• DocumentCode
    1082404
  • Title

    The hybrid model: a new pharmacokinetic model for computer-controlled infusion pumps

  • Author

    Wada, D. Russell ; Ward, Denham S.

  • Author_Institution
    Dept. of Anesthesia, Stanford Univ. Sch. of Med., Palo Alto, CA, USA
  • Volume
    41
  • Issue
    2
  • fYear
    1994
  • Firstpage
    134
  • Lastpage
    142
  • Abstract
    Classical pharmacokinetic models used in computer-controlled infusion pumps (CCIPs) assume instantaneous mixing of drug in blood; however, the average recirculation time of blood in man is approximately one minute. To investigate the effects of recirculation dynamics on the transient performance of CCIPs the authors propose a hybrid physiologically-based pharmacokinetic model for the narcotic alfentanil. A three-compartment model was derived from the response of the hybrid model to a short infusion and used to compute a CCIP infusion targeting 450 μg/l. For this infusion, the hybrid model predicts that the arterial plasma concentration will overshoot the target concentration by 39 percent with an average prediction error of 3 percent. The overshoot and average prediction error increase to 100 and 25 percent respectively when using a three-compartment pharmacokinetic model derived from a bolus. The overshoot can be reduced by decreasing the maximum possible infusion rate, or by increasing the zero-order hold infusion interval.
  • Keywords
    biomedical equipment; computerised control; patient treatment; physiological models; pumps; 1 min; alfentanil; computer-controlled infusion pumps; hybrid model; instantaneous drug/blood mixing; intravenous drugs; narcotic; pharmacokinetic model; prediction error; recirculation dynamics; zero-order hold infusion interval; Anesthesia; Blood; Centralized control; Committee on Communications and Information Policy; Control systems; Differential equations; Drugs; History; Plasma simulation; Predictive models; Alfentanil; Computer Simulation; Drug Therapy, Computer-Assisted; Infusion Pumps; Infusions, Intravenous; Models, Biological; Pharmacokinetics;
  • fLanguage
    English
  • Journal_Title
    Biomedical Engineering, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0018-9294
  • Type

    jour

  • DOI
    10.1109/10.284924
  • Filename
    284924