Development of a semimechanistic model to describe the pharmacokinetics of gentamicin in patients receiving Hemodialysis


Autoria(s): Dang, Lily; Duffull, Stephen
Contribuinte(s)

Dr Lisa L von Moltke

Data(s)

01/01/2006

Resumo

The aim of this study was to ascertain the most suitable dosing schedule for gentamicin in patients receiving hemodialysis. We developed a model to describe the concentrationtime course of gentamicin in patients receiving hemodialysis. Using the model, an optimal dosing schedule was evaluated. Various dosing regimens were compared in their ability to achieve maximum concentration (C-max, >= 8 mg/L) and area under the concentration time-curve (AUC >= 70 mg(.)h/L and <= 120 mg(.)h/L per 24 hours). The model was evaluated by comparing model predictions against real data collected retrospectively. Simulations from the model confirmed the benefits of predialysis dosing. The mean optimal dose was 230 mg administered immediately before dialysis. The model was found to have good predictive performance when simulated data were compared to data observed in real patients. In summary, a model was developed that describes gentamicin pharmacokinetics in patients receiving hemodialysis. Predialysis dosing provided a superior pharmacokinetic profile than did postdialysis dosing.

Identificador

http://espace.library.uq.edu.au/view/UQ:79848

Idioma(s)

eng

Publicador

Sage Publications Inc

Palavras-Chave #Gentamicin #Pharmacokinetics #Hemodialysis #Pharmacology & Pharmacy #Daily Aminoglycoside Therapy #Stage Renal-disease #Dialysis #Failure #Nephrotoxicity #Ototoxicity #Tobramycin #Clearance #Regimen #Rates #C1 #320501 Pharmaceutical Sciences and Pharmacy #730103 Blood disorders
Tipo

Journal Article