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一项关于头孢噻肟、头孢呋辛、头孢他啶、氧氟沙星和环丙沙星对血液及尿液病原体体外活性的多中心研究。

A multicentre study of the in-vitro activity of cefotaxime, cefuroxime, ceftazidime, ofloxacin and ciprofloxacin against blood and urinary pathogens.

作者信息

Amyes S G, Baird D R, Crook D W, Gillespie S H, Howard A J, Oppenhiem B A, Pedler S J, Paull A, Tompkins D S, Lawrie S A

机构信息

Scottish Antibiotic Reference Laboratory, Department of Medical Microbiology, University of Edinburgh.

出版信息

J Antimicrob Chemother. 1994 Nov;34(5):639-48. doi: 10.1093/jac/34.5.639.

Abstract

The in-vitro susceptibilities of aerobic bacteria isolated from 1804 blood and 4529 urine specimens collected at nine hospitals in the UK were examined. An agar dilution method was used to determine the MICs of each isolate to three cephalosporins, cefotaxime, cefuroxime and ceftazidime, and to two fluoroquinolones, ofloxacin and ciprofloxacin. Sensitivities were then calculated using British Society for Antimicrobial Chemotherapy recommended breakpoints. Of the cephalosporins tested cefotaxime was the most active against the Enterobacteriaceae. All the systemic staphylococcus isolates collected were sensitive to both cefotaxime and cefuroxime. As expected, ceftazidime was the only cephalosporin active against the Pseudomonas isolates. Both quinolones were highly active against the Enterobacteriaceae and Pseudomonas spp. They also demonstrated good Gram-positive activity, particularly against Staphylococcus aureus and Enterococcus spp.

摘要

对从英国九家医院采集的1804份血液样本和4529份尿液样本中分离出的需氧菌进行了体外药敏试验。采用琼脂稀释法测定每种分离菌对三种头孢菌素(头孢噻肟、头孢呋辛和头孢他啶)以及两种氟喹诺酮类药物(氧氟沙星和环丙沙星)的最低抑菌浓度(MIC)。然后使用英国抗菌化疗协会推荐的断点计算敏感性。在所测试的头孢菌素中,头孢噻肟对肠杆菌科细菌活性最强。收集的所有全身性葡萄球菌分离株对头孢噻肟和头孢呋辛均敏感。正如预期的那样,头孢他啶是唯一对假单胞菌分离株有活性的头孢菌素。两种喹诺酮类药物对肠杆菌科细菌和假单胞菌属均具有高活性。它们对革兰氏阳性菌也表现出良好的活性,尤其是对金黄色葡萄球菌和肠球菌属。

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