Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review
The use of the Wampole Isolator 1.5-ml pediatric blood culture tube for the detection of fungemia in children was assessed by a 10-year retrospective review at two pediatric hospitals, The Hospital for Sick Children in Toronto, Canada, and the Children's Medical Center of Dallas, Texas. Over th...
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Veröffentlicht in: | Journal of clinical microbiology 2016-09, Vol.54 (9), p.2284-2287 |
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description | The use of the Wampole Isolator 1.5-ml pediatric blood culture tube for the detection of fungemia in children was assessed by a 10-year retrospective review at two pediatric hospitals, The Hospital for Sick Children in Toronto, Canada, and the Children's Medical Center of Dallas, Texas. Over this period, a total of 9,442 pediatric Isolator specimens were processed, with yeast or yeast-like organisms recovered in 297 (3.1%) of the specimens (151 [1.6%] unique clinical episodes) and filamentous or dimorphic fungi recovered in 31 (0.3%) of the specimens (25 unique clinical episodes). Only 18 of the 151 clinical episodes of fungemia attributable to yeast were not detected by automated blood culture systems. The majority of isolated yeast were Candida spp., which were usually detected by automated systems, whereas the most common non-Candida yeast was Malassezia furfur, which the automated system failed to detect. Filamentous or dimorphic fungi were detected in 25 episodes, of which only 9 (36%) episodes were deemed clinically significant after chart review, indicating that in the majority of cases (16/25, 64%) fungal isolation represented contamination. In five of the nine clinically significant episodes, the isolated fungus (Histoplasma capsulatum, Coccidioides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.) was also identified in other clinical specimens. Over the 10-year study period, the use of the pediatric Isolator system, at the discretion of the treating physician, only rarely provided useful clinical information for the diagnosis of fungemia in children, with the exception of M. furfur and possibly endemic mycoses. |
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W.</contributor><creatorcontrib>Campigotto, Aaron ; Richardson, Susan E ; Sebert, Michael ; McElvania TeKippe, Erin ; Chakravarty, Aparna ; Doern, Christopher D ; Warnock, D. W.</creatorcontrib><description>The use of the Wampole Isolator 1.5-ml pediatric blood culture tube for the detection of fungemia in children was assessed by a 10-year retrospective review at two pediatric hospitals, The Hospital for Sick Children in Toronto, Canada, and the Children's Medical Center of Dallas, Texas. Over this period, a total of 9,442 pediatric Isolator specimens were processed, with yeast or yeast-like organisms recovered in 297 (3.1%) of the specimens (151 [1.6%] unique clinical episodes) and filamentous or dimorphic fungi recovered in 31 (0.3%) of the specimens (25 unique clinical episodes). Only 18 of the 151 clinical episodes of fungemia attributable to yeast were not detected by automated blood culture systems. The majority of isolated yeast were Candida spp., which were usually detected by automated systems, whereas the most common non-Candida yeast was Malassezia furfur, which the automated system failed to detect. Filamentous or dimorphic fungi were detected in 25 episodes, of which only 9 (36%) episodes were deemed clinically significant after chart review, indicating that in the majority of cases (16/25, 64%) fungal isolation represented contamination. In five of the nine clinically significant episodes, the isolated fungus (Histoplasma capsulatum, Coccidioides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.) was also identified in other clinical specimens. Over the 10-year study period, the use of the pediatric Isolator system, at the discretion of the treating physician, only rarely provided useful clinical information for the diagnosis of fungemia in children, with the exception of M. furfur and possibly endemic mycoses.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.00578-16</identifier><identifier>PMID: 27307462</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Adolescent ; Aspergillus ; Bipolaris ; Blood Culture - methods ; Canada ; Candida ; Child ; Child, Preschool ; Coccidioides immitis ; Female ; Fungemia - diagnosis ; Fungi - classification ; Fungi - isolation & purification ; Fusarium oxysporum ; Histoplasma capsulatum ; Humans ; Infant ; Infant, Newborn ; Malassezia furfur ; Male ; Mycology ; Retrospective Studies ; Specimen Handling - methods ; Texas</subject><ispartof>Journal of clinical microbiology, 2016-09, Vol.54 (9), p.2284-2287</ispartof><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright © 2016, American Society for Microbiology. All Rights Reserved. 2016 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-9e65f4b13f1a48584a2f88ef7daa71ef7f51f8ebea53821e87e9fa6ee213e3fe3</citedby><cites>FETCH-LOGICAL-c483t-9e65f4b13f1a48584a2f88ef7daa71ef7f51f8ebea53821e87e9fa6ee213e3fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005482/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005482/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27307462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Warnock, D. W.</contributor><creatorcontrib>Campigotto, Aaron</creatorcontrib><creatorcontrib>Richardson, Susan E</creatorcontrib><creatorcontrib>Sebert, Michael</creatorcontrib><creatorcontrib>McElvania TeKippe, Erin</creatorcontrib><creatorcontrib>Chakravarty, Aparna</creatorcontrib><creatorcontrib>Doern, Christopher D</creatorcontrib><title>Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><description>The use of the Wampole Isolator 1.5-ml pediatric blood culture tube for the detection of fungemia in children was assessed by a 10-year retrospective review at two pediatric hospitals, The Hospital for Sick Children in Toronto, Canada, and the Children's Medical Center of Dallas, Texas. Over this period, a total of 9,442 pediatric Isolator specimens were processed, with yeast or yeast-like organisms recovered in 297 (3.1%) of the specimens (151 [1.6%] unique clinical episodes) and filamentous or dimorphic fungi recovered in 31 (0.3%) of the specimens (25 unique clinical episodes). Only 18 of the 151 clinical episodes of fungemia attributable to yeast were not detected by automated blood culture systems. The majority of isolated yeast were Candida spp., which were usually detected by automated systems, whereas the most common non-Candida yeast was Malassezia furfur, which the automated system failed to detect. Filamentous or dimorphic fungi were detected in 25 episodes, of which only 9 (36%) episodes were deemed clinically significant after chart review, indicating that in the majority of cases (16/25, 64%) fungal isolation represented contamination. In five of the nine clinically significant episodes, the isolated fungus (Histoplasma capsulatum, Coccidioides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.) was also identified in other clinical specimens. Over the 10-year study period, the use of the pediatric Isolator system, at the discretion of the treating physician, only rarely provided useful clinical information for the diagnosis of fungemia in children, with the exception of M. furfur and possibly endemic mycoses.</description><subject>Adolescent</subject><subject>Aspergillus</subject><subject>Bipolaris</subject><subject>Blood Culture - methods</subject><subject>Canada</subject><subject>Candida</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Coccidioides immitis</subject><subject>Female</subject><subject>Fungemia - diagnosis</subject><subject>Fungi - classification</subject><subject>Fungi - isolation & purification</subject><subject>Fusarium oxysporum</subject><subject>Histoplasma capsulatum</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Malassezia furfur</subject><subject>Male</subject><subject>Mycology</subject><subject>Retrospective Studies</subject><subject>Specimen Handling - methods</subject><subject>Texas</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1v1DAQxS0EarelN87IRw6keOI4djgglfSDokWtgEpwsrzJuDVy4tZ2Wu1_T7YtFdw4vcP7zdPMPEJeAdsHKNW7z-2XfcaEVAXUz8gCWKOKumY_npMFY40oALjcJjsp_WIMqkqILbJdSs5kVZcLMi7DHb3Izru8psHSc-ydydF19DQFb3KI9KMPoaft5PMUkX5bp4wDtbNxiBm77MK4GTyexkscnKFupO2V833E8T01FFjxE02kX_HW4d1L8sIan3DvUXfJxfHR9_ZTsTw7OW0PlkVXKZ6LBmthqxVwC6ZSQlWmtEqhlb0xEma1AqzCFRrBVQmoJDbW1IglcOQW-S758JB7Pa0G7DscczReX0c3mLjWwTj9rzO6K30ZbrWYX1mpcg548xgQw82EKevBpQ69NyOGKWlQpWyAs_9CQTQSeL1B3z6gXQwpRbRPGwHTmzb13Ka-b1NDPeOv_77iCf5TH_8NXcCbsQ</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Campigotto, Aaron</creator><creator>Richardson, Susan E</creator><creator>Sebert, Michael</creator><creator>McElvania TeKippe, Erin</creator><creator>Chakravarty, Aparna</creator><creator>Doern, Christopher D</creator><general>American Society for Microbiology</general><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>M7N</scope><scope>5PM</scope></search><sort><creationdate>20160901</creationdate><title>Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review</title><author>Campigotto, Aaron ; Richardson, Susan E ; Sebert, Michael ; McElvania TeKippe, Erin ; Chakravarty, Aparna ; Doern, Christopher D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-9e65f4b13f1a48584a2f88ef7daa71ef7f51f8ebea53821e87e9fa6ee213e3fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Aspergillus</topic><topic>Bipolaris</topic><topic>Blood Culture - methods</topic><topic>Canada</topic><topic>Candida</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Coccidioides immitis</topic><topic>Female</topic><topic>Fungemia - diagnosis</topic><topic>Fungi - classification</topic><topic>Fungi - isolation & purification</topic><topic>Fusarium oxysporum</topic><topic>Histoplasma capsulatum</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Malassezia furfur</topic><topic>Male</topic><topic>Mycology</topic><topic>Retrospective Studies</topic><topic>Specimen Handling - methods</topic><topic>Texas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Campigotto, Aaron</creatorcontrib><creatorcontrib>Richardson, Susan E</creatorcontrib><creatorcontrib>Sebert, Michael</creatorcontrib><creatorcontrib>McElvania TeKippe, Erin</creatorcontrib><creatorcontrib>Chakravarty, Aparna</creatorcontrib><creatorcontrib>Doern, Christopher D</creatorcontrib><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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Campigotto, Aaron</au><au>Richardson, Susan E</au><au>Sebert, Michael</au><au>McElvania TeKippe, Erin</au><au>Chakravarty, Aparna</au><au>Doern, Christopher D</au><au>Warnock, D. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review</atitle><jtitle>Journal of clinical microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>54</volume><issue>9</issue><spage>2284</spage><epage>2287</epage><pages>2284-2287</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><abstract>The use of the Wampole Isolator 1.5-ml pediatric blood culture tube for the detection of fungemia in children was assessed by a 10-year retrospective review at two pediatric hospitals, The Hospital for Sick Children in Toronto, Canada, and the Children's Medical Center of Dallas, Texas. Over this period, a total of 9,442 pediatric Isolator specimens were processed, with yeast or yeast-like organisms recovered in 297 (3.1%) of the specimens (151 [1.6%] unique clinical episodes) and filamentous or dimorphic fungi recovered in 31 (0.3%) of the specimens (25 unique clinical episodes). Only 18 of the 151 clinical episodes of fungemia attributable to yeast were not detected by automated blood culture systems. The majority of isolated yeast were Candida spp., which were usually detected by automated systems, whereas the most common non-Candida yeast was Malassezia furfur, which the automated system failed to detect. Filamentous or dimorphic fungi were detected in 25 episodes, of which only 9 (36%) episodes were deemed clinically significant after chart review, indicating that in the majority of cases (16/25, 64%) fungal isolation represented contamination. In five of the nine clinically significant episodes, the isolated fungus (Histoplasma capsulatum, Coccidioides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.) was also identified in other clinical specimens. Over the 10-year study period, the use of the pediatric Isolator system, at the discretion of the treating physician, only rarely provided useful clinical information for the diagnosis of fungemia in children, with the exception of M. furfur and possibly endemic mycoses.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27307462</pmid><doi>10.1128/JCM.00578-16</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Aspergillus Bipolaris Blood Culture - methods Canada Candida Child Child, Preschool Coccidioides immitis Female Fungemia - diagnosis Fungi - classification Fungi - isolation & purification Fusarium oxysporum Histoplasma capsulatum Humans Infant Infant, Newborn Malassezia furfur Male Mycology Retrospective Studies Specimen Handling - methods Texas |
title | Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review |
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