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 Blondeau, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Blondeau, J. M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (1999) 43, Suppl. B, 1-11
© 1999 The British Society for Antimicrobial Chemotherapy

A review of the comparative in-vitro activities of 12 antimicrobial agents, with a focus on five new `respiratory quinolones'

Joseph M. Blondeau*

Departments of Clinical Microbiology and Pathology, Saskatoon District Health, St Paul's Hospital (Grey Nuns'), Royal University Hospital and the University of Saskatchewan, Saskatoon, Saskatchewan, S7N 0W8, Canada

The efficacies of many antimicrobial agents are being threatened by a global increase in the numbers of resistant bacterial pathogens—microorganisms that were once susceptible to some of these agents. In particular, antimicrobial resistance amongst strains of Haemophilus influenzae, Moraxella catarrhalis and Streptococcus pneumoniae has limited the usefulness of first-line agents in some clinical settings. Quinolones were introduced in the 1980s and represented a significant therapeutic advancement in the treatment of patients with infectious diseases. While these compounds possessed potent in-vitro activities against a wide range of Gram-negative pathogens, their activities against some Gram-positive and `atypical' pathogens remained borderline. Further advancement in the development of quinolones has overcome some of these problems. The `respiratory quinolones' represent a new generation within this class of molecules and comprise compounds possessing broad spectrum activities against Gram-negative, Gram-positive and atypical pathogens. This review will focus on the in-vitro activities of five new respiratory quinolones (gatifloxacin, grepafloxacin, levofloxacin, moxifloxacin and trovafloxacin), ciprofloxacin and six non-quinolone agents (azithromycin, clarithromycin, amoxycillin, co-amoxiclav, cefuroxime and co-trimoxazole) against a range of bacterial and atypical pathogens, including those that are now resistant to several of these compounds.

* Corresponding address. Department of Clinical Microbiology, Royal University Hospital, 103 Hospital Drive, Saskatoon, Saskatchewan, S7N 0W8, Canada. Tel: +1-306-655-6943; Fax: +1-306-655-6947; E-mail: blondeauj{at}sdh.sk.ca


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


This article has been cited by other articles:


Home page
J Antimicrob ChemotherHome page
P. Silley, B. Stephan, H. A. Greife, and A. Pridmore
Comparative activity of pradofloxacin against anaerobic bacteria isolated from dogs and cats
J. Antimicrob. Chemother., November 1, 2007; 60(5): 999 - 1003.
[Abstract] [Full Text] [PDF]


Home page
Arch OphthalmolHome page
J. J. Fuller and D. M. Marcus
Vitreous and Aqueous Penetration of Orally Administered Gatifloxacin in Humans
Arch Ophthalmol, September 1, 2004; 122(9): 1408 - 1409.
[Full Text] [PDF]



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.