Abdul-Aziz Mohd H, McDonald Craig, McWhinney Brett, Ungerer Jacobus P J, Lipman Jeffrey, Roberts Jason A
The University of Queensland, Brisbane, Australia
Royal Brisbane and Women's Hospital, Brisbane, Australia.
Ann Pharmacother. 2014 Oct;48(10):1380-4. doi: 10.1177/1060028014540610. Epub 2014 Jun 20.
To report the difficulty in achieving and maintaining target antibiotic exposure in critically ill patients with deep-seeded infections.
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; MIC, 1 µg/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 µg/mL), and the corresponding CSF concentrations were undetectable (<0.1 µg/mL) with standard intermittent bolus dosing of 2 g every 4 hours. By administering flucloxacillin by continuous infusion (CI) and increasing the dose to 20 g daily, the plasma (2.2-5.7 µg/mL) and CSF (0.1 µg/mL) levels were increased, albeit lower than the predefined targets (plasma, 40 µg/mL; CSF, 4 µg/mL).
The presence of physiological changes associated with critical illness-namely, hypoalbuminemia and augmented renal clearance-may significantly alter antibiotic pharmacokinetics, and this phenomenon may lead to suboptimal antibiotic exposure if they are not accounted for. This case also highlights the value of applying CI in such patient groups and demonstrates the significance of monitoring plasma and CSF drug concentrations in optimizing antibiotic delivery.
Future research should aim to evaluate the utility of such drug monitoring with regard to patient outcomes and cost-effectiveness.
报告在患有深部感染的重症患者中实现并维持目标抗生素暴露水平的困难。
我们报告一例36岁男性,因弥漫性中枢神经系统及外周耐甲氧西林金黄色葡萄球菌感染(最低抑菌浓度;MIC,1μg/mL)入住重症监护病房。由于感染情况复杂,我们测定了血浆和脑脊液(CSF)中游离氟氯西林的连续浓度,并以此指导抗生素给药。不出所料,采用每4小时2g的标准间歇性推注给药时,氟氯西林的血浆谷浓度低于MIC(0.2 - 0.4μg/mL),相应的脑脊液浓度未检测到(<0.1μg/mL)。通过持续输注(CI)氟氯西林并将剂量增加至每日20g,血浆(2.2 - 5.7μg/mL)和脑脊液(0.1μg/mL)水平有所升高,尽管仍低于预定义目标(血浆,40μg/mL;脑脊液,4μg/mL)。
与危重病相关的生理变化,即低白蛋白血症和肾清除率增加,可能会显著改变抗生素的药代动力学,如果不加以考虑,这种现象可能导致抗生素暴露不足。该病例还凸显了在这类患者群体中应用持续输注的价值,并证明了监测血浆和脑脊液药物浓度对优化抗生素给药的重要性。
未来的研究应旨在评估这种药物监测在患者预后和成本效益方面的效用。