Department of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Department of Internal Medicine I, Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
Antimicrob Agents Chemother. 2018 Jan 25;62(2). doi: 10.1128/AAC.02164-17. Print 2018 Feb.
Effective concentrations of antibiotics in brain tissue are essential for antimicrobial therapy of brain infections. However, data concerning cerebral penetration properties of antibiotics for treatment or prophylaxis of central nervous system infections are rare. Six patients suffering subarachnoid hemorrhage and requiring cerebral microdialysis for neurochemical monitoring were included in this study. Free interstitial concentrations of cefuroxime after intravenous application of 1,500 mg were measured by microdialysis in brain tissue, as well as in plasma at steady-state ( = 6) or after single-dose administration ( = 1). At steady state, free area under the concentration-time curve from 0 to 24 h (AUC) values of 389.0 ± 210.3 mg/liter·h and 131.4 ± 72.8 mg/liter·h were achieved for plasma and brain, respectively, resulting in a brain tissue penetration ratio (AUC/AUC) of 0.33 ± 0.1. Plasma and brain tissue concentrations at individual time points correlated well ( = 0.59, = 0.001). At steady-state time over MIC (>MIC) values of >40% of dosing interval were achieved up to an MIC of 16 mg/liter for plasma and 4 mg/liter for brain tissue. Although MIC values could not be achieved in brain tissue for relevant bacteria, current dosing strategies of cefuroxime might be sufficient to treat pathogens with MIC values up to 4 mg/liter. The activity of cefuroxime in brain tissue might be overestimated when relying exclusively on plasma levels. Although currently insufficient data after single dose administration exist, lower brain-plasma ratios observed after the first dose might warrant a loading dose for treatment and perioperative prophylaxis.
抗生素在脑组织中的有效浓度对于脑感染的抗菌治疗至关重要。然而,关于抗生素治疗或预防中枢神经系统感染的脑穿透特性的数据很少。本研究纳入了 6 例蛛网膜下腔出血患者,这些患者需要进行脑微透析以进行神经化学监测。通过微透析测量静脉应用 1500mg 头孢呋辛后,脑组织和血浆中的游离浓度,在稳态时(n=6)或单次给药后(n=1)。在稳态时,脑和血浆的游离浓度时间曲线下面积(AUC)0 至 24 小时的 389.0±210.3mg/liter·h 和 131.4±72.8mg/liter·h,AUC/AUC 比值为 0.33±0.1。各个时间点的血浆和脑组织浓度相关性良好(r=0.59,P=0.001)。在稳态时,超过 MIC(>MIC)的时间达到给药间隔的 40%以上,对于血浆达到 MIC 为 16mg/liter,对于脑组织达到 MIC 为 4mg/liter。尽管对于相关细菌无法在脑组织中达到 MIC 值,但目前的头孢呋辛剂量策略可能足以治疗 MIC 值高达 4mg/liter 的病原体。当仅依赖于血浆水平时,头孢呋辛在脑组织中的活性可能被高估。尽管目前单次剂量给药后的数据不足,但首次剂量后观察到的较低的脑-血浆比值可能需要负荷剂量进行治疗和围手术期预防。