Optimal antipseudomonal ?-lactam drug dosing recommendations in critically-ill Asian patients receiving CRRT

被引:4
作者
Jang, Soo Min [1 ,2 ]
Lewis, Susan J. [3 ,4 ,7 ]
Rhie, Sandy Jeong [5 ,6 ,8 ]
机构
[1] Loma Linda Univ, Dept Pharm Practice, Sch Pharm, Loma Linda, CA USA
[2] Loma Linda Univ, Dept Internal Med, Sch Med, Loma Linda, CA USA
[3] Univ Findlay, Dept Pharm Practice, Coll Pharm, Findlay, OH USA
[4] Mercy Hlth St Anne Hosp, Dept Pharm, Toledo, OH USA
[5] Ewha Womans Univ, Coll Pharm, Seoul, South Korea
[6] Ewha Womans Univ, Grad Sch Pharmaceut Sci, Seoul, South Korea
[7] 1000 N Main St, Findlay, OH 45840 USA
[8] 52 Ewhayeodae Gil, Seoul 03760, South Korea
基金
新加坡国家研究基金会;
关键词
Continuous renal replacement therapy; Pharmacokinetics; pharmacodynamics; Cefepime; Ceftazidime; Meropenem; Piperacillin; tazobactam; Monte Carlo simulation; RENAL-REPLACEMENT THERAPY; ACUTE KIDNEY INJURY; CEFEPIME PLASMA-CONCENTRATIONS; MORTALITY; PHARMACODYNAMICS; INTENSITY; TOXICITY; OUTCOMES; FAILURE;
D O I
10.1016/j.jcrc.2022.154172
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Available online xxxx Introduction: The average body weight is smaller in Asian patients compared with Western patients, but influence of body weight in antibiotic dosing is unknown. This study was to predict the optimal ceftazidime, cefepime, meropenem, piperacillin/tazobactam doses in Asian patients undergoing continuous venovenous hemofiltration (CVVH). Methods: Monte Carlo simulations (MCS) were performed using published Asian demographics and pharmacokinetics parameters in 5000 virtual patients at three CVVH effluent rates (Qeff; 20, 30, 40 mL/kg/h). Various dosing regimens were assessed for the probability of target attainments using 60% fT > 1 x MIC or 4xMIC and neurotoxicity risk at 48-h using suggested neurotoxicity thresholds. Results: Ceftazidime 1 g q12h, meropenem 1 g q12h, and piperacillin/tazobactam 3.375 g q6h were optimal for all Qeff settings against fT > 1 x MIC. Cefepime 2 g q24h and 2 g q12h were optimal at 20 and 30-40 mL/kg/h respectively. For the aggressive PD target (4 x MIC), optimal ceftazidime regimens were 1.25 g q8h (20-30 mL/kg/h) and 1.5 g q8h (40 mL/kg/h). Cefepime 2 g q8h and meropenem 1 g q8h were optimal at all Qeff settings. No simulated piperacillin doses attained the aggressive PD target. Increased neurotoxicity risk was predicted with ceftazidime and cefepime doses attaining the efficacy. Conclusion: MCS enabled the prediction of optimal beta-lactam dosing regimens for Asian patients receiving CVVH at varying Qeff. Clinical validation is warranted. (c) 2022 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
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页数:7
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