In Vitro Studies of a Novel Antimicrobial Luer-Activated Needleless Connector for Prevention of Catheter-Related Bloodstream Infection

Background. We report in vitro studies of a commercially available novel antimicrobial Luer-activated connector with the inner surface coated with nanoparticle-silver to prevent contaminants from forming biofilm and causing catheter-related bloodstream infection. Methods. Sterile control nonmedicate...

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Veröffentlicht in:Clinical infectious diseases 2010-06, Vol.50 (12), p.1580-1587
1. Verfasser: Maki, Dennis G.
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description Background. We report in vitro studies of a commercially available novel antimicrobial Luer-activated connector with the inner surface coated with nanoparticle-silver to prevent contaminants from forming biofilm and causing catheter-related bloodstream infection. Methods. Sterile control nonmedicated connectors and antimicrobial connectors were filled with ∼1×105 cfu/mL of Staphylococcus epidermidis, methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus, Enterobacter cloacae, Pseudomonas aeruginosa, or Candida albicans; after 24 h of incubation, the numbers of remaining viable microorganisms were quantified and compared with the concentration in control connectors (∼1×107 cfu/mL). In trials simulating clinical use, septal membranes of connectors were inoculated with E. cloacae, were allowed to dry, and were then actuated and infused with lactated ringer's solution for 72 h, with sampling for microorganisms in downstream efferent fluid and for biofilm in the connector. Results. Microorganisms suspended in the intraluminal fluid path of antimicrobial connectors were rapidly killed. For 5 species, there was a 5.23-6.80 mean log10 reduction (>99.999%), and with C. albicans, there was a 99.9% reduction. In clinical simulation trials, heavy contamination of downstream fluid was detected at all time points with control connectors, reaching ∼1×105 cfu/mL at 72 h, and heavy biofilm was uniformly present; with the antimicrobial connectors, there was complete prevention of downstream fluid contamination and total absence of biofilm formation. Conclusions. These simulation experiments show that needleless connectors readily acquire an internal biofilm when microorganisms gain access to the internal fluid path and that biofilm formation allows an exponential buildup of internal contamination, with shedding back into the fluid path and downstream sufficient to cause bacteremia. Incorporation of nanoparticle silver into the lining surfaces of the novel connector kills microorganisms in the fluid pathway and prevents internal biofilm formation, even with high levels of introduced contamination and continuous fluid flow. This technology deserves to be evaluated in a prospective, randomized clinical trial to determine its capacity to prevent catheter-associated bloodstream infection.
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We report in vitro studies of a commercially available novel antimicrobial Luer-activated connector with the inner surface coated with nanoparticle-silver to prevent contaminants from forming biofilm and causing catheter-related bloodstream infection. Methods. Sterile control nonmedicated connectors and antimicrobial connectors were filled with ∼1×105 cfu/mL of Staphylococcus epidermidis, methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus, Enterobacter cloacae, Pseudomonas aeruginosa, or Candida albicans; after 24 h of incubation, the numbers of remaining viable microorganisms were quantified and compared with the concentration in control connectors (∼1×107 cfu/mL). In trials simulating clinical use, septal membranes of connectors were inoculated with E. cloacae, were allowed to dry, and were then actuated and infused with lactated ringer's solution for 72 h, with sampling for microorganisms in downstream efferent fluid and for biofilm in the connector. Results. Microorganisms suspended in the intraluminal fluid path of antimicrobial connectors were rapidly killed. For 5 species, there was a 5.23-6.80 mean log10 reduction (&gt;99.999%), and with C. albicans, there was a 99.9% reduction. In clinical simulation trials, heavy contamination of downstream fluid was detected at all time points with control connectors, reaching ∼1×105 cfu/mL at 72 h, and heavy biofilm was uniformly present; with the antimicrobial connectors, there was complete prevention of downstream fluid contamination and total absence of biofilm formation. Conclusions. These simulation experiments show that needleless connectors readily acquire an internal biofilm when microorganisms gain access to the internal fluid path and that biofilm formation allows an exponential buildup of internal contamination, with shedding back into the fluid path and downstream sufficient to cause bacteremia. Incorporation of nanoparticle silver into the lining surfaces of the novel connector kills microorganisms in the fluid pathway and prevents internal biofilm formation, even with high levels of introduced contamination and continuous fluid flow. This technology deserves to be evaluated in a prospective, randomized clinical trial to determine its capacity to prevent catheter-associated bloodstream infection.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/652764</identifier><identifier>PMID: 20455695</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: The University of Chicago Press</publisher><subject>Adult ; Aged ; Antimicrobials ; ARTICLES AND COMMENTARIES ; Bacteremia - diagnosis ; Bacteremia - prevention &amp; control ; Bacteria - isolation &amp; purification ; Bacterial diseases ; Bacterial infections ; Bacterial sepsis ; Biofilms ; Biological and medical sciences ; Blood ; Candida albicans ; Catheter-Related Infections - diagnosis ; Catheter-Related Infections - prevention &amp; control ; Catheterization - instrumentation ; Catheters ; Clinical trials ; Colony Count, Microbial ; Disease prevention ; Enterobacter cloacae ; Enterococcus ; Female ; Fungemia - diagnosis ; Fungemia - prevention &amp; control ; General aspects ; Health care industry ; Human bacterial diseases ; Human infectious diseases. Experimental studies and models ; Humans ; Infections ; Infectious diseases ; Male ; Medical sciences ; Microorganisms ; Middle Aged ; Pseudomonas aeruginosa ; Retrospective Studies ; Septum ; Silver ; Staphylococcus aureus ; Staphylococcus epidermidis ; Yeasts - isolation &amp; purification</subject><ispartof>Clinical infectious diseases, 2010-06, Vol.50 (12), p.1580-1587</ispartof><rights>2010 Infectious Diseases Society of America</rights><rights>2010 by the Infectious Diseases Society of America 2010</rights><rights>2015 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Jun 15, 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-2b166f0832281f35974d48f375c169fb87f1f3960cd2bd2a3c51bb13e49d1fd63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25679920$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25679920$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,778,782,801,27911,27912,58004,58237</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22853968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20455695$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maki, Dennis G.</creatorcontrib><title>In Vitro Studies of a Novel Antimicrobial Luer-Activated Needleless Connector for Prevention of Catheter-Related Bloodstream Infection</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><addtitle>Clinical Infectious Diseases</addtitle><description>Background. We report in vitro studies of a commercially available novel antimicrobial Luer-activated connector with the inner surface coated with nanoparticle-silver to prevent contaminants from forming biofilm and causing catheter-related bloodstream infection. Methods. Sterile control nonmedicated connectors and antimicrobial connectors were filled with ∼1×105 cfu/mL of Staphylococcus epidermidis, methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus, Enterobacter cloacae, Pseudomonas aeruginosa, or Candida albicans; after 24 h of incubation, the numbers of remaining viable microorganisms were quantified and compared with the concentration in control connectors (∼1×107 cfu/mL). In trials simulating clinical use, septal membranes of connectors were inoculated with E. cloacae, were allowed to dry, and were then actuated and infused with lactated ringer's solution for 72 h, with sampling for microorganisms in downstream efferent fluid and for biofilm in the connector. Results. Microorganisms suspended in the intraluminal fluid path of antimicrobial connectors were rapidly killed. For 5 species, there was a 5.23-6.80 mean log10 reduction (&gt;99.999%), and with C. albicans, there was a 99.9% reduction. In clinical simulation trials, heavy contamination of downstream fluid was detected at all time points with control connectors, reaching ∼1×105 cfu/mL at 72 h, and heavy biofilm was uniformly present; with the antimicrobial connectors, there was complete prevention of downstream fluid contamination and total absence of biofilm formation. Conclusions. These simulation experiments show that needleless connectors readily acquire an internal biofilm when microorganisms gain access to the internal fluid path and that biofilm formation allows an exponential buildup of internal contamination, with shedding back into the fluid path and downstream sufficient to cause bacteremia. Incorporation of nanoparticle silver into the lining surfaces of the novel connector kills microorganisms in the fluid pathway and prevents internal biofilm formation, even with high levels of introduced contamination and continuous fluid flow. 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Experimental studies and models</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microorganisms</topic><topic>Middle Aged</topic><topic>Pseudomonas aeruginosa</topic><topic>Retrospective Studies</topic><topic>Septum</topic><topic>Silver</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus epidermidis</topic><topic>Yeasts - isolation &amp; purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maki, Dennis G.</creatorcontrib><collection>Istex</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maki, Dennis G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Studies of a Novel Antimicrobial Luer-Activated Needleless Connector for Prevention of Catheter-Related Bloodstream Infection</atitle><jtitle>Clinical infectious diseases</jtitle><stitle>Clinical Infectious Diseases</stitle><addtitle>Clinical Infectious Diseases</addtitle><date>2010-06-15</date><risdate>2010</risdate><volume>50</volume><issue>12</issue><spage>1580</spage><epage>1587</epage><pages>1580-1587</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. We report in vitro studies of a commercially available novel antimicrobial Luer-activated connector with the inner surface coated with nanoparticle-silver to prevent contaminants from forming biofilm and causing catheter-related bloodstream infection. Methods. Sterile control nonmedicated connectors and antimicrobial connectors were filled with ∼1×105 cfu/mL of Staphylococcus epidermidis, methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus, Enterobacter cloacae, Pseudomonas aeruginosa, or Candida albicans; after 24 h of incubation, the numbers of remaining viable microorganisms were quantified and compared with the concentration in control connectors (∼1×107 cfu/mL). In trials simulating clinical use, septal membranes of connectors were inoculated with E. cloacae, were allowed to dry, and were then actuated and infused with lactated ringer's solution for 72 h, with sampling for microorganisms in downstream efferent fluid and for biofilm in the connector. Results. Microorganisms suspended in the intraluminal fluid path of antimicrobial connectors were rapidly killed. For 5 species, there was a 5.23-6.80 mean log10 reduction (&gt;99.999%), and with C. albicans, there was a 99.9% reduction. In clinical simulation trials, heavy contamination of downstream fluid was detected at all time points with control connectors, reaching ∼1×105 cfu/mL at 72 h, and heavy biofilm was uniformly present; with the antimicrobial connectors, there was complete prevention of downstream fluid contamination and total absence of biofilm formation. Conclusions. These simulation experiments show that needleless connectors readily acquire an internal biofilm when microorganisms gain access to the internal fluid path and that biofilm formation allows an exponential buildup of internal contamination, with shedding back into the fluid path and downstream sufficient to cause bacteremia. Incorporation of nanoparticle silver into the lining surfaces of the novel connector kills microorganisms in the fluid pathway and prevents internal biofilm formation, even with high levels of introduced contamination and continuous fluid flow. This technology deserves to be evaluated in a prospective, randomized clinical trial to determine its capacity to prevent catheter-associated bloodstream infection.</abstract><cop>Oxford</cop><pub>The University of Chicago Press</pub><pmid>20455695</pmid><doi>10.1086/652764</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Antimicrobials
ARTICLES AND COMMENTARIES
Bacteremia - diagnosis
Bacteremia - prevention & control
Bacteria - isolation & purification
Bacterial diseases
Bacterial infections
Bacterial sepsis
Biofilms
Biological and medical sciences
Blood
Candida albicans
Catheter-Related Infections - diagnosis
Catheter-Related Infections - prevention & control
Catheterization - instrumentation
Catheters
Clinical trials
Colony Count, Microbial
Disease prevention
Enterobacter cloacae
Enterococcus
Female
Fungemia - diagnosis
Fungemia - prevention & control
General aspects
Health care industry
Human bacterial diseases
Human infectious diseases. Experimental studies and models
Humans
Infections
Infectious diseases
Male
Medical sciences
Microorganisms
Middle Aged
Pseudomonas aeruginosa
Retrospective Studies
Septum
Silver
Staphylococcus aureus
Staphylococcus epidermidis
Yeasts - isolation & purification
title In Vitro Studies of a Novel Antimicrobial Luer-Activated Needleless Connector for Prevention of Catheter-Related Bloodstream Infection
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