Literature DB >> 32601155

Population Pharmacokinetics and Target Attainment of Cefepime in Critically Ill Patients and Guidance for Initial Dosing.

Mohammad H Al-Shaer1,2, Michael N Neely3, Jiajun Liu4,5,6, Kartikeya Cherabuddi7, Veena Venugopalan2, Nathaniel J Rhodes4,5,6, Kenneth Klinker2, Marc H Scheetz4,5,6, Charles A Peloquin8,2.   

Abstract

Cefepime is commonly used in the intensive care unit (ICU) to treat bacterial infections. The time during which the free cefepime concentration is above the MIC (fT>MIC) should be optimized to increase the efficacy of the regimen. We aim to optimize the exposure of cefepime in ICU patients by using population pharmacokinetic (PK) modeling and simulations. Two data sets were included in this study. The first was a prospective study of pediatric patients who received cefepime at 50 mg/kg of body weight and had extensive PK sampling. The second study comprised retrospective data for adult ICU patients admitted to UF Health Shands Hospital who received cefepime and had their cefepime concentrations measured. The population PK model was developed, and simulations were performed, using Pmetrics. The target exposures were 100% fT>MIC and 100% fT>4×MIC The studies included a total of 266 patients, and the mean ages were 3.9 years in the pediatric group and 55 years in adult group. More than half of the patients were males. The mean (standard deviation [SD]) creatinine clearance (CrCl) was 125 (93) ml/min. The mean (SD) daily dose for adults was 4.9 (1.6) g. Cefepime was well described by a two-compartment model with weight as a covariate on the volume of distribution and elimination rate constant (k el), and CrCl and age group as covariates on k el At a MIC of 8 mg/liter, a cefepime loading dose of 4 g as an extended infusion followed by a 6-g continuous infusion was needed for good target attainment. In conclusion, prolonged or continuous infusions will be needed to achieve optimal cefepime exposure for ICU patients. Given the observed variability, therapeutic drug monitoring can help individualize therapy.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  Monte Carlo simulation; cefepime; clinical therapeutics; population pharmacokinetics; precision dosing

Mesh:

Substances:

Year:  2020        PMID: 32601155      PMCID: PMC7449216          DOI: 10.1128/AAC.00745-20

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  41 in total

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Review 2.  Antibiotic exposure at the site of infection: principles and assessment of tissue penetration.

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Review 3.  The role of pharmacokinetics/pharmacodynamics in setting clinical MIC breakpoints: the EUCAST approach.

Authors:  J W Mouton; D F J Brown; P Apfalter; R Cantón; C G Giske; M Ivanova; A P MacGowan; A Rodloff; C-J Soussy; M Steinbakk; G Kahlmeter
Journal:  Clin Microbiol Infect       Date:  2012-01-20       Impact factor: 8.067

4.  Low plasma cefepime levels in critically ill septic patients: pharmacokinetic modeling indicates improved troughs with revised dosing.

Authors:  J Lipman; S C Wallis; C Rickard
Journal:  Antimicrob Agents Chemother       Date:  1999-10       Impact factor: 5.191

5.  Cefepime neurotoxicity: thresholds and risk factors. A retrospective cohort study.

Authors:  L Boschung-Pasquier; A Atkinson; L K Kastner; S Banholzer; M Haschke; N Buetti; D I Furrer; C Hauser; P Jent; Y A Que; H Furrer; B Babouee Flury
Journal:  Clin Microbiol Infect       Date:  2019-07-05       Impact factor: 8.067

6.  Intrapulmonary pharmacokinetics of antibiotics used to treat nosocomial pneumonia caused by Gram-negative bacilli: A systematic review.

Authors:  Aaron J Heffernan; Fekade B Sime; Jeffrey Lipman; Jayesh Dhanani; Katherine Andrews; David Ellwood; Keith Grimwood; Jason A Roberts
Journal:  Int J Antimicrob Agents       Date:  2018-11-23       Impact factor: 5.283

Review 7.  Pharmacokinetic/pharmacodynamic parameters: rationale for antibacterial dosing of mice and men.

Authors:  W A Craig
Journal:  Clin Infect Dis       Date:  1998-01       Impact factor: 9.079

Review 8.  Antibiotic resistance--what's dosing got to do with it?

Authors:  Jason A Roberts; Peter Kruger; David L Paterson; Jeffrey Lipman
Journal:  Crit Care Med       Date:  2008-08       Impact factor: 7.598

9.  Assessment of Global Incidence and Mortality of Hospital-treated Sepsis. Current Estimates and Limitations.

Authors:  Carolin Fleischmann; André Scherag; Neill K J Adhikari; Christiane S Hartog; Thomas Tsaganos; Peter Schlattmann; Derek C Angus; Konrad Reinhart
Journal:  Am J Respir Crit Care Med       Date:  2016-02-01       Impact factor: 21.405

10.  Defining Clinical Exposures of Cefepime for Gram-Negative Bloodstream Infections That Are Associated with Improved Survival.

Authors:  Nathaniel J Rhodes; Joseph L Kuti; David P Nicolau; Scott Van Wart; Anthony M Nicasio; Jiajun Liu; Benjamin J Lee; Michael N Neely; Marc H Scheetz
Journal:  Antimicrob Agents Chemother       Date:  2015-12-14       Impact factor: 5.191

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2.  Using Machine Learning To Define the Impact of Beta-Lactam Early and Cumulative Target Attainment on Outcomes in Intensive Care Unit Patients with Hospital-Acquired and Ventilator-Associated Pneumonia.

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3.  Cefepime Precision Dosing Tool: from Standard to Precise Dose Using Nonparametric Population Pharmacokinetics.

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Journal:  Antimicrob Agents Chemother       Date:  2021-12-13       Impact factor: 5.938

4.  Estimation of cefepime, piperacillin, and tazobactam clearance with iohexol-based glomerular filtration rate in paediatric patients.

Authors:  Hiie Soeorg; Aveli Noortoots; Maarja Karu; Kadri Saks; Jana Lass; Irja Lutsar; Lenne-Triin Kõrgvee
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