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Surveillance length and validity of benchmarks for central line-associated bloodstream infection incidence rates in intensive care units
Several national and regional central line-associated bloodstream infections (CLABSI) surveillance programs do not require continuous hospital participation. We evaluated the effect of different hospital participation requirements on the validity of annual CLABSI incidence rate benchmarks for intens...
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Published in: | PloS one 2012-05, Vol.7 (5), p.e36582-e36582 |
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description | Several national and regional central line-associated bloodstream infections (CLABSI) surveillance programs do not require continuous hospital participation. We evaluated the effect of different hospital participation requirements on the validity of annual CLABSI incidence rate benchmarks for intensive care units (ICUs).
We estimated the annual pooled CLABSI incidence rates for both a real regional ( |
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We estimated the annual pooled CLABSI incidence rates for both a real regional (<100 ICUs) and a simulated national (600 ICUs) surveillance program, which were used as a reference for the simulations. We simulated scenarios where the annual surveillance participation was randomly or non-randomly reduced. Each scenario's annual pooled CLABSI incidence rate was estimated and compared to the reference rates in terms of validity, bias, and proportion of simulation iterations that presented valid estimates (ideal if ≥ 90%).
All random scenarios generated valid CLABSI incidence rates estimates (bias -0.37 to 0.07 CLABSI/1000 CVC-days), while non-random scenarios presented a wide range of valid estimates (0 to 100%) and higher bias (-2.18 to 1.27 CLABSI/1000 CVC-days). In random scenarios, the higher the number of participating ICUs, the shorter the participation required to generate ≥ 90% valid replicates. While participation requirements in a countrywide program ranged from 3 to 13 surveillance blocks (1 block = 28 days), requirements for a regional program ranged from 9 to 13 blocks.
Based on the results of our model of national CLABSI reporting, the shortening of participation requirements may be suitable for nationwide ICU CLABSI surveillance programs if participation months are randomly chosen. However, our regional models showed that regional programs should opt for continuous participation to avoid biased benchmarks.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0036582</identifier><identifier>PMID: 22586480</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Benchmarking ; Benchmarks ; Bias ; Biology ; Catheter-Related Infections - epidemiology ; Catheter-Related Infections - etiology ; Catheterization, Central Venous - adverse effects ; Children & youth ; Comparative analysis ; Computer simulation ; Cross infection ; Cross Infection - epidemiology ; Datasets ; Disease control ; Epidemiology ; Estimates ; Health aspects ; Hospitals ; Hospitals - statistics & numerical data ; Humans ; Incidence ; Infections ; Intensive care ; Intensive care units ; Intensive Care Units - statistics & numerical data ; Medical statistics ; Medicine ; Nosocomial infections ; Occupational health ; Participation ; Patient safety ; Pediatrics ; Population Surveillance ; Simulation ; Studies ; Surveillance ; Validity</subject><ispartof>PloS one, 2012-05, Vol.7 (5), p.e36582-e36582</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Fontela et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Fontela et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-1ee0849233c4cb3e0178c036431fb430a512c4869dfb0e299e80ccc85ec4004e3</citedby><cites>FETCH-LOGICAL-c692t-1ee0849233c4cb3e0178c036431fb430a512c4869dfb0e299e80ccc85ec4004e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1324602171/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1324602171?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22586480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Morgan, Daniel</contributor><creatorcontrib>Fontela, Patricia S</creatorcontrib><creatorcontrib>Quach, Caroline</creatorcontrib><creatorcontrib>Buckeridge, David</creatorcontrib><creatorcontrib>Pai, Madukhar</creatorcontrib><creatorcontrib>Platt, Robert W</creatorcontrib><title>Surveillance length and validity of benchmarks for central line-associated bloodstream infection incidence rates in intensive care units</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Several national and regional central line-associated bloodstream infections (CLABSI) surveillance programs do not require continuous hospital participation. We evaluated the effect of different hospital participation requirements on the validity of annual CLABSI incidence rate benchmarks for intensive care units (ICUs).
We estimated the annual pooled CLABSI incidence rates for both a real regional (<100 ICUs) and a simulated national (600 ICUs) surveillance program, which were used as a reference for the simulations. We simulated scenarios where the annual surveillance participation was randomly or non-randomly reduced. Each scenario's annual pooled CLABSI incidence rate was estimated and compared to the reference rates in terms of validity, bias, and proportion of simulation iterations that presented valid estimates (ideal if ≥ 90%).
All random scenarios generated valid CLABSI incidence rates estimates (bias -0.37 to 0.07 CLABSI/1000 CVC-days), while non-random scenarios presented a wide range of valid estimates (0 to 100%) and higher bias (-2.18 to 1.27 CLABSI/1000 CVC-days). In random scenarios, the higher the number of participating ICUs, the shorter the participation required to generate ≥ 90% valid replicates. While participation requirements in a countrywide program ranged from 3 to 13 surveillance blocks (1 block = 28 days), requirements for a regional program ranged from 9 to 13 blocks.
Based on the results of our model of national CLABSI reporting, the shortening of participation requirements may be suitable for nationwide ICU CLABSI surveillance programs if participation months are randomly chosen. However, our regional models showed that regional programs should opt for continuous participation to avoid biased benchmarks.</description><subject>Benchmarking</subject><subject>Benchmarks</subject><subject>Bias</subject><subject>Biology</subject><subject>Catheter-Related Infections - epidemiology</subject><subject>Catheter-Related Infections - etiology</subject><subject>Catheterization, Central Venous - adverse effects</subject><subject>Children & youth</subject><subject>Comparative analysis</subject><subject>Computer simulation</subject><subject>Cross infection</subject><subject>Cross Infection - epidemiology</subject><subject>Datasets</subject><subject>Disease control</subject><subject>Epidemiology</subject><subject>Estimates</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Hospitals - statistics & numerical data</subject><subject>Humans</subject><subject>Incidence</subject><subject>Infections</subject><subject>Intensive care</subject><subject>Intensive care units</subject><subject>Intensive Care Units - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fontela, Patricia S</au><au>Quach, Caroline</au><au>Buckeridge, David</au><au>Pai, Madukhar</au><au>Platt, Robert W</au><au>Morgan, Daniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surveillance length and validity of benchmarks for central line-associated bloodstream infection incidence rates in intensive care units</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-05-07</date><risdate>2012</risdate><volume>7</volume><issue>5</issue><spage>e36582</spage><epage>e36582</epage><pages>e36582-e36582</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Several national and regional central line-associated bloodstream infections (CLABSI) surveillance programs do not require continuous hospital participation. We evaluated the effect of different hospital participation requirements on the validity of annual CLABSI incidence rate benchmarks for intensive care units (ICUs).
We estimated the annual pooled CLABSI incidence rates for both a real regional (<100 ICUs) and a simulated national (600 ICUs) surveillance program, which were used as a reference for the simulations. We simulated scenarios where the annual surveillance participation was randomly or non-randomly reduced. Each scenario's annual pooled CLABSI incidence rate was estimated and compared to the reference rates in terms of validity, bias, and proportion of simulation iterations that presented valid estimates (ideal if ≥ 90%).
All random scenarios generated valid CLABSI incidence rates estimates (bias -0.37 to 0.07 CLABSI/1000 CVC-days), while non-random scenarios presented a wide range of valid estimates (0 to 100%) and higher bias (-2.18 to 1.27 CLABSI/1000 CVC-days). In random scenarios, the higher the number of participating ICUs, the shorter the participation required to generate ≥ 90% valid replicates. While participation requirements in a countrywide program ranged from 3 to 13 surveillance blocks (1 block = 28 days), requirements for a regional program ranged from 9 to 13 blocks.
Based on the results of our model of national CLABSI reporting, the shortening of participation requirements may be suitable for nationwide ICU CLABSI surveillance programs if participation months are randomly chosen. However, our regional models showed that regional programs should opt for continuous participation to avoid biased benchmarks.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22586480</pmid><doi>10.1371/journal.pone.0036582</doi><tpages>e36582</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Benchmarking Benchmarks Bias Biology Catheter-Related Infections - epidemiology Catheter-Related Infections - etiology Catheterization, Central Venous - adverse effects Children & youth Comparative analysis Computer simulation Cross infection Cross Infection - epidemiology Datasets Disease control Epidemiology Estimates Health aspects Hospitals Hospitals - statistics & numerical data Humans Incidence Infections Intensive care Intensive care units Intensive Care Units - statistics & numerical data Medical statistics Medicine Nosocomial infections Occupational health Participation Patient safety Pediatrics Population Surveillance Simulation Studies Surveillance Validity |
title | Surveillance length and validity of benchmarks for central line-associated bloodstream infection incidence rates in intensive care units |
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