Abstract
The antimicrobial spectrum of activity of the early quinolones (i.e., norfloxacin, ofloxacin, ciprofloxacin) favor potency against Gram-negative microorganisms [1, 2]. The newer agents (levofloxacin, gatifloxacin, moxifloxacin) have expanded activity against the Gram-positive microorganisms [3, 4] and some of these newer agents which are currently available or in clinical trial (moxifloxacin, gatifloxacin, garenoxacin) also demonstrate excellent in vitro activity against the Gram-negative, Gram-positive, anaerobic, and atypical microorganisms [5-7]. Ciprofloxacin and levofloxacin have only moderate activity against the group A streptococci, with MIC90s of 0.5 pg/ml, however, reports of resistance to these agents have been rare [8, 9]. In a nationwide multicenter susceptibility surveillance study in Spain [10], 70 (3.4%) of 2,039 isolates of Streptococcus pyogenes had a ciprofloxacin MIC >_ 4 pg/ml. These microorganisms were found to be equally distributed between children and adults [10]. The early investigations with the then new fluoroquinolones, particularly ciprofloxacin, demonstrated in vitro activity against both methicillinsusceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA), although the activity was marginal with MIC90s of 0.5 pg/ml [11, 12]. A single mutation in the primary target would increase the MIC of ciprofloxacin four-to 16-fold, a level of resistance at or above peak drug concentrations achievable in serum, providing an opportunity for such first-step mutants to survive and emerge when a patient was exposed to fluoroquinolones [13]. Fluoroquinolone resistance in MRSA and the coagulase-negative staphylococci is now >50% worldwide [14-16]. Fluoroquinolone resistance in methicillin-susceptible staphylococci vary from <5% to 22%, depending on the location of the study [17, 18]. An international study with isolates provided from countries in Europe, Asia, and Latin America demonstrated ciprofloxacin resistant rates in MRSA, MSSA, methicillin-resistant and -susceptible coagulase-negative staphylococci of 90%, 21%, 50% and 22% respectively [15]. Susceptibility testing was carried out
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Embil, J.M. (2003). Quinolones for the treatment of skin, soft tissue, bone and prosthetic joint infections. In: Ronald, A.R., Low, D.E. (eds) Fluoroquinolone Antibiotics. Milestones in Drug Therapy. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8103-6_12
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DOI: https://doi.org/10.1007/978-3-0348-8103-6_12
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