Pharmacodynamic modeling of propofol-induced general anesthesia in young adults.

Sourish Chakravarty, Ksenia Nikolaeva, Devika Kishnan, Francisco J Flores, Patrick L Purdon, Emery N Brown
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引用次数: 6

Abstract

Target controlled infusion (TCI) of intraveneous anesthetics can assist clinical practitioners to provide improved care for General Anesthesia (GA). Pharmacokinetic/Pharmacodynamic (PK/PD) models help in relating the anesthetic drug infusion to observed brain activity inferred from electroencephalogram (EEG) signals. The parameters in popular population PK/PD models for propofol-induced GA (Marsh and Schnider models) are either verified based on proprietary functions of the EEG signal which are difficult to correlate with the neurophysiological models of anesthesia, or the marker itself needs to be estimated simultaneously with the PD model. Both these factors make these existing paradigms challenging to apply in real-time context where a patient-specific tuning of parameters is desired. In this work, we propose a simpler EEG marker from frequency domain description of EEG and develop two corresponding PK/PD modeling approaches which differ in whether they use existing population-level PK models (approach 1) or not (approach 2). We use a simple deterministic parameter estimation approach to identify the unknown PK/PD model parameters from an existing human EEG data-set. We infer that both approaches 1 and 2 yield similar and reasonably good fits to the marker data. This work can be useful in developing patient-specific TCI strategies to induce GA.

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异丙酚诱导青少年全身麻醉的药效学模型。
静脉麻醉药靶控输注(TCI)可以帮助临床医生为全身麻醉(GA)提供更好的护理。药代动力学/药效学(PK/PD)模型有助于将麻醉药物输注与从脑电图(EEG)信号推断的观察到的脑活动联系起来。常用的异丙酚诱导GA的群体PK/PD模型(Marsh和Schnider模型)中的参数要么是基于脑电图信号的专有函数来验证的,而这些函数很难与麻醉的神经生理模型相关联,要么是标记物本身需要与PD模型同时估计。这两个因素使得现有的范例难以在实时环境中应用,因为在实时环境中需要对特定于患者的参数进行调整。在这项工作中,我们从EEG的频域描述中提出了一种更简单的EEG标记,并开发了两种相应的PK/PD建模方法,不同的是它们是否使用现有的群体水平的PK模型(方法1)或不使用方法2)。我们使用一种简单的确定性参数估计方法从现有的人类EEG数据集中识别未知的PK/PD模型参数。我们推断,两种方法1和2产生相似的,相当好的拟合标记数据。这项工作可用于制定患者特异性TCI策略以诱导GA。
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