Which virus is treated with ganciclovir?

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Ganciclovir is Used to Treat Cytomegalovirus (CMV)

The correct answer is D. Cytomegalovirus - ganciclovir is specifically indicated for CMV disease treatment and prophylaxis in immunocompromised patients, including transplant recipients and those with HIV/AIDS. 1

Primary Indication and Mechanism

  • Ganciclovir is an acyclic nucleoside analogue that inhibits CMV replication by preferentially phosphorylating in CMV-infected cells and competitively inhibiting viral DNA polymerase 1
  • The drug achieves 100-fold greater triphosphate concentrations in CMV-infected cells compared to uninfected cells, demonstrating its selective antiviral activity 1
  • FDA-approved indications include prevention of CMV disease in solid organ transplant recipients, prevention in advanced HIV patients at risk, and maintenance treatment of CMV retinitis 1

Clinical Efficacy Evidence

Treatment of Active CMV Disease:

  • In transplant recipients with severe CMV infection, ganciclovir demonstrates clinical improvement rates of 84% for CMV retinitis, 83% for gastrointestinal CMV, and 72% for CMV pneumonia 2
  • Virologic response occurs in 92% of patients with sequential cultures showing clearance of CMV from blood, urine, or throat washings 2
  • In liver and kidney transplant recipients with severe CMV infection, 90% of evaluable patients survived with resolution of fever (mean 5.3 days), improved liver function, and cleared pulmonary infiltrates 3

Prophylaxis Strategy:

  • KDIGO guidelines recommend all kidney transplant recipients (except donor/recipient both CMV-negative) receive oral ganciclovir or valganciclovir prophylaxis for at least 3 months post-transplant and 6 weeks after T-cell-depleting antibody treatment 4
  • Pre-emptive therapy initiated when BKV plasma levels exceed 10,000 copies/ml or with positive CMV monitoring reduces disease incidence to 1-3% 4

Dosing Protocols by Clinical Scenario

Serious/Tissue-Invasive CMV Disease:

  • Intravenous ganciclovir 5 mg/kg every 12 hours for 2-3 weeks is recommended for CMV encephalitis, though therapeutic failures are common with monotherapy 4
  • Combination therapy with ganciclovir (5 mg/kg IV q12h) plus foscarnet (60 mg/kg IV q8h or 90 mg/kg IV q12h) for 3 weeks achieves improvement/stabilization in 74% of HIV patients with CMV encephalitis or myelitis 4

Non-Serious CMV Disease in Adults:

  • Either IV ganciclovir or oral valganciclovir can be used for mild CMV disease 4
  • Oral valganciclovir 900 mg twice daily for 21 days is noninferior to IV ganciclovir for CMV disease treatment in solid organ transplant recipients, with comparable viremia eradication rates (45.1% vs 48.4% at Day 21) 5

Pediatric Considerations:

  • All CMV disease in pediatric transplant recipients requires IV ganciclovir treatment 4
  • For congenital CMV, valganciclovir for 6 months improves developmental outcomes and prevents hearing loss progression, superior to 6-week courses 6

Why Not the Other Options

Influenza A (Option A):

  • Treated with neuraminidase inhibitors (oseltamivir, zanamivir), not ganciclovir 4

Herpes Simplex (Option B):

  • Acyclovir is the drug of choice, with dosing of 10-20 mg/kg IV every 8 hours for 14-21 days for HSV encephalitis 4
  • While ganciclovir has activity against HSV in vitro, it is not indicated for HSV treatment 1

Herpes Zoster (Option C):

  • Treated with acyclovir, valacyclovir, or famciclovir 4
  • Ganciclovir is not the standard treatment despite activity against herpes viruses 1

Critical Adverse Effects to Monitor

  • Neutropenia occurs in 35-42% of patients, with higher rates (60%) in bone marrow transplant recipients 2, 7
  • Thrombocytopenia develops in 19% of patients 2
  • Dose modification may be required for neutropenia; granulocyte colony-stimulating factor can be used for severe cases 6
  • Weekly monitoring of CMV by nucleic acid testing or pp65 antigenemia is recommended during treatment 4

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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