Literature DB >> 10098102

Rapid attainment of steady state plasma drug concentrations within precise limits.

B Korman1, L S Jennings, J R Rigg.   

Abstract

We describe a method of rapidly obtaining a specified steady state plasma concentration of an intravenous drug within precise limits. The technique requires an initial bolus to raise the plasma concentration to the upper limit followed by a series of constant-rate infusions each of which is associated with a minimum plasma concentration equal to the lower limit. The infusion rate is stepped down when the plasma concentration returns to the upper limit. Computer simulation, based on the method, is used to generate plasma concentration-time curves with fluctuations of up to 10% about selected steady state concentrations of amrinone, esmolol, lidocaine, midazolam, propofol, and theophylline. The utility of this general approach to intravenous dosing and potential limitations of the method are discussed.

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Year:  1998        PMID: 10098102     DOI: 10.1023/a:1023285426388

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  22 in total

1.  General derivation of the ideal intravenous drug input required to achieve and maintain a constant plasma drug concentration. Theoretical application to lignocaine therapy.

Authors:  D P Vaughan; G T Tucker
Journal:  Eur J Clin Pharmacol       Date:  1976       Impact factor: 2.953

2.  The diposi tion of morphine in surgical patients.

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Journal:  Clin Pharmacol Ther       Date:  1975-06       Impact factor: 6.875

3.  Induction and maintenance of propofol anaesthesia. A manual infusion scheme.

Authors:  F L Roberts; J Dixon; G T Lewis; R M Tackley; C Prys-Roberts
Journal:  Anaesthesia       Date:  1988-03       Impact factor: 6.955

4.  Rapidly achieved plasma concentration plateaus, with observations on theophylline kinetics.

Authors:  P A Mitenko; R I Ogilvie
Journal:  Clin Pharmacol Ther       Date:  1972 May-Jun       Impact factor: 6.875

5.  A method for achieving rapidly steady-state blood concentrations of I.V. drugs.

Authors:  J R Rigg; T Y Wong
Journal:  Br J Anaesth       Date:  1981-12       Impact factor: 9.166

6.  Intravenous propofol anaesthesia using a computerised infusion system.

Authors:  M White; G N Kenny
Journal:  Anaesthesia       Date:  1990-03       Impact factor: 6.955

7.  Pharmacokinetics of midazolam in total i.v. anaesthesia.

Authors:  P Persson; A Nilsson; P Hartvig; A Tamsen
Journal:  Br J Anaesth       Date:  1987-05       Impact factor: 9.166

8.  Pharmacokinetics as applied to total intravenous anaesthesia. Practical implications.

Authors:  J Schüttler; H Schwilden; H Stoekel
Journal:  Anaesthesia       Date:  1983-07       Impact factor: 6.955

9.  Propofol administered by a manual infusion regimen.

Authors:  J W Sear; J B Glen
Journal:  Br J Anaesth       Date:  1995-04       Impact factor: 9.166

10.  Pharmacokinetics of amrinone during cardiac surgery.

Authors:  J M Bailey; J H Levy; H G Rogers; F Szlam; C C Hug
Journal:  Anesthesiology       Date:  1991-12       Impact factor: 7.892

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  1 in total

1.  Rapid attainment of steady-state plasma drug concentrations within precise limits in multicompartment mammillary systems.

Authors:  B Korman; L S Jennings
Journal:  J Pharmacokinet Biopharm       Date:  1999-06
  1 in total

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