Abstract
The availability of valganciclovir (VGCV) has significantly simplified the treatment of human cytomegalovirus (HCMV) infection after solid-organ transplantation. We show that there was no difference in the kinetics of the decrease in HCMV load after preemptive therapy with VGCV in 22 solid-organ transplant recipients (T1/2=2.16 days), compared with that in 23 patients treated with intravenous ganciclovir (GCV) (T(1/2) = 1.73 days; P=.63). Preemptive therapy with VGCV provides control of HCMV replication that is comparable to that achieved with preemptive intravenous therapy with GCV.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Administration, Oral
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Adult
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Antiviral Agents / administration & dosage
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Antiviral Agents / therapeutic use*
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Cytomegalovirus / drug effects*
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Cytomegalovirus Infections / drug therapy
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Cytomegalovirus Infections / prevention & control*
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Cytomegalovirus Infections / virology
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Female
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Ganciclovir / administration & dosage
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Ganciclovir / analogs & derivatives*
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Ganciclovir / therapeutic use*
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Humans
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Injections, Intravenous
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Kinetics
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Male
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Middle Aged
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Retrospective Studies
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Transplants*
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Valganciclovir
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Viral Load
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Virus Replication / drug effects
Substances
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Antiviral Agents
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Valganciclovir
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Ganciclovir