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Adv Exp Med Biol ; 696: 401-10, 2011.
Article in English | MEDLINE | ID: mdl-21431580

ABSTRACT

Peritoneal dialysis-associated peritonitis (PDAP) can be treated using very different regimens of antimicrobial administration, regimens that result in different pharmacokinetic outcomes and systemic exposure levels. Currently, there is no population-level pharmacokinetic framework germane to the treatment of PDAP. We coupled a differential-equation-based model of antimicrobial kinetics to a Monte Carlo simulation framework, and conducted "in silico" clinical trials to explore the anticipated effects of different antimicrobial dosing regimens on relevant pharmacokinetic parameters (AUC/MIC and time greater than 5 ×MIC) and the level of systemic exposure.


Subject(s)
Anti-Infective Agents/pharmacokinetics , Peritonitis/drug therapy , Peritonitis/metabolism , Anti-Infective Agents/administration & dosage , Area Under Curve , Ascitic Fluid/metabolism , Cefazolin/administration & dosage , Cefazolin/pharmacokinetics , Ceftazidime/administration & dosage , Ceftazidime/pharmacokinetics , Clinical Trials as Topic , Computational Biology , Computer Simulation , Dialysis Solutions , Humans , Microbial Sensitivity Tests , Models, Biological , Monte Carlo Method , Peritoneal Dialysis/adverse effects , Peritonitis/etiology , User-Computer Interface
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