GRIPE, School of Medicine, University of Antioquia, Medellin, Colombia.
Laboratorio Integrado de Medicina Especializada, School of Medicine, IPS Universitaria, University of Antioquia, Medellín, Colombia.
Antimicrob Agents Chemother. 2023 Feb 16;67(2):e0096622. doi: 10.1128/aac.00966-22. Epub 2023 Jan 25.
Combination therapy with ampicillin plus ceftriaxone (AMP+CRO) is the first-line therapy for treating severe infections due to Enterococcus faecalis. However, the pharmacokinetic/pharmacodynamic (PK/PD) index linked to the efficacy of the combination is not yet defined, hindering dose optimization in the clinic. Because classical PK/PD indices are not directly applicable to antimicrobial combinations, two novel indices were tested in the optimized murine model of infection by E. faecalis to delineate the potentiation of AMP by CRO: the time above the CRO threshold (T) and the time above the AMP instantaneous MIC (T). The potential clinical relevance was evaluated by simulating human doses of AMP and CRO. Hill's equation fitted well the exposure-response data in terms of T, with a CRO threshold of 1 mg/L. The required exposures were 46%, 49%, and 52% for stasis and 1- and 2-log killing, respectively. Human ceftriaxone doses of 2 g every 12 h (q12h) would reach the target in >90% of strains with thresholds ≤64 mg/L. The AMP T index also fitted well, and the required exposures were 37%, 41%, and 46% for stasis and 1- and 2-log killing, respectively. In humans, the addition of CRO would allow use of lower AMP doses to reach the same T and to treat strains with higher MICs. This is the first report of the PK/PD indices and required magnitudes linked to AMP+CRO against E. faecalis; these results can be used as the basis to guide the design of clinical trials to improve combined therapy against enterococci.
氨苄西林联合头孢曲松(AMP+CRO)联合治疗是治疗粪肠球菌引起的严重感染的一线治疗方法。然而,与联合疗效相关的药代动力学/药效学(PK/PD)指标尚未确定,这阻碍了临床优化剂量。由于经典的 PK/PD 指标不能直接应用于抗菌药物联合治疗,因此在优化的粪肠球菌感染小鼠模型中测试了两种新的指标来描述 CRO 对 AMP 的增效作用:CRO 阈值以上时间(T)和 AMP 瞬时 MIC 以上时间(T)。通过模拟人类 AMP 和 CRO 剂量来评估潜在的临床相关性。Hill 方程在 T 方面很好地拟合了暴露-反应数据,CRO 阈值为 1mg/L。对于停滞和 1-和 2-对数杀伤,分别需要 46%、49%和 52%的暴露。每 12 小时(q12h)给予 2g 的头孢曲松将达到阈值≤64mg/L 的>90%菌株的目标。AMP T 指数也很好地拟合,对于停滞和 1-和 2-对数杀伤,分别需要 37%、41%和 46%的暴露。在人类中,添加 CRO 可以降低 AMP 剂量以达到相同的 T,并治疗 MIC 更高的菌株。这是首次报道与粪肠球菌相关的 AMP+CRO 的 PK/PD 指标和所需强度,这些结果可用于指导临床试验设计,以改善针对肠球菌的联合治疗。