TY - JOUR
T1 - Colonisation and infection due to Enterobacteriaceae producing plasmid-mediated AmpC β-lactamases
AU - Rodríguez-Baño, Jesús
AU - Miró, Elisenda
AU - Villar, Macarena
AU - Coelho, Alicia
AU - Gozalo, Mónica
AU - Borrell, Nuria
AU - Bou, Germán
AU - Conejo, M. Carmen
AU - Pomar, Virginia
AU - Aracil, Belén
AU - Larrosa, Nieves
AU - Agüero, Jesús
AU - Oliver, Antonio
AU - Fernández, Ana
AU - Oteo, Jesús
AU - Pascual, Alvaro
AU - Navarro, Ferran
PY - 2012/2/1
Y1 - 2012/2/1
N2 - Objectives: To investigate the epidemiology and clinical features of infections caused by Enterobacteria producing plasmid-mediated AmpC β-lactamases (pAmpC), which are emerging as a cause of resistance to extended-spectrum cephalosporins. Methods: A prospective multicentre cohort of patients with infection/colonisation due to pAmpC-producing Enterobacteriaceae was performed in 7 Spanish hospitals from February throughout July 2009. pAmpCs were characterised by PCR and sequencing. Results: 140 patients were included; organisms isolated were Escherichia coli (n=100), Proteus mirabilis (n=20), Klebsiella pneumoniae (n=17), and others (n=3). Overall, 90% had a chronic underlying condition. The acquisition was nosocomial in 43%, healthcare-associated in 41% (14% of those were nursing home residents), and community in 16%. Only 5% of patients had no predisposing feature for infection with multidrug-resistant bacteria. Nineteen percent of patients were bacteraemic. Inappropriate empirical therapy was administered to 81% of bacteraemic patients, who had a crude mortality rate of 48%. The most frequent enzyme was CMY-2 (70%, predominantly in E. coli and P. mirabilis) followed by DHA-1 (19%, predominantly in K. pneumoniae). Conclusion: pAmpC-producing Enterobacteriaceae caused nosocomial, healthcare-associated and community infections mainly in predisposed patients. Invasive infections were associated with high mortality which might be partly related to inappropriate empirical therapy. © 2011 The British Infection Association.
AB - Objectives: To investigate the epidemiology and clinical features of infections caused by Enterobacteria producing plasmid-mediated AmpC β-lactamases (pAmpC), which are emerging as a cause of resistance to extended-spectrum cephalosporins. Methods: A prospective multicentre cohort of patients with infection/colonisation due to pAmpC-producing Enterobacteriaceae was performed in 7 Spanish hospitals from February throughout July 2009. pAmpCs were characterised by PCR and sequencing. Results: 140 patients were included; organisms isolated were Escherichia coli (n=100), Proteus mirabilis (n=20), Klebsiella pneumoniae (n=17), and others (n=3). Overall, 90% had a chronic underlying condition. The acquisition was nosocomial in 43%, healthcare-associated in 41% (14% of those were nursing home residents), and community in 16%. Only 5% of patients had no predisposing feature for infection with multidrug-resistant bacteria. Nineteen percent of patients were bacteraemic. Inappropriate empirical therapy was administered to 81% of bacteraemic patients, who had a crude mortality rate of 48%. The most frequent enzyme was CMY-2 (70%, predominantly in E. coli and P. mirabilis) followed by DHA-1 (19%, predominantly in K. pneumoniae). Conclusion: pAmpC-producing Enterobacteriaceae caused nosocomial, healthcare-associated and community infections mainly in predisposed patients. Invasive infections were associated with high mortality which might be partly related to inappropriate empirical therapy. © 2011 The British Infection Association.
KW - β-Lactamases
KW - Bloodstream infections
KW - Escherichia coli
KW - Klebsiella pneumoniae
KW - Plasmid-mediated AmpC
KW - Proteus mirabilis
KW - Risk factors
U2 - 10.1016/j.jinf.2011.11.016
DO - 10.1016/j.jinf.2011.11.016
M3 - Article
SN - 0163-4453
VL - 64
SP - 176
EP - 183
JO - Journal of Infection
JF - Journal of Infection
IS - 2
ER -