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VetCAST Method for Determination of the Pharmacokinetic-Pharmacodynamic Cut-Off Values of a Long-Acting Formulation of Florfenicol to Support Clinical Breakpoints for Florfenicol Antimicrobial Susceptibility Testing in Cattle

机译:VetCAST方法测定氟苯尼考长效制剂的药代动力学-药效学临界值以支持牛氟苯尼考抗菌敏感性试验的临床断点

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摘要

The PK/PD cut-off (PK/PDCO) value of florfenicol for calf pathogens was determined for long acting formulations (MSD Nuflor® and a bioequivalent generic product). PK/PDCO is one of the three MICs considered by VetCAST, a sub-committee of the European Committee on Susceptibility Testing (EUCAST), to establish a Clinical Breakpoint for interpreting Antimicrobial Susceptibility Testing (AST). A population model was built by pooling three pharmacokinetic data sets, obtained from 50 richly sampled calves, receiving one of two formulations (the pioneer product and a generic formulation). A virtual population of 5,000 florfenicol disposition curves was generated by Monte Carlo Simulations (MCS) over the 96 h of the assumed duration of action of the formulations. From this population, the maximum predicted MIC, for which 90% of calves can achieve some a priori selected critical value for two PK/PD indices, AUC/MIC and T>MIC, was established. Numerical values were established for two bacterial species of the bovine respiratory disease (BRD) complex, Pasteurella multocida and Mannheimia haemolytica. It was concluded that the PK/PDCO of florfenicol for both AUC/MIC and T>MIC was 1 mg/L.
机译:对于长效制剂(MSDNuflor®和生物等效的通用产品),确定了氟苯尼考对小牛病原体的PK / PD截止值(PK / PDCO)值。 PK / PDCO是欧洲药敏试验委员会(EUCAST)的子委员会VetCAST所考虑的三个MIC之一,以建立解释抗生素药敏试验(AST)的临床断点。通过汇总三个药代动力学数据集(从50个丰富的牛犊中获得)来建立种群模型,并接收两种配方(先驱产品和通用配方)之一。通过蒙特卡洛模拟(MCS)在假设的制剂作用持续时间96小时内生成了5,000份氟苯尼考配置曲线的虚拟种群。从这个种群中,建立了最大预测MIC,对于两个PK / PD指数AUC / MIC和T> MIC,90%的犊牛可以达到一些先验选择的临界值。建立了牛呼吸道疾病(BRD)复合体的两种细菌物种多杀巴斯德氏菌和溶血曼海姆氏菌的数值。结论是氟苯尼考的​​AUC / MIC和T> MIC的PK / PDCO为1 mg / L。

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