Literature DB >> 28910514

Pharmacokinetics of single-dose ceftaroline fosamil in children with cystic fibrosis.

Jennifer Le1, John S Bradley2,3, Sara Hingtgen3, Shannon Skochko3, Nanette Black3, Ronald N Jones4, Meerana Lim5, Edmund V Capparelli1,2.   

Abstract

BACKGROUND: Single-dose pharmacokinetics (PK) and safety of ceftaroline fosamil with population pharmacokinetic/pharmacodynamic (PK/PD) modeling for staphylococcal pneumonia was performed in children with CF.
METHODS: Subjects between 6 and 18 years old were evaluated in this phase 1, open-label, single-dose, prospective study using 10 mg/kg (up to 600 mg). Non-compartmental analysis and population-based PK analyses with Monte Carlo simulation (for doses 8-20 mg/kg every 8 h, infused over 1-4 h) were conducted.
RESULTS: A total of 20 subjects were enrolled. The median age and weight were 12 yr (range 6.3-17.4) and 38.7 kg (range 17.8-94.3), respectively. A 3-compartment linear model incorporating age and weight provided the best fit for the data. Comparing children 6 to <12 years to those 12 to <18 years, the mean posthoc Bayesian parameter estimates for total volume of distribution (VT ) were 0.32 ± 0.05 L/kg versus 0.32 ± 0.04 L/kg, P = 0.7; and total Clearance (CLT ), 0.50 ± 0.10 L/h/kg versus 0.30 ± 0.07 L/h/kg, P = 0.001. Using susceptibility data from pediatric MRSA lower respiratory tract isolates, 8 mg/kg (maximum of 1000 mg per dose) infused over 1 h every 8 h achieved free-drug plasma concentrations above the minimum inhibitory concentration for ≥60% of the dosing interval in at least 95% of virtual subjects.
CONCLUSIONS: Since children with CF have increased ceftaroline CL compared with published data from non-CF children; greater dosages may be required in children with CF to achieve adequate exposure in the treatment of MRSA pneumonia. Pharmacodynamic-based dosing predicts that dosing should also be based on the patient's MRSA MIC.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  ceftaroline; cystic fibrosis; methicillin-resistant Staphylococcus aureus; pharmacokinetic children

Mesh:

Substances:

Year:  2017        PMID: 28910514     DOI: 10.1002/ppul.23827

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  4 in total

Review 1.  Pharmacokinetic and Pharmacodynamic Optimization of Antibiotic Therapy in Cystic Fibrosis Patients: Current Evidences, Gaps in Knowledge and Future Directions.

Authors:  Charlotte Roy; Manon Launay; Sophie Magréault; Isabelle Sermet-Gaudelus; Vincent Jullien
Journal:  Clin Pharmacokinet       Date:  2021-01-24       Impact factor: 6.447

Review 2.  One Size Fits All? Application of Susceptible-Dose-Dependent Breakpoints to Pediatric Patients and Laboratory Reporting.

Authors:  Lindsey E Nielsen; Jeanne B Forrester; Jennifer Ellis Girotto; Aimee M Dassner; Romney Humphries
Journal:  J Clin Microbiol       Date:  2019-12-23       Impact factor: 5.948

Review 3.  Antimicrobial Treatment of Staphylococcus aureus in Patients With Cystic Fibrosis.

Authors:  Susanna Esposito; Guido Pennoni; Valeria Mencarini; Nicola Palladino; Laura Peccini; Nicola Principi
Journal:  Front Pharmacol       Date:  2019-08-07       Impact factor: 5.810

Review 4.  Ceftaroline Fosamil for Treatment of Pediatric Complicated Skin and Soft Tissue Infections and Community-Acquired Pneumonia.

Authors:  Susanna Esposito; Timothy J Carrothers; Todd Riccobene; Gregory G Stone; Michal Kantecki
Journal:  Paediatr Drugs       Date:  2021-08-31       Impact factor: 3.022

  4 in total

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