TABLE 10.
• We recommend routine screening for BKPyV-DNAemia using the strategies proposed in this current guideline because it is associated with an improvement in clinical outcomes and is cost-effective in kidney transplant recipients in robust models up to the seventh decade of life (strong, B) |
• We suggest not decreasing the frequency of screening because it may reduce the efficacy of intervention by reducing immunosuppression, thereby increasing the overall direct healthcare costs (weak, B) |
Future directions |
➢ Evaluate different screening strategies (modality and frequency) on cost-effectiveness, particularly because they relate to different geographic areas, ethnicities, and limited access to laboratory testing |
➢ Determine the cost-effectiveness ratio of duration and frequency of monitoring of patients not clearing BKPyV-DNAemia at the lowest possible level of immunosuppression (persistent low plasma viral loads with or without biopsy-proven BKPyV-nephropathy) |
➢ Evaluate the cost-effectiveness ratio of BKPyV-specific immunity, such as serotype-specific antibodies, neutralizing antibodies, or CMI, to shorten or extend screening for BKPyV-DNAemia |
➢ Evaluate the cost-effectiveness ratio of novel interventions such as neutralizing antibodies, novel antivirals, or adoptive T-cell therapies for prevention and therapy of BKPyV-DNAemia/-nephropathy |
➢ Assess the benefits of customized screening strategies based on immunosuppression exposure, including choice of induction agent and need for additional therapy for desensitization |
BKPyV, BK polyomavirus; CMI, cell-mediated immunity.