Population pharmacokinetics of tobramycin in patients with and without cystic fibrosis

Hennig, S., Standing, J.F., Staatz, C.E. and Thomson, A.H. (2013) Population pharmacokinetics of tobramycin in patients with and without cystic fibrosis. Clinical Pharmacokinetics, 52(4), pp. 289-301. (doi: 10.1007/s40262-013-0036-y)

Abstract

Background and Objectives: While several studies have examined the pharmacokinetics of tobramycin in patients with cystic fibrosis (CF), there is no consensus on whether they differ in patients with and without CF. The objectives of this study were to identify covariates which explain pharmacokinetic variability and to examine whether having the disease CF in itself alters these relationships and drug dose requirements. Methods: To investigate this issue, a population pharmacokinetic meta-analysis of data from eight centres was undertaken. NONMEM® 7.2 was used to analyse the data, which comprised 4,514 concentration–time measurements from 465 adults and children with CF and 1,095 concentration–time measurements from 267 adults and children without CF. Results: Tobramycin disposition was well described by a two-compartment model with first-order elimination. Patient age, fat-free mass, serum creatinine concentration and sex were identified as significant covariates in the final model. Fat-free mass was superior to total bodyweight as a descriptor of clearance, volume of distribution of the central and peripheral compartments and inter-compartmental clearance. CF as an independent disease-specific factor had no significant influence on the pharmacokinetics of tobramycin at any stage during covariate model building. An optimal dose of 11 mg/kg every 24 h was defined for CF patients using a utility function approach. Conclusion: The pharmacokinetics of tobramycin do not differ significantly in CF patients compared with patients without CF when subject age, fat-free mass, sex and renal function are taken into consideration. Variations in tobramycin dosing between CF and non-CF patients should therefore reflect target concentrations or exposures based on differences in expected pathogen sensitivity and not the presence of CF.

• Item Type: Articles
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Thomson, Miss Alison
• Authors: Hennig, S., Standing, J.F., Staatz, C.E., and Thomson, A.H.
• College/School: College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
• Journal Name: Clinical Pharmacokinetics
• ISSN: 0312-5963
• ISSN (Online): 1179-1926