Low Flucloxacillin Concentrations in a Patient With Central Nervous System Infection: The Need for Plasma and Cerebrospinal Fluid Drug Monitoring in the ICu

被引:19
作者
Abdul-Aziz, Mohd H. [1 ]
McDonald, Craig [2 ]
McWhinney, Brett [3 ]
Ungerer, Jacobus P. J. [3 ]
Lipman, Jeffrey [1 ,2 ]
Roberts, Jason A. [1 ,2 ]
机构
[1] Univ Queensland, Brisbane, Qld, Australia
[2] Royal Brisbane & Womens Hosp, Brisbane, Qld, Australia
[3] Queensland Pathol, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
beta-lactanns; cerebrospinal fluid; intensive care unit; pharmacokinetics; therapeutic drug monitoring; CRITICALLY-ILL PATIENTS; PHARMACOKINETICS; HYPOALBUMINEMIA; ANTIBIOTICS; CEFEPIME; INFUSION;
D O I
10.1177/1060028014540610
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective:To report the difficulty in achieving and maintaining target antibiotic exposure in critically ill patients with deep-seeded infections. Case Summary: We present a case of a 36-year-old man who was admitted to the intensive care unit with diffuse central nervous system and peripheral methicillin-sensitive Staphylococcus aureus infection (minimum inhibitory concentration; M IC, I mu g/mL). Owing to the complicated nature of the infection, sequential concentrations of free flucloxacillin were measured in plasma and cerebrospinal fluid (CSF) and used to direct antibiotic dosing. Unsurprisingly, the trough plasma concentrations of flucloxacillin were below the MIC (0.2-0.4 mu g/nnL), and the corresponding CSF concentrations were undetectable (<0. I mu g/mL) with standard intermittent bolus dosing of 2 g every 4 hours. By administering flucloxacillin by continuous infusion (Cl) and increasing the dose to 20 g daily, the plasma (2.2-5.7 mu g/mL) and CSF (0.1 mu g/mL) levels were increased, albeit lower than the predefined targets (plasma, 40 pg/nnL; CSF, 4 mu g/mL). Discussion: The presence of physiological changes associated with critical illness namely, hypoalbunninemia and augmented renal clearance may significantly alter antibiotic pharnnacokinetics, and this phenomenon may lead to suboptimal antibiotic exposure if they are not accounted for. This case also highlights the value of applying Cl in such patient groups and demonstrates the significance of monitoring plasma and CSF drug concentrations in optimizing antibiotic delivery. Conclusions: Future research should aim to evaluate the utility of such drug monitoring with regard to patient outcomes and cost-effectiveness.
引用
收藏
页码:1380 / 1384
页数:5
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