• Lijec̆nic̆ki vjesnik · Jan 2010

    Review

    [Lipopeptides and oxazolidinones--novel antibiotics in MRSA infection treatment].

    • Ana Pangercić, Suzana Bukovski-Simonoski, and Bruno Barsić.
    • Zavod za intenzivnu medicinu i neuroinfektologiju, Klinika za infektivne bolesti "Dr. Fran Mihaljević", Zagreb.
    • Lijec Vjesn. 2010 Jan 1;132 Suppl 1:11-3.

    AbstractLast few years vancomycin-intermediate S. aureus and vancomycin-resistent S. aureus have emerged, giving us a task to reevaluate susceptiblity to vancomycin in treatment of methicillin-resistent S. aureus (MRSA) infections. It is also oportunity to review necessity for new generation of antibiotics in treatment of MRSA infections. Efficacy of vancomycin treatment in MRSA bacteriemia is associated with minimal inhibitory concentration (MIC) and speed of killing colonies. There is an increased probability of failure in treatment of MRSA bacteremia when there are high vancomycin MIC in vitro. That's one of the reasons why there is novel antibiotic therapy for MRSA investigated, especially daptomycin and linezolid. Daptomycin is lipopeptide and an important optional antibiotic in MRSA infections treatment: bacteremia and endocarditis, even the tricuspidal valve endocarditis. Linezolid, as novel oxazolidinon, has shown good activity against gram-positive bacteria, especially in treatment of nosocomial pneumonia and complicated skin and soft tissue infections caused by MRSA.

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