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Modeling the respiratory depressant effect of opioids: application to fentanyl

机译:模拟阿片类药物的呼吸抑制作用:应用于芬太尼

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The respiratory depressant effect of fentanyl is described quantitatively by using a mathematical model. The model is an extension of a previous one reproducing the human ventilatory control system on physiological bases. The model includes three compartments (lung, body tissue and brain tissue), the main mechanisms involved in respiratory regulation (peripheral and central chemoreceptors, and the central hypoxic depression), and local blood flow regulation. Fentanyl effects on respiratory system include a weakening of the peripheral and central chemoreceptor gains on ventilation, a depression of body metabolism, and a direct inhibition of respiratory activity. All parameter values in the model have been chosen in accordance with clinical data from the literature. The model, with suitable values of its parameters, is able to reproduce the main respiratory variables in a wide range of fentanyl plasma concentrations, showing that minute ventilation in spontaneously breathing subjects depends on two antagonistic actions: opiod inhibitory influences, which abate ventilation, and the consequent chemoreflex stimulation. Simulations of resumption of spontaneous breathing after artificial ventilation in anesthetized patients indicate that a safe resumption can be achieved through approaches that increase patient CO/sub 2/ tension, since they shorten the time for chemoreceptor activation to overcome fentanyl-induced inhibition of respiratory activity.
机译:使用数学模型定量描述芬太尼的呼吸抑制作用。该模型是在生理基础上重现人类通风控制系统的前一个模型的扩展。该模型包括三个部分(肺,身体组织和脑组织),参与呼吸调节的主要机制(周围和中央化学感受器以及中枢低氧抑郁症)和局部血流调节。芬太尼对呼吸系统的影响包括通气时周围和中央化学感受器增益的减弱,身体新陈代谢的降低以及呼吸活动的直接抑制。已根据文献中的临床数据选择了模型中的所有参数值。该模型具有适当的参数值,能够在很宽的芬太尼血浆浓度范围内重现主要的呼吸变量,表明自发呼吸的受试者的微小通气取决于两种拮抗作用:阿片类药物的抑制作用,减轻了通气量;以及随之而来的化学反射刺激。对麻醉患者进行人工通气后恢复自主呼吸的模拟表明,通过增加患者CO / sub 2 /张力的方法可以实现安全的恢复,因为它们缩短了化学感受器激活的时间,从而克服了芬太尼诱导的呼吸活动抑制作用。

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