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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical microbiology 2016-09, Vol.54 (9), p.2284-2287
Hauptverfasser: Campigotto, Aaron, Richardson, Susan E, Sebert, Michael, McElvania TeKippe, Erin, Chakravarty, Aparna, Doern, Christopher D
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2287
container_issue 9
container_start_page 2284
container_title Journal of clinical microbiology
container_volume 54
creator Campigotto, Aaron
Richardson, Susan E
Sebert, Michael
McElvania TeKippe, Erin
Chakravarty, Aparna
Doern, Christopher D
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.
doi_str_mv 10.1128/JCM.00578-16
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5005482</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1827913082</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-9e65f4b13f1a48584a2f88ef7daa71ef7f51f8ebea53821e87e9fa6ee213e3fe3</originalsourceid><addsrcrecordid>eNqNkc1v1DAQxS0EarelN87IRw6keOI4djgglfSDokWtgEpwsrzJuDVy4tZ2Wu1_T7YtFdw4vcP7zdPMPEJeAdsHKNW7z-2XfcaEVAXUz8gCWKOKumY_npMFY40oALjcJjsp_WIMqkqILbJdSs5kVZcLMi7DHb3Izru8psHSc-ydydF19DQFb3KI9KMPoaft5PMUkX5bp4wDtbNxiBm77MK4GTyexkscnKFupO2V833E8T01FFjxE02kX_HW4d1L8sIan3DvUXfJxfHR9_ZTsTw7OW0PlkVXKZ6LBmthqxVwC6ZSQlWmtEqhlb0xEma1AqzCFRrBVQmoJDbW1IglcOQW-S758JB7Pa0G7DscczReX0c3mLjWwTj9rzO6K30ZbrWYX1mpcg548xgQw82EKevBpQ69NyOGKWlQpWyAs_9CQTQSeL1B3z6gXQwpRbRPGwHTmzb13Ka-b1NDPeOv_77iCf5TH_8NXcCbsQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1815971362</pqid></control><display><type>article</type><title>Low Utility of Pediatric Isolator Blood Culture System for Detection of Fungemia in Children: a 10-Year Review</title><source>American Society for Microbiology</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Campigotto, Aaron ; Richardson, Susan E ; Sebert, Michael ; McElvania TeKippe, Erin ; Chakravarty, Aparna ; Doern, Christopher D</creator><contributor>Warnock, D. 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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0095-1137
ispartof Journal of clinical microbiology, 2016-09, Vol.54 (9), p.2284-2287
issn 0095-1137
1098-660X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5005482
source American Society for Microbiology; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A02%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Low%20Utility%20of%20Pediatric%20Isolator%20Blood%20Culture%20System%20for%20Detection%20of%20Fungemia%20in%20Children:%20a%2010-Year%20Review&rft.jtitle=Journal%20of%20clinical%20microbiology&rft.au=Campigotto,%20Aaron&rft.date=2016-09-01&rft.volume=54&rft.issue=9&rft.spage=2284&rft.epage=2287&rft.pages=2284-2287&rft.issn=0095-1137&rft.eissn=1098-660X&rft_id=info:doi/10.1128/JCM.00578-16&rft_dat=%3Cproquest_pubme%3E1827913082%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1815971362&rft_id=info:pmid/27307462&rfr_iscdi=true