作者: Stephen P Hawser , Samuel K Bouchillon , Christine Lascols , Meredith Hackel , Daryl J Hoban
DOI: 10.1128/AAC.00070-11
关键词: Amikacin 、 Klebsiella pneumoniae 、 Antibiotic resistance 、 Virology 、 Abdominal Infection 、 Antibiotics 、 Drug resistance 、 Biology 、 Imipenem 、 Ertapenem 、 Microbiology
摘要: A total of 2,841 clinical isolates Klebsiella pneumoniae from intra-abdominal infections worldwide were collected in the Study for Monitoring Antimicrobial Resistance Trends (SMART) during 2008 and 2009. Overall, 22.4% had extended-spectrum β-lactamases (ESBLs). The most active antibiotics among 11 tested imipenem, amikacin, ertapenem, though even these, like all other comparators, less consistently against ESBL-positive than ESBL-negative isolates. Globally, 6.5% ertapenem resistant based on June 2010 breakpoints published by Clinical Laboratory Standards Institute, with MICs ≥1 μg/ml. Molecular characterization 43 ≥4 μg/ml showed that they variously produced CTX-M or SHV ESBLs combined altered impermeability and/or KPC (n = 28), OXA-48 3), VIM 1) carbapenemases. Further monitoring susceptibility molecular ertapenem-resistant are needed.