Source:http://linkedlifedata.com/resource/pubmed/id/17468776
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-6-20
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pubmed:abstractText |
The use of quantitative cytomegalovirus (CMV) real-time polymerase chain reaction (RT-PCR) and preemptive ganciclovir therapy is replacing prophylaxis as the management of choice in high-risk patients undergoing stem cell transplantation (SCT). However, there are limited data defining its role in this setting. In the current retrospective single-centre study, quantitative RT-PCR was used to determine CMV in 577 consecutive patients undergoing SCT (172 allogeneic and 405 autologous) over a 5-year period. CMV RT-PCR was performed weekly until cessation of immunosuppression (allogeneic) or for 30 days post-SCT (autologous). Treatment was commenced after two consecutive positive results or a high copy on the first occasion (> 1000 copies/ml, > 3 log). The overall CMV reactivation rate in patients undergoing allogeneic SCT was 30%, with reactivation observed in 72% of high-risk patients (recipient positive patients). CMV end-organ disease was observed in eight patients (1%); of these, four were CMV RT-PCR negative at the time of diagnosis of end-organ CMV disease, with three remaining negative throughout the course of the disease. CMV-related mortality was recorded in three patients. The current data support a preemptive treatment strategy-based CMV RT-PCR, but indicate that in symptomatic patients, a negative CMV PCR result does not exclude CMV end-organ disease.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0268-3369
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
55-61
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pubmed:meshHeading |
pubmed-meshheading:17468776-Adolescent,
pubmed-meshheading:17468776-Adult,
pubmed-meshheading:17468776-Aged,
pubmed-meshheading:17468776-Cytomegalovirus,
pubmed-meshheading:17468776-Cytomegalovirus Infections,
pubmed-meshheading:17468776-Female,
pubmed-meshheading:17468776-Humans,
pubmed-meshheading:17468776-Male,
pubmed-meshheading:17468776-Middle Aged,
pubmed-meshheading:17468776-Reproducibility of Results,
pubmed-meshheading:17468776-Retrospective Studies,
pubmed-meshheading:17468776-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:17468776-Stem Cell Transplantation,
pubmed-meshheading:17468776-Transplantation, Autologous,
pubmed-meshheading:17468776-Transplantation, Homologous,
pubmed-meshheading:17468776-Viral Load
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pubmed:year |
2007
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pubmed:articleTitle |
Active CMV disease does not always correlate with viral load detection.
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pubmed:affiliation |
Department of Haematology, University of Manchester, Christie Hospital, Manchester, UK. jruell@aol.com
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pubmed:publicationType |
Journal Article
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