Fedrigo Nayara Helisandra, Mazucheli Josmar, Albiero James, Shinohara Danielle Rosani, Lodi Fernanda Gomes, Machado Ana Cristina Dos Santos, Sy Sherwin K B, Tognim Maria Cristina Bronharo
Departamento de Ciências Básicas da Saúde, Universidade Estadual de Maringá, Maringá, PR, Brazil.
Programa de Pós-Graduação em Bioestatística, Departamento de Estatística, Universidade Estadual de Maringá, Maringá, PR, Brazil.
Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.02498-16. Print 2017 Aug.
Fosfomycin is widely used for the treatment of uncomplicated urinary tract infection (UTI), and it has recently been recommended that fosfomycin be used to treat infections caused by multidrug-resistant (MDR) Gram-negative bacilli. Whether urine acidification can improve bacterial susceptibility to fosfomycin oral dosing regimens has not been analyzed. The MIC of fosfomycin for 245 Gram-negative bacterial isolates, consisting of 158 isolates and 87 isolates which were collected from patients with urinary tract infections, were determined at pH 6.0 and 7.0 using the agar dilution method. Monte Carlo simulation of the urinary fosfomycin area under the concentration-time curve (AUC) after a single oral dose of 3,000 mg fosfomycin and the MIC distribution were used to determine the probability of target attainment (PTA). Fosfomycin was effective against (MIC ≤ 16 μg/ml) but not against spp. (MIC > 512 μg/ml). Acidification of the environment increased the susceptibility of 71% of the bacterial isolates and resulted in a statistically significant decrease in bacterial survival. The use of a regimen consisting of a single oral dose of fosfomycin against an isolate with an MIC of ≤64 mg/liter was able to achieve a PTA of ≥90% for a target pharmacodynamic index (AUC/MIC) of 23 in urine; PTA was not achieved when the MIC was higher than 64 mg/liter. The cumulative fractions of the bacterial responses (CFR) were 99% and 55% against and spp., respectively, based on simulated drug exposure in urine with an acidic pH of 6.0. A decrease of the pH from 7.0 to 6.0 improved the PTA and CFR of the target pharmacodynamic index in both and isolates.
磷霉素广泛用于治疗非复杂性尿路感染(UTI),最近有人建议使用磷霉素治疗由多重耐药(MDR)革兰氏阴性杆菌引起的感染。尿液酸化是否能提高细菌对磷霉素口服给药方案的敏感性尚未得到分析。使用琼脂稀释法在pH 6.0和7.0条件下测定了从尿路感染患者中收集的245株革兰氏阴性细菌分离株(包括158株大肠埃希菌分离株和87株肺炎克雷伯菌分离株)对磷霉素的最低抑菌浓度(MIC)。采用蒙特卡洛模拟法,对单次口服3000 mg磷霉素后尿中磷霉素浓度-时间曲线下面积(AUC)和MIC分布进行分析,以确定达标概率(PTA)。磷霉素对大肠埃希菌有效(MIC≤16 μg/ml),但对肺炎克雷伯菌属无效(MIC>512 μg/ml)。环境酸化使71%的细菌分离株敏感性增加,并导致细菌存活率在统计学上显著降低。对于MIC≤64 mg/L的肺炎克雷伯菌分离株,采用单次口服磷霉素的给药方案,对于尿中目标药效学指标(AUC/MIC)为23时能够达到≥90%的PTA;当MIC高于64 mg/L时则无法达到PTA。基于pH值为6.0的尿液中模拟药物暴露情况,对大肠埃希菌和肺炎克雷伯菌属的细菌反应累积分数(CFR)分别为99%和55%。pH从7.0降至6.0可改善大肠埃希菌和肺炎克雷伯菌属分离株中目标药效学指标的PTA和CFR。