Optimizing target control of the vessel rich group with volatile anesthetics.

The ability to monitor the inspired and expired concentrations of volatile anesthetic gases in real time makes these drugs implicitly targetable. However, the end-tidal concentration only represents the concentration within the brain and the vessel rich group (VRG) at steady state, and very poorly a...

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Publicado en:Journal of Clinical Monitoring & Computing Vol. 33; no. 3; pp. 445 - 455
Autor principal: Connor, Christopher W.
Formato: Journal Article
Publicado: Springer Nature Jun2019
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2019
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      pub: Springer Nature
      place: New York, New York
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        atl: Optimizing target control of the vessel rich group with volatile anesthetics.
      aug:
        au: Connor, Christopher W.
        affil: Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, 75 Francis Street, CWN L1, 02115, Boston, MA, USA
      sug:
        subj:
          Isoflurane Pharmacodynamics
          Anesthetics, Inhalation Pharmacokinetics
          Anesthesia, Inhalation Methods
          Models, Theoretical
          Anesthetics
          Gases
          Signal Processing, Computer Assisted
          Tidal Volume
          Regression
          Algorithms
          Nebulizers and Vaporizers
          Psychological Tests
          Scales
      ab: The ability to monitor the inspired and expired concentrations of volatile anesthetic gases in real time makes these drugs implicitly targetable. However, the end-tidal concentration only represents the concentration within the brain and the vessel rich group (VRG) at steady state, and very poorly approximates the VRG concentration during common dynamic situations such as initial uptake and emergence. How should the vaporization of anesthetic gases be controlled in order to optimally target VRG concentration in clinical practice? Using a generally accepted pharmacokinetic model of uptake and redistribution, a transfer function from the vaporizer setting to the VRG is established and transformed to the time domain. Targeted actuation of the vaporizer in a time-optimal manner is produced by a variable structure, sliding mode controller. Direct mathematical application of the controller produces rapid cycling at the limits of the vaporizer, further prolonged by low fresh gas flows. This phenomenon, known as "chattering", is unsuitable for operating real equipment. Using a simple and clinically intuitive modification to the targeting algorithm, a variable low-pass boundary layer is applied to the actuation, smoothing discontinuities in the control law and practically eliminating chatter without prolonging the time taken to reach the VRG target concentration by any clinically significant degree. A model is derived for optimum VRG-targeted control of anesthetic vaporizers. An alternate and further application is described, in which deliberate perturbation of the vaporization permits non-invasive estimation of parameters such as cardiac output that are otherwise difficult to measure intra-operatively.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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