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Clinical and virologic outcomes in high‐risk adult Epstein‐Barr virus mismatched organ transplant recipients
Author(s) -
Kumar Deepali,
Patil Nikhil,
Husain Shahid,
Chaparro Cecilia,
Bhat Mamatha,
Kim S. Joseph,
Humar Atul
Publication year - 2017
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/ctr.13000
Subject(s) - medicine , valganciclovir , immunosuppression , viral load , viremia , gastroenterology , immunology , population , transplantation , virus , ganciclovir , environmental health , human cytomegalovirus
Epstein‐Barr virus ( EBV ) D+/R− organ transplant recipients are a high‐risk group for developing post‐transplant lymphoproliferative disease ( PTLD ). Little data are available for prevention in the adult EBV mismatched population. We conducted a retrospective study of EBV D+/R− organ transplants performed during 2002‐2014. Of the 153 patients identified, 82.4% patients received antiviral prophylaxis with valganciclovir for a median of 4.5 months (range: 0.8‐22 months) and 36.6% underwent viral load monitoring in the first post‐transplant year. EBV viremia developed in 67.2% monitored patients. In viremic patients, immunosuppression was reduced in 20/37(54.1%) in response to viremia and 17/37 (45.9%) received therapeutic dose valganciclovir. In patients with EBV viremia who received valganciclovir and/or had a reduction in immunosuppression and had sufficient viral load time points (n=31), 28 (90.3%) had a significant decline in viral load at day 14 (median log decline 0.49 (0.24‐0.64), P <.001) and at day 30 (0.87 (0.52‐1.21), P <.001). PTLD developed in 27 (15%) patients (biopsy proven=25, possible=2) at median 8 months (range: 2.4‐130) post‐transplant with the majority (81.5%) within the first year. In multivariate analysis, viral load monitoring and use of mycophenolate were associated with a lower incidence of PTLD . Antiviral prophylaxis was not associated with a lower risk of PTLD , but viral load monitoring and use of mycophenolate mofetil were protective.