exhibited objective symptoms of toxicity, either local or systemic, after release of the tourniquet, nor were there any subjective complaints. No changes in blood pressure, heart rate or oxygen saturation were observed at any time during the procedure, or after deflation of the tourniquet. After releasing the tourniquet lignocaine is rapidly and biexponentially eliminated, with a t1/2a of 4.3 +/- 2.1 min and a t1/2 beta of 79.1 +/- 31.2 min. Total body clearance was 0.86 +/- 0.39 L min-1. Eight patients showed rapid release of lignocaine from the exsanguinated area. In two patients the systemic plasma concentration of lignocaine increased more slowly than in the remaining eight. This can be explained by a greater degree of lignocaine absorbtion in the tissues of the arm. Pharmacokinetic constants after rapid and slow absorption were calculated.

摘要

利多卡因是一种适用于静脉区域麻醉(IVRA)的安全药物,其起效迅速,能产生良好的手术麻醉效果。利多卡因局部麻醉作用的起效时间为11.2±5.1分钟。在20分钟内可达到满意的手术条件,表现为良好的感觉阻滞,无需额外使用镇痛药。感觉阻滞的发展不存在固定顺序,如桡神经、正中神经和尺神经的阻滞顺序。松开止血带后,没有患者出现局部或全身毒性的客观症状,也没有任何主观不适。在手术过程中或止血带放气后,任何时候均未观察到血压、心率或血氧饱和度的变化。松开止血带后,利多卡因迅速以双指数方式消除,α半衰期为4.3±2.1分钟,β半衰期为79.1±31.2分钟。全身清除率为0.86±0.39 L·min⁻¹。8例患者利多卡因从放血区域快速释放。2例患者利多卡因的全身血浆浓度升高速度比其余8例患者慢。这可以用手臂组织对利多卡因的吸收程度更高来解释。计算了快速吸收和缓慢吸收后的药代动力学常数。

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