Literature DB >> 1815045

An approximate model-independent method to maintain constant plasma levels of intravenous drugs.

J M Bailey1.   

Abstract

To rapidly achieve and maintain constant plasma concentrations most intravenous drugs must be administered as an initial bolus followed by a combination of exponentially declining plus constant-rate infusions. In the clinical practice of anesthesia and critical care medicine this is often not practical without specialized equipment. In this paper a simpler approach of maintaining approximately constant plasma concentrations is developed using a loading dose with a two-stage infusion scheme (an initial rapid infusion reduced at a given time to a lower rate). Equations are developed for determining the rate of the infusions as well as the duration of the initial infusion by equating moments of the Laplace transform of the approximate infusion to the moments of the Laplace transform of an exact solution. This approach is independent of models and uses as parameters the moments of the curve relating the concentration following a single iv dose of unit magnitude as a function of time. The accuracy of this technique was assessed by computer simulation.

Mesh:

Year:  1991        PMID: 1815045     DOI: 10.1007/BF01080871

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


  10 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.  A linear recirculation model for drug disposition.

Authors:  D J Cutler
Journal:  J Pharmacokinet Biopharm       Date:  1979-02

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Authors:  J G Wagner
Journal:  Clin Pharmacol Ther       Date:  1974-10       Impact factor: 6.875

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Authors:  E Krüger-Thiemer
Journal:  Eur J Pharmacol       Date:  1968-10       Impact factor: 4.432

5.  Computer-assisted continuous infusions of fentanyl during cardiac anesthesia: comparison with a manual method.

Authors:  J M Alvis; J G Reves; A V Govier; P G Menkhaus; C E Henling; J A Spain; E Bradley
Journal:  Anesthesiology       Date:  1985-07       Impact factor: 7.892

6.  Automated gas chromatography for studies of midazolam pharmacokinetics.

Authors:  D J Greenblatt; A Locniskar; H R Ochs; P M Lauven
Journal:  Anesthesiology       Date:  1981-08       Impact factor: 7.892

7.  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

8.  Pharmacokinetics of fentanyl administered by computer-controlled infusion pump.

Authors:  S L Shafer; J R Varvel; N Aziz; J C Scott
Journal:  Anesthesiology       Date:  1990-12       Impact factor: 7.892

9.  Pharmacokinetic model-driven infusion of fentanyl: assessment of accuracy.

Authors:  P S Glass; J R Jacobs; L R Smith; B Ginsberg; T J Quill; S A Bai; J G Reves
Journal:  Anesthesiology       Date:  1990-12       Impact factor: 7.892

10.  Intravenous fentanyl kinetics.

Authors:  D A McClain; C C Hug
Journal:  Clin Pharmacol Ther       Date:  1980-07       Impact factor: 6.875

  10 in total
  1 in total

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

Authors:  B Korman; L S Jennings; J R Rigg
Journal:  J Pharmacokinet Biopharm       Date:  1998-06
  1 in total

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