Population Pharmacokinetic Modeling of Total and Free Ceftriaxone in Critically Ill Children and Young Adults and Monte Carlo Simulations Support Twice Daily Dosing for Target Attainment

Author:

Tang Girdwood Sonya123ORCID,Dong Min23ORCID,Tang Peter34,Stoneman Erin5,Jones Rhonda5,Yunger Toni5,Ostermeier Austin13,Curry Calise1,Forton Melissa1,Hail Traci1,Mullaney Randi1,Lahni Patrick5ORCID,Punt Nieko67ORCID,Kaplan Jennifer35ORCID,Vinks Alexander A.23ORCID

Affiliation:

1. Division of Hospital Medicine, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

2. Division of Clinical Pharmacology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

3. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA

4. Division of Pathology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

5. Division of Critical Care Medicine, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

6. Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands

7. Medimatics, Maastricht, the Netherlands

Abstract

Critical illness, including sepsis, causes significant pathophysiologic changes that alter the pharmacokinetics (PK) of antibiotics. Ceftriaxone is one of the most prescribed antibiotics in patients admitted to the pediatric intensive care unit (PICU).

Funder

HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

HHS | NIH | National Center for Advancing Translational Sciences

Cincinnati Children's Hospital Medical Center

Gerber Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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