Pokorná Pavla, Michaličková Danica, Tibboel Dick, Berner Jonas
Institute of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital, 128 00 Prague, Czech Republic.
Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, 128 00 Prague, Czech Republic.
Antibiotics (Basel). 2024 May 3;13(5):419. doi: 10.3390/antibiotics13050419.
This study aimed to characterize the impact of extracorporeal membrane oxygenation (ECMO) on the pharmacokinetics (PK) of meropenem in neonates and children and to provide recommendations for meropenem dosing in this specific population of patients. Therapeutic drug monitoring (152 meropenem plasma concentrations) data from 45 patients (38 received ECMO) with a body weight (BW) of 7.88 (3.62-11.97) kg (median (interquartile range)) and postnatal age of 3 (0-465) days were collected. The population PK analysis was performed using NONMEM V7.3.0. Monte Carlo simulations were performed to assess the probability of target achievement (PTA) for 40% of time the free drug remained above the minimum inhibitory concentration (fT > MIC) and 100% fT > MIC. BW was found to be a significant covariate for the volume of distribution (Vd) and clearance (CL). Additionally, continuous renal replacement therapy (CRRT) was associated with a two-fold increase in Vd. In the final model, the CL and Vd for a typical patient with a median BW of 7.88 kg that was off CRRT were 1.09 L/h (RSE = 8%) and 3.98 L (14%), respectively. ECMO did not affect meropenem PK, while superimposed CRRT significantly increased Vd. We concluded that current dosing regimens provide acceptably high PTA for MIC ≤ 4 mg/L for 40% fT > MIC, but individual dose adjustments are needed for 100% fT > MIC.
本研究旨在描述体外膜肺氧合(ECMO)对美罗培南在新生儿和儿童体内药代动力学(PK)的影响,并为这一特定患者群体的美罗培南给药提供建议。收集了45例体重为7.88(3.62 - 11.97)kg(中位数(四分位间距))、出生后年龄为3(0 - 465)天的患者(38例接受ECMO)的治疗药物监测(152次美罗培南血浆浓度)数据。使用NONMEM V7.3.0进行群体PK分析。进行蒙特卡洛模拟以评估游离药物在40%的时间内保持高于最低抑菌浓度(fT > MIC)和100% fT > MIC时达到目标的概率(PTA)。发现体重是分布容积(Vd)和清除率(CL)的显著协变量。此外,持续肾脏替代疗法(CRRT)与Vd增加两倍相关。在最终模型中,体重中位数为7.88 kg且未接受CRRT的典型患者的CL和Vd分别为1.09 L/h(相对标准误差 = 8%)和3.98 L(14%)。ECMO不影响美罗培南的PK,而叠加的CRRT显著增加Vd。我们得出结论,当前给药方案对于40% fT > MIC且MIC≤4 mg/L时能提供可接受的高PTA,但对于100% fT > MIC则需要进行个体化剂量调整。