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Prospective observational study on the role of catheter colonization and multidrug-resistance associated with catheter-related bloodstream infections

dc.contributor.authorPinto, Miguel
dc.contributor.authorBorges, Vitor
dc.contributor.authorNascimento, Maria
dc.contributor.authorMartins, Filomena
dc.contributor.authorPessanha, Maria Ana
dc.contributor.authorFaria, Isabel
dc.contributor.authorRodrigues, Joao
dc.contributor.authorMatias, Rui
dc.contributor.authorJoao Paulo, Gomes
dc.contributor.authorJordao, Luisa
dc.date.accessioned2022-06-24T16:19:20Z
dc.date.available2022-06-24T16:19:20Z
dc.date.issued2022-04
dc.description.abstractBackground: Central venous catheter (CVC)-related bloodstream infection (CRBSI) is a huge public health consern with considerable impact on mortality and health costs. The emergence of antimicrobial resistant microorganisms associated or not with CVC colonization by biofilms makes the treatment of CRBSI even more challeging. Methods:A 3-year observational study enrolling 3 tertiary hospitals located in Lisbon (Portugal) was designed to identify the major etiological agent of 58 CRBSI, their ability to colonize CVCs and their antimicrobial resistance profiles. Etiological agents of CRBSI were idebtified by VITEK-2. Whole-genome sequencing was used to confirm CRBSI by the most prevalent etiological agents and characteriza their resistome. CVC's colonization (namely by biofilm assembly) was monitored by scanning electron microscopy. Results: Staphylococci were the most prevalent causative agent (36/58, 62%), with S. aureus and coagulase negative S. epidermidis accounting for 24.1% and 36.2% of CRBSIs, respectively. Comparative genomic analysis of CVCs/hemoculture pairs of isolates revealed genomic matches for 35/36 pairs and a good correlation between antibiotic susceptibility phenotype and the presence of antimicrobials resistance genetic determinants. CVCs colonization was observed mainly in the catheter lumen and presented different phenotypes ranging from isolated attached microorganisms to mature biofilms. The latest phenotype, mature biofilms of S. epidermidis and S. aureus were found for 50.0% and 48.6% of the CVCs, respectively. Nevertheless, no statistical significant association was established between biofilm assembly and CRBSI highlighting the need for further studies to elucidate biofilms' role on this HAI. Conclusion: WGS proved to be a valuable tool to confirm CRBSI. Despite staphylococci biofilms identification on a considerable number of CVCs, no statistically significant association was found between CRBSI and biofilms.pt_PT
dc.description.sponsorshipFCT/487/15/01/2019/Spt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/8041
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectBiofilmspt_PT
dc.subjectCRBSI (catheter related bloodstream infection)pt_PT
dc.subjectCentral Venous Catheterpt_PT
dc.subjectSthaphylococcuspt_PT
dc.subjectAntimicrobials Resistancept_PT
dc.subjectResistência aos Antimicrobianospt_PT
dc.titleProspective observational study on the role of catheter colonization and multidrug-resistance associated with catheter-related bloodstream infectionspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugal (online)pt_PT
oaire.citation.title32nd European Congress of Clinical Microbiology & Infectious Diseases (ECCMID), 23-26 April 2022pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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