Department of Intensive Care, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Department of Intensive Care and Perioperative Medicine, Skane University Hospital, Malmö, Lund University, Lund, Sweden.
J Antimicrob Chemother. 2018 Jan 1;73(1):191-198. doi: 10.1093/jac/dkx330.
To use a population pharmacokinetic approach to define maximally effective meropenem dosing recommendations for treatment of Acinetobacter baumannii and Pseudomonas aeruginosa infections in a large cohort of patients with septic shock.
Adult patients with septic shock and conserved renal function, treated with meropenem, were eligible for inclusion. Seven blood samples were collected during a single dosing interval and meropenem concentrations were measured by a validated HPLC-MS/MS method. Monte Carlo simulations were employed to define optimum dosing regimens for treatment of empirical or targeted therapy of A. baumannii and P. aeruginosa. EudraCT-no. 2014-002555-26 and NCT02240277.
Fifty patients were included, 26 male and 24 female, with a median age of 64 years with an all-cause 90 day mortality of 34%. A two-compartment linear model including creatinine clearance (CLCR) as a covariate best described meropenem pharmacokinetics. For empirical treatment of A. baumannii, 2000 mg/6 h was required by intermittent (30 min) or prolonged (3 h) infusion, whereas 6000 mg/day was required with continuous infusion. For P. aeruginosa, 2000 mg/8 h or 1000 mg/6 h was required for both empirical and targeted treatment. In patients with a CLCR of ≤ 100 mL/min, successful concentration targets could be reached with intermittent dosing of 1000 mg/8 h.
In patients with septic shock and possible augmented renal clearance, doses should be increased and/or administration should be performed by prolonged or continuous infusion to increase the likelihood of achieving therapeutic drug concentrations. In patients with normal renal function, however, standard dosing seems to be sufficient.
采用群体药代动力学方法,为大量感染鲍曼不动杆菌和铜绿假单胞菌的脓毒性休克患者制定最大有效美罗培南剂量推荐方案。
纳入使用美罗培南治疗、合并脓毒性休克且肾功能正常的成年患者。在单次给药间隔内采集 7 份血样,采用经验证的高效液相色谱-串联质谱法(HPLC-MS/MS)测定美罗培南浓度。采用蒙特卡罗模拟法确定经验性或靶向治疗鲍曼不动杆菌和铜绿假单胞菌的最佳给药方案。EudraCT-no.2014-002555-26 和 NCT02240277。
共纳入 50 例患者,男 26 例,女 24 例,中位年龄 64 岁,全因 90 天死亡率为 34%。以肌酐清除率(CLCR)为协变量的两室线性模型可最佳描述美罗培南的药代动力学特征。经验性治疗鲍曼不动杆菌时,间歇性(30 分钟)或延长输注(3 小时)需输注 2000mg/6h,而连续输注则需 6000mg/天。对于铜绿假单胞菌,经验性和靶向治疗均需 2000mg/8h 或 1000mg/6h。CLCR≤100ml/min 的患者,间歇性 1000mg/8h 给药可达到有效浓度目标。
合并有代偿性肾功能清除增加的脓毒性休克患者,应增加剂量和/或通过延长或持续输注给药,以提高达到治疗药物浓度的可能性。然而,对于肾功能正常的患者,标准剂量似乎已足够。