Kovarik J M, Hoepelman I M, Verhoef J
Department of Clinical Microbiology and Infectious Diseases, University Hospital Utrecht, The Netherlands.
Eur J Clin Microbiol Infect Dis. 1989 Sep;8(9):761-9. doi: 10.1007/BF02185842.
Considerable in vitro and clinical research has been conducted concerning once-daily administration of aminoglycosides. Inherent to such regimens are elevated peak concentrations and prolonged periods during which concentrations are below the MIC for the pathogen. High peak concentration to MIC ratios may maximize bactericidal rates but the problem of toxicity remains. Although sustained exposure to sublethal concentrations could undermine efficacy, antimicrobial activity may be prolonged by the post-antibiotic effect. A wide variety of animal toxicity and efficacy models has been investigated. Findings suggest that less frequent administration is associated with less toxicity while efficacy remains unaltered. Elevated doses appeared to be well tolerated in studies in volunteers and patients, however relatively few critically ill patients have been assessed. Efficacy in the treatment of urinary tract, respiratory and other infections appears unaffected by administration frequency. In an attempt to standardize dosage regimens to allow comparisons among diverse patient groups in clinical trials, guidelines for dosage adjustment based on renal function are outlined.
关于氨基糖苷类药物每日一次给药,已经进行了大量的体外和临床研究。此类给药方案的固有特点是峰值浓度升高,且在较长时间段内浓度低于病原体的最低抑菌浓度(MIC)。高峰浓度与MIC的比值较高可能会使杀菌率最大化,但毒性问题依然存在。尽管持续暴露于亚致死浓度可能会削弱疗效,但抗生素后效应可能会延长抗菌活性。已经研究了各种各样的动物毒性和疗效模型。研究结果表明,给药频率较低与毒性较小相关,而疗效保持不变。在志愿者和患者的研究中,高剂量似乎耐受性良好,然而接受评估的重症患者相对较少。治疗尿路感染、呼吸道感染和其他感染的疗效似乎不受给药频率的影响。为了使给药方案标准化,以便在临床试验中对不同患者群体进行比较,概述了基于肾功能的剂量调整指南。