首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Similar motor block effects with different disposition kinetics between lidocaine and (+ or -) articaine in patients undergoing axillary brachial plexus block during day case surgery.
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Similar motor block effects with different disposition kinetics between lidocaine and (+ or -) articaine in patients undergoing axillary brachial plexus block during day case surgery.

机译:在日间病例手术中,接受腋窝臂丛神经阻滞的患者在利多卡因和(+或-)青蒿素之间具有不同的处置动力学,具有相似的运动阻滞效果。

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AIM: The aim of this investigation was to compare the clinical effects and pharmacokinetics of lidocaine and articaine in two groups of 15 patients undergoing axillary brachial plexus anesthesia. METHOD: The study had a randomized design. Thirty patients were allocated to one of the two groups. Each patient received either lidocaine (600 mg = 2.561 mMol + 5 microg/ml adrenaline) or articaine (600 mg = 2.113 mMol + 5 microg/ml adrenaline), injected via the axilla of the brachial plexus over a period of 30 seconds. Onset of surgical analgesia was defined as the period from the end of the injection of the local anesthetic to the loss of pinprick sensation in the distribution of all three nerves. RESULTS: The mean onset time of sensory block of the median nerve of both lidocaine and articaine were approximately 10 min. Lidocaine is biexponentially eliminated with a t1/2alpha of 9.95 +/- 14.3 min and a t1/2beta of 2.86 +/- 1.55 h. Lidocaine is metabolized into MEGX (mono-ethyl-glycyl-xilidide) (t(max) 2.31 +/- 0.84 h; C(max) 0.32 +/- 0.13 mg/l; t1/2beta 2.36 +/- 2.35 h). Lidocaine total body clearance was 67.9 +/- 28.9 l/h. Articaine is rapidly and monoexponentially eliminated with a t1/2beta of 0.95 +/- 0.39 h. The total body clearance of articaine is higher than that of lidocaine, 1,133 +/- 582 l/h vs 67.9 +/- 28.9 l/h, respectively (p < 0.0001). The volume of distribution (V(d)), of articaine is a factor 16 higher times than that of lidocaine (p < 0.0001). CONCLUSION: For the axillary administration, lidocaine and articaine show similar pharmacodynamics with a different pharmacokinetic behavior and can therefore be used to the clinical preference for this regional anesthetic technique.
机译:目的:本研究的目的是比较利多卡因和青蒿素在两组接受腋下臂丛神经麻醉的15例患者中的临床效果和药代动力学。方法:该研究采用随机设计。 30名患者被分配到两组之一。每位患者接受利多卡因(600 mg = 2.561 mMol + 5 microg / ml肾上腺素)或青蒿素(600 mg = 2.113 mMol + 5 microg / ml肾上腺素),经臂丛神经腋下注射,持续30秒。手术镇痛的发作定义为从局部麻醉剂注射结束到所有三条神经的分布失去针刺感的时间。结果:利多卡因和青蒿素的正中神经感觉阻滞平均发作时间约为10分钟。利多卡因以9.95 +/- 14.3分钟的t1 / 2alpha和2.86 +/- 1.55 h的t1 / 2beta双指数消除。利多卡因被代谢成MEGX(单乙基缩水甘油基己糖苷)(t(最大)2.31 +/- 0.84小时; C(最大)0.32 +/- 0.13毫克/升; t1 / 2beta 2.36 +/- 2.35小时)。利多卡因的全身清除率为67.9 +/- 28.9 l / h。 Articaine被迅速和单指数消除,t1 / 2beta为0.95 +/- 0.39 h。青蒿素的全身清除率高于利多卡因,分别为1133 +/- 582 l / h和67.9 +/- 28.9 l / h(p <0.0001)。青蒿素的分布体积(V(d))比利多卡因的分布体积高出16倍(p <0.0001)。结论:对于腋窝给药,利多卡因和青蒿素显示出相似的药效学,具有不同的药代动力学行为,因此可用于该区域麻醉技术的临床偏爱。

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