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Prospective Surveillance for Invasive Fungal Infections in Hematopoietic Stem Cell Transplant Recipients, 2001-2006: Overview of the Transplant-Associated Infection Surveillance Network (TRANSNET) Database

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dc.contributor.author Alexander, Barbara en_US
dc.date.accessioned 2011-06-21T17:27:21Z
dc.date.available 2011-06-21T17:27:21Z
dc.date.issued 2010 en_US
dc.identifier.citation Kontoyiannis,Dimitrios P.;Marr,Kieren A.;Park,Benjamin J.;Alexander,Barbara D.;Anaissie,Elias J.;Walsh,Thomas J.;Ito,James;Andes,David R.;Baddley,John W.;Brown,Janice M.;Brumble,Lisa M.;Freifeld,Alison G.;Hadley,Susan;Herwaldt,Loreen A.;Kauffman,Carol A.;Knapp,Katherine;Lyon,G. Marshall;Morrison,Vicki A.;Papanicolaou,Genovefa;Patterson,Thomas F.;Perl,Trish M.;Schuster,Mindy G.;Walker,Randall;Wannemuehler,Kathleen A.;Wingard,John R.;Chiller,Tom M.;Pappas,Peter G.. 2010. Prospective Surveillance for Invasive Fungal Infections in Hematopoietic Stem Cell Transplant Recipients, 2001-2006: Overview of the Transplant-Associated Infection Surveillance Network (TRANSNET) Database. Clinical Infectious Diseases 50(8): 1091-1100. en_US
dc.identifier.issn 1058-4838 en_US
dc.identifier.uri http://hdl.handle.net/10161/4145
dc.description.abstract Background. The incidence and epidemiology of invasive fungal infections (IFIs), a leading cause of death among hematopoeitic stem cell transplant (HSCT) recipients, are derived mainly from single-institution retrospective studies. Methods. The Transplant Associated Infections Surveillance Network, a network of 23 US transplant centers, prospectively enrolled HSCT recipients with proven and probable IFIs occurring between March 2001 and March 2006. We collected denominator data on all HSCTs preformed at each site and clinical, diagnostic, and outcome information for each IFI case. To estimate trends in IFI, we calculated the 12-month cumulative incidence among 9 sequential subcohorts. Results. We identified 983 IFIs among 875 HSCT recipients. The median age of the patients was 49 years; 60% were male. Invasive aspergillosis (43%), invasive candidiasis (28%), and zygomycosis (8%) were the most common IFIs. Fifty-nine percent and 61% of IFIs were recognized within 60 days of neutropenia and graft-versus-host disease, respectively. Median onset of candidiasis and aspergillosis after HSCT was 61 days and 99 days, respectively. Within a cohort of 16,200 HSCT recipients who received their first transplants between March 2001 and September 2005 and were followed up through March 2006, we identified 718 IFIs in 639 persons. Twelve-month cumulative incidences, based on the first IFI, were 7.7 cases per 100 transplants for matched unrelated allogeneic, 8.1 cases per 100 transplants for mismatched-related allogeneic, 5.8 cases per 100 transplants for matched-related allogeneic, and 1.2 cases per 100 transplants for autologous HSCT. Conclusions. In this national prospective surveillance study of IFIs in HSCT recipients, the cumulative incidence was highest for aspergillosis, followed by candidiasis. Understanding the epidemiologic trends and burden of IFIs may lead to improved management strategies and study design. en_US
dc.language.iso en_US en_US
dc.publisher UNIV CHICAGO PRESS en_US
dc.relation.isversionof doi:10.1086/651263 en_US
dc.subject risk-factors en_US
dc.subject mold infections en_US
dc.subject prophylactic fluconazole en_US
dc.subject prognostic-factors en_US
dc.subject aspergillosis en_US
dc.subject epidemiology en_US
dc.subject autopsy en_US
dc.subject outcomes en_US
dc.subject blood en_US
dc.subject immunology en_US
dc.subject infectious diseases en_US
dc.subject microbiology en_US
dc.title Prospective Surveillance for Invasive Fungal Infections in Hematopoietic Stem Cell Transplant Recipients, 2001-2006: Overview of the Transplant-Associated Infection Surveillance Network (TRANSNET) Database en_US
dc.title.alternative en_US
dc.description.version Version of Record en_US
duke.date.pubdate 2010-4-15 en_US
duke.description.endpage 1100 en_US
duke.description.issue 8 en_US
duke.description.startpage 1091 en_US
duke.description.volume 50 en_US
dc.relation.journal Clinical Infectious Diseases en_US

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