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Identification and antimicrobial susceptibility of Staphylococcus from home-treated peritoneal dialysis patients

dc.contributor.authorBatalha, J. E. N. [UNESP]
dc.contributor.authorCunha, M. L. R. S. [UNESP]
dc.contributor.authorMontelli, A. C. [UNESP]
dc.contributor.authorBarretti, Pasqual [UNESP]
dc.contributor.authorCaramori, Jacqueline Socorro Costa Teixeira [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:51:04Z
dc.date.available2014-05-20T13:51:04Z
dc.date.issued2010-01-01
dc.description.abstractStaphylococcus aureus is the main agent of infections during peritoneal dialysis (PD). The presence of S. aureus in the nasal cavity has been extensively studied and suggested as a risk factor of dialysis-related infections, whereas coagulase-negative Staphylococcus (CNS) species are frequently considered part of the normal human microbiota. The aim of this study was to identify Staphylococcus in the nasal cavity, pericatheter skin and peritoneal effluent from PD patients, as well as to evaluate the antimicrobial activity evolution in vitro. Thirty-two chronic PD patients were observed during 12 months and had nasal and pericatheter skin samples collected for culture. When peritonitis was detected, samples were also collected from the peritoneal effluent for culture. The activity of several antimicrobial drugs (penicillin G, oxacillin, cephalothin, ofloxacin, netilmicin and vancomycin) against different Staphylococcus species was measured by using the agar drug diffusion assay (Kirby-Bauer method). Staphylococcus was separated into S. aureus, S. epidermidis and other CNS species in order to determine the in vitro resistance level. S. epidermidis resistance to oxacillin progressively increased during the study period (p < 0.05). Resistance to ofloxacin was inexpressive, whereas resistance to netilmicin and vancomycin was not detected. of the oxacillin-resistant species (n = 74), 83% were S. epidermidis, 13% other CNS and 4% S. aureus (p < 0.05). Regarding multidrug resistant strains (n = 45), 82% were S. epidermidis, 13% other CNS, and 5% S. aureus (p < 0.05). This study shows the relevance of resistance to oxacillin and CNS multi-drug resistance, particularly concerning S. epidermidis, in PD patients.en
dc.description.affiliationSão Paulo State Univ, UNESP, Univ Estadual Paulista, Dept Microbiol & Immunol,Botucatu Biosci Inst, Botucatu, SP, Brazil
dc.description.affiliationSão Paulo State Univ, UNESP, Univ Estadual Paulista, Dept Internal Med,Botucatu Med Sch, Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Univ Estadual Paulista, Dept Microbiol & Immunol,Botucatu Biosci Inst, Botucatu, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Univ Estadual Paulista, Dept Internal Med,Botucatu Med Sch, Botucatu, SP, Brazil
dc.format.extent212-222
dc.identifierhttp://dx.doi.org/10.1590/S1678-91992010000200005
dc.identifier.citationJournal of Venomous Animals and Toxins Including Tropical Diseases. Botucatu: Cevap-unesp, v. 16, n. 2, p. 212-222, 2010.
dc.identifier.fileS1678-91992010000200005-en.pdf
dc.identifier.issn1678-9199
dc.identifier.lattes5496411983893479
dc.identifier.orcid0000-0003-4979-4836
dc.identifier.scieloS1678-91992010000200005
dc.identifier.urihttp://hdl.handle.net/11449/18235
dc.identifier.wosWOS:000278873100005
dc.language.isoeng
dc.publisherUniversidade Estadual Paulista (Unesp), Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP)
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseases
dc.relation.ispartofjcr1.782
dc.relation.ispartofsjr0,573
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectperitoneal dialysis (PD)en
dc.subjectperitonitisen
dc.subjectrisk factoren
dc.subjectStaphylococcusen
dc.subjectcoagulase-negative Staphylococcus (CNS)en
dc.titleIdentification and antimicrobial susceptibility of Staphylococcus from home-treated peritoneal dialysis patientsen
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/jvatitd/iaboutj.htm
dcterms.rightsHolderCevap-unesp
dspace.entity.typePublication
unesp.author.lattes5496411983893479[4]
unesp.author.orcid0000-0003-4979-4836[4]
unesp.author.orcid0000-0001-9079-2723[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt
unesp.departmentMicrobiologia e Imunologia - IBBpt

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