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Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants.

Publication ,  Conference
Ganguly, S; Edginton, AN; Gerhart, JG; Cohen-Wolkowiez, M; Greenberg, RG; Gonzalez, D ...
Published in: Clin Pharmacokinet
December 2021

BACKGROUND: Meropenem is a broad-spectrum carbapenem antibiotic approved by the US Food and Drug Administration for use in pediatric patients, including treating complicated intra-abdominal infections in infants < 3 months of age. The impact of maturation in glomerular filtration rate and tubular secretion by renal transporters on meropenem pharmacokinetics, and the effect on meropenem dosing, remains unknown. We applied physiologically based pharmacokinetic (PBPK) modeling to characterize the disposition of meropenem in preterm and term infants. METHODS: An adult meropenem PBPK model was developed in PK-Sim® (Version 8) and scaled to infants accounting for renal transporter ontogeny and glomerular filtration rate maturation. The PBPK model was evaluated using 645 plasma concentrations from 181 infants (gestational age 23-40 weeks; postnatal age 1-95 days). The PBPK model-based simulations were performed to evaluate meropenem dosing in the product label for infants < 3 months of age treated for complicated intra-abdominal infections. RESULTS: Our model predicted plasma concentrations in infants in agreement with the observed data (average fold error of 0.90). The PBPK model-predicted clearance in a virtual infant population was successfully able to capture the post hoc estimated clearance of meropenem in this population, estimated by a previously published model. For 90% of virtual infants, a 4-mg/L target plasma concentration was achieved for > 50% of the dosing interval following product label-recommended dosing. CONCLUSIONS: Our PBPK model supports the meropenem dosing regimens recommended in the product label for infants <3 months of age.

Duke Scholars

Published In

Clin Pharmacokinet

DOI

EISSN

1179-1926

Publication Date

December 2021

Volume

60

Issue

12

Start / End Page

1591 / 1604

Location

Switzerland

Related Subject Headings

  • Young Adult
  • Pharmacology & Pharmacy
  • Models, Biological
  • Middle Aged
  • Meropenem
  • Kidney
  • Intraabdominal Infections
  • Infant, Newborn
  • Infant
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Ganguly, S., Edginton, A. N., Gerhart, J. G., Cohen-Wolkowiez, M., Greenberg, R. G., Gonzalez, D., & Best Pharmaceuticals for Children Act-Pediatric Trials Network Steering Committee. (2021). Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants. In Clin Pharmacokinet (Vol. 60, pp. 1591–1604). Switzerland. https://doi.org/10.1007/s40262-021-01046-6
Ganguly, Samit, Andrea N. Edginton, Jacqueline G. Gerhart, Michael Cohen-Wolkowiez, Rachel G. Greenberg, Daniel Gonzalez, and Best Pharmaceuticals for Children Act-Pediatric Trials Network Steering Committee. “Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants.” In Clin Pharmacokinet, 60:1591–1604, 2021. https://doi.org/10.1007/s40262-021-01046-6.
Ganguly S, Edginton AN, Gerhart JG, Cohen-Wolkowiez M, Greenberg RG, Gonzalez D, et al. Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants. In: Clin Pharmacokinet. 2021. p. 1591–604.
Ganguly, Samit, et al. “Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants.Clin Pharmacokinet, vol. 60, no. 12, 2021, pp. 1591–604. Pubmed, doi:10.1007/s40262-021-01046-6.
Ganguly S, Edginton AN, Gerhart JG, Cohen-Wolkowiez M, Greenberg RG, Gonzalez D, Best Pharmaceuticals for Children Act-Pediatric Trials Network Steering Committee. Physiologically Based Pharmacokinetic Modeling of Meropenem in Preterm and Term Infants. Clin Pharmacokinet. 2021. p. 1591–1604.
Journal cover image

Published In

Clin Pharmacokinet

DOI

EISSN

1179-1926

Publication Date

December 2021

Volume

60

Issue

12

Start / End Page

1591 / 1604

Location

Switzerland

Related Subject Headings

  • Young Adult
  • Pharmacology & Pharmacy
  • Models, Biological
  • Middle Aged
  • Meropenem
  • Kidney
  • Intraabdominal Infections
  • Infant, Newborn
  • Infant
  • Humans