Effect of severity disease on the pharmacokinetics of cefuroxime in children with multiple organ system failure

9Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

The aim of the present study was to investigate if the severity of illness affected the pharmacokinetics of cefuroxime in 11 children diagnosed with multiple organ system failure. The patients were assigned to a severely ill group (group 1), a very severely ill group (group 2), or a control group (group 0). Blood samples were taken and cefuroxime concentrations were measured in plasma by HPLC after the first intravenous infusion of 100 mg of cefuroxime per kg of body weight. The pharmacokinetic profile of cefuroxime exhibited both one and two compartmental distribution. Statistically significant differences between the pharmacokinetic parameters of the severe (group 1) and the very severe patients (group 2) were found, and significant differences (p<0.05) in the pharmacokinetic parameters between groups 1 and 2 vs. the control group were observed for most of the parameters analyzed. However, there was no statistical difference in clearance between group 1 and the control group. The data indicate that the pharmacokinetic differences determined by severity of disease are useful for establishing an individualized regimen dosage in children with multiple organ system failure. © 2008 Pharmaceutical Society of Japan.

Cite

CITATION STYLE

APA

Olguín, H. J., Asseff, I. L., Vieyra, A. C., Pérez, A. G., Saldaña, N. G., Quesada, A. C., & Guillé, G. P. (2008). Effect of severity disease on the pharmacokinetics of cefuroxime in children with multiple organ system failure. Biological and Pharmaceutical Bulletin, 31(2), 316–320. https://doi.org/10.1248/bpb.31.316

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free