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. 2020 Oct 28;9(11):3479. doi: 10.3390/jcm9113479

Table 2.

Complications after conversion to belatacept.

Total
Patients
N = 453
Early Conversion a
N = 121
Late Conversion a
N = 332
p-Value
Renal complications
Kidney allograft failure n (%) 42 (9.3) 23 (19.0) 19 (5.7) <0.001
Rejection post-conversion n (%) 24 (5.3) 10 (8.3) 14 (4.2) 0.143
Viral complications
CMV DNAemia n (%) 74 (16.9) 37 (31.6) 37 (11.5) <0.001
CMV disease n (%) 22 (4.8) 14 (11.6) 8 (2.4) <0.001
Time between belatacept conversion to CMV disease—months 10.7 ± 9 9.6 ± 10 12.7 ± 8 0.188
EBV DNAemia n (%) 133 (36.0) 13 (14.8) 120 (42.7) <0.001
BK virus DNAemia n (%) 6 (2.0) 4 (7.2) 2 (0.8) 1
BK nephropathy n (%) 0 0 0 -
JC Virus n (%) 2 (0.4) 2 (1.6) 0 0.121
VZV n (%) 5 (1.1) 2 (1.6) 3 (0.9) 0.610
Bacterial complications
Tuberculosis n (%) 2 (0.4) 1 (0.8) 1 (0.3) 0.458
Fungal complications
Pneumocystis pneumonia n (%) 13 (2.8) 6 (4.9) 7 (2.1) 0.557
Aspergillosis pneumonia n (%) 2 (0.4) 2 (1.6) 0 0.121
Other complications
Death n (%) 22 (4.8) 10 (8.3) 12 (3.6) 0.073

Results are expressed according to N (%). Missing data are not taken into account for the calculation of percentages. CMV, Cytomegalovirus; EBV, Epstein–Barr virus; VZV: varicella zoster virus. a Early conversion was considered as belatacept conversion before 6 months after kidney transplantation, and later conversion was >6 months after transplantation.