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[临床实践中的现有抗生素]

[Current antibiotics for clinical practice].

作者信息

Zimmerli W

机构信息

Departement für Innere Medizin, Universitätskliniken, Kantonsspital Basel.

出版信息

Praxis (Bern 1994). 1996 Oct 1;85(40):1240-4.

PMID:8966413
Abstract

During the last decade a large number of novel antimicrobial agents has been developed and marketed. For the practitioner, three groups of oral substances are important, namely cephalosporins, fluoroquinolones and macrolides. The new oral cephalosporins have an improved beta-lactamase stability. Their serum half-life of 2 to 4 h is more than twice as long as that of older substances; however, their oral bioavailability is lower than that of older cephalosporins. They have an excellent activity against gram-negative bacteria, but no or only little activity against staphylococci. They are especially indicated in ENT and UT infections. The fluoroquinolones have an excellent bioavailability and are therefore ideal as oral drugs. Their microbiological spectrum is best against gram negative microorganisms. Pneumococci are not very susceptible to quinolones, with the exception of sparfloxacin. There is an increasing emergency of resistance due to a broad use of these substances. Main indications are UT infections, febrile enterocolitis, and bone and joint infections. New macrolides give less side effects and improved pharmacokinetics. Clarithromycin and azithromycin have high tissue concentrations. The main indications are upper respiratory tract infections and the community-acquired pneumonia. Newer indications for clarithromycin and azithromycin are non-tuberculous mycobacteriosis and in special cases toxoplasmosis in AIDS patients. Despite the different advantages of the new oral antibiotics, older substances such as aminopenicillins and cotrimoxazole are still important agents in the outpatient treatment.

摘要

在过去十年中,大量新型抗菌药物已被研发并投放市场。对于从业者而言,有三类口服药物很重要,即头孢菌素、氟喹诺酮类和大环内酯类。新型口服头孢菌素对β-内酰胺酶的稳定性有所提高。它们的血清半衰期为2至4小时,比旧药物长两倍多;然而,它们的口服生物利用度低于旧的头孢菌素。它们对革兰氏阴性菌有出色的活性,但对葡萄球菌无活性或活性很小。它们特别适用于耳鼻喉科和泌尿系统感染。氟喹诺酮类具有出色的生物利用度,因此是理想的口服药物。它们的微生物谱对革兰氏阴性微生物最佳。除司帕沙星外,肺炎球菌对喹诺酮类不太敏感。由于这些药物的广泛使用,耐药性出现的情况越来越多。主要适应症为泌尿系统感染、发热性小肠结肠炎以及骨和关节感染。新型大环内酯类副作用较少,药代动力学有所改善。克拉霉素和阿奇霉素具有较高的组织浓度。主要适应症为上呼吸道感染和社区获得性肺炎。克拉霉素和阿奇霉素的新适应症是非结核分枝杆菌病,在特殊情况下还包括艾滋病患者的弓形虫病。尽管新型口服抗生素有不同优势,但旧药物如氨基青霉素和复方新诺明在门诊治疗中仍然是重要药物。

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