Smits A, De Cock R F W, Allegaert K, Vanhaesebrouck S, Danhof M, Knibbe C A J
Neonatal Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium Department of Development and Regeneration, KU Leuven, Leuven, Belgium
Division of Pharmacology, LACDR, Leiden University, Leiden, Netherlands.
Antimicrob Agents Chemother. 2015 Oct;59(10):6344-51. doi: 10.1128/AAC.01157-15. Epub 2015 Jul 27.
Based on a previously derived population pharmacokinetic model, a novel neonatal amikacin dosing regimen was developed. The aim of the current study was to prospectively evaluate this dosing regimen. First, early (before and after second dose) therapeutic drug monitoring (TDM) observations were evaluated for achieving target trough (<3 mg/liter) and peak (>24 mg/liter) levels. Second, all observed TDM concentrations were compared with model-predicted concentrations, whereby the results of a normalized prediction distribution error (NPDE) were considered. Subsequently, Monte Carlo simulations were performed. Finally, remaining causes limiting amikacin predictability (i.e., prescription errors and disease characteristics of outliers) were explored. In 579 neonates (median birth body weight, 2,285 [range, 420 to 4,850] g; postnatal age 2 days [range, 1 to 30 days]; gestational age, 34 weeks [range, 24 to 41 weeks]), 90.5% of the observed early peak levels reached 24 mg/liter, and 60.2% of the trough levels were <3 mg/liter (93.4% ≤5 mg/liter). Observations were accurately predicted by the model without bias, which was confirmed by the NPDE. Monte Carlo simulations showed that peak concentrations of >24 mg/liter were reached at steady state in almost all patients. Trough values of <3 mg/liter at steady state were documented in 78% to 100% and 45% to 96% of simulated cases with and without ibuprofen coadministration, respectively; suboptimal trough levels were found in patients with postnatal age <14 days and current weight of >2,000 g. Prospective evaluation of a model-based neonatal amikacin dosing regimen resulted in optimized peak and trough concentrations in almost all patients. Slightly adapted dosing for patient subgroups with suboptimal trough levels was proposed. This model-based approach improves neonatal dosing individualization.
基于先前推导的群体药代动力学模型,开发了一种新型的新生儿阿米卡星给药方案。本研究的目的是前瞻性地评估该给药方案。首先,评估早期(第二剂前后)治疗药物监测(TDM)观察结果,以实现目标谷浓度(<3毫克/升)和峰浓度(>24毫克/升)。其次,将所有观察到的TDM浓度与模型预测浓度进行比较,并考虑标准化预测分布误差(NPDE)的结果。随后,进行了蒙特卡洛模拟。最后,探究了限制阿米卡星预测性的其他原因(即处方错误和异常值的疾病特征)。在579名新生儿中(出生体重中位数为2285[范围为420至4850]克;出生后年龄为2天[范围为1至30天];胎龄为34周[范围为24至41周]),90.5%的观察到的早期峰浓度达到24毫克/升,60.2%的谷浓度<3毫克/升(93.4%≤5毫克/升)。模型对观察结果进行了无偏差的准确预测,NPDE证实了这一点。蒙特卡洛模拟表明,几乎所有患者在稳态时峰浓度均>24毫克/升。在分别有和没有布洛芬合用的模拟病例中,稳态时谷值<3毫克/升的情况分别记录在78%至100%和45%至96%的病例中;出生后年龄<14天且当前体重>2000克的患者谷浓度未达最佳水平。对基于模型的新生儿阿米卡星给药方案进行前瞻性评估,几乎所有患者的峰浓度和谷浓度都得到了优化。针对谷浓度未达最佳水平的患者亚组,提出了略微调整的给药方案。这种基于模型的方法改善了新生儿给药个体化。