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Management of Glycopeptide-Resistant Staphylococcus aureus Infections

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Book cover Management of Multiple Drug-Resistant Infections

Part of the book series: Infectious Disease ((ID))

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Abstract

Before the introduction of penicillin, invasive Staphylococcus aureus infections were associated with mortality rates over 90% (1). Although penicillin was initially effective, resistance because of β-lactamase appeared quickly and spread. Within 10 yr, strains were resistant to erythromycin, tetracycline, and chloramphenicol. Methicillin resistance associated with modified penicillin-binding proteins (PBPs) appeared within 2 yr of the introduction of methicillin (2), and over the subsequent decades, strains resistant to an increasing number of antibiotics have spread worldwide. In hospitals, S. aureus resistant to multiple antibiotics commonly exceeds the susceptible strains. The emergence of glycopeptide-intermediate S. aureus (GISA) and vancomycin-resistant S. aureus (VRSA) raised the possibility of infections untreatable by standard antibiotic combinations. New agents are under investigation, but few fulfill the role.

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Peter, A., Wilson, R. (2004). Management of Glycopeptide-Resistant Staphylococcus aureus Infections. In: Gillespie, S.H. (eds) Management of Multiple Drug-Resistant Infections. Infectious Disease. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-738-3_4

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  • DOI: https://doi.org/10.1007/978-1-59259-738-3_4

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61737-438-8

  • Online ISBN: 978-1-59259-738-3

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