Efficacy of low-dose valganciclovir in Cytomegalovirus R+ lung transplant recipients: a retrospective comparative analysis

Efficacy of low-dose valganciclovir in Cytomegalovirus R+ lung transplant recipients: a retrospective comparative analysis

Authors

  • Jessica Hunt Department of Pharmacy, St. Joseph Hospital and Medical Center, Phoenix AZ https://orcid.org/0000-0001-6392-927X
  • Kristina M. Chapple Department of Biostatistics and Neurosurgery, St. Joseph Hospital and Medical Center, Phoenix AZ
  • Aasya Nasar Department of Pharmacy, St. Joseph Hospital and Medical Center, Phoenix AZ https://orcid.org/0000-0002-7011-9694
  • Lauren Cherrier Department of Pharmacy, St. Joseph Hospital and Medical Center, Phoenix AZ https://orcid.org/0000-0002-5042-0236
  • Rajat Walia Department of Pulmonology, St. Joseph Hospital and Medical Center, Phoenix AZ

Keywords:

Cytomegalovirus, lung transplantation, valganciclovir

Abstract

Background: Cytomegalovirus (CMV) infection is extremely common after lung transplant and can be associated with significant morbidity and mortality. Current practice suggests the use of 900 mg daily of valganciclovir for CMV prophylaxis, but there is no literature assessing whether 450 mg daily of valganciclovir is sufficient in intermediate CMV risk lung transplant recipients. Therefore, we sought to assess the role of low-dose valganciclovir (LDV) versus high-dose valganciclovir (HDV) prophylaxis in intermediate-risk (R+) recipients.
Methods: We conducted a retrospective analysis on lung transplant recipients at the Norton Thoracic Institute in Phoenix, Arizona looking at intermediate-risk patients that received either valganciclovir 450 mg per day (LDV) or 900 mg/day (HDV). All patients were followed for 1 year posttransplant for incidence of CMV viremia. The primary outcome was the rate of CMV viremia as determined by a positive CMV polymerase chain reaction ([PCR] >2.7 log copies/mL). Secondary outcomes included rate of adverse events, acute cellular rejection, and mortality.
Results: The primary analysis included 103 patients (55 in the LDV group, 48 in the HDV group). In the LDV group, 9 patients (16.4%) developed CMV viremia compared to 4 (8.3%) in the HDV group (p=0.221) with no difference observed in adverse event rates between groups.
Conclusion: There was no statistical difference between groups for the primary outcome. However, the effect size demonstrated in this analysis may be of clinical relevance and valganciclovir 450 mg daily would not be recommended in intermediate risk lung transplant recipients at this time. To confirm our results, further prospective studies enrolling larger patient populations are necessary.

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Published

25-01-2021

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Original Research Articles

How to Cite

1.
Hunt J, Chapple KM, Nasar A, Cherrier L, Walia R. Efficacy of low-dose valganciclovir in Cytomegalovirus R+ lung transplant recipients: a retrospective comparative analysis. Multidiscip Respir Med [Internet]. 2021 Jan. 25 [cited 2024 Dec. 21];16. Available from: https://mrmjournal.org/index.php/mrm/article/view/706