Departments of Pharmacology.
Microbiology.
Ther Drug Monit. 2020 Dec;42(6):841-847. doi: 10.1097/FTD.0000000000000800.
Amikacin is a semisynthetic antibiotic used in the treatment of gram-negative bacterial infections and has a narrow therapeutic index. Although therapeutic drug monitoring is recommended for amikacin, it is not routinely performed because of the use of a less toxic once-daily regimen. Only few studies have evaluated the role of therapeutic drug monitoring in patients treated with amikacin. The objective of our study was to find an association between the pharmacokinetic parameters of amikacin and the time required for a clinical cure, creatinine clearance, and frequency of ototoxicity in patients with urinary tract infection treated for 7 or more days.
A prospective study was conducted on patients with urinary tract infections who were administered amikacin for 7 or more days. Blood samples were obtained from the patients to measure the maximum drug concentration (Cmax) and trough concentration (Ctrough). Minimum inhibitory concentration (MIC) values were determined for patients with positive urine cultures. Serum creatinine levels were estimated every 3 days. The auditory assessment was performed using pure tone audiometry at baseline and weekly until the patients were discharged. Levels of amikacin were analyzed using a validated liquid chromatography-tandem mass spectrometry method.
Of 125 patients analyzed, the median time required for a clinical cure was less in the group of patients who achieved a Cmax/MIC ratio ≥8 than it was in those who did not achieve this level [7 versus 8 days (P = 0.02)]. The Ctrough of amikacin was associated with the change in serum creatinine level (P = 0.01) and the incidence of nephrotoxicity (P = 0.004).
In patients receiving short-term amikacin therapy, Cmax/MIC value can be used to predict the time required for a clinical cure. Ctrough can be used to predict the occurrence of nephrotoxicity in patients receiving amikacin therapy.
阿米卡星是一种半合成抗生素,用于治疗革兰氏阴性菌感染,治疗指数较窄。尽管推荐对阿米卡星进行治疗药物监测,但由于使用毒性较小的每日一次方案,因此并未常规进行。只有少数研究评估了治疗药物监测在接受阿米卡星治疗的患者中的作用。我们的研究目的是在接受阿米卡星治疗 7 天以上的尿路感染患者中,寻找阿米卡星药代动力学参数与临床治愈所需时间、肌酐清除率和耳毒性发生率之间的关联。
对接受阿米卡星治疗 7 天以上的尿路感染患者进行前瞻性研究。从患者中采集血样以测量最大药物浓度(Cmax)和谷浓度(Ctrough)。对尿液培养阳性的患者测定最小抑菌浓度(MIC)值。每 3 天估计一次血清肌酐水平。在基线和每周进行听觉评估,直到患者出院。使用经验证的液相色谱-串联质谱法分析阿米卡星水平。
在分析的 125 名患者中,达到 Cmax/MIC 比值≥8 的患者的临床治愈所需时间中位数明显短于未达到此水平的患者[7 天比 8 天(P = 0.02)]。阿米卡星的 Ctrough 与血清肌酐水平的变化(P = 0.01)和肾毒性的发生率(P = 0.004)相关。
在接受短期阿米卡星治疗的患者中,Cmax/MIC 值可用于预测临床治愈所需的时间。Ctrough 可用于预测接受阿米卡星治疗的患者发生肾毒性的情况。