Pharmacokinetics of ganciclovir in haematopoietic stem cell transplantation recipients with or without renal impairment

J Antimicrob Chemother. 2006 May;57(5):1004-7. doi: 10.1093/jac/dkl089. Epub 2006 Mar 21.

Abstract

Objectives: We investigated the pharmacokinetics of ganciclovir in 12 haematopoietic stem cell transplantation (HSCT) recipients to evaluate the validity of a 50% reduction in the ganciclovir dosage for mild renal impairment.

Patients and methods: Ganciclovir at 5 mg/kg/day was pre-emptively infused in patients with estimated CL(CR) > or = 70 mL/min (Group A), whereas the dose was reduced to 2.5 mg/kg/day in patients with CL(CR) between 50 and 70 mL/min (Group B).

Results: The peak concentration was significantly higher in Group A (P < 0.01). However, the decrease in the plasma ganciclovir concentration was slower in Group B (P = 0.09), and the AUC of all patients in both groups was distributed within a narrow range (25.6 +/- 4.77 microg x h/mL), when two patients with exceptionally high AUC values were excluded.

Conclusions: A 50% reduction in ganciclovir appeared to be appropriate for patients with mild renal impairment. Measuring the ganciclovir concentration at 4 h after starting infusion may be adequate for evaluating AUC.

MeSH terms

  • Adult
  • Antiviral Agents / blood
  • Antiviral Agents / pharmacokinetics*
  • Antiviral Agents / therapeutic use
  • Area Under Curve
  • Cytomegalovirus Infections / prevention & control
  • Dose-Response Relationship, Drug
  • Female
  • Ganciclovir / blood
  • Ganciclovir / pharmacokinetics*
  • Ganciclovir / therapeutic use
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Infusions, Intravenous
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Renal Insufficiency / metabolism*

Substances

  • Antiviral Agents
  • Ganciclovir