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 (T-1/2 = 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 pro vides control of HCMV replication that is comparable to that achieved with preemptive intravenous therapy with GCV.
机构:
Northwestern Univ, Div Infect Dis, Feinberg Sch Med, Chicago, IL 60611 USA
Northwestern Univ, Div Organ Transplantat, Feinberg Sch Med, Chicago, IL 60611 USANorthwestern Univ, Div Infect Dis, Feinberg Sch Med, Chicago, IL 60611 USA
机构:
Univ Utah, Div Pediat Infect Dis, Salt Lake City, UT USA
Primary Childrens Med Ctr, Div Transplant Immunocompromised Infect Dis, Salt Lake City, UT USAUniv Utah, Div Pediat Infect Dis, Salt Lake City, UT USA
Knackstedt, Elizabeth Doby
Danziger-Isakov, Lara
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机构:
Univ Cincinnati, Div Pediat Infect Dis, Immunocompromised Host Infect Dis, Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USAUniv Utah, Div Pediat Infect Dis, Salt Lake City, UT USA