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  • Mullins, Victor M.
     
     Subjects
     
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  • Biological control systems -- Mathematical models.
     
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  • Heart -- Mechanical properties -- Computer simulation
     
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  • Heart -- Effect of drugs on
     
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  • Cardiovascular pharmacology
     
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  • MSP Thesis.
     
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  •  Design and applicati...
     
     
     
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    Design and application of a pharmacological control module for a perfusion simulator / by Victor M. Mullins.
    by Mullins, Victor M.
    Subjects
  • Biological control systems -- Mathematical models.
  •  
  • Heart -- Mechanical properties -- Computer simulation
  •  
  • Heart -- Effect of drugs on
  •  
  • Cardiovascular pharmacology
  •  
  • MSP Thesis.
  • Description: 
    iv, 86 leaves : Ill. ; 28 cm.
    Contents: 
    Clinical advisor: Michael Gough
    Committee members: Dr. Vincent Canino, Dr. Steven Barnicki, Daniel Minkel
    Introduction -- Materials & methods -- Results -- Discussion -- References -- Appendix A) Instructions for authors B) List of changes to software code C) Software code added of changed.
    The Perfusion Simulator being developed at the Milwaukee School of Engineering is comprised of computer software as well as hydraulic and electronic hardware. A cardiopulmonary bypass simulator can be useful to train a perfusion student without an element of risk to a patient. Cardiopulmonary bypass alters the pharmacology of drugs. This is caused by such factors as hypothermia, hemodilution, and contact with the cardiopulmonary bypass apparatus. Much of the changes in pharmacology of drugs while on bypass has not been quantitatively studied. There is a large degree of variability in drug pharmacokinetics and pharmacodynamics among patients during cardiopulmonary bypass as well as among patients in general. Mathematical models were developed to simulate the actions of three drugs which affect the systemic vascular resistance of a patient. The drugs modeled are isoflurane, nitroglycerin, and phenylephrine. For isoflurane, a pharmacodynamic model was used. Both nitroglycerin and phenylephrine were modeled with pharmacokinetic-pharmacodynamic models.
    After a dose of a specific drug is selected, the resulting effect occurs which in turn interacts with the main module of perfusion software to control a fluid valve which decreases or increases the resistance in the patient model.
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    Walter Schroeder LibraryMaster's ThesesAC805 .M85 1996AvailableAdd Copy to MyList

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