Treatment of Significant CMV Counts in Renal Transplant Patients
For renal transplant patients with significant CMV counts, intravenous ganciclovir is recommended for serious or tissue-invasive disease, while either intravenous ganciclovir or oral valganciclovir is recommended for non-serious disease, with therapy continuing until CMV is no longer detectable by plasma nucleic acid testing. 1
Treatment Algorithm Based on Disease Severity
Serious/Tissue-Invasive CMV Disease
- First-line treatment: Intravenous ganciclovir 5 mg/kg once daily 1, 2
- Duration: Continue until CMV is no longer detectable by plasma NAT or pp65 antigenemia 1
- Immunosuppression: Consider reducing immunosuppressive medication in life-threatening CMV disease or persistent disease 1
- Monitoring: Weekly monitoring of CMV by NAT or pp65 antigenemia during treatment 1
Non-Serious CMV Disease (mild clinical symptoms)
- Treatment options:
- Duration: Continue until CMV is no longer detectable by plasma NAT or pp65 antigenemia 1
- Monitoring: Weekly monitoring of CMV by NAT or pp65 antigenemia 1
Special Considerations
Pediatric Patients
- All CMV disease in pediatric kidney transplant recipients should be treated with intravenous ganciclovir 1
- Dosing should be calculated based on body surface area and modified creatinine clearance 4
Treatment-Resistant CMV
For cases that fail to respond to standard therapy:
- Consider foscarnet 90-120 mg/kg once daily 2
- Cidofovir for highly resistant cases 2
- Maribavir for refractory cases 2
Monitoring During Treatment
- Monitor graft function closely during CMV disease 1
- Weekly complete blood counts during the first month of treatment 2
- Monthly renal function tests 2
- Continue viral load monitoring until clearance 1, 2
Prevention of Recurrence
After successful treatment of CMV disease, consider secondary prophylaxis:
- Valganciclovir 900 mg once daily for 1-3 months 2, 4
- For high-risk patients (D+/R-), extending prophylaxis to 200 days post-transplant has been shown to significantly reduce the incidence of CMV disease compared to 100 days (16.1% vs 36.8%) 5
Important Caveats
- Dose adjustment: Valganciclovir and ganciclovir doses must be adjusted for renal function 2
- Monitoring for toxicity: Regular monitoring for neutropenia, thrombocytopenia, and renal dysfunction is essential 2
- Drug interactions: Be aware of potential interactions with immunosuppressive medications 2
- Low-dose vs. high-dose valganciclovir: While some centers use valganciclovir 450 mg daily for prophylaxis with similar efficacy to 900 mg daily 6, 7, 8, for active CMV disease treatment, the higher dose (900 mg twice daily) is recommended 3
Remember that early detection and appropriate management of CMV infection in renal transplant recipients is essential to optimize transplant outcomes and patient survival 2.