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Population Pharmacokinetics of Trimethoprim-Sulfamethoxazole in Infants and Children

Authors :
Ram Yogev
Barrie Harper
Jeffrey Peter Mitchell
Daniel Gonzalez
Susan R. Mendley
Andrew M. Atz
Julie Autmizguine
Janice E. Sullivan
Andrew Lewandowski
Paula Delmore
Brenda B. Poindexter
Michael Cohen-Wolkowiez
Chiara Melloni
Christoph P. Hornik
Samantha H Dallefeld
Amira Al-Uzri
Source :
Antimicrobial Agents and Chemotherapy. 62
Publication Year :
2018
Publisher :
American Society for Microbiology, 2018.

Abstract

Trimethoprim (TMP)-sulfamethoxazole (SMX) is used to treat various types of infections, including community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) and Pneumocystis jirovecii infections in children. Pharmacokinetic (PK) data for infants and children are limited, and the optimal dosing is not known. We performed a multicenter, prospective PK study of TMP-SMX in infants and children. Separate population PK models were developed for TMP and SMX administered by the enteral route using nonlinear mixed-effects modeling. Optimal dosing was determined on the basis of the matching adult TMP exposure and attainment of the surrogate pharmacodynamic (PD) target for efficacy, a free TMP concentration above the MIC over 50% of the dosing interval. Data for a total of 153 subjects (240 samples for PK analysis) with a median postnatal age of 8 years (range, 0.1 to 20 years) contributed to the analysis for both drugs. A one-compartment model with first-order absorption and elimination characterized the TMP and SMX PK data well. Weight was included in the base model for clearance (CL/ F ) and volume of distribution ( V / F ). Both TMP and SMX CL/ F increased with age. In addition, TMP and SMX CL/ F were inversely related to the serum creatinine and albumin concentrations, respectively. The exposure achieved in children after oral administration of TMP-SMX at 8/40 mg/kg of body weight/day divided into administration every 12 h matched the exposure achieved in adults after administration of TMP-SMX at 320/1,600 mg/day divided into administration every 12 h and achieved the PD target for bacteria with an MIC of 0.5 mg/liter in >90% of infants and children. The exposure achieved in children after oral administration of TMP-SMX at 12/60 and 15/75 mg/kg/day divided into administration every 12 h matched the exposure achieved in adults after administration of TMP-SMX at 640/3,200 mg/day divided into administration every 12 h in subjects 6 to

Details

ISSN :
10986596 and 00664804
Volume :
62
Database :
OpenAIRE
Journal :
Antimicrobial Agents and Chemotherapy
Accession number :
edsair.doi.dedup.....852b9bec0565aa27465e740415e34be0
Full Text :
https://doi.org/10.1128/aac.01813-17