April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
ARMOR, a New Prospective, Multicenter Surveillance Study to Determine the in vitro Activity Profile of Besifloxacin and Comparators Against Ocular Pathogens From the US
Author Affiliations & Notes
  • W. Haas
    R & D Microbiology, Bausch & Lomb Inc, Rochester, New York
  • C. Pillar
    Eurofins Medinet, Inc., Chantilly, Virginia
  • M. Torres
    Eurofins Medinet, Inc., Chantilly, Virginia
  • T. W. Morris
    R & D Microbiology, Bausch & Lomb Inc, Rochester, New York
  • D. Sahm
    Eurofins Medinet, Inc., Chantilly, Virginia
  • Footnotes
    Commercial Relationships  W. Haas, Bausch + Lomb, E; C. Pillar, Bausch + Lomb, C; M. Torres, Bausch + Lomb, C; T.W. Morris, Bausch + Lomb, E; D. Sahm, Bausch + Lomb, C.
  • Footnotes
    Support  This study was supported by Bausch and Lomb
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 2417. doi:
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      W. Haas, C. Pillar, M. Torres, T. W. Morris, D. Sahm; ARMOR, a New Prospective, Multicenter Surveillance Study to Determine the in vitro Activity Profile of Besifloxacin and Comparators Against Ocular Pathogens From the US. Invest. Ophthalmol. Vis. Sci. 2010;51(13):2417.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract
 
Purpose:
 

It is important to track resistance trends among target pathogens to current agents and monitor for the emergence of resistance to recently approved agents such as besifloxacin (BES). This study reports susceptibility data for BES and comparators against ocular isolates of Gram-positive and -negative ocular pathogens collected across the US.

 
Methods:
 

In 2009, ocular isolates (144 S. aureus, 112 coagulase-negative staphylococci (CNS), 92 P. aeruginosa, 47 H. influenzae, and 41 S. pneumoniae) were collected from 21 hospitals across the US and were tested against BES, ciprofloxacin (CIP), moxifloxacin (MXF), azithromycin (AZM), and tobramycin (TOB).

 
Results:
 

Table 1 shows MIC50/MIC90 (µg/mL) values for five of the test agents. Against methicillin resistant S. aureus (MRSA) and CIP non-susceptible (NS) isolates BES had an MIC50/MIC90 of 1/4, relative to 4/16 for MXF and 64/256 for CIP. Against MR-CNS and CIP-NS isolates, BES had an MIC50/MIC90 of 0.25/4 and 0.5/4 respectively, several fold more potent than MXF (MR-CNS: 1/32; CIP-NS: 2/32) and CIP (MR-CNS: 16/64; CIP-NS: 64/64).

 
Conclusions:
 

BES was the most potent agent evaluated against Gram-positive cocci and was several-fold more potent against methicillin and fluoroquinolone resistant isolates. BES was comparable to other fluoroquinolones against H. influenzae, and was similar to MXF but less potent than CIP against P. aeruginosa. These results highlight the potential of BES for the treatment of ocular infections. Continued surveillance to monitor the emergence of resistance to current topical ophthalmic agents, including BES, is warranted.  

 
Keywords: antibiotics/antifungals/antiparasitics • bacterial disease • Staphylococcus 
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