Cefepime pharmacokinetics in adult extracorporeal membrane oxygenation patients

被引:3
|
作者
Zheng, Lily [1 ]
Alshaer, Mohammad H. [2 ]
Peloquin, Charles [2 ]
Venugopalan, Veena [2 ]
Alnuaimat, Hassan M. [3 ]
Converse, Maureen [4 ]
机构
[1] Univ Florida Hlth Jacksonville North, Dept Pharm Serv, Max Leggett Pkwy, Jacksonville, FL 15255 USA
[2] Univ Florida, Pharmacotherapy & Translat Res, Coll Pharm, Med Sci Bldg Rm P4 05,1600 SW Archer Rd, Gainesville, FL USA
[3] Univ Florida, Coll Med, Div Pulm Crit Care & Sleep Med, 1600 SW Archer Rd, Gainesville, FL 32608 USA
[4] Cleveland Clin, Dept Pharm, 9500 Euclid Ave, Cleveland, OH USA
关键词
Therapeutic drug monitoring; Extracorporeal membrane oxygenation; Antibiotics; Pharmacokinetics; Pharmacodynamics; Cefepime;
D O I
10.1016/j.pupt.2023.102271
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The impact of extracorporeal membrane oxygenation (ECMO) on the pharmacokinetics/dynamics (PK/PD) of beta-lactam antibiotics have not been well studied in general, but cefepime specifically has the least amount of data. We aimed to investigate whether ECMO alters the PK of cefepime in adult intensive care unit (ICU) patients. Methods: This single-center, retrospective case-control study evaluated cefepime therapeutic drug monitoring (TDM) results from ECMO patients that were matched 1:1 with TDM results in non-ECMO patients for drug regimen and renal function. The primary outcome was the difference in PK/PD of cefepime in ECMO compared with non-ECMO ICU patients. Secondary outcomes included hospital length of stay, treatment failure, superinfection, bacterial resistance, and survival to discharge. Results: Eighty-two patients were included with 44 matched cefepime concentrations in each group. ECMO patients had higher free maximum concentrations (fCmax) (p = 0.003), lower free minimum concentration (fCmin)/1x minimum inhibitory concentration (MIC) ratios (p = 0.040), and lower attainment of free Cmin/4x MIC (p = 0.010). There were no differences between the groups for free Cmin, time above 1xMIC or 4x MIC, and pharmacokinetic parameters (ke, half-life, and Vd). Of those who survived to discharge, hospital length of stay was longer in the ECMO group (p < 0.001). Patients on ECMO were more likely to experience treatment failure (p = 0.036). The incidence of bacterial resistance, superinfection, or survival were similar among the groups. Conclusion: These data suggest that more aggressive empiric dosing may be warranted in patients on ECMO. Therapeutic drug monitoring and future prospective studies would provide more evidence to guide decision making regarding dose adjustments.
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页数:5
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