Yourassowsky E
Département de Microbiologie, Hôpital universitaire Brugmann, Bruxelles, Belgique.
Ann Biol Clin (Paris). 1988;46(2):138-43.
Even though antibiotic in vivo and in vitro modes of action are not superposable, laboratory studies allow a logical approach to the treatment of infections. The answer to the question "What dose and for how long?" frequently asked during the treatment of a severe infection is not necessarily "The maximum dose for a long duration". The following points among many others, should be taken into consideration. The rate of bacterial action of beta-lactams on Gram negative bacilli is concentration dependent for ampicillin and amoxicillin for instance. This rate is hardly concentration dependent for ureidopenicillins (azlocillin, mezlocillin and piperacillin) and azthreonam which bind principally on PBP3. With third generation cephalosporins, in relation to concentrations, two steps in bactericidal rate may be observed. The post-antibiotic effect is often short (1 hour). The rate of bactericidal action of beta-lactams on Staphylococcus aureus is hardly concentration dependent. The post-antibiotic effect may be long (4 to 6 hours). A paradoxical effect may be observed namely with Streptococcus faecalis. The killing rate of beta-lactams is inoculum dependent. The aminoglycosides have a very high bactericidal activity rate on Gram positive and Gram negative bacteria. The post-antibiotic effect is long (4 to 6 hours). The antibacterial effect is little inoculum dependent. These conclusions are driven from experiences performed on cultures in growth phase. One of the controversial point related to the in vitro in vivo relationship is the ignorance of the multiplication rate of the bacteria in the infected site.(ABSTRACT TRUNCATED AT 250 WORDS)
尽管抗生素的体内和体外作用模式并不完全相同,但实验室研究为感染治疗提供了合理的方法。在严重感染治疗过程中经常问到的“用多大剂量、用多久?”这个问题,答案不一定是“长时间用最大剂量”。在诸多要点中,以下几点应予以考虑。例如,β-内酰胺类药物对革兰氏阴性杆菌的抗菌作用速率对于氨苄西林和阿莫西林而言是浓度依赖性的。而对于主要结合在PBP3上的脲基青霉素(阿洛西林、美洛西林和哌拉西林)和氨曲南,该速率几乎不依赖于浓度。对于第三代头孢菌素,就浓度而言,可观察到杀菌速率的两个阶段。抗生素后效应通常较短(1小时)。β-内酰胺类药物对金黄色葡萄球菌的杀菌作用速率几乎不依赖于浓度。抗生素后效应可能较长(4至6小时)。对于粪肠球菌可能会观察到一种矛盾效应。β-内酰胺类药物的杀菌速率取决于接种菌量。氨基糖苷类药物对革兰氏阳性和革兰氏阴性细菌具有非常高的杀菌活性速率。抗生素后效应较长(4至6小时)。抗菌作用对接种菌量依赖性较小。这些结论源于对生长阶段培养物所做的实验。与体外-体内关系相关的一个有争议的点是对感染部位细菌繁殖速率的忽视。(摘要截选至250词)