Purpose: To determine if incidence of CMV disease differs based on recipient IgG quantification.
Methods: A single-center, retrospective review was performed on all renal transplants between 7/2006 and 6/2010 with one year follow-up. Patients were included if they were 18–75 years old with a D+/R low+ or D+/R+ seromatch; and were excluded if they received a multi-organ transplant or had HIV, HCV, or HBV co-infection. The primary outcome was incidence of documented CMV disease. Secondary outcomes included time to CMV disease, patient and graft survival, acute rejection, and infections.
Results: Of 250 renal transplants performed, 107 met inclusion criteria. Demographics between groups were similar. The patient population had a median age of 55 (IQR 44–61) years. The majority of patients were D+/R low+ (n=78, 73%) and the remainder were D+/R+ (n=29, 27%). Rabbit antithymocyte globulin was used for induction in 24% and rejection in 7% of recipients. Most patients received valganciclovir 450 mg daily for prophylaxis (n=98, 92%); nine received acyclovir. Median duration of prophylaxis was 6 months. CMV disease rates were similar between D+/R low+ and D+/R+ groups (2.5% vs. 0%, p = 1). No significant difference was identified between serogroups regarding acute rejection, patient survival, or graft survival. D+/R low+ transplants had significantly greater infections than D+/R+ (22% vs. 4%, p = 0.02).
Conclusion: Incidence of CMV disease wasn’t significantly different between serogroups. Quantification of recipient CMV IgG didn’t significantly affect the incidence of acute rejection or patient and graft survival. However, D+/R low+ transplants had an increased rate of infections.