Literature DB >> 6509862

Two prospective dosing methods for nortriptyline.

P J Perry, J L Browne, B Alexander, M T Tsuang, A D Sherman, F J Dunner.   

Abstract

This study compared two prospective pharmacokinetic dosing methods to predict steady-state concentrations of nortriptyline. One method required multiple determinations of the nortriptyline plasma concentration to estimate the drug's steady-state concentration. The second method required a single nortriptyline concentration drawn at a fixed time, preferably 36 hours, following a nortriptyline test dose. The 36-hour nortriptyline plasma concentrations (NTP 36h) were substituted into the straight-line equation of Cssav = 17.2 + 3.74 (NTP 36h), where Cssav is the average steady-state concentration for a 100 mg/day dose of nortriptyline. No differences were noted between the observed steady-state nortriptyline concentration of 121 +/- 19 ng/ml, the 36-hour single-point prediction mean concentration of 121 +/- 21 ng/ml, or the multiple-point prediction mean concentration of 122 +/- 19 ng/ml. Because of the similar findings between the two methods, the clinical advantages and disadvantages of each kinetic approach are discussed to put these prospective dosing protocols into their proper perspective.

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Year:  1984        PMID: 6509862     DOI: 10.2165/00003088-198409060-00005

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  11 in total

1.  Pharmacokinetics of nortriptyline in man after single and multiple oral doses: the predictability of steady-state plasma concentrations from single-dose plasma-level data.

Authors:  B Alexanderson
Journal:  Eur J Clin Pharmacol       Date:  1972-03       Impact factor: 2.953

2.  Pharmacokinetic protocol for predicting plasma nortriptyline levels.

Authors:  J L Browne; P J Perry; B Alexander; A D Sherman; M T Tsuang; F J Dunner; B M Pfohl
Journal:  J Clin Psychopharmacol       Date:  1983-12       Impact factor: 3.153

3.  Nortriptyline in depressed patients with high plasma levels. II.

Authors:  R Braithwaite; S Montgomery; S Dawling
Journal:  Clin Pharmacol Ther       Date:  1978-03       Impact factor: 6.875

4.  Indications and guidelines for plasma tricyclic antidepressant concentration monitoring.

Authors:  S C Risch; N H Kalin; D S Janowsky; L Y Huey
Journal:  J Clin Psychopharmacol       Date:  1981-03       Impact factor: 3.153

5.  Prediction of maintenance dose required to attain a desired drug concentration at steady-state from a single determination of concentration after an initial dose.

Authors:  J T Slattery; M Gibaldi; J R Koup
Journal:  Clin Pharmacokinet       Date:  1980 Jul-Aug       Impact factor: 6.447

6.  Nortriptyline therapy in elderly patients: dosage prediction after single dose pharmacokinetic study.

Authors:  S Dawling; P Crome; R A Braithwaite; R R Lewis
Journal:  Eur J Clin Pharmacol       Date:  1980-08       Impact factor: 2.953

7.  Prediction of individual dosage of nortriptyline.

Authors:  T B Cooper; G M Simpson
Journal:  Am J Psychiatry       Date:  1978-03       Impact factor: 18.112

8.  A sensitive method for the determination of amitriptyline and nortriptyline in human plasma.

Authors:  T B Cooper; D Allen; G M Simpson
Journal:  Psychopharmacol Commun       Date:  1976

9.  Single-dose kinetics predict steady-state concentrations on imipramine and desipramine.

Authors:  W Z Potter; A P Zavadil; I J Kopin; F K Goodwin
Journal:  Arch Gen Psychiatry       Date:  1980-03

10.  Factors influencing nortriptyline steady-state kinetics: plasma and saliva levels.

Authors:  P Kragh-Sørensen; N E Larsen
Journal:  Clin Pharmacol Ther       Date:  1980-12       Impact factor: 6.875

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  1 in total

Review 1.  Clinical pharmacokinetic considerations in the elderly. An update.

Authors:  S Dawling; P Crome
Journal:  Clin Pharmacokinet       Date:  1989-10       Impact factor: 6.447

  1 in total

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