Skip to main content
. 2020 May 2;9(5):1320. doi: 10.3390/jcm9051320

Table 2.

Graft function outcomes of the r-ATG and basiliximab groups.

Total
(n = 268)
Low Dose
r-ATG (n = 37)
Basiliximab
(n = 231)
p-Value
DGF (%) 2 (0.7) 0 2 (0.9) 0.898
Graft failure (%) 12 (4.5) 1 (2.7) 11 (4.8) 0.737
Patient death (%) 3 (1.1) 0 3 (1.3) 0.657
Total BPAR (%) 125 (46.6) 19 (51.4) 106 (45.9) 0.335
Clinical BPAR
TCMR (%) 53 (19.8) 4 (10.8) 49 (21.2) * 0.355
Borderline change (%) 29 (10.8) 9 (24.3) 20 (8.7)
Subclinical BPAR
TCMR (%) 11 (4.1) 2 (5.4) * 9 (3.9) *
Borderline change (%) 32 (11.9) 4 (10.8) 28 (12.1)
No rejection 143 (53.4) 18 (48.6) 125 (54.1)
de novo DSA (total n = 245) 10 (4.1) 5 (14.3) 5 (2.4) 0.004
e-GFR, mean (mL/min/1.73m2) 0.120
1 month 68.5 68.2 68.6
1 year 62.2 63.0 62.1
2 years 67.1 66.5 67.1
3 years 66.0 65.9 66.0
5 years 64.7 63.0 64.9

r-ATG, rabbit anti-thymocyte globulin; DGF, delayed graft function; BPAR, biopsy-proven acute rejection; TCMR, T-cell mediated acuter rejection; DSA, donor specific antibody; e-GFR, estimated-glomerular filtration rate; : total 159 patients received protocol biopsy (34 and 125 in the r-ATG group and the basiliximab group, respectively); : 35 and 210 patients were screened for de novo DSA in the r-ATG group and the basiliximab groups (2 and 21 patients omitted), respectively; *: Two patients had spontaneous AMR and clinical TCMR in the basiliximab group. Each one patient had spontaneous AMR and subclinical TCMR in the r-ATG and the basiliximab group.