What is the recommended treatment for Cytomegalovirus (CMV) infection after lung transplant?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 4, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Management of CMV Infection Post Lung Transplant

For post-lung transplant CMV infection, first-line treatment should be oral valganciclovir or intravenous ganciclovir for at least 2 weeks and until CMV is no longer detectable by PCR. 1

First-Line Treatment Options

  • Oral valganciclovir at 900 mg twice daily for 21 days (induction phase), followed by 900 mg once daily as maintenance until CMV is no longer detectable 2, 3
  • Intravenous ganciclovir at 5 mg/kg twice daily for at least 2 weeks and until CMV is no longer detectable 1, 4
  • Typically, therapy is initiated with oral valganciclovir unless there are absorption or toxicity issues 1
  • The choice between oral valganciclovir and IV ganciclovir depends on:
    • Severity of infection
    • Gastrointestinal absorption capacity
    • Renal function 2

Monitoring During Treatment

  • Weekly quantitative CMV viral load monitoring by PCR 1
  • Complete blood counts to monitor for myelosuppression (particularly with ganciclovir/valganciclovir) 4, 3
  • Renal function monitoring, especially with foscarnet 1
  • Continue treatment until CMV is no longer detectable by PCR 1, 2

Second-Line Treatment Options

  • For ganciclovir-resistant CMV or when ganciclovir is not tolerated (e.g., ganciclovir-induced myelosuppression):
    • Intravenous foscarnet 1, 2
    • Intravenous cidofovir (with caution due to nephrotoxicity) 1
  • For CMV infection refractory to ganciclovir/valganciclovir, foscarnet, or cidofovir:
    • Oral maribavir (shown to achieve CMV viremia clearance in 56% of patients vs. 24% with other agents) 1
  • Infectious disease consultation is highly recommended for resistant or refractory cases 1

Important Considerations and Potential Complications

  • Dose adjustments are necessary for patients with renal impairment 4, 3
  • Common adverse effects to monitor:
    • Ganciclovir/valganciclovir: neutropenia, thrombocytopenia, anemia 1, 5
    • Foscarnet: nephrotoxicity and electrolyte abnormalities 1
    • Cidofovir: substantial nephrotoxicity and possible ocular toxicity 1
  • Risk factors for CMV disease in lung transplant recipients include:
    • Advanced age 5
    • Reduced-dose valganciclovir (less than 900 mg/day) 5
    • Less than 6 months of prophylaxis 5
    • Single-lung transplant 5

Special Considerations for Lung Transplant Recipients

  • Lung transplant recipients are at particularly high risk for CMV disease, with incidence rates of 27% reported even with prophylaxis 5
  • Breakthrough CMV disease can occur during prophylaxis (9% of cases) 5
  • Ganciclovir-resistant CMV has been associated with high mortality (100% in one study) 5
  • For patients with significant gastrointestinal GVHD, IV ganciclovir may be preferred over oral valganciclovir 1

Duration of Treatment

  • Treatment should continue for at least 2 weeks 1
  • Therapy should be maintained until CMV is no longer detectable by PCR 1, 2
  • For patients with high-risk factors, longer treatment courses may be necessary 1

Remember that acyclovir and valacyclovir have excellent safety profiles but are only weakly active against CMV and are not recommended for treatment of CMV infection 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Tratamiento para Hepatoesplenomegalia por Citomegalovirus (CMV)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cytomegalovirus disease among donor-positive/recipient-negative lung transplant recipients in the era of valganciclovir prophylaxis.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2010

Related Questions

What is the recommended management for Cytomegalovirus (CMV) post lung transplant?
What is the indication for filgrastim (Granulocyte-Colony Stimulating Factor) in a patient with leukopenia (low Total Leukocyte Count) receiving valganciclovir (Valcyte, antiviral medication) post lung transplant?
What is the recommended dose of IV ganciclovir for a 50 kg female patient on dialysis?
How do I manage a patient with elevated White Blood Cell (WBC) count, positive Cytomegalovirus (CMV), and negative mononucleosis (mono)?
What is the principal side effect of ganciclovir (antiviral medication) therapy?
What does a positive Babinski sign indicate and how is it managed?
What is the primary action of secretin (a hormone) in the digestive system?
What is the association between laboratory markers (platelet count, transaminases (liver enzymes), albumin, C-Reactive Protein (CRP)) and Acute Kidney Injury (AKI) severity in patients with Tropical Acute Febrile Illness?
What is the association between laboratory markers (platelet count, transaminases (liver enzymes), albumin, C-Reactive Protein (CRP)) and Acute Kidney Injury (AKI) severity in patients with Tropical Acute Febrile Illness?
What is the preferred treatment between Mirabegron (Myrbetriq) and Flavoxate for overactive bladder?
What is the association between laboratory markers (platelet count, transaminases (liver enzymes), albumin, C-Reactive Protein (CRP)) and Acute Kidney Injury (AKI) severity in patients with Tropical Acute Febrile Illness?

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.