Sader Helio S, Jacobs Michael R, Fritsche Thomas R
JMI Laboratories, North Liberty, IA 52317, USA.
Diagn Microbiol Infect Dis. 2007 Mar;57(3 Suppl):5S-12S. doi: 10.1016/j.diagmicrobio.2006.12.014. Epub 2007 Feb 9.
The antimicrobial spectrum and in vitro potency of the most frequently prescribed orally administered cephalosporins (cefaclor, cefdinir, cefpodoxime, cefprozil, cefuroxime axetil, cephalexin) and amoxicillin/clavulanate are reviewed. These beta-lactam agents have been widely used in the outpatient arena for the treatment of community-acquired respiratory tract and other mild-to-moderate infections. The data presented here were obtained from critical review articles on each of these compounds. Cephalexin and cefaclor were among the least potent and had the narrowest antimicrobial spectrums against the pathogens evaluated. In contrast, cefdinir, cefpodoxime, cefprozil, and cefuroxime were highly active against penicillin-susceptible Streptococcus pneumoniae and retained some activity against penicillin-intermediate strains, whereas amoxicillin/clavulanate was the most active against S. pneumoniae, including most penicillin nonsusceptible strains. Amoxicillin/clavulanate and cefdinir were the most potent compounds against methicillin (oxacillin)-susceptible Staphylococcus aureus, whereas cefpodoxime was the most potent compound against Haemophilus influenzae. Amoxicillin/clavulanate, cefdinir, and cefpodoxime were also active against Moraxella catarrhalis, including beta-lactamase-producing strains. In summary, orally administered "3rd-generation" or extended spectrum cephalosporins exhibited more balanced spectrums of activity against the principal bacterial pathogens responsible for outpatient respiratory tract and other infections when compared with other widely used oral cephalosporins of earlier generations or amoxicillin alone.
本文综述了最常处方的口服头孢菌素(头孢克洛、头孢地尼、头孢泊肟酯、头孢丙烯、头孢呋辛酯、头孢氨苄)和阿莫西林/克拉维酸的抗菌谱及体外抗菌效力。这些β-内酰胺类药物已广泛用于门诊治疗社区获得性呼吸道感染及其他轻至中度感染。此处呈现的数据来自对这些化合物的批判性综述文章。头孢氨苄和头孢克洛对所评估病原体的抗菌效力最低且抗菌谱最窄。相比之下,头孢地尼、头孢泊肟酯、头孢丙烯和头孢呋辛对青霉素敏感的肺炎链球菌高度活跃,对青霉素中介菌株仍保留一定活性,而阿莫西林/克拉维酸对肺炎链球菌活性最强,包括大多数青霉素不敏感菌株。阿莫西林/克拉维酸和头孢地尼对甲氧西林(苯唑西林)敏感的金黄色葡萄球菌是最有效的化合物,而头孢泊肟酯对流感嗜血杆菌是最有效的化合物。阿莫西林/克拉维酸、头孢地尼和头孢泊肟酯对卡他莫拉菌也有活性,包括产β-内酰胺酶的菌株。总之,与其他广泛使用的早期口服头孢菌素或单独使用的阿莫西林相比,口服“第三代”或广谱头孢菌素对引起门诊呼吸道及其他感染的主要细菌病原体展现出更平衡的活性谱。