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Rationale for Eliminating Staphylococcus Breakpoints for -Lactam Agents Other Than Penicillin, Oxacillin or Cefoxitin, and Ceftaroline
Author(s) -
Jennifer Dien Bard,
Janet A. Hindler,
Howard S. Gold,
Brandi Limbago
Publication year - 2014
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 - 10.1093/cid/ciu043
Subject(s) - cefoxitin , penicillin , medicine , cephalosporin , antibiotics , microbiology and biotechnology , penicillin binding proteins , staphylococcus aureus , staphylococcal infections , staphylococcus , biology , bacteria , genetics
Due to the ongoing concern about the reliability of Staphylococcus breakpoints (interpretive criteria) for other β-lactam agents, the Clinical and Laboratory Standards Institute recently approved the elimination of all breakpoints for antistaphylococcal β-lactams except for penicillin, oxacillin or cefoxitin, and ceftaroline. Routine testing of penicillin and oxacillin or cefoxitin should be used to infer susceptibility for all β-lactams with approved clinical indications for staphylococcal infections. It is critical for laboratories to reject requests for susceptibility testing of other β-lactams against staphylococci and to indicate that susceptibility to these agents can be predicted from the penicillin and oxacillin or cefoxitin results. This article reviews β-lactam resistance mechanisms in staphylococci, current antimicrobial susceptibility testing and reporting recommendations for β-lactams and staphylococci, and microbiologic data and clinical data supporting the elimination of staphylococcal breakpoints for other β-lactam agents.

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