Cargando…

Length of stay and odds of MRSA acquisition: a dose–response relationship?

The association between methicillin-resistant Staphylococcus aureus (MRSA) colonisation and/or infection with increased morbidity and mortality among hospital patients has long been recognised. We sought to build on previous studies to identify modifiable risk factors associated with the acquisition...

Descripción completa

Detalles Bibliográficos
Autores principales: Loke, H. Y., Kyaw, W. M., Chen, M. I. C., Lim, J. W., Ang, B., Chow, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625199/
https://www.ncbi.nlm.nih.gov/pubmed/31364542
http://dx.doi.org/10.1017/S0950268819001110
_version_ 1783434368685965312
author Loke, H. Y.
Kyaw, W. M.
Chen, M. I. C.
Lim, J. W.
Ang, B.
Chow, A.
author_facet Loke, H. Y.
Kyaw, W. M.
Chen, M. I. C.
Lim, J. W.
Ang, B.
Chow, A.
author_sort Loke, H. Y.
collection PubMed
description The association between methicillin-resistant Staphylococcus aureus (MRSA) colonisation and/or infection with increased morbidity and mortality among hospital patients has long been recognised. We sought to build on previous studies to identify modifiable risk factors associated with the acquisition of MRSA colonisation and infection by conducting a retrospective cohort study on patients admitted through the Emergency Department of an acute tertiary-care general hospital in Singapore which implemented universal on-admission MRSA screening. Patients were assigned to the acquisition or non-acquisition group depending on whether they acquired MRSA during their admission. We used logistic regression models with a patient being in the acquisition group as the binary outcome to identify factors associated with MRSA acquisition. A total of 1302 acquisition and 37 949 non-acquisition group patients were analysed. Fifteen variables were included in the multivariate model. A dose–response relationship between length of stay and odds of MRSA acquisition was observed, with a length of stay 3 weeks or more (Adj OR 11.78–57.36, all P < 0.001) being the single biggest predictor of MRSA acquisition. Other variables significantly associated with MRSA acquisition were: male gender, age 65 or greater, previous MRSA colonisation or infection, exposure to certain antibiotics and surgery, and history of diabetes.
format Online
Article
Text
id pubmed-6625199
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Cambridge University Press
record_format MEDLINE/PubMed
spelling pubmed-66251992019-07-17 Length of stay and odds of MRSA acquisition: a dose–response relationship? Loke, H. Y. Kyaw, W. M. Chen, M. I. C. Lim, J. W. Ang, B. Chow, A. Epidemiol Infect Original Paper The association between methicillin-resistant Staphylococcus aureus (MRSA) colonisation and/or infection with increased morbidity and mortality among hospital patients has long been recognised. We sought to build on previous studies to identify modifiable risk factors associated with the acquisition of MRSA colonisation and infection by conducting a retrospective cohort study on patients admitted through the Emergency Department of an acute tertiary-care general hospital in Singapore which implemented universal on-admission MRSA screening. Patients were assigned to the acquisition or non-acquisition group depending on whether they acquired MRSA during their admission. We used logistic regression models with a patient being in the acquisition group as the binary outcome to identify factors associated with MRSA acquisition. A total of 1302 acquisition and 37 949 non-acquisition group patients were analysed. Fifteen variables were included in the multivariate model. A dose–response relationship between length of stay and odds of MRSA acquisition was observed, with a length of stay 3 weeks or more (Adj OR 11.78–57.36, all P < 0.001) being the single biggest predictor of MRSA acquisition. Other variables significantly associated with MRSA acquisition were: male gender, age 65 or greater, previous MRSA colonisation or infection, exposure to certain antibiotics and surgery, and history of diabetes. Cambridge University Press 2019-06-21 /pmc/articles/PMC6625199/ /pubmed/31364542 http://dx.doi.org/10.1017/S0950268819001110 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Loke, H. Y.
Kyaw, W. M.
Chen, M. I. C.
Lim, J. W.
Ang, B.
Chow, A.
Length of stay and odds of MRSA acquisition: a dose–response relationship?
title Length of stay and odds of MRSA acquisition: a dose–response relationship?
title_full Length of stay and odds of MRSA acquisition: a dose–response relationship?
title_fullStr Length of stay and odds of MRSA acquisition: a dose–response relationship?
title_full_unstemmed Length of stay and odds of MRSA acquisition: a dose–response relationship?
title_short Length of stay and odds of MRSA acquisition: a dose–response relationship?
title_sort length of stay and odds of mrsa acquisition: a dose–response relationship?
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625199/
https://www.ncbi.nlm.nih.gov/pubmed/31364542
http://dx.doi.org/10.1017/S0950268819001110
work_keys_str_mv AT lokehy lengthofstayandoddsofmrsaacquisitionadoseresponserelationship
AT kyawwm lengthofstayandoddsofmrsaacquisitionadoseresponserelationship
AT chenmic lengthofstayandoddsofmrsaacquisitionadoseresponserelationship
AT limjw lengthofstayandoddsofmrsaacquisitionadoseresponserelationship
AT angb lengthofstayandoddsofmrsaacquisitionadoseresponserelationship
AT chowa lengthofstayandoddsofmrsaacquisitionadoseresponserelationship