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Relapsing cytomegalovirus infection in solid organ transplant recipients

dc.contributor.authorShanahan, A.en_US
dc.contributor.authorMalani, Preeti N.en_US
dc.contributor.authorKaul, D. R.en_US
dc.date.accessioned2010-06-01T19:52:56Z
dc.date.available2010-06-01T19:52:56Z
dc.date.issued2009-12en_US
dc.identifier.citationShanahan, A.; Malani, P.N.; Kaul, D.R. (2009). "Relapsing cytomegalovirus infection in solid organ transplant recipients." Transplant Infectious Disease 11(6): 513-518. <http://hdl.handle.net/2027.42/73013>en_US
dc.identifier.issn1398-2273en_US
dc.identifier.issn1399-3062en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/73013
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19735385&dopt=citationen_US
dc.description.abstractEfforts to prevent relapsed cytomegalovirus (CMV) disease among solid organ transplant (SOT) recipients present clinical challenges. Historically, SOT recipients treated with short courses of ganciclovir, without documented clearance of viremia, had relapse rates of 23–33%. Current treatment often includes much longer courses of valganciclovir, and persistence of viremia at the end of treatment is rare. We sought to determine the rate and risk factors for relapse under those treatment conditions. Records of 1760 SOT recipients from January 2003 to June 2007 were reviewed; 105 cases of CMV viremia were identified. Relapse occurred in 20/105 (19%); 50% had end-organ disease at the time of relapse. Most patients received approximately 3 months of valganciclovir. Clearance of viremia was documented in 19/20 patients with relapse. Multivariable analysis identified receipt of a thoracic organ and diabetes mellitus as risk factors for relapse. Despite long treatment courses with valganciclovir and documented clearance of viremia, CMV relapse remains common among SOT recipients. Better understanding of the epidemiology of CMV among SOT recipients and validation of risk factors for disease relapse should be the focus of future prospective trials. Such trials should include different treatment durations and extended monitoring for relapse.en_US
dc.format.extent119150 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherBlackwell Publishing Incen_US
dc.rights© 2009 John Wiley & Sons A/Sen_US
dc.subject.otherCMV Infectionen_US
dc.subject.otherCytomegalovirusen_US
dc.subject.otherSolid Organ Transplantationen_US
dc.subject.otherCMV Relapseen_US
dc.titleRelapsing cytomegalovirus infection in solid organ transplant recipientsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USA ,en_US
dc.contributor.affiliationumDivision of Infectious Diseases, University of Michigan Medical School, Ann Arbor, Michigan, USA ,en_US
dc.contributor.affiliationumGeriatric Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USA ,en_US
dc.contributor.affiliationumVeterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan, USA ,en_US
dc.contributor.affiliationumGeriatric Research Education and Clinical Center (GRECC), Ann Arbor, Michigan, USAen_US
dc.identifier.pmid19735385en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/73013/1/j.1399-3062.2009.00443.x.pdf
dc.identifier.doi10.1111/j.1399-3062.2009.00443.xen_US
dc.identifier.sourceTransplant Infectious Diseaseen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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