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

被引:27
作者
Al-Shaer, Mohammad H. [1 ,2 ]
Neely, Michael N. [3 ]
Liu, Jiajun [4 ,5 ,6 ]
Cherabuddi, Kartikeya [7 ]
Venugopalan, Veena [2 ]
Rhodes, Nathaniel J. [4 ,5 ,6 ]
Klinker, Kenneth [2 ]
Scheetz, Marc H. [4 ,5 ,6 ]
Peloquin, Charles A. [1 ,2 ]
机构
[1] Univ Florida, Emerging Pathogens Inst, Infect Dis Pharmacokinet Lab, Gainesville, FL 32611 USA
[2] Univ Florida, Coll Pharm, Dept Pharmacotherapy & Translat Res, Gainesville, FL 32611 USA
[3] Childrens Hosp Los Angeles, Lab Appl Pharmacokinet & Bioinformat, Los Angeles, CA 90027 USA
[4] Midwestern Univ Chicago, Coll Pharm, Downers Grove, IL USA
[5] Northwestern Mem Hosp, Chicago, IL 60611 USA
[6] Midwestern Univ Chicago, Pharmacometr Ctr Excellence, Coll Pharm, Downers Grove, IL USA
[7] Univ Florida, Coll Med, Div Infect Dis, Gainesville, FL USA
关键词
Monte Carlo simulation; cefepime; clinical therapeutics; population pharmacokinetics; precision dosing; BETA-LACTAM CONCENTRATIONS; PHARMACODYNAMICS; RESISTANCE; PLASMA; INFECTIONS; SIMULATION; CLEARANCE; RATIONALE; EXPOSURE;
D O I
10.1128/AAC.00745-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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(>4xMIC). 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.
引用
收藏
页数:13
相关论文
共 44 条
  • [1] Beta-Lactam Infusion in Severe Sepsis (BLISS): a prospective, two-centre, open-labelled randomised controlled trial of continuous versus intermittent beta-lactam infusion in critically ill patients with severe sepsis
    Abdul-Aziz, Mohd H.
    Sulaiman, Helmi
    Mat-Nor, Mohd-Basri
    Rai, Vineya
    Wong, Kang K.
    Hasan, Mohd S.
    Abd Rahman, Azrin N.
    Jamal, Janattul A.
    Wallis, Steven C.
    Lipman, Jeffrey
    Staatz, Christine E.
    Roberts, Jason A.
    [J]. INTENSIVE CARE MEDICINE, 2016, 42 (10) : 1535 - 1545
  • [2] Meropenem, Cefepime, and Piperacillin Protein Binding in Patient Samples
    Al-Shaer, Mohammad H.
    Alghamdi, Wael A.
    Graham, Emily
    Peloquin, Charles A.
    [J]. THERAPEUTIC DRUG MONITORING, 2020, 42 (01) : 129 - 132
  • [3] [Anonymous], 2019, Antibiotic Resistance Threats in the United States
  • [4] HIGH-PRESSURE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BMY-28142 IN PLASMA AND URINE
    BARBHAIYA, RH
    FORGUE, ST
    SHYU, WC
    PAPP, EA
    PITTMAN, KA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (01) : 55 - 59
  • [5] Intrapulmonary concentrations of meropenem administered by continuous infusion in critically ill patients with nosocomial pneumonia: a randomized pharmacokinetic trial
    Benitez-Cano, Adela
    Luque, Sonia
    Sorli, Luisa
    Carazo, Jesus
    Ramos, Isabel
    Campillo, Nuria
    Curull, Victor
    Sanchez-Font, Albert
    Vilaplana, Carles
    Horcajada, Juan P.
    Adalia, Ramon
    Bermejo, Silvia
    Samso, Enric
    Hope, William
    Grau, Santiago
    [J]. CRITICAL CARE, 2020, 24 (01):
  • [6] Beumier M, 2015, MINERVA ANESTESIOL, V81, P497
  • [7] Cefepime neurotoxicity: thresholds and risk factors. A retrospective cohort study
    Boschung-Pasquier, L.
    Atkinson, A.
    Kastner, L. K.
    Banholzer, S.
    Haschke, M.
    Buetti, N.
    Furrer, D., I
    Hauser, C.
    Jent, P.
    Que, Y. A.
    Furrer, H.
    Flury, B. Babouee
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2020, 26 (03) : 333 - 339
  • [8] Bristol-Myers Squibb, 2007, MAX CAF PACK INS MAX CAF PACK INS
  • [9] Prospective monitoring of cefepime in intensive care unit adult patients
    Chapuis, Thomas M.
    Giannoni, Eric
    Majcherczyk, Paul A.
    Chiolero, Rene
    Schaller, Marie-Denise
    Berger, Mette M.
    Bolay, Saskia
    Decosterd, Laurent A.
    Bugnon, Denis
    Moreillon, Philippe
    [J]. CRITICAL CARE, 2010, 14 (02):
  • [10] PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE
    COCKCROFT, DW
    GAULT, MH
    [J]. NEPHRON, 1976, 16 (01) : 31 - 41