目标控制输注中异丙酚快速和缓慢诱导的比较研究:作用区域异丙酚浓度预测。随机临床试验

Ricardo Francisco Simoni , Luiz Eduardo de Paula Gomes Miziara , Luis Otávio Esteves , Diógenes de Oliveira Silva , Cristina Alves Ribeiro , Mariana Oki Smith , Leonardo Ferreira de Paula , Luis Henrique Cangiani
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In slow induction group, target-controlled infusion of propofol with plasma, Marsh pharmacokinetic model (ke0 0.26<!--> <!-->min<sup>−1</sup>) with target concentration (Tc) at 2.0<!--> <!-->μg.mL<sup>−1</sup> were administered. When the predicted propofol concentration at the Es reached half of Es value, Es was increased to previous Es +1<!--> <!-->μg.mL<sup>−1</sup>, successively, until loss of consciousness. 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引用次数: 0

摘要

背景与目的研究表明,异丙酚输注速率可能影响作用部位的预测异丙酚浓度(Es)。本研究的目的是评估Marsh药代动力学模型(ke0 0.26 min−1)预测的快速或缓慢诱导时意识丧失的Es。方法28例患者随机分为2组。慢诱导组,靶控血浆输注异丙酚,建立Marsh药代动力学模型(ke0 0.26 min−1),靶浓度(Tc) 2.0 μg。给药mL−1。当Es处的预测异丙酚浓度达到Es值的一半时,Es增加到原来的Es +1 μg。mL−1,连续,直到失去意识。快速诱导组在Es时靶控血浆输注异丙酚(6.0 μg.ml−1)诱导,等待至意识丧失。结果快速诱导组意识丧失e值显著低于慢速诱导组(1.67±0.76、2.50±0.56 μg)。mL−1,P = 0.004)。结论在异丙酚药动学模型相同、血浆与作用部位平衡常数相同的情况下,快速诱导与慢速诱导对意识丧失的e级预测异丙酚浓度不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estudio comparativo entre inducción rápida y lenta de propofol en infusión objetivo-controlada: concentración de propofol prevista en la región de acción. Ensayo clínico aleatorizado

Background and objective

Studies have shown that rate of propofol infusion may influence the predicted propofol concentration at the effect site (Es). The aim of this study was to evaluate the Es predicted by the Marsh pharmacokinetic model (ke0 0.26 min−1) in loss of consciousness during fast or slow induction.

Method

The study included 28 patients randomly divided into 2 equal groups. In slow induction group, target-controlled infusion of propofol with plasma, Marsh pharmacokinetic model (ke0 0.26 min−1) with target concentration (Tc) at 2.0 μg.mL−1 were administered. When the predicted propofol concentration at the Es reached half of Es value, Es was increased to previous Es +1 μg.mL−1, successively, until loss of consciousness. In rapid induction group, patients were induced with target-controlled infusion of propofol with plasma (6.0 μg.ml−1) at Es, and waited until loss of consciousness.

Results

In rapid induction group, Es for loss of consciousness was significantly lower compared to slow induction group (1.67 ± 0.76 and 2.50 ± 0.56 μg.mL−1, respectively, P = 0.004).

Conclusion

The predicted propofol concentration at the Es for loss of consciousness is different for rapid induction and slow induction, even with the same pharmacokinetic model of propofol and the same balance constant between plasma and effect site.

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