Clinical outcomes of valganciclovir prophylaxis in high-risk (D+/R-) renal transplant recipients experiencing delayed graft function

Transpl Infect Dis. 2019 Aug;21(4):e13125. doi: 10.1111/tid.13125. Epub 2019 Jun 25.

Abstract

Background: Cytomegalovirus (CMV) outcomes with valganciclovir prophylaxis in renal transplant recipients experiencing delayed graft function (DGF) are unclear.

Methods: This single center, retrospective, cohort study of CMV high-risk (D+/R- with alemtuzumab induction) deceased donor renal transplant recipients receiving valganciclovir prophylaxis assessed CMV outcomes in patients experiencing DGF (n = 72) versus those with immediate graft function (IGF; n = 66).

Results: Cytomegalovirus viremia by 12 months occurred at similar rates in the IGF and DGF groups (30.3% vs 26.4%, respectively, P = 0.71) with 89.7% (35/39) of all cases classified as CMV disease. The median time to CMV viremia post transplant was day 141 and 138 in the IGF and DGF groups, respectively (P = 0.30). The incidence of biopsy-proven acute rejection (BPAR) was higher in the DGF group (18.1% vs 4.6%, P = 0.02) with BPAR preceding CMV in only 1 patient. There was no significant difference in graft loss (1.5% vs 4.2%, P = 0.62) or patient survival (98.5% vs 95.8%, P = 0.62) at 1 year between the IGF and DGF groups, respectively.

Conclusion: Valganciclovir prophylaxis in patients experiencing DGF yielded similar CMV outcomes up to 1-year post transplant when compared to use in patients with IGF.

Keywords: cytomegalovirus; delayed graft function; hemodialysis; renal transplant; valganciclovir.

MeSH terms

  • Adult
  • Antiviral Agents / administration & dosage*
  • Cytomegalovirus Infections / virology
  • Delayed Graft Function*
  • Electronic Health Records
  • Female
  • Graft Rejection / prevention & control*
  • Graft Survival
  • Humans
  • Kidney Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Risk Factors
  • Transplant Recipients*
  • Treatment Outcome
  • Valganciclovir / administration & dosage*
  • Viremia

Substances

  • Antiviral Agents
  • Valganciclovir