Lu Cheng, Zhang Yuyi, Chen Mingyu, Zhong Ping, Chen Yuancheng, Yu Jicheng, Wu Xiaojie, Wu Jufang, Zhang Jing
Institute of Antibiotics, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Key Laboratory of Clinical Pharmacology of Antibiotics, Ministry of Health, Shanghai, China.
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6619-6625. doi: 10.1128/AAC.00997-16. Print 2016 Nov.
Meropenem is used to manage postneurosurgical meningitis, but its population pharmacokinetics (PPK) in plasma and cerebrospinal fluid (CSF) in this patient group are not well-known. Our aims were to (i) characterize meropenem PPK in plasma and CSF and (ii) recommend favorable dosing regimens in postneurosurgical meningitis patients. Eighty-two patients were enrolled to receive meropenem infusions of 2 g every 8 h (q8h), 1 g q8h, or 1 g q6h for at least 3 days. Serial blood and CSF samples were collected, and concentrations were determined and analyzed via population modeling. Probabilities of target attainment (PTA) were predicted via Monte Carlo simulations, using the target of unbound meropenem concentrations above the MICs for at least 40% of dosing intervals in plasma and at least of 50% or 100% of dosing intervals in CSF. A two-compartment model plus another CSF compartment best described the data. The central, intercentral/peripheral, and intercentral/CSF compartment clearances were 22.2 liters/h, 1.79 liters/h, and 0.01 liter/h, respectively. Distribution volumes of the central and peripheral compartments were 17.9 liters and 3.84 liters, respectively. The CSF compartment volume was fixed at 0.13 liter, with its clearance calculated by the observed drainage amount. The multiplier for the transfer from the central to the CSF compartment was 0.172. Simulation results show that the PTAs increase as infusion is prolonged and as the daily CSF drainage volume decreases. A 4-hour infusion of 2 g q8h with CSF drainage of less than 150 ml/day, which provides a PTA of >90% for MICs of ≤8 mg/liter in blood and of ≤0.5 mg/liter or 0.25 mg/liter in CSF, is recommended. (This study has been registered at ClinicalTrials.gov under identifier NCT02506686.).
美罗培南用于治疗神经外科术后脑膜炎,但其在该患者群体血浆和脑脊液(CSF)中的群体药代动力学(PPK)尚不清楚。我们的目的是:(i)描述美罗培南在血浆和脑脊液中的PPK;(ii)为神经外科术后脑膜炎患者推荐合适的给药方案。82例患者入组,接受每8小时(q8h)2g、q8h 1g或q6h 1g的美罗培南输注,持续至少3天。采集系列血液和脑脊液样本,通过群体建模确定并分析浓度。通过蒙特卡洛模拟预测达到目标的概率(PTA),血浆中游离美罗培南浓度在至少40%的给药间隔高于最低抑菌浓度(MIC),脑脊液中在至少50%或100%的给药间隔高于MIC作为目标。一个二室模型加另一个脑脊液室能最好地描述数据。中央室、中央/外周室和中央/脑脊液室的清除率分别为22.2升/小时、1.79升/小时和0.01升/小时。中央室和外周室的分布容积分别为17.9升和3.84升。脑脊液室容积固定为0.13升,其清除率通过观察到的引流量计算。从中央室到脑脊液室的转移系数为0.172。模拟结果表明,随着输注时间延长和每日脑脊液引流量减少,PTA增加。建议采用q8h 2g 4小时输注,脑脊液引流量小于150ml/天,对于血液中MIC≤8mg/升、脑脊液中MIC≤0.5mg/升或0.25mg/升可提供>90% 的PTA。(本研究已在ClinicalTrials.gov注册,标识符为NCT02506686。)