头孢噻肟
头孢匹罗
头孢曲松
青霉素
头孢他啶
微生物学
肺炎链球菌
头孢菌素
抗生素
抗菌剂
生物
细菌
亚胺培南
抗生素耐药性
遗传学
铜绿假单胞菌
作者
A L Barry,S D Brown,William J. Novick
标识
DOI:10.1128/aac.39.10.2193
摘要
The in vitro activities of four extended-spectrum cephalosporins and benzyl penicillin were evaluated against 698 clinical isolates of Streptococcus pneumoniae, including 130 (19%) penicillin-intermediate and 84 (12%) penicillin-resistant strains. Cefotaxime and ceftriaxone were essentially identical in their antipneumococcal activities: both were active against penicillin-susceptible strains and most penicillin-intermediate strains. Cefpirome was twice as potent as cefotaxime and ceftriaxone against penicillin-resistant strains. Ceftazidime was 8- to 16-fold less active than cefotaxime and ceftriaxone against S. pneumoniae in vitro, and thus, its spectrum included only penicillin-susceptible strains.
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