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[新型氟喹诺酮类药物司帕沙星对医院感染菌的体外抗菌活性及协同曲线]

[In vitro antibacterial activity of a new fluoroquinolone, sparfloxacin, against nosocomial bacteria, and concordance curve].

作者信息

Soussy C J, Cluzel M, Derlot E, Exmelin L, Kitzis M D, Dabernat H, Le Noc P, Muller-Serieys C, Reverdy M E, Scheftel J M, Thabaut A

机构信息

Service de Bactériologie, CHU Henri-Mondor, Créteil, France.

出版信息

Pathol Biol (Paris). 1996 Apr;44(4):241-8.

PMID:8763585
Abstract

Minimal inhibitory concentrations (MICs) of sparfloxacin (SFX) were determined by agar dilution for 3,164 bacterial strains isolated in 10 university hospitals; in addition, antibiograms by agar diffusion were performed with 5 micrograms disks. Activity of SFX against nalidixic acid (NAL) susceptible (S) Enterobacteriaceae was close to that of other fluoroquinolones (FQ) (MIC 50 and 90: 0.06-0.5 microgram/ml); like for other FQ, this activity was reduced against NAL intermediate and resistant (R) Enterobacteriaceae (2-16). MICs of SFX against P. aeruginosa were between 0.12 and 16 (1-32). SFX had also a good activity against NAL-S A. baumannii (CMI < or = 0.25) but this activity is reduced against NAL-R Acinetobacter (16). SFX was highly active against Haemophilus (0.016-0.06) gonococci (0.008), meningococci (0.008) and B. catarrhalis (0.008-0.03). SFX showed activity superior to the currently available FQ against methicillin susceptible staphylococci (0.06); the resistant strains [8] are usually methicillin resistant. SFX is more effective against enterococci (0.5), streptococci (0.25-0.5) and particularly pneumococci (0.25-0.5) including penicillin-resistant strains. The coefficient correlation of the regression curve is 0.876; for MIC breakpoints of 1 and 2 micrograms/ml, zone diameter breakpoints should be 20 and 16 mm.

摘要

采用琼脂稀释法测定了10所大学医院分离出的3164株细菌对司帕沙星(SFX)的最低抑菌浓度(MIC);此外,还使用含5微克药物的纸片通过琼脂扩散法进行了药敏试验。司帕沙星对萘啶酸(NAL)敏感(S)的肠杆菌科细菌的活性与其他氟喹诺酮类药物(FQ)相近(MIC50和MIC90:0.06 - 0.5微克/毫升);与其他氟喹诺酮类药物一样,对NAL中介及耐药(R)的肠杆菌科细菌,其活性降低(2 - 16)。司帕沙星对铜绿假单胞菌的MIC在0.12至16之间(1 - 32)。司帕沙星对NAL敏感的鲍曼不动杆菌也有良好活性(CMI≤0.25),但对NAL耐药的不动杆菌,其活性降低(16)。司帕沙星对流感嗜血杆菌(0.016 - 0.06)、淋球菌(0.008)、脑膜炎球菌(0.008)和卡他莫拉菌(0.008 - 0.03)有高度活性。司帕沙星对甲氧西林敏感葡萄球菌的活性优于目前可用的氟喹诺酮类药物(0.06);耐药菌株[8]通常为甲氧西林耐药。司帕沙星对肠球菌(0.5)、链球菌(0.25 - 0.5),尤其是对包括耐青霉素菌株在内的肺炎球菌(0.25 - 0.5)更有效。回归曲线的系数相关性为0.876;对于MIC断点为1和2微克/毫升,抑菌圈直径断点应为20和16毫米。

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