Koloskoff Kevin, Thirion Daniel J G, Matouk Elias, Marsot Amélie
Faculty of Pharmacy, Université de Montréal.
Laboratoire STP2, Faculty of Pharmacy, Université de Montréal; and.
Ther Drug Monit. 2023 Apr 1;45(2):251-258. doi: 10.1097/FTD.0000000000001021.
Acute pulmonary exacerbations (APEs) in patients with adult cystic fibrosis (CF) are treated with a beta-lactam and an aminoglycoside for activity against Pseudomonas aeruginosa (PA). Emerging drug resistance and changing pharmacokinetic profile in an aging population involve a reevaluation of tobramycin dosing recommendations. The objective of this study was to develop a population pharmacokinetic model and establish optimal dosing recommendations for tobramycin using Monte Carlo simulations.
This retrospective clinical study and data collection were performed at the CF center of the McGill University Health Center (MUHC), Canada. Model development and simulations were performed using a nonlinear mixed-effect modeling approach (NONMEM, version 7.4.2). The ratios of maximal concentration (C max ) to the minimal inhibitory concentration (MIC) (C max /MIC ≥8 and ≥10) and area under the curve (AUC) to the MIC (AUC/MIC ≥70 and ≥100) were evaluated.
Adult patients with CF (n = 51) treated with tobramycin were included in the study. Plasma concentrations of tobramycin were obtained for 699 samples from the MUHC database. The two-compartmental model best described the pharmacokinetics of tobramycin. The association of patient height with the central volume of distribution significantly improved this model. Height, rather than weight, induced the best reduction in objective function. According to simulations, doses between 3.4 mg/cm and 4.4 mg/cm were necessary to achieve C max /MIC values of ≥8 and ≥10, respectively. However, higher doses were required to achieve the AUC/MIC targets.
This study demonstrated that height of the patients seems to be more suitable than their weight for dosing adjustments in adult patients with CF. According to this model, initial doses of tobramycin between 3.4 and 4.4 mg/cm should be recommended for patients with a median height of 164 cm and weight of 55 kg to achieve the target plasma concentrations.
成年囊性纤维化(CF)患者的急性肺部加重期(APE)采用β-内酰胺类药物和氨基糖苷类药物治疗,以对抗铜绿假单胞菌(PA)。在老龄化人群中,新出现的耐药性和不断变化的药代动力学特征涉及对妥布霉素给药建议的重新评估。本研究的目的是建立一个群体药代动力学模型,并使用蒙特卡洛模拟确定妥布霉素的最佳给药建议。
这项回顾性临床研究和数据收集在加拿大麦吉尔大学健康中心(MUHC)的CF中心进行。使用非线性混合效应建模方法(NONMEM,版本7.4.2)进行模型开发和模拟。评估最大浓度(Cmax)与最低抑菌浓度(MIC)的比值(Cmax/MIC≥8和≥10)以及曲线下面积(AUC)与MIC的比值(AUC/MIC≥70和≥100)。
本研究纳入了51例接受妥布霉素治疗的成年CF患者。从MUHC数据库中获取了699份妥布霉素血浆浓度样本。二室模型最能描述妥布霉素的药代动力学。患者身高与中央分布容积的关联显著改善了该模型。身高而非体重导致目标函数的最佳降低。根据模拟,分别需要3.4mg/cm至4.4mg/cm的剂量才能达到Cmax/MIC值≥8和≥10。然而,需要更高的剂量才能达到AUC/MIC目标。
本研究表明,对于成年CF患者,在调整剂量时,患者的身高似乎比体重更合适。根据该模型,对于身高中位数为164cm、体重为55kg的患者,应推荐初始剂量为3.4至4.4mg/cm的妥布霉素,以达到目标血浆浓度。