Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Soussy, C.-J.
Right arrow Articles by Courvalin, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Soussy, C.-J.
Right arrow Articles by Courvalin, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (1999) 43, Suppl. C, 43-50
© 1999 The British Society for Antimicrobial Chemotherapy

In-vitro antibacterial activity of levofloxacin against hospital isolates: a multicentre study

C.-J. Soussya,*, M. Cluzelb, M.-C. Ployc, M.-D. Kitzisd, C. Morele, A. Bryskierf and P. Courvaling

a Service de Bacteriologie, Hôpital Henri Mondor, Créteil b Department of bacteriology, CHU Clermont-Ferrand c Department of Bacteriology, CHU Limoges d department of Bacteriology, Hôpital Saint-Joseph, Paris e Department of Bacteriology, CHU Caen f Direction des Recherches Anti-infectieux, Clinical Pharmacology, Division Santé Hoechst Marion Roussel, Romainville g Unité des Agents Antibactériens, Institut Pasteur, Paris, France

The objective of this study was to evaluate the activity of the fluoroquinolone, levofloxacin, against hospital isolates of bacteria. MICs of levofloxacin were determined for 2154 strains by agar dilution. Breakpoints for susceptibility testing were calculated using the agar diffusion technique with 5 µg discs. The activity of levofloxacin against nalidixic acid- and pefloxacin-susceptible Enterobacteriaceae (n = 668) was higher (MIC 50/90 0.06–0.12 mg/L) than previously reported for ofloxacin. As seen with other fluoroquinolones, this activity was reduced against nalidixic acid-resistant and pefloxacin-intermediate and -resistant strains (MIC 1–8 mg/L). MICs for Pseudomonas aeruginosa (n = 104) were between 0.12 and 128 mg/L. Levofloxacin had good activity against nalidixic acid- and pefloxacin-susceptible Acinetobacter baumannii (n = 12; MIC 0.06–0.25 mg/L), but the activity was reduced against nalidixic acid- and pefloxacin-resistant strains (n = 80; MIC 1–32 mg/L). Haemophilus influenzae (n = 70), Haemophilus parainfluenzae (n = 47) and Moraxella catarrhalis (n = 64) were inhibited by low concentrations of levofloxacin (MICs 0.016–0.03 mg/L, 0.03–0.12 mg/L and 0.03–0.12 mg/L, respectively). Clostridium perfringens (n = 23; MIC 0.25–1 mg/L) was more susceptible than Bacteroides fragilis (n = 60; MIC 0.5–4 mg/L). Levofloxacin showed superior activity compared with ofloxacin against methicillin-susceptible staphylococci (n = 107; MIC 0.03–0.5 mg/L); the resistant strains (MICs 2–32 mg/L) were usually also resistant to methicillin. Levofloxacin was less effective against enterococci (n = 105; MIC 1–32 mg/L), but streptococci (n = 192) and pneumococci (n = 129), including 58 penicillin-non-susceptible strains, were inhibited by low concentrations (MICs 0.5–2 mg/L). According to the regression curve, zone diameters were usually 20–22 mm, 17–19 mm and 15–16 mm for MICs of 1, 2 and 4 mg/L, respectively. In conclusion, this study, performed on a large number of strains, confirms the superior antibacterial activity of levofloxacin compared with ofloxacin, especially against pathogens isolated from respiratory tract infections.

* Correspondence address. Service de Bacteriologie, Hôpital Henri Mondor, 51 Avenue du Maréchal de Lattre de Tassigny, 94010 Créteil Cedex, France. Tel: +33-1-49-81-28-31; Fax: +33-1-49-81-28-39.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.