静脉麻醉药之间的相互作用

MD M.J. Mertens (Resident in Anaesthesia), MD, PhD J. Vuyk (Staff Anaesthesiologist)
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引用次数: 6

摘要

静脉麻醉药之间的相互作用可以是药代动力学的也可以是药效学的。药代动力学药物-药物相互作用的临床意义将取决于药物作用部位药物浓度变化的幅度。静脉麻醉药可影响其他共施静脉麻醉药的分布、消除和/或效果。由于与药代动力学变异性(60-80%)相比,药效学变异性(300-400%)更大,因此在临床上,药效学相互作用比药代动力学相互作用更重要。涉及静脉麻醉的许多药效学相互作用是协同的,这允许使用较低的剂量或浓度来达到足够的麻醉深度,并相应减少副作用的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
6 Interactions between intravenous anaesthetic agents

Interactions between intravenous anaesthetic agents can be either pharmacokinetic or pharmacodynamic. The clinical significance of a pharmacokinetic drug-drug interaction will depend on the magnitude of the change in the concentration of the drug at the site of pharmacological action. Intravenous anaesthetic agents can influence the distribution and elimination and/or the effect of other co-administered intravenous anaesthetic agents. Because of the larger pharmacodynamic variability (300–400%) compared to the pharmacokinetic variability (60–80%), pharmacodynamic interactions are more important clinically than pharmacokinetic interactions. Many pharmacodynamic interactions involving intravenous anaesthetics are synergistic, and this allows lower doses or concentrations to be used to achieve adequate depth of anaesthesia, with a corresponding reduction in the incidence of side-effects.

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