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Automated multi-variable anesthesia : from physiological model to control strategies Hosseinirad, Sara
Abstract
The automation of intravenous anesthesia is a complex control problem hindered by significant inter-individual variability, model uncertainty, and surgical disturbances. While classical systems improve precision, their reliance on generalized population-based models limits adaptation to individual patient responses. This thesis systematically overcomes these challenges, progressing from an analysis of population-based models to the development and validation of a novel, adaptive framework for multi-variable anesthesia. We critically evaluate whether more complex Pharmacokinetic (PK) models are inherently superior for control system design due to their ability to capture demographic-based variability in response. A rigorous comparison reveals that the choice of the PK model does not significantly reduce
control-relevant variability. This highlights the fundamental need for robust, adaptive feedback systems rather than sole reliance on achieving model perfection. To facilitate the development of such a system, we designed and validated the Anesthesia Response Simulator (AReS). AReS provides a realistic in-silico environment by incorporating state-of-the-art models for nonlinear drug interactions, simulating surgical disturbances, and including a diverse set of patient-specific models to simulate variability beyond demographics. The primary contribution of this thesis is a novel, hierarchical control framework that merges model-based control with data-driven intelligence. This architecture features a safety-constrained Generalized Predictive Controller (GPC) to manage the multi-variable administration of drugs for hypnosis, nociception, and hemodynamics. A high-level Reinforcement Learning agent acts as an intelligent supervisor, learning an adaptive policy to dynamically tune the GPC’s parameters. Evaluated using AReS across a diverse cohort of virtual patients and surgical scenarios, this adaptive framework demonstrated superior performance over a fixed-parameter baseline. It achieved faster induction and maintained physiological stability more consistently despite surgical stimuli. The system successfully adapts to different phases of anesthesia despite inter-individual response variability, demonstrating a capacity for personalization that presents a viable pathway toward safer, more reliable automated anesthesia. Furthermore, a theoretical investigation within a multi-agent framework demonstrated that formulating the problem to guarantee convergence of data-driven algorithms would require an overly simplistic formulation of this complex problem. This finding justifies our focus on rigorous experimental validation for the proposed hierarchical framework.
Item Metadata
| Title |
Automated multi-variable anesthesia : from physiological model to control strategies
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| Creator | |
| Supervisor | |
| Publisher |
University of British Columbia
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| Date Issued |
2025
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| Description |
The automation of intravenous anesthesia is a complex control problem hindered by significant inter-individual variability, model uncertainty, and surgical disturbances. While classical systems improve precision, their reliance on generalized population-based models limits adaptation to individual patient responses. This thesis systematically overcomes these challenges, progressing from an analysis of population-based models to the development and validation of a novel, adaptive framework for multi-variable anesthesia. We critically evaluate whether more complex Pharmacokinetic (PK) models are inherently superior for control system design due to their ability to capture demographic-based variability in response. A rigorous comparison reveals that the choice of the PK model does not significantly reduce
control-relevant variability. This highlights the fundamental need for robust, adaptive feedback systems rather than sole reliance on achieving model perfection. To facilitate the development of such a system, we designed and validated the Anesthesia Response Simulator (AReS). AReS provides a realistic in-silico environment by incorporating state-of-the-art models for nonlinear drug interactions, simulating surgical disturbances, and including a diverse set of patient-specific models to simulate variability beyond demographics. The primary contribution of this thesis is a novel, hierarchical control framework that merges model-based control with data-driven intelligence. This architecture features a safety-constrained Generalized Predictive Controller (GPC) to manage the multi-variable administration of drugs for hypnosis, nociception, and hemodynamics. A high-level Reinforcement Learning agent acts as an intelligent supervisor, learning an adaptive policy to dynamically tune the GPC’s parameters. Evaluated using AReS across a diverse cohort of virtual patients and surgical scenarios, this adaptive framework demonstrated superior performance over a fixed-parameter baseline. It achieved faster induction and maintained physiological stability more consistently despite surgical stimuli. The system successfully adapts to different phases of anesthesia despite inter-individual response variability, demonstrating a capacity for personalization that presents a viable pathway toward safer, more reliable automated anesthesia. Furthermore, a theoretical investigation within a multi-agent framework demonstrated that formulating the problem to guarantee convergence of data-driven algorithms would require an overly simplistic formulation of this complex problem. This finding justifies our focus on rigorous experimental validation for the proposed hierarchical framework.
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| Genre | |
| Type | |
| Language |
eng
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| Date Available |
2026-01-05
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| Provider |
Vancouver : University of British Columbia Library
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| Rights |
Attribution-NonCommercial-NoDerivatives 4.0 International
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| DOI |
10.14288/1.0451115
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| URI | |
| Degree (Theses) | |
| Program (Theses) | |
| Affiliation | |
| Degree Grantor |
University of British Columbia
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| Graduation Date |
2026-05
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| Campus | |
| Scholarly Level |
Graduate
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| Rights URI | |
| Aggregated Source Repository |
DSpace
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Rights
Attribution-NonCommercial-NoDerivatives 4.0 International