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The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection

BACKGROUND: Staphylococcus aureus (SA) colonisation is associated with development of bloodstream infection (BSI), with the majority of colonising and infecting strains identical by pulsed-field gel electrophoresis (PFGE). We examined SA colonisation in patients with SABSI to delineate better the re...

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Autores principales: Marshall, Caroline, McBryde, Emma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099385/
https://www.ncbi.nlm.nih.gov/pubmed/24996783
http://dx.doi.org/10.1186/1756-0500-7-428
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author Marshall, Caroline
McBryde, Emma
author_facet Marshall, Caroline
McBryde, Emma
author_sort Marshall, Caroline
collection PubMed
description BACKGROUND: Staphylococcus aureus (SA) colonisation is associated with development of bloodstream infection (BSI), with the majority of colonising and infecting strains identical by pulsed-field gel electrophoresis (PFGE). We examined SA colonisation in patients with SABSI to delineate better the relationship between the two. METHODS: Patients with SABSI were swabbed in the nose, throat, groin, axilla and rectum. Isolates were typed using PFGE. Logistic regression was performed to determine factors associated with positive swabs. RESULTS: 79 patients with SABSI had swabs taken. 46 (58%) had ≥ 1 screening swab positive for S. aureus; of these 37 (80%) were in the nose, 11 (24%) in the throat, 12 (26%) in the groin, 11 (24%) in the axilla and 8 (17%) in the rectum. On multivariate analysis, days from blood culture to screening swabs (OR 0.5, 95% CI 0.32-0.78, P = 0.003) and methicillin resistance (OR 9.5, 95% CI 1.07-84.73, P = 0.04) were associated with having positive swabs. Of 46 participants who had a blood sample and 1 other sample subtyped, 33 (72%, 95% CI 57-84%) had all identical subtypes, 1 (2%) had subtypes varying by 1–3 bands and 12 (26%) had subtypes ≥ 3 bands different. 30/36 (83%) blood-nose pairs were identical. CONCLUSION: Overall, 58% of patients with SABSI had positive screening swabs. Of these, only 80% had a positive nose swab ie less than half (37/79, 47%) of all SABSI patients were nasally colonised. This may explain why nasal mupirocin alone has not been effective in preventing SA infection. Measures to eradicate non-nasal carriage should also be included.
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spelling pubmed-40993852014-07-17 The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection Marshall, Caroline McBryde, Emma BMC Res Notes Research Article BACKGROUND: Staphylococcus aureus (SA) colonisation is associated with development of bloodstream infection (BSI), with the majority of colonising and infecting strains identical by pulsed-field gel electrophoresis (PFGE). We examined SA colonisation in patients with SABSI to delineate better the relationship between the two. METHODS: Patients with SABSI were swabbed in the nose, throat, groin, axilla and rectum. Isolates were typed using PFGE. Logistic regression was performed to determine factors associated with positive swabs. RESULTS: 79 patients with SABSI had swabs taken. 46 (58%) had ≥ 1 screening swab positive for S. aureus; of these 37 (80%) were in the nose, 11 (24%) in the throat, 12 (26%) in the groin, 11 (24%) in the axilla and 8 (17%) in the rectum. On multivariate analysis, days from blood culture to screening swabs (OR 0.5, 95% CI 0.32-0.78, P = 0.003) and methicillin resistance (OR 9.5, 95% CI 1.07-84.73, P = 0.04) were associated with having positive swabs. Of 46 participants who had a blood sample and 1 other sample subtyped, 33 (72%, 95% CI 57-84%) had all identical subtypes, 1 (2%) had subtypes varying by 1–3 bands and 12 (26%) had subtypes ≥ 3 bands different. 30/36 (83%) blood-nose pairs were identical. CONCLUSION: Overall, 58% of patients with SABSI had positive screening swabs. Of these, only 80% had a positive nose swab ie less than half (37/79, 47%) of all SABSI patients were nasally colonised. This may explain why nasal mupirocin alone has not been effective in preventing SA infection. Measures to eradicate non-nasal carriage should also be included. BioMed Central 2014-07-05 /pmc/articles/PMC4099385/ /pubmed/24996783 http://dx.doi.org/10.1186/1756-0500-7-428 Text en Copyright © 2014 Marshall and McBryde; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Marshall, Caroline
McBryde, Emma
The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title_full The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title_fullStr The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title_full_unstemmed The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title_short The role of Staphylococcus aureus carriage in the pathogenesis of bloodstream infection
title_sort role of staphylococcus aureus carriage in the pathogenesis of bloodstream infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099385/
https://www.ncbi.nlm.nih.gov/pubmed/24996783
http://dx.doi.org/10.1186/1756-0500-7-428
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