基于模拟的 PID 和 LQG 闭环麻醉控制比较分析。

Sourish Chakravarty, Ayan S Waite, John H Abel, Emery N Brown
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摘要

闭环麻醉给药(CLAD)系统可以帮助麻醉医生在较长时间内有效地达到并维持所需的麻醉深度。典型的闭环麻醉给药系统将根据生理信号计算出的麻醉标记作为实时反馈,调整麻醉剂量以达到所需的标记设定点。由于近期文献中报道的 CLAD 系统的控制策略各不相同,因此对常见控制策略进行比较分析非常有用。对于一个非线性植物模型,我们基于成熟的分区药代动力学和西格玛-最大药效学模型,对三种输出反馈线性控制策略的设定点跟踪性能进行了数值分析:比例-积分-派生(PID)控制、线性二次高斯(LQG)控制和具有积分作用的 LQG(ILQG)。具体来说,我们对多个 CLAD 会话进行了数值模拟,模拟的情况是:患者无法获得工厂模型参数,控制器根据标称模型设计,控制器增益在整个会话期间保持不变。根据我们对模型和控制器的选择进行的数值分析,我们推断在精度和偏差方面,PID 控制优于 ILQG,而 ILQG 又优于 LQG。在观测到噪声的情况下,ILQG 可以调整为提供更平滑的输液率,同时获得与 PID 相当的稳态响应。本文报告的数值分析框架和研究结果可帮助 CLAD 开发人员选择控制策略。本文也可作为 CLAD 控制理论的教学论文。
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A simulation-based comparative analysis of PID and LQG control for closed-loop anesthesia delivery.

Closed loop anesthesia delivery (CLAD) systems can help anesthesiologists efficiently achieve and maintain desired anesthetic depth over an extended period of time. A typical CLAD system would use an anesthetic marker, calculated from physiological signals, as real-time feedback to adjust anesthetic dosage towards achieving a desired set-point of the marker. Since control strategies for CLAD vary across the systems reported in recent literature, a comparative analysis of common control strategies can be useful. For a nonlinear plant model based on well-established models of compartmental pharmacokinetics and sigmoid-Emax pharmacodynamics, we numerically analyze the set-point tracking performance of three output-feedback linear control strategies: proportional-integral-derivative (PID) control, linear quadratic Gaussian (LQG) control, and an LQG with integral action (ILQG). Specifically, we numerically simulate multiple CLAD sessions for the scenario where the plant model parameters are unavailable for a patient and the controller is designed based on a nominal model and controller gains are held constant throughout a session. Based on the numerical analyses performed here, conditioned on our choice of model and controllers, we infer that in terms of accuracy and bias PID control performs better than ILQG which in turn performs better than LQG. In the case of noisy observations, ILQG can be tuned to provide a smoother infusion rate while achieving comparable steady state response with respect to PID. The numerical analysis framework and findings reported here can help CLAD developers in their choice of control strategies. This paper may also serve as a tutorial paper for teaching control theory for CLAD.

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