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False-positive Aspergillus galactomannan antigenaemia after haematopoietic stem cell transplantation
Objectives Although Aspergillus galactomannan (GM) antigen detection is widely applied in the diagnosis of invasive aspergillosis (IA), false-positive reactions with fungus-derived antibiotics, other fungal genera or the passage of dietary GM through injured mucosa are a matter of concern. The aim o...
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Published in: | Journal of antimicrobial chemotherapy 2008-02, Vol.61 (2), p.411-416 |
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creator | Asano-Mori, Yuki Kanda, Yoshinobu Oshima, Kumi Kako, Shinichi Shinohara, Akihito Nakasone, Hideki Kaneko, Makoto Sato, Hiroyuki Watanabe, Takuro Hosoya, Noriko Izutsu, Koji Asai, Takashi Hangaishi, Akira Motokura, Toru Chiba, Shigeru Kurokawa, Mineo |
description | Objectives Although Aspergillus galactomannan (GM) antigen detection is widely applied in the diagnosis of invasive aspergillosis (IA), false-positive reactions with fungus-derived antibiotics, other fungal genera or the passage of dietary GM through injured mucosa are a matter of concern. The aim of this study was to investigate the cumulative incidence and risk factors for false-positive GM antigenaemia. Patients and methods The records of 157 adult allogeneic haematopoietic stem cell transplantation (HSCT) recipients were retrospectively analysed. Episodes of positive GM antigenaemia, defined as two consecutive GM results with an optical density index above 0.6, were classified into true, false and inconclusive GM antigenaemia by reviewing the clinical course. Results Twenty-five patients developed proven or probable IA with a 1 year cumulative incidence of 12.9%, whereas 50 experienced positive GM antigenaemia with an incidence of 32.2%. Among the total 58 positive episodes of the 50 patients, 29 were considered false-positive. The positive predictive value (PPV) was lower during the first 100 days than beyond 100 days after HSCT (37.5% versus 58.8%). Gastrointestinal chronic graft-versus-host disease (GVHD) was identified as the only independent significant factor for the increased incidence of false-positive GM antigenaemia (PPV 0% versus 66.7%, P = 0.02). Conclusions GM antigen results must be considered cautiously in conjunction with other diagnostic procedures including computed tomography scans, especially during the first 100 days after HSCT and in patients with gastrointestinal chronic GVHD. |
doi_str_mv | 10.1093/jac/dkm463 |
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The aim of this study was to investigate the cumulative incidence and risk factors for false-positive GM antigenaemia. Patients and methods The records of 157 adult allogeneic haematopoietic stem cell transplantation (HSCT) recipients were retrospectively analysed. Episodes of positive GM antigenaemia, defined as two consecutive GM results with an optical density index above 0.6, were classified into true, false and inconclusive GM antigenaemia by reviewing the clinical course. Results Twenty-five patients developed proven or probable IA with a 1 year cumulative incidence of 12.9%, whereas 50 experienced positive GM antigenaemia with an incidence of 32.2%. Among the total 58 positive episodes of the 50 patients, 29 were considered false-positive. The positive predictive value (PPV) was lower during the first 100 days than beyond 100 days after HSCT (37.5% versus 58.8%). Gastrointestinal chronic graft-versus-host disease (GVHD) was identified as the only independent significant factor for the increased incidence of false-positive GM antigenaemia (PPV 0% versus 66.7%, P = 0.02). Conclusions GM antigen results must be considered cautiously in conjunction with other diagnostic procedures including computed tomography scans, especially during the first 100 days after HSCT and in patients with gastrointestinal chronic GVHD.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkm463</identifier><identifier>PMID: 18055488</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Aged ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Aspergillosis - diagnosis ; Aspergillosis - etiology ; Aspergillosis - metabolism ; Aspergillus ; Aspergillus - metabolism ; Biological and medical sciences ; Chemotherapy ; chronic GVHD ; False Positive Reactions ; Female ; Follow-Up Studies ; Fungal infections ; gastrointestinal tract ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic Stem Cell Transplantation - trends ; Human mycoses ; Humans ; Infectious diseases ; invasive aspergillosis ; Male ; Mannans - analysis ; Mannans - metabolism ; Medical sciences ; Microbiology ; Middle Aged ; Miscellaneous mycoses ; mucosal damage ; Mycoses ; Pharmacology. Drug treatments ; Retrospective Studies ; Stem cells ; Transplants & implants</subject><ispartof>Journal of antimicrobial chemotherapy, 2008-02, Vol.61 (2), p.411-416</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org 2008</rights><rights>2008 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c543t-a5759443569b5ad8183080c814950b7033526e152e0d2323a5804c2bdaaba25b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20048947$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18055488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asano-Mori, Yuki</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><creatorcontrib>Oshima, Kumi</creatorcontrib><creatorcontrib>Kako, Shinichi</creatorcontrib><creatorcontrib>Shinohara, Akihito</creatorcontrib><creatorcontrib>Nakasone, Hideki</creatorcontrib><creatorcontrib>Kaneko, Makoto</creatorcontrib><creatorcontrib>Sato, Hiroyuki</creatorcontrib><creatorcontrib>Watanabe, Takuro</creatorcontrib><creatorcontrib>Hosoya, Noriko</creatorcontrib><creatorcontrib>Izutsu, Koji</creatorcontrib><creatorcontrib>Asai, Takashi</creatorcontrib><creatorcontrib>Hangaishi, Akira</creatorcontrib><creatorcontrib>Motokura, Toru</creatorcontrib><creatorcontrib>Chiba, Shigeru</creatorcontrib><creatorcontrib>Kurokawa, Mineo</creatorcontrib><title>False-positive Aspergillus galactomannan antigenaemia after haematopoietic stem cell transplantation</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Objectives Although Aspergillus galactomannan (GM) antigen detection is widely applied in the diagnosis of invasive aspergillosis (IA), false-positive reactions with fungus-derived antibiotics, other fungal genera or the passage of dietary GM through injured mucosa are a matter of concern. The aim of this study was to investigate the cumulative incidence and risk factors for false-positive GM antigenaemia. Patients and methods The records of 157 adult allogeneic haematopoietic stem cell transplantation (HSCT) recipients were retrospectively analysed. Episodes of positive GM antigenaemia, defined as two consecutive GM results with an optical density index above 0.6, were classified into true, false and inconclusive GM antigenaemia by reviewing the clinical course. Results Twenty-five patients developed proven or probable IA with a 1 year cumulative incidence of 12.9%, whereas 50 experienced positive GM antigenaemia with an incidence of 32.2%. Among the total 58 positive episodes of the 50 patients, 29 were considered false-positive. The positive predictive value (PPV) was lower during the first 100 days than beyond 100 days after HSCT (37.5% versus 58.8%). Gastrointestinal chronic graft-versus-host disease (GVHD) was identified as the only independent significant factor for the increased incidence of false-positive GM antigenaemia (PPV 0% versus 66.7%, P = 0.02). Conclusions GM antigen results must be considered cautiously in conjunction with other diagnostic procedures including computed tomography scans, especially during the first 100 days after HSCT and in patients with gastrointestinal chronic GVHD.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Aspergillosis - diagnosis</subject><subject>Aspergillosis - etiology</subject><subject>Aspergillosis - metabolism</subject><subject>Aspergillus</subject><subject>Aspergillus - metabolism</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy</subject><subject>chronic GVHD</subject><subject>False Positive Reactions</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Fungal infections</subject><subject>gastrointestinal tract</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hematopoietic Stem Cell Transplantation - trends</subject><subject>Human mycoses</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>invasive aspergillosis</subject><subject>Male</subject><subject>Mannans - analysis</subject><subject>Mannans - metabolism</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Middle Aged</subject><subject>Miscellaneous mycoses</subject><subject>mucosal damage</subject><subject>Mycoses</subject><subject>Pharmacology. Drug treatments</subject><subject>Retrospective Studies</subject><subject>Stem cells</subject><subject>Transplants & implants</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqF0U9rFDEYBvAgil2rFz-ADIIehLFv_k7mWKptxQUvCqWX8E4mu2Y7MxmTjOi3N8suLXjQUwj88j5JHkJeUnhPoeVnO7Rn_d0oFH9EVlQoqBm09DFZAQdZN0LyE_IspR0AKKn0U3JCNUgptF6R_hKH5Oo5JJ_9T1edp9nFrR-GJVVbHNDmMOI04VThlP3WTehGjxVusovV97LBHObgXfa2StmNlXXDUOWIU5qHcgSzD9Nz8mSzj3lxXE_Jt8uPXy-u6_WXq08X5-vaSsFzjbKRrRBcqraT2GuqOWiwmopWQtcA55IpRyVz0DPOOEoNwrKuR-yQyY6fkreHuXMMPxaXshl92l8IJxeWZBpgtFWg_wsZSKZLWIGv_4K7sMSpPMIw2ijFhRIFvTsgG0NK0W3MHP2I8behYPYNmdKQOTRU8KvjxKUbXf9Aj5UU8OYIMFkcNuUrrU_3jgEI3YrmwYVl_ndgfXC-9PPrXmK8M6rhjTTXN7fmqrkVH8TntbnhfwAaY7Vr</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Asano-Mori, Yuki</creator><creator>Kanda, Yoshinobu</creator><creator>Oshima, Kumi</creator><creator>Kako, Shinichi</creator><creator>Shinohara, Akihito</creator><creator>Nakasone, Hideki</creator><creator>Kaneko, Makoto</creator><creator>Sato, Hiroyuki</creator><creator>Watanabe, Takuro</creator><creator>Hosoya, Noriko</creator><creator>Izutsu, Koji</creator><creator>Asai, Takashi</creator><creator>Hangaishi, Akira</creator><creator>Motokura, Toru</creator><creator>Chiba, Shigeru</creator><creator>Kurokawa, Mineo</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20080201</creationdate><title>False-positive Aspergillus galactomannan antigenaemia after haematopoietic stem cell transplantation</title><author>Asano-Mori, Yuki ; Kanda, Yoshinobu ; Oshima, Kumi ; Kako, Shinichi ; Shinohara, Akihito ; Nakasone, Hideki ; Kaneko, Makoto ; Sato, Hiroyuki ; Watanabe, Takuro ; Hosoya, Noriko ; Izutsu, Koji ; Asai, Takashi ; Hangaishi, Akira ; Motokura, Toru ; Chiba, Shigeru ; Kurokawa, Mineo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c543t-a5759443569b5ad8183080c814950b7033526e152e0d2323a5804c2bdaaba25b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Aspergillosis - diagnosis</topic><topic>Aspergillosis - etiology</topic><topic>Aspergillosis - metabolism</topic><topic>Aspergillus</topic><topic>Aspergillus - metabolism</topic><topic>Biological and medical sciences</topic><topic>Chemotherapy</topic><topic>chronic GVHD</topic><topic>False Positive Reactions</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Fungal infections</topic><topic>gastrointestinal tract</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic Stem Cell Transplantation - trends</topic><topic>Human mycoses</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>invasive aspergillosis</topic><topic>Male</topic><topic>Mannans - analysis</topic><topic>Mannans - metabolism</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>Miscellaneous mycoses</topic><topic>mucosal damage</topic><topic>Mycoses</topic><topic>Pharmacology. Drug treatments</topic><topic>Retrospective Studies</topic><topic>Stem cells</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asano-Mori, Yuki</creatorcontrib><creatorcontrib>Kanda, Yoshinobu</creatorcontrib><creatorcontrib>Oshima, Kumi</creatorcontrib><creatorcontrib>Kako, Shinichi</creatorcontrib><creatorcontrib>Shinohara, Akihito</creatorcontrib><creatorcontrib>Nakasone, Hideki</creatorcontrib><creatorcontrib>Kaneko, Makoto</creatorcontrib><creatorcontrib>Sato, Hiroyuki</creatorcontrib><creatorcontrib>Watanabe, Takuro</creatorcontrib><creatorcontrib>Hosoya, Noriko</creatorcontrib><creatorcontrib>Izutsu, Koji</creatorcontrib><creatorcontrib>Asai, Takashi</creatorcontrib><creatorcontrib>Hangaishi, Akira</creatorcontrib><creatorcontrib>Motokura, Toru</creatorcontrib><creatorcontrib>Chiba, Shigeru</creatorcontrib><creatorcontrib>Kurokawa, Mineo</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>Biotechnology Research Abstracts</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 & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asano-Mori, Yuki</au><au>Kanda, Yoshinobu</au><au>Oshima, Kumi</au><au>Kako, Shinichi</au><au>Shinohara, Akihito</au><au>Nakasone, Hideki</au><au>Kaneko, Makoto</au><au>Sato, Hiroyuki</au><au>Watanabe, Takuro</au><au>Hosoya, Noriko</au><au>Izutsu, Koji</au><au>Asai, Takashi</au><au>Hangaishi, Akira</au><au>Motokura, Toru</au><au>Chiba, Shigeru</au><au>Kurokawa, Mineo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>False-positive Aspergillus galactomannan antigenaemia after haematopoietic stem cell transplantation</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>61</volume><issue>2</issue><spage>411</spage><epage>416</epage><pages>411-416</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives Although Aspergillus galactomannan (GM) antigen detection is widely applied in the diagnosis of invasive aspergillosis (IA), false-positive reactions with fungus-derived antibiotics, other fungal genera or the passage of dietary GM through injured mucosa are a matter of concern. The aim of this study was to investigate the cumulative incidence and risk factors for false-positive GM antigenaemia. Patients and methods The records of 157 adult allogeneic haematopoietic stem cell transplantation (HSCT) recipients were retrospectively analysed. Episodes of positive GM antigenaemia, defined as two consecutive GM results with an optical density index above 0.6, were classified into true, false and inconclusive GM antigenaemia by reviewing the clinical course. Results Twenty-five patients developed proven or probable IA with a 1 year cumulative incidence of 12.9%, whereas 50 experienced positive GM antigenaemia with an incidence of 32.2%. Among the total 58 positive episodes of the 50 patients, 29 were considered false-positive. The positive predictive value (PPV) was lower during the first 100 days than beyond 100 days after HSCT (37.5% versus 58.8%). Gastrointestinal chronic graft-versus-host disease (GVHD) was identified as the only independent significant factor for the increased incidence of false-positive GM antigenaemia (PPV 0% versus 66.7%, P = 0.02). Conclusions GM antigen results must be considered cautiously in conjunction with other diagnostic procedures including computed tomography scans, especially during the first 100 days after HSCT and in patients with gastrointestinal chronic GVHD.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18055488</pmid><doi>10.1093/jac/dkm463</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antibiotics. Antiinfectious agents. Antiparasitic agents Aspergillosis - diagnosis Aspergillosis - etiology Aspergillosis - metabolism Aspergillus Aspergillus - metabolism Biological and medical sciences Chemotherapy chronic GVHD False Positive Reactions Female Follow-Up Studies Fungal infections gastrointestinal tract Hematopoietic Stem Cell Transplantation - adverse effects Hematopoietic Stem Cell Transplantation - trends Human mycoses Humans Infectious diseases invasive aspergillosis Male Mannans - analysis Mannans - metabolism Medical sciences Microbiology Middle Aged Miscellaneous mycoses mucosal damage Mycoses Pharmacology. Drug treatments Retrospective Studies Stem cells Transplants & implants |
title | False-positive Aspergillus galactomannan antigenaemia after haematopoietic stem cell transplantation |
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