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Braz. j. infect. dis ; 20(6): 556-563, Nov.-Dec. 2016. tab
Article in English | LILACS | ID: biblio-828166

ABSTRACT

ABSTRACT Background: Carbapenem-resistant Acinetobacter baumannii (CRAb) is an important cause of nosocomial infections especially in intensive care units. This study aimed to assess clinical aspects and the genetic background of CRAb among ICU patients at a Brazilian teaching hospital. Methods: 56 critically ill patients colonized or infected by CRAb, during ICU stay, were prospectively assessed. Based on imipenem MIC ≥ 4 µg/mL, 28 CRAB strains were screened for the presence of genes encoding metallo-β-lactamases and OXA-type β-lactamases. The blaOXA-type genes were characterized by PCR using primers targeting ISAba-1 or -3. Genetic diversity of blaOXA-positive strains was determined by ERIC-PCR analysis. Results: Patient's mean age (±SD) was 61 (±15.1), and 58.9% were male. Eighty-percent of the patients presented risk factors for CRAb colonization, mainly invasive devices (87.5%) and previous antibiotic therapy (77.6%). Thirty-three patients died during hospital stay (59.0%). Resistance to carbapenems was associated with a high prevalence of blaOXA-23 (51.2%) and/or blaOXA-143 (18.6%) genes. ERIC-PCR genotyping identified 10 clusters among OXA-producing CRAb. Three CRAb strains exhibited additional resistance to polymyxin B (MIC ≥ 4 µg/mL), whereas 10 CRAb strains showed tigecycline MICs > 2 µg/mL. Conclusions: In this study, clonally unrelated OXA-123- and OXA-143-producing A. baumannii strains in ICU patients were strongly correlated to colonization with infected patients being associated with a poor outcome.


Subject(s)
Humans , Male , Female , Middle Aged , beta-Lactamases/biosynthesis , Acinetobacter Infections/microbiology , Cross Infection/microbiology , Acinetobacter baumannii/enzymology , Anti-Bacterial Agents/pharmacology , beta-Lactamases/genetics , Brazil , Microbial Sensitivity Tests , Prospective Studies , Acinetobacter baumannii/drug effects , Acinetobacter baumannii/genetics , Multiplex Polymerase Chain Reaction , Genotype , Hospitals, Teaching , Intensive Care Units
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