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Time of effect duration and administration interval for sitagliptin in patients with kidney failure.
Keller, Frieder; Hartmann, Bertram; Czock, David.
Afiliação
  • Keller F; Division of Nephrology, Department of Internal Medicine 1, University Hospital, Albert Einstein Allee 23, 89070, Ulm, Germany, frieder.keller@uni-ulm.de.
Eur J Drug Metab Pharmacokinet ; 39(2): 77-85, 2014 Jun.
Article em En | MEDLINE | ID: mdl-24353117
ABSTRACT
A measure correlating the time course of the effect with the time course of concentrations could be helpful in drug dosing. We propose a new equation with explicit solutions for calculating the effect duration. A specific effect fraction is selected (fr) and the time of fractional effect duration (TED.fr) can be derived as a function of the elimination half-life by combining linear elimination kinetics with sigmoid effect dynamics. This new measure is applied to the example of sitagliptin, whose elimination half-life increases from 10.1 to 28.4 h in patients with kidney failure. Under normal multiple-dose conditions, the 24-h sitagliptin administration interval corresponds to a 0.90 time of fractional effect duration (TED.90). A dose reduction to one-fourth or 25 mg every 24 h is proposed for patients with kidney failure; this results in a TED.90 of 45 h, i.e. 21 h longer than the proposed 24-h administration interval (+88 %). The proportional dosing alternative of 100 mg every 96 h would result in a TED.90 of 64 h, which is 32 h less than the 96-h administration interval (-33 %). With a half dose of 50 mg and a doubled administration interval of 48 h, the TED.90 is 51 h in kidney failure, only 3 h longer than the latter administration interval (+6 %). We conclude that our general equation can be applied to rapidly calculate the specific time of effect duration for the different dose schedules.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazinas / Triazóis / Insuficiência Renal Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazinas / Triazóis / Insuficiência Renal Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article