In vitro evaluation of meropenem-vaborbactam against clinical CRE isolates at a tertiary care center with low KPC-mediated carbapenem resistance
The in vitro activity of meropenem-vaborbactam was examined against clinical carbapenem-resistant Enterobacteriaceae isolates collected over 3 years at our medical center. Only 3 KPC-producers were identified. Susceptibility to meropenem-vaborbactam was noted in 15/16 (94%) isolates (MIC90 2 mg/L) t...
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Published in | Diagnostic microbiology and infectious disease Vol. 93; no. 3; pp. 258 - 260 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.03.2019
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Subjects | |
Online Access | Get full text |
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Summary: | The in vitro activity of meropenem-vaborbactam was examined against clinical carbapenem-resistant Enterobacteriaceae isolates collected over 3 years at our medical center. Only 3 KPC-producers were identified. Susceptibility to meropenem-vaborbactam was noted in 15/16 (94%) isolates (MIC90 2 mg/L) that were nonsusceptible to meropenem. Meropenem-vaborbactam may have utility at centers where non–KPC-producers are more frequent.
•Meropenem-vaborbactam is a novel drug combination that is particularly potent against KPC-producing CRE.•Meropenem-vaborbactam susceptibility testing by gradient diffusion and disk diffusion was evaluated against 44 clinical CRE isolates from patients at our health care center collected over a 3-year period.•Meropenem-vaborbactam susceptibility testing results were congruent using CLSI-approved gradient diffusion and disk diffusion testing methods.•Meropenem-vaborbactam had relatively potent in vitro activity (MIC90 2 mg/L) against CRE isolates at our center despite a very low incidence of KPC-producing CRE.•Individual health care centers should evaluate novel drugs in the context of the local epidemiology of circulating strains at their center. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0732-8893 1879-0070 |
DOI: | 10.1016/j.diagmicrobio.2018.09.017 |