Nicodemo A C, Mendes C M, Oplustil C P, Sinto S
Medical Investigation Laboragory (LIM-54) - University of São Paulo Medical School, São Paulo, São Paulo, Brazil.
Braz J Infect Dis. 2001 Apr;5(2):50-2. doi: 10.1590/s1413-86702001000200001. Epub 2001 Aug 3.
In recent years, the level of resistance of S. pneumoniae to beta-lactam and/or macrolides has increased around the world including some countries in South America. Because of this resistance, it is necessary to test the therapeutic alternatives for treating this pathogen, including the newer quinolones. This study was carried out in order to compare the in vitro activity of fluoroquinolones gatifloxacin, levofloxacin and trovafloxacin, to penicillin G, amoxicillin, amoxicillin-clavulanate, cufuroxime sodium, ceftriaxone, azithromycin and clarithromycin, against 300 strains of S. pneumoniae. Of the 300 samples tested, 18.6% were not susceptible to penicillin (56 strains) and 7% (21 strains) were resistant to the second generation cephalosporin. Among the macrolides, resistance ranged from 6.7% for clarithromycin to 29.6% for azithromycin. Susceptibility to the newer quinolones was 100% including the 56 strains not susceptible to penicillin. Among the 10 antibiotics evaluated, the fluoroquinolones gatifloxacin, levofloxacin, and trovafloxacin displayed high levels of in vitro activity against S. pneumoniae.
近年来,肺炎链球菌对β-内酰胺类和/或大环内酯类药物的耐药水平在全球范围内有所上升,包括南美洲的一些国家。由于这种耐药性,有必要测试治疗这种病原体的替代疗法,包括新型喹诺酮类药物。本研究旨在比较加替沙星、左氧氟沙星和曲伐沙星这三种氟喹诺酮类药物,与青霉素G、阿莫西林、阿莫西林-克拉维酸、头孢呋辛钠、头孢曲松、阿奇霉素和克拉霉素对300株肺炎链球菌的体外活性。在测试的300个样本中,18.6%(56株)对青霉素不敏感,7%(21株)对第二代头孢菌素耐药。在大环内酯类药物中,克拉霉素的耐药率为6.7%,阿奇霉素为29.6%。包括56株对青霉素不敏感的菌株在内,对新型喹诺酮类药物的敏感性为100%。在评估的10种抗生素中,加替沙星、左氧氟沙星和曲伐沙星这三种氟喹诺酮类药物对肺炎链球菌显示出高水平的体外活性。