Treatment of CMV Pneumonia
For CMV pneumonia, first-line treatment is ganciclovir (IV) or foscarnet (IV), with valganciclovir (oral) as an alternative when absorption is adequate; adjunctive IVIG can be considered but is not routinely recommended. 1
First-Line Antiviral Therapy
The cornerstone of treatment involves antiviral agents targeting CMV replication:
- Ganciclovir (IV) or Foscarnet (IV) are the first-choice antiviral options 1
- Valganciclovir (oral) is typically initiated when absorption is not a concern, though some centers prefer IV ganciclovir 1
- Treatment duration is at least 2 weeks and should continue until CMV is no longer detected by PCR 1
Choosing Between Agents
The selection between ganciclovir and foscarnet depends on the patient's clinical profile:
- Foscarnet causes less myelosuppression, making it preferable in patients with baseline cytopenias 1
- Ganciclovir avoids the reversible nephrotoxicity and electrolyte abnormalities associated with foscarnet 1
- Choice may depend on institutional preference and concern for specific toxicities (myelosuppression vs nephrotoxicity) 1
Adjunctive Immunoglobulin Therapy
IVIG can be administered adjunctively for CMV pneumonitis, but is not routinely recommended due to cost and limited evidence of benefit 1:
- When used, IVIG is commonly administered every other day for 3 to 5 doses 1
- CMV-specific IVIG has not proven more efficacious than standard IVIG 1
- A large retrospective study found that adding IVIG to antiviral treatment did not improve overall or attributable mortality in hematopoietic cell transplant recipients 2
Treatment Outcomes and Prognosis
CMV pneumonia remains challenging despite antiviral therapy:
- In immunocompromised patients, treatment benefits 10%-72% of patients, making it more difficult to treat than CMV retinitis or gastrointestinal disease 3
- Among hematopoietic cell transplant recipients, 6-month survival improved to approximately 30% in recent years 2
- Improvements appear due to antiviral treatment and changes in transplant practices rather than immunoglobulin-based treatments 2
- In immunocompetent hosts with severe CMV pneumonia, prognosis is generally good with antiviral treatment 4
Risk Factors for Poor Outcome
Independent predictors of mortality include:
- High APACHE II score (>16) at onset of CMV pneumonia 5
- Development of antiviral toxicity 5
- Lymphopenia and mechanical ventilation 2
- Female sex and elevated bilirubin 2
Special Populations
Immunocompetent Patients
While CMV pneumonia is rare in immunocompetent individuals, antiviral treatment should be considered in severe cases:
- Ganciclovir treatment may positively shorten the course of CMV pneumonia 6
- Consider CMV pneumonia in patients with atypical lymphocytes and mildly elevated transaminases 4
- Treatment with ganciclovir 6 mg/kg/day IV divided twice daily has shown dramatic response 6
Patients with Lymphoma
CMV pneumonia incidence is increasing in lymphoma patients:
- Most patients (92%) had received chemotherapy and corticosteroids (89%) before onset 5
- CMV-attributed mortality rate was 30% 5
- Coinfections were present in 31% of cases at onset of CMV pneumonia 5
Monitoring and Resistance
- Consider testing for drug resistance if clinically significant breakthrough infection is detected 1
- For refractory or resistant infections, infectious disease consultation is recommended 1
- CMV surveillance consists of weekly monitoring by PCR, though thresholds for treatment vary by institution 1
Common Pitfalls
- Do not use acyclovir or valacyclovir for CMV pneumonia treatment—they are only weakly active against CMV 1
- Ensure adequate diagnostic sampling: CMV detection in bronchoalveolar lavage specimens is better with culture methods than cytologic or immunohistochemical methods 5
- Avoid delaying treatment while awaiting confirmatory testing in high-risk patients with compatible clinical presentation 1