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抗生素给药方案对实验性心内膜炎疗效的影响。

Impact of the antibiotic dosage schedule on efficacy in experimental endocarditis.

作者信息

Carbon C

机构信息

Department of Internal Medicine, Hôpital Bichat, Université Paris VII, France.

出版信息

Scand J Infect Dis Suppl. 1990;74:163-72.

PMID:2097705
Abstract

The animal model of endocarditis provides a reliable and reproducible model of acute infection and appears appropriate for studying the parameters involved in the in vivo efficacy of antibiotic therapy. The following points are discussed: (i) beta-lactam antibiotics exhibit a time-dependent bactericidal effect which explains the importance of t1/2 beta in the determination of dosing intervals and the need for large unitary doses for increasing efficacy through extending the period of serum levels greater than MIC (ii). The impact of unitary doses and dosing intervals of aminoglycosides on their in vivo synergism with beta-lactams has been investigated in Escherichia coli and streptococcal infections. Once- daily dosing of netilmicin appears very synergistic with ceftriaxone on E. coli, and the aminoglycoside has a significant dose effect. Conversely, divided doses are necessary to exhibit full synergistic effect with penicillin G on E. faecalis. Different patterns of in vivo synergism can therefore be individualized (iii). The rapid bactericidal effect of quinolones and their in vivo post-antibiotic effect allowing large intervals between doses have been investigated with ciprofloxacin (iv). The importance of t1/2 beta on the in vivo effect of glycopeptides is illustrated by data comparing teicoplanin and vancomycin. It is concluded that in vitro killing rate within 3 h is the major factor interfering with the dose interval, followed by t1/2 beta which is of major importance for those drugs whose bactericidal effect is time-dependent. These parameters appear to have a similar importance in experimental endocarditis to that in other experimental models. However, infected vegetations represent a particular focus of infection incorporating heterogeneity of antibiotic distribution, high density of bacteria and reduced metabolic activity of microorganisms. These factors may explain the lack of in vivo postantibiotic effect observed with some antibiotics, correspondingly shorter dosage intervals in endocarditis than in other types of infections and a need for high unitary doses.

摘要

心内膜炎动物模型为急性感染提供了一个可靠且可重复的模型,似乎适合用于研究抗生素治疗体内疗效相关的参数。讨论了以下几点:(i)β-内酰胺类抗生素表现出时间依赖性杀菌作用,这解释了t1/2β在确定给药间隔中的重要性,以及通过延长血清水平高于MIC的时间来增加疗效所需的大剂量单次给药的必要性(ii)。在大肠杆菌和链球菌感染中,研究了氨基糖苷类抗生素的单次剂量和给药间隔对其与β-内酰胺类抗生素体内协同作用的影响。奈替米星每日一次给药在大肠杆菌感染中与头孢曲松显示出很强的协同作用,且该氨基糖苷类抗生素有显著的剂量效应。相反,在粪肠球菌感染中,需分次给药才能与青霉素G发挥充分的协同作用。因此,不同的体内协同模式可以个体化(iii)。用环丙沙星研究了喹诺酮类药物的快速杀菌作用及其体内抗生素后效应,该效应允许较大的给药间隔(iv)。比较替考拉宁和万古霉素的数据说明了t1/2β对糖肽类药物体内效应的重要性。得出的结论是,3小时内的体外杀菌率是干扰给药间隔的主要因素,其次是t1/2β,对于杀菌作用具有时间依赖性的药物而言,t1/2β至关重要。这些参数在实验性心内膜炎中的重要性似乎与其他实验模型中的相似。然而,感染性赘生物是感染的一个特殊焦点,其包含抗生素分布的异质性、细菌的高密度以及微生物代谢活性的降低。这些因素可能解释了某些抗生素缺乏体内抗生素后效应、心内膜炎中给药间隔相应短于其他类型感染以及需要高剂量单次给药的原因。

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