Table 1.
| Medication | Prophylaxis | Prophylaxis dosea | Treatment | Treatment dosea |
|---|---|---|---|---|
| Ganciclovir | Y | 5 mg/kg/dose IV q24 h | Y | 5 mg/kg/dose IV q12 h |
| Valganciclovir | Y | 7 × BSAb × CrClc PO q24 h (max 900 mg/day) | Y | 7 × BSAb × CrClc PO q12 h (max: 900 mg/dose) |
| Foscarnetd | Y | 60 mg/kg/dose IV q12 h for 7 days then 90–120 mg/kg/dose qDay | Y | 60 mg/kg/dose IV q8 h; Maintenance: 90 mg/kg qDay |
| Cidofovire | Yf | 5 mg/kg/dose qWeek × 2 weeks then 5 mg/kg/dose every other week | Y | 5 mg/kg/dose qWeek × 2 weeks then 5 mg/kg/dose every other week |
| Letermovir (≥18 years) | Y | 480 mg PO IV q24 h | N | NA |
| Maribavir (≥12 years and ≥35 kg) | N | NA | Y | 400 mg PO BID |
Dosing given is for patients with normal renal function.
BSA, body surface area.
CrCl, creatinine clearance, using modified Schwartz formula which bases k constant on age.
IV hydration should be given as 10–20 ml/kg (max 1,000 ml) prior to initial infusion and then 10–20 ml/kg (max 1,000 ml) given concurrently with subsequent doses.
Should be given with probenecid (25–40 mg/kg/dose (max 2,000mg) PO 3 h prior to cidofovir and 10–20 mg/kg/dose (max 1,000 mg) 2–3 h and 8–9 h after cidofovir) as well as IV hydration (10–20 ml/kg pre- and post-cidofovir OR increase maintenance IVF by 1.5–2×).
Less commonly used due to availability of other agents with more favorable side effect profiles.