[Pharmacokinetic basis of constant-flow administration of drugs during long-lasting anesthesia].

J C Mathieu-Daudé, J Deschodt, J du Cailar
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Abstract

The criteria for intravenous administration of anesthetics or their adjunctives in continuous and constant flow remain imprecise and incompletely understood. Drugs with a very short half-life are usually preferred, without this being a restrictive notion. The theoretical bases for the kinetics of constant flow intravenous infusion are well known but not the practical carrying out, and the practitioner remains confronted with various fundamental questions. Indeed, the quantity administered must take in account it's elimination, but what happens in cases of destructive metabolism, above all when the metabolites are toxic? On the other hand, can the kinetics observed for a given dose be extrapolated to any dose that is administered? Using real examples during constant-flow anestesia, we reconsider a simple calculation method based on the total clearance for a given substance and providing the theoretical constant-concentration level. This study shows how complex the kinetics of constant-flow administration area. All these techniques should be preceded before human application, by serious research on adequate experimental models.

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[长期麻醉中恒流量给药的药代动力学基础]。
麻醉药物或其辅助药物连续和恒定静脉给药的标准仍然不精确和不完全理解。半衰期很短的药物通常是首选,这并不是一个限制性的概念。恒流量静脉输液动力学的理论基础是众所周知的,但在实际操作中尚不清楚,从业者仍然面临着各种基本问题。的确,给药的量必须考虑到它的消除,但在破坏性代谢的情况下,尤其是当代谢物有毒时,会发生什么呢?另一方面,在给定剂量下观察到的动力学是否可以外推到任何给药剂量?结合恒流麻醉过程中的实际例子,我们重新考虑了一种基于给定物质的总间隙并提供理论恒定浓度水平的简单计算方法。该研究表明,恒流量给药区域的动力学是多么复杂。所有这些技术都应该在人类应用之前,通过对适当的实验模型进行认真的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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