Clinical Infectious Diseases · 2016 · 402 citations · 22 references
Life SciencesInfectious DiseasesMicrobiologyAntimicrobial ResistanceBacteriologyMedical MicrobiologyAntibacterial ResistanceAntibiotic ResistanceAntimicrobial Susceptibility TestingBacterial EpidemiologyBeta-lactam ResistanceCarbapenem Resistance28-Day MortalityBeta-lactamase GenesCarbapenem AntibioticsCarbapenem Resistance MechanismsMicroarray-based DetectionMinimum Inhibitory Concentration DeterminationMinimum Inhibitory Concentration TestingResistance Gene Mechanisms
BACKGROUND: Carbapenem-resistant Enterobacteriaceae (CRE) are associated with considerable mortality. As mechanisms of carbapenem resistance are heterogeneous, it is unclear if mortality differs based on resistance mechanisms. We sought to determine whether CRE resistance mechanism determination is prognostically informative. METHODS: We conducted an observational study comparing 14-day mortality between patients with carbapenemase-producing (CP)-CRE compared with non-CP-CRE bacteremia. Clinical data were collected on all patients. A comprehensive DNA microarray-based assay was performed on all isolates to identify β-lactamase-encoding genes. RESULTS: (3%). CP-CRE isolates were more likely to have meropenem minimum inhibitory concentrations (MICs) ≥16 µg/mL, while non-CP-CRE isolates were more likely to have meropenem MICs ≤1 µg/mL (P value < .001). A total of 18 (22%) patients died within 14 days, including 12 (32%) in the CP-CRE group and 6 (13%) in the non-CP-CRE group. Adjusting for severity of illness on day 1 of bacteremia, underlying medical conditions, and differences in antibiotic treatment administered, the odds of dying within 14 days were more than 4 times greater for CP-CRE compared with non-CP-CRE bacteremic patients (adjusted odds ratio, 4.92; 95% confidence interval, 1.01-24.81). CONCLUSION: Our findings suggest that CP-CRE may be more virulent than non-CP-CRE and are associated with poorer outcomes. This underscores the added importance of delineating underlying resistance mechanisms of CRE to direct antibiotic treatment decisions.
22
Mario Tumbarello, Pierluigi Viale, Claudio Viscoli et al. · Clinical Infectious Diseases · 2012 · 1K citations
Helen W. Boucher, George H. Talbot, Daniel K. Benjamin et al. · Clinical Infectious Diseases · 2013 · 696 citations · Full text
George L. Daikos, Sophia Tsaousi, L. S. Tzouvelekis et al. · Antimicrobial Agents and Chemotherapy · 2014 · 602 citations · Full text
Zubair Qureshi, David L. Paterson, Brian A. Potoski et al. · Antimicrobial Agents and Chemotherapy · 2012 · 563 citations · Full text