Tailored Pharmacokinetic model to predict drug trapping in long-term anesthesia

被引:11
作者
Copot, Dana [1 ]
Ionescu, Clara [1 ,2 ]
机构
[1] Univ Ghent, Dept Electromech Syst & Met Engn, Res Grp Dynam Syst & Control, B-9052 Ghent, Belgium
[2] Tech Univ Cluj Napoca, Dept Automat, Cluj Napoca 400114, Romania
关键词
ICU patients; Covid-19; Pandemic context; Patient simulator; Pharmacokinetic model; Calibratio; Fractal inetics; Anomalous diffusion; Anesthesia; DIFFUSION;
D O I
10.1016/j.jare.2021.04.004
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: In long-term induced general anesthesia cases such as those uniquely defined by the ongo-ing Covid-19 pandemic context, the clearance of hypnotic and analgesic drugs from the body follows anomalous diffusion with afferent drug trapping and escape rates in heterogeneous tissues. Evidence exists that drug molecules have a preference to accumulate in slow acting compartments such as muscle and fat mass volumes. Currently used patient dependent pharmacokinetic models do not take into account anomalous diffusion resulted from heterogeneous drug distribution in the body with time vary-ing clearance rates. Objectives: This paper proposes a mathematical framework for drug trapping estimation in PK models for estimating optimal drug infusion rates to maintain long-term anesthesia in Covid-19 patients. We also propose a protocol for measuring and calibrating PK models, along with a methodology to minimize blood sample collection. Methods: We propose a framework enabling calibration of the models during the follow up of Covid-19 patients undergoing anesthesia during their treatment and recovery period in ICU. The proposed model can be easily updated with incoming information from clinical protocols on blood plasma drug concen-tration profiles. Already available pharmacokinetic and pharmacodynamic models can be then calibrated based on blood plasma concentration measurements. Results: The proposed calibration methodology allow to minimize risk for potential over-dosing as clear-ance rates are updated based on direct measurements from the patient. Conclusions: The proposed methodology will reduce the adverse effects related to over-dosing, which allow further increase of the success rate during the recovery period. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of Cairo University.
引用
收藏
页码:27 / 36
页数:10
相关论文
共 67 条
[1]  
A.S. of Health-System Pharmacists, CURR DRUG SHORT PROP
[2]   An efficient algorithm for solving the fractional optimal control of SIRV epidemic model with a combination of vaccination and treatment [J].
Ameen, I ;
Baleanu, Dumitru ;
Ali, Hegagi Mohamed .
CHAOS SOLITONS & FRACTALS, 2020, 137
[3]  
[Anonymous], 2013, HUMAN RESP SYSTEM AN
[4]   Evaluation of respiratory properties by means of fractional order models [J].
Assadi, I. ;
Charef, A. ;
Copot, D. ;
De Keyser, R. ;
Bensouici, T. ;
Ionescu, C. .
BIOMEDICAL SIGNAL PROCESSING AND CONTROL, 2017, 34 :206-213
[5]   Modeling attractors of chaotic dynamical systems with fractal-fractional operators [J].
Atangana, Abdon ;
Qureshi, Sania .
CHAOS SOLITONS & FRACTALS, 2019, 123 :320-337
[6]   NEW FRACTIONAL DERIVATIVES WITH NON-LOCAL AND NON-SINGULAR KERNEL Theory and Application to Heat Transfer Model [J].
Atangana, Abdon ;
Baleanu, Dumitru .
THERMAL SCIENCE, 2016, 20 (02) :763-769
[7]   A new fractional model and optimal control of a tumor-immune surveillance with non-singular derivative operator [J].
Baleanu, D. ;
Jajarmi, A. ;
Sajjadi, S. S. ;
Mozyrska, D. .
CHAOS, 2019, 29 (08)
[8]   Planar System-Masses in an Equilateral Triangle: Numerical Study within Fractional Calculus [J].
Baleanu, Dumitru ;
Ghanbari, Behzad ;
Asad, Jihad H. ;
Jajarmi, Amin ;
Pirouz, Hassan Mohammadi .
CMES-COMPUTER MODELING IN ENGINEERING & SCIENCES, 2020, 124 (03) :953-968
[9]   The fractional features of a harmonic oscillator with position-dependent mass [J].
Baleanu, Dumitru ;
Jajarmi, Amin ;
Sajjadi, Samaneh Sadat ;
Asad, Jihad H. .
COMMUNICATIONS IN THEORETICAL PHYSICS, 2020, 72 (05)
[10]  
Berg J, BIOCHEMISTR