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酰胺类局部麻醉药对有效不应期时间离散度的影响:与室性心律失常的关系。

Amide local anesthetic alterations of effective refractory period temporal dispersion: relationship to ventricular arrhythmias.

作者信息

Kasten G W

出版信息

Anesthesiology. 1986 Jul;65(1):61-6. doi: 10.1097/00000542-198607000-00010.

DOI:10.1097/00000542-198607000-00010
PMID:3729059
Abstract

The hemodynamic and electrophysiologic effects of bupivacaine, etidocaine, mepivacaine, and lidocaine were investigated in 32 pentobarbital-anesthetized adult mongrel dogs. Following equipotent dosing, all four agents produced similar hemodynamic effects: decrease in stroke volume and cardiac output, heart rate slowing, increase in systemic vascular resistance, and increases in pulmonary arterial pressure (PAP) and pulmonary capillary wedge pressure (PCWP). The effects of the various agents on the ECG were different. Compared with the control period, mepivacaine and lidocaine produced slight increases and etidocaine and bupivacaine much greater increases in: the area under the curve of the T-wave; lengthening of the QTU interval; and enhancement of the "slow wave" or U-wave following the T-wave. The effects of the various agents on effective refractory period (ERP) temporal dispersion were dramatically different. The ERP temporal dispersion increased to 48.3 +/- 36.0 ms following mepivacaine, 37.4 +/- 10.1 ms following lidocaine, 97.1 +/- 36.2 ms following bupivacaine, and 92.5 +/- 30.5 ms following etidocaine. Six of seven bupivacaine, six of seven etidocaine, two of eight mepivacaine, and none of eight lidocaine animals sustained a polymorphic, undulating ventricular tachycardia similar to Torsades de Pointes following burst ventricular pacing. The results of this study suggest that bupivacaine, etidocaine, and occasionally mepivacaine can result in a Torsades de Pointes-like syndrome following intravenous administration. The magnitude of ERP temporal dispersion differences between the various agents appears to explain their differential arrhythmogenicity.

摘要

在32只戊巴比妥麻醉的成年杂种犬中研究了布比卡因、依替卡因、甲哌卡因和利多卡因的血流动力学和电生理效应。给予等效剂量后,所有四种药物产生相似的血流动力学效应:每搏量和心输出量降低、心率减慢、全身血管阻力增加以及肺动脉压(PAP)和肺毛细血管楔压(PCWP)升高。各种药物对心电图的影响不同。与对照期相比,甲哌卡因和利多卡因使T波曲线下面积、QTU间期延长以及T波后“慢波”或U波增强有轻微增加,而依替卡因和布比卡因的增加幅度大得多。各种药物对有效不应期(ERP)时间离散的影响差异显著。甲哌卡因给药后ERP时间离散增加至48.3±36.0毫秒,利多卡因给药后为37.4±10.1毫秒,布比卡因给药后为97.1±36.2毫秒,依替卡因给药后为92.5±30.5毫秒。七只布比卡因动物中有六只、七只依替卡因动物中有六只、八只甲哌卡因动物中有两只、八只利多卡因动物中无一在心室快速起搏后出现类似于尖端扭转型室性心动过速的多形性、起伏性室性心动过速。本研究结果表明,布比卡因、依替卡因以及偶尔的甲哌卡因静脉给药后可导致类似尖端扭转型室性心动过速的综合征。各种药物之间ERP时间离散差异的大小似乎可以解释它们不同的致心律失常性。

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The effects of volatile induction and maintenance of anesthesia and selective spinal anesthesia on QT interval, QT dispersion, and arrhythmia incidence.挥发性诱导和维持麻醉以及选择性脊髓麻醉对 QT 间期、QT 离散度和心律失常发生率的影响。
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[Long QT syndrome and anaesthesia].
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Adverse effects of spinal and epidural anaesthesia.脊髓麻醉和硬膜外麻醉的不良反应。
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