Chihara Shinya, Ishigo Tomoyuki, Kazuma Satoshi, Matsumoto Kana, Morita Kunihiko, Masuda Yoshiki
Department of Intensive Care Medicine, Sapporo Medical University, School of Medicine, Sapporo 060-8543, Japan.
Department of Clinical Engineering, Japan Health Care University Faculty of Health Sciences, Sapporo 062-0053, Japan.
Antibiotics (Basel). 2024 Aug 11;13(8):755. doi: 10.3390/antibiotics13080755.
Aggressive pharmacokinetic (PK)/pharmacodynamic (PD) targets have shown better microbiological eradication rates and a lower propensity to develop resistant strains than conservative targets. We investigated whether meropenem blood levels, including aggressive PK/PD, were acceptable in terms of efficacy and safety using a meropenem regimen of 1 g infusion every 8 h over 3 h in patients undergoing continuous renal replacement therapy (CRRT) for septic acute kidney injury (AKI). Aggressive PK/PD targets were defined as the percentage of time that the free concentration (%fT) > 4 × minimal inhibitory concentration (MIC), the toxicity threshold was defined as a trough concentration >45 mg/L, and the percentage of achievement at each MIC was evaluated. The 100% fT > 4 × MIC for a pathogen with an MIC of 0.5 mg/L was 89%, and that for a pathogen with an MIC of 2 mg/L was 56%. The mean steady-state trough concentration of meropenem was 11.9 ± 9.0 mg/L and the maximum steady-state trough concentration was 29.2 mg/L. Simulations using Bayesian estimation showed the probability of achieving 100% fT > 4 × MIC for up to an MIC of 2 mg/L for the administered administration via continuous infusion at 3 g/24 h. We found that an aggressive PK/PD could be achieved up to an MIC of 0.5 mg/L with a meropenem regimen of 1 g infused every 8 h over 3 h for patients receiving CRRT for septic AKI. In addition, the risk of reaching the toxicity range with this regimen is low. In addition, if the MIC was 1-2 mg/L, the simulation results indicated that aggressive PK/PD can be achieved by continuous infusion at 3 g/24 h without increasing the daily dose.
与保守目标相比,积极的药代动力学(PK)/药效学(PD)目标已显示出更好的微生物清除率和更低的耐药菌株产生倾向。我们研究了在接受连续性肾脏替代治疗(CRRT)的脓毒症急性肾损伤(AKI)患者中,使用美罗培南每8小时1g、输注3小时的方案时,包括积极PK/PD在内的美罗培南血药浓度在疗效和安全性方面是否可接受。积极的PK/PD目标定义为游离浓度(%fT)>4×最低抑菌浓度(MIC)的时间百分比,毒性阈值定义为谷浓度>45mg/L,并评估每个MIC水平下的达标百分比。对于MIC为0.5mg/L的病原体,100% fT>4×MIC为89%,对于MIC为2mg/L的病原体,该比例为56%。美罗培南的平均稳态谷浓度为11.9±9.0mg/L,最大稳态谷浓度为29.2mg/L。使用贝叶斯估计的模拟显示,通过持续输注3g/24h给药,对于高达2mg/L的MIC,实现100% fT>4×MIC的概率。我们发现,对于接受CRRT治疗脓毒症AKI的患者,每8小时1g、输注3小时的美罗培南方案在MIC高达0.5mg/L时可实现积极的PK/PD。此外,该方案达到毒性范围的风险较低。此外,如果MIC为1 - 2mg/L,模拟结果表明,通过持续输注3g/24h且不增加每日剂量即可实现积极的PK/PD。