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dc.creatorVillar, Macarenaes
dc.creatorCano, María Elicieres
dc.creatorGato, Evaes
dc.creatorGarnacho Montero, Josées
dc.creatorCisneros, José Migueles
dc.creatorRuiz de Alegría, C.es
dc.creatorPascual Hernández, Álvaroes
dc.creatorRodríguez-Baño, Jesúses
dc.date.accessioned2017-05-18T09:37:49Z
dc.date.available2017-05-18T09:37:49Z
dc.date.issued2014
dc.identifier.citationVillar, M., Cano, M.E., Gato, E., Garnacho Montero, J., Cisneros, J.M., Ruiz de Alegría, C.,...,Rodríguez-Baño, J. (2014). Epidemiologic and Clinical Impact of Acinetobacter baumannii Colonization and Infection: A Reappraisal. Medicine, 93 (5), 202-210.
dc.identifier.issn0025-7974es
dc.identifier.urihttp://hdl.handle.net/11441/60014
dc.description.abstractAcinetobacter baumannii is one of the most important antibiotic-resistant nosocomial bacteria. We investigated changes in the clinical and molecular epidemiology of A. baumannii over a 10-year period. We compared the data from 2 prospective multicenter cohort studies in Spain, one performed in 2000 (183 patients) and one in 2010 (246 patients), which included consecutive patients infected or colonized by A. baumannii. Molecular typing was performed by repetitive extragenic palindromic polymerase chain reaction (REP-PCR), pulsed-field gel electrophoresis (PFGE), and multilocus sequence typing (MLST). The incidence density of A. baumannii colonization or infection increased significantly from 0.14 in 2000 to 0.52 in 2010 in medical services (p<0.001). The number of non-nosocomial health careassociated cases increased from 1.2% to 14.2%, respectively (p<0.001). Previous exposure to carbapenems increased in 2010 (16.9% in 2000 vs 27.3% in 2010, p¼0.03). The drugs most frequently used for definitive treatment of patients with infections were carbapenems in 2000 (45%) and colistin in 2010 (50.3%). There was molecular-typing evidence of an increase in the frequency of A. baumannii acquisition in non-intensive care unit wards in 2010 (7.6% in 2000 vs 19.2% in 2010, p¼0.01). By MSLT, the ST2 clonal group predominated and increased in 2010. This epidemic clonal group was more frequently resistant to imipenem and was associated with an increased risk of sepsis, although not with severe sepsis or mortality. Some significant changes were noted in the epidemiology of A. baumannii, which is increasingly affecting patients admitted to conventional wards and is also the cause of non-nosocomial health care-associated infections. Epidemic clones seem to combine antimicrobial resistance and the ability to spread, while maintaining their clinical virulence.es
dc.description.sponsorshipMinisterio de Ciencia e Innovaciónes
dc.description.sponsorshipInstituto de Salud Carlos IIIes
dc.description.sponsorshipEuropean Development Regional Fund “A way to achieve Europe” ERDFes
dc.description.sponsorshipSpanish Network for the Research in Infectious Diseases REIPI RD06/0008es
dc.description.sponsorshipFIS PI 10/00056 and PI 11/02046es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherLippincott Williams & Wilkinses
dc.relation.ispartofMedicine, 93 (5), 202-210.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAcinetobacter baumanniies
dc.subjectNosocomial bacteriaes
dc.subjectMicrobiologic studieses
dc.subjectInfectiones
dc.titleEpidemiologic and Clinical Impact of Acinetobacter baumannii Colonization and Infection: A Reappraisales
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Microbiologíaes
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinau
dc.identifier.doi10.1097/MD.0000000000000036es
dc.contributor.groupUniversidad de Sevilla. CTS210: Adherencia Bacteriana a Nuevos Biomaterialeses
idus.format.extent9es
dc.journaltitleMedicinees
dc.publication.volumen93es
dc.publication.issue5es
dc.publication.initialPage202es
dc.publication.endPage210es

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