[Pharmacokinetics of articaine in mandibular nerve block].

IF 1.9 Q2 POLITICAL SCIENCE Regional-Anaesthesie Pub Date : 1991-05-01
W P Müller, P Weiser, K L Scholler
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Abstract

Up to now, mandibular nerve blocks have been carried out without knowing the exact blood concentrations resulting from the use of the local anesthetics. Due to the high vascularity a rapid increase in serum local anesthetic levels is to be expected. Due to analytical problems, the literature provides controversial statements about the pharmacokinetics of articaine which is generally used for this block. The given half-life periods following intramuscular application range from 39 min [8] to 31 h [6]. For this reason, mandibular nerve blocks with 2 ml 4% articaine with 1:200,000 epinephrine were carried out in 10 awake patients and 10 patients during intubation anesthesia. RESULTS. Blood samples from peripheral veins showed an average maximum concentration of 2.1 +/- 1.3 mg/l after 12.5 +/- 2.5 min. After 8 h the value had fallen below the minimum detection limit of 0.05 mg/l. In the present study, a half-life of approximately 20 min was determined for articaine after conduction anesthesia. This local anesthetic holds an exceptional position because as an amide-type local anesthetic it contains an additional ester group that is hydrolytically metabolized in the blood. The concentration of the resulting metabolite reaches a maximum value of 2.6 +/- 1.6 mg/l after 40 to 50 min. CONCLUSIONS. Compared to other amide-type local anesthetics, whose terminal plasma half-life varies between 1 and 3.6 h [5], the value of 20 min found for articaine is very low. This is in part due to its structure, as the ester group is rapidly metabolized by plasma esterases. Because of its rapid breakdown articaine is very suitable for use in oral surgery. The HPLC method represents an uncomplicated analytical technique for the determination of local anesthetics levels in blood and other body fluids.

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[阿替卡因在下颌神经阻滞中的药代动力学]。
到目前为止,在不知道使用局部麻醉剂导致的确切血液浓度的情况下进行下颌神经阻滞。由于高血管性,预期血清局部麻醉水平会迅速增加。由于分析上的问题,文献对阿替卡因的药代动力学提出了有争议的说法,阿替卡因通常用于该阻滞。肌肉注射后的半衰期为39分钟[8]至31小时[6]。为此,我们对10例清醒患者和10例插管麻醉患者分别进行了2 ml 4%阿替卡因加1:20万肾上腺素的下颌神经阻滞。结果。外周静脉血样在12.5 +/- 2.5 min后平均最高浓度为2.1 +/- 1.3 mg/l, 8 h后降至最低检出限0.05 mg/l以下。在本研究中,测定了传导麻醉后阿替卡因的半衰期约为20分钟。这种局部麻醉剂具有特殊的地位,因为作为一种酰胺型局部麻醉剂,它含有在血液中水解代谢的额外酯基。40 ~ 50 min后,代谢产物浓度达到2.6 +/- 1.6 mg/l的最大值。其他酰胺类局麻药的终末血浆半衰期在1 ~ 3.6 h之间[5],与之相比,阿替卡因的20 min很低。这部分是由于它的结构,因为酯群被血浆酯酶迅速代谢。由于其快速分解的特性,阿替卡因非常适合用于口腔外科。高效液相色谱法是测定血液和其他体液中局部麻醉剂含量的一种简单的分析技术。
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[An epidural spinal abscess as a lethal complication of peridural anesthesia]. [Knotting of a peridural catheter]. [A simple technique for estimating the level of analgesia in regional anesthesia]. [CSE--the combination of spinal and epidural anesthesia]. [Comments on the paper by R. Schürg et al. Maternal and neonatal plasma concentrations of bupivacaine during peridural anesthesia for cesarean section].
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