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Staphylococcus aureus Nasal Colonization and Subsequent Infection in Intensive Care Unit Patients: Does Methicillin Resistance Matter?
Staphylococcus aureus is an important cause of infection in intensive care unit (ICU) patients. Colonization with methicillin-resistant S. aureus (MRSA) is a risk factor for subsequent S. aureus infection. However, MRSA-colonized patients may have more comorbidities than methicillin-susceptible S. a...
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Published in: | Infection control and hospital epidemiology 2010-06, Vol.31 (6), p.584-591 |
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description | Staphylococcus aureus is an important cause of infection in intensive care unit (ICU) patients. Colonization with methicillin-resistant S. aureus (MRSA) is a risk factor for subsequent S. aureus infection. However, MRSA-colonized patients may have more comorbidities than methicillin-susceptible S. aureus (MSSA)-colonized or noncolonized patients and therefore may be more susceptible to infection on that basis.
To determine whether MRSA-colonized patients who are admitted to medical and surgical ICUs are more likely to develop any S. aureus infection in the ICU, compared with patients colonized with MSSA or not colonized with S. aureus, independent of predisposing patient risk factors.
Prospective cohort study.
A 24-bed surgical ICU and a 19-bed medical ICU of a 1,252-bed, academic hospital.
A total of 9,523 patients for whom nasal swab samples were cultured for S. aureus at ICU admission during the period from December 2002 through August 2007.
Patients in the ICU for more than 48 hours were examined for an ICU-acquired S. aureus infection, defined as development of S. aureus infection more than 48 hours after ICU admission.
S. aureus colonization was present at admission for 1,433 (27.8%) of 5,161 patients (674 [47.0%] with MRSA and 759 [53.0%] with MSSA). An ICU-acquired S. aureus infection developed in 113 (2.19%) patients, of whom 75 (66.4%) had an infection due to MRSA. Risk factors associated with an ICU-acquired S. aureus infection included MRSA colonization at admission (adjusted hazard ratio, 4.70 [95% confidence interval, 3.07-7.21]) and MSSA colonization at admission (adjusted hazard ratio, 2.47 [95% confidence interval, 1.52-4.01]).
ICU patients colonized with S. aureus were at greater risk of developing a S. aureus infection in the ICU. Even after adjusting for patient-specific risk factors, MRSA-colonized patients were more likely to develop S. aureus infection, compared with MSSA-colonized or noncolonized patients. |
doi_str_mv | 10.1086/652530 |
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To determine whether MRSA-colonized patients who are admitted to medical and surgical ICUs are more likely to develop any S. aureus infection in the ICU, compared with patients colonized with MSSA or not colonized with S. aureus, independent of predisposing patient risk factors.
Prospective cohort study.
A 24-bed surgical ICU and a 19-bed medical ICU of a 1,252-bed, academic hospital.
A total of 9,523 patients for whom nasal swab samples were cultured for S. aureus at ICU admission during the period from December 2002 through August 2007.
Patients in the ICU for more than 48 hours were examined for an ICU-acquired S. aureus infection, defined as development of S. aureus infection more than 48 hours after ICU admission.
S. aureus colonization was present at admission for 1,433 (27.8%) of 5,161 patients (674 [47.0%] with MRSA and 759 [53.0%] with MSSA). An ICU-acquired S. aureus infection developed in 113 (2.19%) patients, of whom 75 (66.4%) had an infection due to MRSA. Risk factors associated with an ICU-acquired S. aureus infection included MRSA colonization at admission (adjusted hazard ratio, 4.70 [95% confidence interval, 3.07-7.21]) and MSSA colonization at admission (adjusted hazard ratio, 2.47 [95% confidence interval, 1.52-4.01]).
ICU patients colonized with S. aureus were at greater risk of developing a S. aureus infection in the ICU. Even after adjusting for patient-specific risk factors, MRSA-colonized patients were more likely to develop S. aureus infection, compared with MSSA-colonized or noncolonized patients.</description><identifier>ISSN: 0899-823X</identifier><identifier>EISSN: 1559-6834</identifier><identifier>DOI: 10.1086/652530</identifier><identifier>PMID: 20426656</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Artificial respiration ; Bacterial diseases ; Biological and medical sciences ; Carrier State - diagnosis ; Carrier State - epidemiology ; Central venous catheterization ; Cohort Studies ; Cross Infection - prevention & control ; Female ; Hospital admissions ; Hospital units ; Hospitalization ; Hospitals, University ; Human bacterial diseases ; Humans ; Infections ; Infectious diseases ; Intensive Care Units ; Male ; Mass Screening ; Medical sciences ; Methicillin-Resistant Staphylococcus aureus - isolation & purification ; Microbial colonization ; Middle Aged ; Miscellaneous ; Missouri - epidemiology ; Nasal Cavity - microbiology ; Nursing ; Original Article ; Patient Admission ; Pharmacology. Drug treatments ; Predisposing factors ; Prospective Studies ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Staphylococcal Infections - diagnosis ; Staphylococcal Infections - epidemiology ; Staphylococcal Infections - etiology ; Staphylococcal infections, streptococcal infections, pneumococcal infections ; Staphylococcus aureus ; Staphylococcus aureus - isolation & purification ; Young Adult</subject><ispartof>Infection control and hospital epidemiology, 2010-06, Vol.31 (6), p.584-591</ispartof><rights>2010 by The Society for Healthcare Epidemiology of America. All rights reserved.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-fa80250fe6aff17720675804b10aa64c44821f27ba27dce78c1942061cf5e7843</citedby><cites>FETCH-LOGICAL-c423t-fa80250fe6aff17720675804b10aa64c44821f27ba27dce78c1942061cf5e7843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22773603$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20426656$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Honda, Hitoshi</creatorcontrib><creatorcontrib>Krauss, Melissa J.</creatorcontrib><creatorcontrib>Coopersmith, Craig M.</creatorcontrib><creatorcontrib>Kollef, Marin H.</creatorcontrib><creatorcontrib>Richmond, Amy M.</creatorcontrib><creatorcontrib>Fraser, Victoria J.</creatorcontrib><creatorcontrib>Warren, David K.</creatorcontrib><title>Staphylococcus aureus Nasal Colonization and Subsequent Infection in Intensive Care Unit Patients: Does Methicillin Resistance Matter?</title><title>Infection control and hospital epidemiology</title><addtitle>Infect Control Hosp Epidemiol</addtitle><description>Staphylococcus aureus is an important cause of infection in intensive care unit (ICU) patients. Colonization with methicillin-resistant S. aureus (MRSA) is a risk factor for subsequent S. aureus infection. However, MRSA-colonized patients may have more comorbidities than methicillin-susceptible S. aureus (MSSA)-colonized or noncolonized patients and therefore may be more susceptible to infection on that basis.
To determine whether MRSA-colonized patients who are admitted to medical and surgical ICUs are more likely to develop any S. aureus infection in the ICU, compared with patients colonized with MSSA or not colonized with S. aureus, independent of predisposing patient risk factors.
Prospective cohort study.
A 24-bed surgical ICU and a 19-bed medical ICU of a 1,252-bed, academic hospital.
A total of 9,523 patients for whom nasal swab samples were cultured for S. aureus at ICU admission during the period from December 2002 through August 2007.
Patients in the ICU for more than 48 hours were examined for an ICU-acquired S. aureus infection, defined as development of S. aureus infection more than 48 hours after ICU admission.
S. aureus colonization was present at admission for 1,433 (27.8%) of 5,161 patients (674 [47.0%] with MRSA and 759 [53.0%] with MSSA). An ICU-acquired S. aureus infection developed in 113 (2.19%) patients, of whom 75 (66.4%) had an infection due to MRSA. Risk factors associated with an ICU-acquired S. aureus infection included MRSA colonization at admission (adjusted hazard ratio, 4.70 [95% confidence interval, 3.07-7.21]) and MSSA colonization at admission (adjusted hazard ratio, 2.47 [95% confidence interval, 1.52-4.01]).
ICU patients colonized with S. aureus were at greater risk of developing a S. aureus infection in the ICU. Even after adjusting for patient-specific risk factors, MRSA-colonized patients were more likely to develop S. aureus infection, compared with MSSA-colonized or noncolonized patients.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Artificial respiration</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Carrier State - diagnosis</subject><subject>Carrier State - epidemiology</subject><subject>Central venous catheterization</subject><subject>Cohort Studies</subject><subject>Cross Infection - prevention & control</subject><subject>Female</subject><subject>Hospital admissions</subject><subject>Hospital units</subject><subject>Hospitalization</subject><subject>Hospitals, University</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Intensive Care Units</subject><subject>Male</subject><subject>Mass Screening</subject><subject>Medical sciences</subject><subject>Methicillin-Resistant Staphylococcus aureus - isolation & purification</subject><subject>Microbial colonization</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Missouri - epidemiology</subject><subject>Nasal Cavity - microbiology</subject><subject>Nursing</subject><subject>Original Article</subject><subject>Patient Admission</subject><subject>Pharmacology. Drug treatments</subject><subject>Predisposing factors</subject><subject>Prospective Studies</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Staphylococcal Infections - diagnosis</subject><subject>Staphylococcal Infections - epidemiology</subject><subject>Staphylococcal Infections - etiology</subject><subject>Staphylococcal infections, streptococcal infections, pneumococcal infections</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - isolation & purification</subject><subject>Young Adult</subject><issn>0899-823X</issn><issn>1559-6834</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqF0d1qVDEQAOAgil2rPoIERL1azX9yeqHI-ldoVawF7w6zaeKmZJM1ySnUB_C5je5a9UK8Gob5MhlmELpLyWNKjHqiJJOcXEMzKuUwV4aL62hGzDDMDeOf9tCtWs8JIXoY6E20x4hgSkk1Q99OGmxWlzHbbO1UMUzF9fAWKkS8yDGn8BVayAlDOsMn07K6L5NLDR8m7-zPQkg9aS7VcOHwAorDpyk0_L4_67Ae4BfZVXzs2irYEGPnH1wNtUGyDh9Da648u41ueIjV3dnFfXT66uXHxZv50bvXh4vnR3MrGG9zD4YwSbxT4D3VmhGlpSFiSQmAElYIw6hneglMn1mnjaWD6IhaL3sm-D56uu27mZZr10lqBeK4KWEN5XLMEMa_Kymsxs_5YhRUCmlUb_Bo16DkvojaxnWo1sUIyeWpjlrIQRvdl_5fyfnAjSGmy4dbaUuutTh_NQ8l44_rjtvrdnjvz-mv2K9zdvBgB6BaiL70HYf62zGtuSK8u_tbd15bLv_67jskNrlI</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Honda, Hitoshi</creator><creator>Krauss, Melissa J.</creator><creator>Coopersmith, Craig M.</creator><creator>Kollef, Marin H.</creator><creator>Richmond, Amy M.</creator><creator>Fraser, Victoria J.</creator><creator>Warren, David K.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7U1</scope><scope>7U2</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>20100601</creationdate><title>Staphylococcus aureus Nasal Colonization and Subsequent Infection in Intensive Care Unit Patients: Does Methicillin Resistance Matter?</title><author>Honda, Hitoshi ; Krauss, Melissa J. ; Coopersmith, Craig M. ; Kollef, Marin H. ; Richmond, Amy M. ; Fraser, Victoria J. ; Warren, David K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-fa80250fe6aff17720675804b10aa64c44821f27ba27dce78c1942061cf5e7843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Artificial respiration</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Carrier State - diagnosis</topic><topic>Carrier State - epidemiology</topic><topic>Central venous catheterization</topic><topic>Cohort Studies</topic><topic>Cross Infection - prevention & control</topic><topic>Female</topic><topic>Hospital admissions</topic><topic>Hospital units</topic><topic>Hospitalization</topic><topic>Hospitals, University</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Intensive Care Units</topic><topic>Male</topic><topic>Mass Screening</topic><topic>Medical sciences</topic><topic>Methicillin-Resistant Staphylococcus aureus - isolation & purification</topic><topic>Microbial colonization</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Missouri - epidemiology</topic><topic>Nasal Cavity - microbiology</topic><topic>Nursing</topic><topic>Original Article</topic><topic>Patient Admission</topic><topic>Pharmacology. Drug treatments</topic><topic>Predisposing factors</topic><topic>Prospective Studies</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Staphylococcal Infections - diagnosis</topic><topic>Staphylococcal Infections - epidemiology</topic><topic>Staphylococcal Infections - etiology</topic><topic>Staphylococcal infections, streptococcal infections, pneumococcal infections</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - isolation & purification</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Honda, Hitoshi</creatorcontrib><creatorcontrib>Krauss, Melissa J.</creatorcontrib><creatorcontrib>Coopersmith, Craig M.</creatorcontrib><creatorcontrib>Kollef, Marin H.</creatorcontrib><creatorcontrib>Richmond, Amy M.</creatorcontrib><creatorcontrib>Fraser, Victoria J.</creatorcontrib><creatorcontrib>Warren, David K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection control and hospital epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Honda, Hitoshi</au><au>Krauss, Melissa J.</au><au>Coopersmith, Craig M.</au><au>Kollef, Marin H.</au><au>Richmond, Amy M.</au><au>Fraser, Victoria J.</au><au>Warren, David K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Staphylococcus aureus Nasal Colonization and Subsequent Infection in Intensive Care Unit Patients: Does Methicillin Resistance Matter?</atitle><jtitle>Infection control and hospital epidemiology</jtitle><addtitle>Infect Control Hosp Epidemiol</addtitle><date>2010-06-01</date><risdate>2010</risdate><volume>31</volume><issue>6</issue><spage>584</spage><epage>591</epage><pages>584-591</pages><issn>0899-823X</issn><eissn>1559-6834</eissn><abstract>Staphylococcus aureus is an important cause of infection in intensive care unit (ICU) patients. Colonization with methicillin-resistant S. aureus (MRSA) is a risk factor for subsequent S. aureus infection. However, MRSA-colonized patients may have more comorbidities than methicillin-susceptible S. aureus (MSSA)-colonized or noncolonized patients and therefore may be more susceptible to infection on that basis.
To determine whether MRSA-colonized patients who are admitted to medical and surgical ICUs are more likely to develop any S. aureus infection in the ICU, compared with patients colonized with MSSA or not colonized with S. aureus, independent of predisposing patient risk factors.
Prospective cohort study.
A 24-bed surgical ICU and a 19-bed medical ICU of a 1,252-bed, academic hospital.
A total of 9,523 patients for whom nasal swab samples were cultured for S. aureus at ICU admission during the period from December 2002 through August 2007.
Patients in the ICU for more than 48 hours were examined for an ICU-acquired S. aureus infection, defined as development of S. aureus infection more than 48 hours after ICU admission.
S. aureus colonization was present at admission for 1,433 (27.8%) of 5,161 patients (674 [47.0%] with MRSA and 759 [53.0%] with MSSA). An ICU-acquired S. aureus infection developed in 113 (2.19%) patients, of whom 75 (66.4%) had an infection due to MRSA. Risk factors associated with an ICU-acquired S. aureus infection included MRSA colonization at admission (adjusted hazard ratio, 4.70 [95% confidence interval, 3.07-7.21]) and MSSA colonization at admission (adjusted hazard ratio, 2.47 [95% confidence interval, 1.52-4.01]).
ICU patients colonized with S. aureus were at greater risk of developing a S. aureus infection in the ICU. Even after adjusting for patient-specific risk factors, MRSA-colonized patients were more likely to develop S. aureus infection, compared with MSSA-colonized or noncolonized patients.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>20426656</pmid><doi>10.1086/652530</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Artificial respiration Bacterial diseases Biological and medical sciences Carrier State - diagnosis Carrier State - epidemiology Central venous catheterization Cohort Studies Cross Infection - prevention & control Female Hospital admissions Hospital units Hospitalization Hospitals, University Human bacterial diseases Humans Infections Infectious diseases Intensive Care Units Male Mass Screening Medical sciences Methicillin-Resistant Staphylococcus aureus - isolation & purification Microbial colonization Middle Aged Miscellaneous Missouri - epidemiology Nasal Cavity - microbiology Nursing Original Article Patient Admission Pharmacology. Drug treatments Predisposing factors Prospective Studies Public health. Hygiene Public health. Hygiene-occupational medicine Staphylococcal Infections - diagnosis Staphylococcal Infections - epidemiology Staphylococcal Infections - etiology Staphylococcal infections, streptococcal infections, pneumococcal infections Staphylococcus aureus Staphylococcus aureus - isolation & purification Young Adult |
title | Staphylococcus aureus Nasal Colonization and Subsequent Infection in Intensive Care Unit Patients: Does Methicillin Resistance Matter? |
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