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Insertion Site Inflammation Is Associated with Central-Line–Associated Bloodstream Infection
Background: Central lines (CL) are widely used in the inpatient setting and central-line–associated bloodstream infection (CLABSI) is a serious complication of CL use. Because CL insertion site inflammation (ISI) may precede the onset of CLABSI, we aimed to define ISI, to determine whether ISI was a...
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Published in: | Infection control and hospital epidemiology 2020-10, Vol.41 (S1), p.s302-s303 |
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creator | Salinas, Jorge Clore, Gosia Kukla, Mary AlZunitan, Mohammed Abosi, Oluchi Puig-Asensio, Mireia Marra, Alexandre Diekema, Daniel Edmond, Michael |
description | Background:
Central lines (CL) are widely used in the inpatient setting and central-line–associated bloodstream infection (CLABSI) is a serious complication of CL use. Because CL insertion site inflammation (ISI) may precede the onset of CLABSI, we aimed to define ISI, to determine whether ISI was associated with CLABSI, and to develop an automated surveillance system for ISI.
Methods:
We extracted electronic medical records (EMRs) of adult patients hospitalized at the University of Iowa Hospitals & Clinics during January 2015–December 2018. Nurses routinely document CL insertion-site characteristics in specifically designed flow sheets in the EMR. An ISI was counted every time ≥1 of the following signs were documented during CL assessments: edema, erythema, induration, tenderness, or drainage. A 1:2 case-control investigation was performed by matching nonmucosal barrier injury (non-MBI) CLABSI patients (cases) to patients without a CLABSI diagnosis (controls). We matched for age (±10 years), sex, date (±30 days), inpatient unit, central-line days, and central-line type (temporary vs permanent). The main exposure of interest was having an ISI on or before CLABSI onset. CLABSIs were determined using CDC NHSN definitions. We then created a metric: ISI days (defined as the number of days with ≥1 ISI documented) and plotted ISI incidence (ISI days per central-line days) to quantify the burden of ISIs and to determine whether ISI and non-MBI CLABSI incidences were collinear. An automated surveillance system for ISI was created using structured query language queries to the EMR data repository and Tableau software.
Results:
During 2015–2018, we detected 194 CLABSI cases that were matched to 338 controls. CLABSI patients had greater odds of having an ISI (OR, 2.3; 95% CI, 1.3–4.0). Over the study period, ISI incidence decreased from ~80 to ~50 ISI days per 1,000 CL days. Non-MBI CLABSI rates also decreased from ~1.5 to ~1.0 CLABSIs per 1,000 CL days.
Conclusions:
ISI incidence is associated with non-MBI CLABSI incidence. Because ISI incidence is higher than CLABSI incidence, surveillance for ISI could be a more sensitive indicator for monitoring the impact of CLABSI prevention practices. Automated surveillance for novel process metrics is a promising infection prevention tool.
Funding:
None
Disclosures:
None |
doi_str_mv | 10.1017/ice.2020.885 |
format | article |
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Central lines (CL) are widely used in the inpatient setting and central-line–associated bloodstream infection (CLABSI) is a serious complication of CL use. Because CL insertion site inflammation (ISI) may precede the onset of CLABSI, we aimed to define ISI, to determine whether ISI was associated with CLABSI, and to develop an automated surveillance system for ISI.
Methods:
We extracted electronic medical records (EMRs) of adult patients hospitalized at the University of Iowa Hospitals & Clinics during January 2015–December 2018. Nurses routinely document CL insertion-site characteristics in specifically designed flow sheets in the EMR. An ISI was counted every time ≥1 of the following signs were documented during CL assessments: edema, erythema, induration, tenderness, or drainage. A 1:2 case-control investigation was performed by matching nonmucosal barrier injury (non-MBI) CLABSI patients (cases) to patients without a CLABSI diagnosis (controls). We matched for age (±10 years), sex, date (±30 days), inpatient unit, central-line days, and central-line type (temporary vs permanent). The main exposure of interest was having an ISI on or before CLABSI onset. CLABSIs were determined using CDC NHSN definitions. We then created a metric: ISI days (defined as the number of days with ≥1 ISI documented) and plotted ISI incidence (ISI days per central-line days) to quantify the burden of ISIs and to determine whether ISI and non-MBI CLABSI incidences were collinear. An automated surveillance system for ISI was created using structured query language queries to the EMR data repository and Tableau software.
Results:
During 2015–2018, we detected 194 CLABSI cases that were matched to 338 controls. CLABSI patients had greater odds of having an ISI (OR, 2.3; 95% CI, 1.3–4.0). Over the study period, ISI incidence decreased from ~80 to ~50 ISI days per 1,000 CL days. Non-MBI CLABSI rates also decreased from ~1.5 to ~1.0 CLABSIs per 1,000 CL days.
Conclusions:
ISI incidence is associated with non-MBI CLABSI incidence. Because ISI incidence is higher than CLABSI incidence, surveillance for ISI could be a more sensitive indicator for monitoring the impact of CLABSI prevention practices. Automated surveillance for novel process metrics is a promising infection prevention tool.
Funding:
None
Disclosures:
None</description><identifier>ISSN: 0899-823X</identifier><identifier>EISSN: 1559-6834</identifier><identifier>DOI: 10.1017/ice.2020.885</identifier><language>eng</language><publisher>Cambridge: Cambridge University Press</publisher><subject>Automation ; Disease control ; Edema ; Health surveillance ; Infections ; Prevention ; Surveillance</subject><ispartof>Infection control and hospital epidemiology, 2020-10, Vol.41 (S1), p.s302-s303</ispartof><rights>2020 by The Society for Healthcare Epidemiology of America. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Salinas, Jorge</creatorcontrib><creatorcontrib>Clore, Gosia</creatorcontrib><creatorcontrib>Kukla, Mary</creatorcontrib><creatorcontrib>AlZunitan, Mohammed</creatorcontrib><creatorcontrib>Abosi, Oluchi</creatorcontrib><creatorcontrib>Puig-Asensio, Mireia</creatorcontrib><creatorcontrib>Marra, Alexandre</creatorcontrib><creatorcontrib>Diekema, Daniel</creatorcontrib><creatorcontrib>Edmond, Michael</creatorcontrib><title>Insertion Site Inflammation Is Associated with Central-Line–Associated Bloodstream Infection</title><title>Infection control and hospital epidemiology</title><description>Background:
Central lines (CL) are widely used in the inpatient setting and central-line–associated bloodstream infection (CLABSI) is a serious complication of CL use. Because CL insertion site inflammation (ISI) may precede the onset of CLABSI, we aimed to define ISI, to determine whether ISI was associated with CLABSI, and to develop an automated surveillance system for ISI.
Methods:
We extracted electronic medical records (EMRs) of adult patients hospitalized at the University of Iowa Hospitals & Clinics during January 2015–December 2018. Nurses routinely document CL insertion-site characteristics in specifically designed flow sheets in the EMR. An ISI was counted every time ≥1 of the following signs were documented during CL assessments: edema, erythema, induration, tenderness, or drainage. A 1:2 case-control investigation was performed by matching nonmucosal barrier injury (non-MBI) CLABSI patients (cases) to patients without a CLABSI diagnosis (controls). We matched for age (±10 years), sex, date (±30 days), inpatient unit, central-line days, and central-line type (temporary vs permanent). The main exposure of interest was having an ISI on or before CLABSI onset. CLABSIs were determined using CDC NHSN definitions. We then created a metric: ISI days (defined as the number of days with ≥1 ISI documented) and plotted ISI incidence (ISI days per central-line days) to quantify the burden of ISIs and to determine whether ISI and non-MBI CLABSI incidences were collinear. An automated surveillance system for ISI was created using structured query language queries to the EMR data repository and Tableau software.
Results:
During 2015–2018, we detected 194 CLABSI cases that were matched to 338 controls. CLABSI patients had greater odds of having an ISI (OR, 2.3; 95% CI, 1.3–4.0). Over the study period, ISI incidence decreased from ~80 to ~50 ISI days per 1,000 CL days. Non-MBI CLABSI rates also decreased from ~1.5 to ~1.0 CLABSIs per 1,000 CL days.
Conclusions:
ISI incidence is associated with non-MBI CLABSI incidence. Because ISI incidence is higher than CLABSI incidence, surveillance for ISI could be a more sensitive indicator for monitoring the impact of CLABSI prevention practices. Automated surveillance for novel process metrics is a promising infection prevention tool.
Funding:
None
Disclosures:
None</description><subject>Automation</subject><subject>Disease control</subject><subject>Edema</subject><subject>Health surveillance</subject><subject>Infections</subject><subject>Prevention</subject><subject>Surveillance</subject><issn>0899-823X</issn><issn>1559-6834</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpNkM1KxDAURoMoOI7ufICCWzvmp22S5Tg4WhhwoYIrQya9wQxtMyYZxJ3v4Bv6JLaOC1cXvvtxLvcgdE7wjGDCr5yBGcUUz4QoD9CElKXMK8GKQzTBQspcUPZ8jE5i3GCMuZRkgl7qPkJIzvfZg0uQ1b1tddfp36SO2TxGb5xO0GTvLr1mC-hT0G2-cj18f379W1-33jcxBdDdSAEzIk7RkdVthLO_OUVPy5vHxV2-ur-tF_NVbghmZU7Z2mIqoJKiKda8aggvmC0sBjCGFdryilFJJBO6aCy3Wq6HtzQfkoaK0rAputhzt8G_7SAmtfG70A8nFRVSsKqUnA-ty33LBB9jAKu2wXU6fCiC1WhQDQbVaFANBtkPtgxlZg</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Salinas, Jorge</creator><creator>Clore, Gosia</creator><creator>Kukla, Mary</creator><creator>AlZunitan, Mohammed</creator><creator>Abosi, Oluchi</creator><creator>Puig-Asensio, Mireia</creator><creator>Marra, Alexandre</creator><creator>Diekema, Daniel</creator><creator>Edmond, Michael</creator><general>Cambridge University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>S0X</scope></search><sort><creationdate>202010</creationdate><title>Insertion Site Inflammation Is Associated with Central-Line–Associated Bloodstream Infection</title><author>Salinas, Jorge ; Clore, Gosia ; Kukla, Mary ; AlZunitan, Mohammed ; Abosi, Oluchi ; Puig-Asensio, Mireia ; Marra, Alexandre ; Diekema, Daniel ; Edmond, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1035-23bf028e698d4b76d1743f4f0eecc34af763291938a4df7fa9b834a7193d285c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Automation</topic><topic>Disease control</topic><topic>Edema</topic><topic>Health surveillance</topic><topic>Infections</topic><topic>Prevention</topic><topic>Surveillance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salinas, Jorge</creatorcontrib><creatorcontrib>Clore, Gosia</creatorcontrib><creatorcontrib>Kukla, Mary</creatorcontrib><creatorcontrib>AlZunitan, Mohammed</creatorcontrib><creatorcontrib>Abosi, Oluchi</creatorcontrib><creatorcontrib>Puig-Asensio, Mireia</creatorcontrib><creatorcontrib>Marra, Alexandre</creatorcontrib><creatorcontrib>Diekema, Daniel</creatorcontrib><creatorcontrib>Edmond, Michael</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Family Health Database (Proquest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Health Management Database (Proquest)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>SIRS Editorial</collection><jtitle>Infection control and hospital epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salinas, Jorge</au><au>Clore, Gosia</au><au>Kukla, Mary</au><au>AlZunitan, Mohammed</au><au>Abosi, Oluchi</au><au>Puig-Asensio, Mireia</au><au>Marra, Alexandre</au><au>Diekema, Daniel</au><au>Edmond, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insertion Site Inflammation Is Associated with Central-Line–Associated Bloodstream Infection</atitle><jtitle>Infection control and hospital epidemiology</jtitle><date>2020-10</date><risdate>2020</risdate><volume>41</volume><issue>S1</issue><spage>s302</spage><epage>s303</epage><pages>s302-s303</pages><issn>0899-823X</issn><eissn>1559-6834</eissn><abstract>Background:
Central lines (CL) are widely used in the inpatient setting and central-line–associated bloodstream infection (CLABSI) is a serious complication of CL use. Because CL insertion site inflammation (ISI) may precede the onset of CLABSI, we aimed to define ISI, to determine whether ISI was associated with CLABSI, and to develop an automated surveillance system for ISI.
Methods:
We extracted electronic medical records (EMRs) of adult patients hospitalized at the University of Iowa Hospitals & Clinics during January 2015–December 2018. Nurses routinely document CL insertion-site characteristics in specifically designed flow sheets in the EMR. An ISI was counted every time ≥1 of the following signs were documented during CL assessments: edema, erythema, induration, tenderness, or drainage. A 1:2 case-control investigation was performed by matching nonmucosal barrier injury (non-MBI) CLABSI patients (cases) to patients without a CLABSI diagnosis (controls). We matched for age (±10 years), sex, date (±30 days), inpatient unit, central-line days, and central-line type (temporary vs permanent). The main exposure of interest was having an ISI on or before CLABSI onset. CLABSIs were determined using CDC NHSN definitions. We then created a metric: ISI days (defined as the number of days with ≥1 ISI documented) and plotted ISI incidence (ISI days per central-line days) to quantify the burden of ISIs and to determine whether ISI and non-MBI CLABSI incidences were collinear. An automated surveillance system for ISI was created using structured query language queries to the EMR data repository and Tableau software.
Results:
During 2015–2018, we detected 194 CLABSI cases that were matched to 338 controls. CLABSI patients had greater odds of having an ISI (OR, 2.3; 95% CI, 1.3–4.0). Over the study period, ISI incidence decreased from ~80 to ~50 ISI days per 1,000 CL days. Non-MBI CLABSI rates also decreased from ~1.5 to ~1.0 CLABSIs per 1,000 CL days.
Conclusions:
ISI incidence is associated with non-MBI CLABSI incidence. Because ISI incidence is higher than CLABSI incidence, surveillance for ISI could be a more sensitive indicator for monitoring the impact of CLABSI prevention practices. Automated surveillance for novel process metrics is a promising infection prevention tool.
Funding:
None
Disclosures:
None</abstract><cop>Cambridge</cop><pub>Cambridge University Press</pub><doi>10.1017/ice.2020.885</doi><oa>free_for_read</oa></addata></record> |
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subjects | Automation Disease control Edema Health surveillance Infections Prevention Surveillance |
title | Insertion Site Inflammation Is Associated with Central-Line–Associated Bloodstream Infection |
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