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Serum and Cerebrospinal Fluid Concentrations of Linezolid in Neurosurgical Patients

机译:神经外科患者中利奈唑胺的血清和脑脊髓液浓度

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Linezolid is a new antimicrobial agent effective against drug-resistant gram-positive pathogens commonly responsible for central nervous system (CNS) infections in neurosurgical patients hospitalized in intensive care units. In order to study the penetration of this antimicrobial into the cerebrospinal fluid (CSF) of such patients, the disposition of linezolid in serum and CSF was studied in 14 neurosurgical patients given linezolid at 600 mg twice daily (1-h intravenous infusion) for the treatment of CNS infections caused by gram-positive pathogens or for prophylactic chemotherapy. Serum and CSF linezolid steady-state concentrations were analyzed by high-pressure liquid chromatography, and the concentration-time profiles obtained were analyzed to estimate pharmacokinetic parameters. The mean ± standard deviation (SD) linezolid maximum and minimum measured concentrations were 18.6 ± 9.6 μg/ml and 5.6 ± 5.0 μg/ml, respectively, in serum and 10.8 ± 5.7 μg/ml and 6.1 ± 4.2 μg/ml, respectively, in CSF. The mean ± SD areas under the concentration-time curves (AUCs) were 128.7 ± 83.9 μg · h/ml for serum and 101.6 ± 59.6 μg · h/ml for CSF, with a mean penetration ratio for the AUC for CSF to the AUC for serum of 0.66. The mean elimination half-life of linezolid in CSF was longer than that in serum (19.1 ± 19.0 h and 6.5 ± 3.6 h, respectively). The serum and CSF linezolid concentrations exceeded the pharmacodynamic breakpoint of 4 μg/ml for susceptible target pathogens for the entire dosing interval in the majority of patients. These findings suggest that linezolid may achieve adequate concentrations in the CSF of patients requiring antibiotics for the management or prophylaxis of CNS infections caused by gram-positive pathogens.
机译:利奈唑胺是一种新的抗微生物药物,可有效抵抗耐药的革兰氏阳性病原体,这些病原体通常导致重症监护病房住院的神经外科患者的中枢神经系统(CNS)感染。为了研究这种抗菌剂在此类患者的脑脊液(CSF)中的渗透性,我们在14名神经外科患者中研究了利奈唑胺在血清和脑脊液中的分布情况,这些患者每天两次接受600 mg利奈唑胺(静注1小时)革兰氏阳性病原体引起的中枢神经系统感染的治疗或预防性化学疗法。通过高压液相色谱分析血清和脑脊液利奈唑胺稳态浓度,并分析获得的浓度-时间曲线以估算药代动力学参数。血清中利奈唑胺最大和最小平均浓度的标准偏差(SD)分别为18.6±9.6μg/ ml和5.6±5.0μg/ ml,血清分别为10.8±5.7μg/ ml和6.1±4.2μg/ ml。在CSF中。浓度-时间曲线(AUC)下的平均值±SD面积,血清为128.7±83.9μg·h / ml,脑脊液为101.6±59.6μg·h / ml,CSF的AUC与AUC的平均渗透率血清为0.66。利奈唑胺在脑脊液中的平均消除半衰期比血清中更长(分别为19.1±19.0 h和6.5±3.6 h)。在大多数患者的整个给药间隔中,易感性靶病原体的血清和CSF利奈唑胺浓度均超过4μg/ ml的药效学临界点。这些发现表明,利奈唑烷可能在需要抗生素治疗或预防革兰氏阳性病原体引起的中枢神经系统感染的患者的脑脊液中达到足够的浓度。

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