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Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?

BACKGROUND: Targeted screening of patients at high risk for methicillin-resistant Staphylococcus aureus (MRSA) carriage is an important component of MRSA control programs, which rely on prediction tools to identify those high-risk patients. Most previous risk studies reported a substantial rate of p...

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Autores principales: Pasricha, Janet, Harbarth, Stephan, Koessler, Thibaud, Camus, Veronique, Schrenzel, Jacques, Cohen, Gilles, Pittet, Didier, Perrier, Arnaud, Iten, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672049/
https://www.ncbi.nlm.nih.gov/pubmed/23721630
http://dx.doi.org/10.1186/2047-2994-2-17
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author Pasricha, Janet
Harbarth, Stephan
Koessler, Thibaud
Camus, Veronique
Schrenzel, Jacques
Cohen, Gilles
Pittet, Didier
Perrier, Arnaud
Iten, Anne
author_facet Pasricha, Janet
Harbarth, Stephan
Koessler, Thibaud
Camus, Veronique
Schrenzel, Jacques
Cohen, Gilles
Pittet, Didier
Perrier, Arnaud
Iten, Anne
author_sort Pasricha, Janet
collection PubMed
description BACKGROUND: Targeted screening of patients at high risk for methicillin-resistant Staphylococcus aureus (MRSA) carriage is an important component of MRSA control programs, which rely on prediction tools to identify those high-risk patients. Most previous risk studies reported a substantial rate of patients who are eligible for screening, but failed to be enrolled. The characteristics of these missed patients are seldom described. We aimed to determine the rate and characteristics of patients who were missed by a MRSA screening programme at our institution to see how the failure to include these patients might impact the accuracy of clinical prediction tools. FINDINGS: From March-June 2010 all patients admitted to 13 internal medicine wards at the University of Geneva Hospital (HUG) were prospectively screened for MRSA carriage. Of 1968 patients admitted to the ward, 267 patients (13.6%) failed to undergo appropriate MRSA screening. Forty-one (2.4%) screened patients were MRSA carriers at admission. On multivariate regression, patients who were missed by screening were more likely to be aged < 50 years (OR 2.4 [1.4-3.9]), transferred to internal medicine from another ward in the hospital (OR 2.8 [1.1-7.1]), and have a history of malignancy (OR 3.2[2.1-5.1]). There was no significant difference in the rate of previous MRSA carriage between screened and unscreened patients. CONCLUSIONS: Our findings highlight the potential bias that “missed” patients may introduce into MRSA risk scores. Reporting on the proportions and characteristics of missed patients is essential for accurate interpretation of MRSA prediction tools.
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spelling pubmed-36720492013-06-05 Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing? Pasricha, Janet Harbarth, Stephan Koessler, Thibaud Camus, Veronique Schrenzel, Jacques Cohen, Gilles Pittet, Didier Perrier, Arnaud Iten, Anne Antimicrob Resist Infect Control Short Report BACKGROUND: Targeted screening of patients at high risk for methicillin-resistant Staphylococcus aureus (MRSA) carriage is an important component of MRSA control programs, which rely on prediction tools to identify those high-risk patients. Most previous risk studies reported a substantial rate of patients who are eligible for screening, but failed to be enrolled. The characteristics of these missed patients are seldom described. We aimed to determine the rate and characteristics of patients who were missed by a MRSA screening programme at our institution to see how the failure to include these patients might impact the accuracy of clinical prediction tools. FINDINGS: From March-June 2010 all patients admitted to 13 internal medicine wards at the University of Geneva Hospital (HUG) were prospectively screened for MRSA carriage. Of 1968 patients admitted to the ward, 267 patients (13.6%) failed to undergo appropriate MRSA screening. Forty-one (2.4%) screened patients were MRSA carriers at admission. On multivariate regression, patients who were missed by screening were more likely to be aged < 50 years (OR 2.4 [1.4-3.9]), transferred to internal medicine from another ward in the hospital (OR 2.8 [1.1-7.1]), and have a history of malignancy (OR 3.2[2.1-5.1]). There was no significant difference in the rate of previous MRSA carriage between screened and unscreened patients. CONCLUSIONS: Our findings highlight the potential bias that “missed” patients may introduce into MRSA risk scores. Reporting on the proportions and characteristics of missed patients is essential for accurate interpretation of MRSA prediction tools. BioMed Central 2013-05-30 /pmc/articles/PMC3672049/ /pubmed/23721630 http://dx.doi.org/10.1186/2047-2994-2-17 Text en Copyright © 2013 Pasricha et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Pasricha, Janet
Harbarth, Stephan
Koessler, Thibaud
Camus, Veronique
Schrenzel, Jacques
Cohen, Gilles
Pittet, Didier
Perrier, Arnaud
Iten, Anne
Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title_full Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title_fullStr Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title_full_unstemmed Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title_short Methicillin-resistant Staphylococcus aureus risk profiling: who are we missing?
title_sort methicillin-resistant staphylococcus aureus risk profiling: who are we missing?
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672049/
https://www.ncbi.nlm.nih.gov/pubmed/23721630
http://dx.doi.org/10.1186/2047-2994-2-17
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