Alternatives to Vancomycin for the Treatment of Methicillin-Resistant Staphylococcus aureus Infections
Author(s) -
Scott T. Micek
Publication year - 2007
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/519471
Subject(s) - dalbavancin , tigecycline , linezolid , daptomycin , medicine , methicillin resistant staphylococcus aureus , vancomycin , quinupristin , dalfopristin , staphylococcus aureus , staphylococcal infections , microbiology and biotechnology , teicoplanin , antibiotics , biology , bacteria , genetics
Vancomycin remains the reference standard for the treatment of systemic infection caused by methicillin-resistant Staphylococcus aureus (MRSA). However, as a result of limited tissue distribution, as well as the emergence of isolates with reduced susceptibility and in vitro resistance to vancomycin, the need for alternative therapies that target MRSA has become apparent. New treatment options for invasive MRSA infections include linezolid, daptomycin, tigecycline, and quinupristin/dalfopristin. Additionally, a number of new anti-MRSA compounds are in development, including novel glycopeptides (dalbavancin, telavancin, and oritavancin), ceftobiprole, and iclaprim. The present article will review clinical issues surrounding the newly marketed and investigational agents with activity against MRSA.
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