Noemí Acedo Alonso
Autonomous University of Barcelona
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Featured researches published by Noemí Acedo Alonso.
Journal of Antimicrobial Chemotherapy | 2015
Vanesa Pascual; Gabriel Ortiz; Maria Simó; Noemí Acedo Alonso; Maria Consol Garcia; Mariona Xercavins; M. A. Morera; Elisenda Miró; Elena Espejo; Ferran Navarro; Mercè Gurguí; Josefa Pérez; Mónica Rodríguez-Carballeira; Javier Garau; Esther Calbo
OBJECTIVES To describe the prevalence and risk factors for infection due to AmpC β-lactamase-producing Escherichia coli (AmpC-EC). METHODS For the prevalence study, all clinical isolates of E. coli with reduced susceptibility to third-generation cephalosporins were prospectively included from June 2010 to November 2011. For risk factor analysis, a case-control study was conducted. Cases were patients with an infection due to AmpC-EC. Controls were patients infected with cephalosporin-susceptible E. coli, matched 1 : 2. Detection of blaAmpC genes was done with a multiplex AmpC-PCR, and hyperproduction of E. coli chromosomal blaAmpC by quantitative RT-PCR. Alteration of the blaAmpC promoter was studied by PCR and sequencing. RESULTS We identified 243 (1.1%) AmpC-EC strains out of 21 563 clinical isolates. Three cases with strains carrying ESBLs, 18 strains that were considered due to colonization and 8 cases lost to clinical follow-up were excluded. Finally, 214 cases were included in the analysis. Ninety-one cases (42.5%) and 269 (62.8%) controls were strictly community acquired (P < 0.001). Thirty-five (16.3%) cases and 186 controls (43.5%) did not have any identifiable risk factor (P < 0.001). Among cases, 158 (73.8%) were found to harbour an acquired AmpC (73.4% CMY-2). Previous use of fluoroquinolones [OR 2.6 (95% CI 1.12-3.36); P = 0.008] was independently associated with AmpC-EC in the multivariate analysis. CONCLUSIONS Prevalence of AmpC in E. coli remains low in our area. Plasmid acquisition (CMY type) represents the main mechanism of AmpC production. A high proportion of community-acquired isolates and patients with no identifiable risk factors were found. Previous use of fluoroquinolones was identified as a risk factor.
Enfermedades Infecciosas Y Microbiologia Clinica | 2017
Inmaculada López-Hernández; Noemí Acedo Alonso; Marta Fernández-Martínez; Laura Zamorano; Antonio Oliver; M. Carmen Conejo; Luis Martínez-Martínez; Ferran Navarro; Álvaro Pascual
INTRODUCTION Antimicrobial resistance in Enterobacteriaceae is increasing worldwide and is making treating infections caused by multidrug-resistant Enterobacteriaceae a challenge. The use of β-lactam agents is compromised by microorganisms harboring extended-spectrum β-lactamases (ESBLs) and other mechanisms of resistance. Avibactam is a non β-lactam agent that inhibits clinically relevant β-lactamases, such as ESBL and AmpC. The ceftazidime-avibactam combination (CAZ-AVI) was recently approved for use in certain complicated infections, and may provide a therapeutic alternative for infections caused by these microorganisms. METHODS The in vitro activity of CAZ and CAZ-AVI (AVI at a fixed concentration of 4mg/L) was tested against 250 clinical isolates of Enterobacteriaceae using broth microdilution. EUCAST breakpoint criteria were used for CAZ, and FDA criteria for CAZ-AVI. Clinical isolates included bacteria producing extended-spectrum β-lactamases (ESBLs) and acquired AmpC β-lactamases (AACBLs). Porin loss in Klebsiella pneumoniae was also evaluated. RESULTS The combination of AVI with CAZ displayed excellent activity against clinical isolates of ESBL-producing Escherichia coli and Klebsiella pneumoniae, rendering all the ceftazidime-resistant isolates susceptible to ceftazidime. CAZ-AVI retained activity against porin-deficient isolates of K. pneumoniae producing ESBLs, AACBLs, or both, although MIC values were higher compared to porin-expressing isolates. CAZ-AVI rendered all the ceftazidime-resistant AACBL-producing Enterobacteriaceae tested susceptible to ceftazidime. CONCLUSION CAZ-AVI showed potent in vitro activity against clinical isolates of Enterobacteriaceae producing ESBLs and/or AACBLs, including K. pneumoniae with loss of porins.
Lectora: Revista de Dones i Textualitat | 2008
Noemí Acedo Alonso
Este articulo1 se presenta como una carta abierta a Flavia Company y a todas las personas que asistieron al seminario organizado por Meri Torras en el Ateneu de Barcelona el pasado invierno. En esta epistola se propone a los/as lectores/as una interpretacion de la novela Melalcor, centrada en conceptos como la identidad, el genero (sexual) o la escritura corporea. Es un breve estudio de algunos de los codigos que configuran el lenguaje de nuestros cuerpos.
International Journal of Antimicrobial Agents | 2016
Noemí Acedo Alonso; Elisenda Miró; Vanesa Pascual; Maria Simó; Maria Consol Garcia; Mariona Xercavins; M. A. Morera; Elena Espejo; Mercè Gurguí; Josefa Pérez; Mónica Rodríguez-Carballeira; Javier Garau; Esther Calbo; Ferran Navarro; Beatriz Mirelis; Pere Coll
European Journal of Clinical Microbiology & Infectious Diseases | 2016
Vanesa Pascual; Noemí Acedo Alonso; Maria Simó; G. Ortiz; Maria Consol Garcia; Mariona Xercavins; M. A. Morera; Elisenda Miró; Elena Espejo; Ferran Navarro; Mercè Gurguí; Josefa Pérez; Mónica Rodríguez-Carballeira; Javier Garau; Esther Calbo
Enrahonar: an international journal of theoretical and practical reason | 2018
Noemí Acedo Alonso
Enrahonar: an international journal of theoretical and practical reason | 2018
Noemí Acedo Alonso
Latinoamérica. Revista de Estudios Latinoamericanos | 2017
Noemí Acedo Alonso
UAB divulga | 2015
Noemí Acedo Alonso
TDX (Tesis Doctorals en Xarxa) | 2015
Noemí Acedo Alonso