Skip to main content
. 2023 Mar 31;107(4):994–1003. doi: 10.1097/TP.0000000000004355

TABLE 2.

Demographics, baseline characteristics, and immunosuppressive treatments of control and prophylactic eculizumab treatment cohorts

Control cohort Prophylactic treatment cohort
  Kidney transplants 33 38
  Transplant recipients 32 38
Demographics
  Mean age in y at transplantation (SD) 28.3 (±15.6)** 38.7 (±13.6)
  Children (<16 y old) (% of those with available data) 9 (27.3) 3 (7.9)
  Female recipients (% of transplants) 25 (75.8) 25 (65.8)
  Median y of transplantation (range) 2007 (2002-2016) *** 2015 (2013-2017)
Recipient complement defect status (% of transplants)
  Nil 0 6 (15.7)
  VUS 10 (30.3) 6 (15.7)
  Pathological variant 21 (63.6) 24 (63.2)
   Complement factor B 0 0
   Complement factor H (CFH) 17 (51.5) 16 (42.1)
   Complement factor I (CFI) 2 (6.1) 0
   CFH + CFI 0 1 (2.6)
   C3 2 (6.1) 7 (18.4)
  Number tested for anti-FH 28 (87.5) 32 (84.2)
   Isolated anti-FH detected 2 2
   Anti-FH detected with genetic variant 5 1
Risk of aHUS recurrence
  Medium 14 (42.4) 12 (31.6)
  High 19 (57.6) 26 (68.4)
Transplant details
  First transplants (%) 26 (78.8) 24 (63)
  Live donor transplants (% of n) n = 2210 (45.5) n = 388 (21)
  Median HLA mismatch (range) not available 3 (0-6)n = 33
Plasma exchange
  Received posttransplant PLEX 7***(n = 11 with available data) 1
Immunosuppression
 Available data on induction immunosuppression not available n = 23
  Basilixumab 19
  Antithymocyte globulin 4
  Alemtuzumab 0
 Available data on maintenance immunosuppression not available n = 33
  Tacrolimus + Mycophenolate mofetil + Prednisolone 28
  Tacrolimus + Mycophenolate mofetil 1
  Ciclosporin + Mycophenolate mofetil 0
  Tacrolimus + Prednisolone 2
  Tacrolimus + Azathioprine + Prednisolone 2
Meningococcal vaccine received before first D of eculizumab treatment
  ACWY serotype (n gives those with available data) not applicable 32 (n = 33)
  B serotype (n gives those with available data) not applicable 26 (n = 32)

Data for kidney transplants received since 2002 at medium or high risk of recurrence of atypical hemolytic uremic syndrome (aHUS) who were not treated with eculizumab (control cohort) and kidney transplants treated with prophylactic eculizumab at the time of transplantation (prophylactic treatment cohort). No recipients had identified pathological variants in noncomplement pathway gene associated with aHUS. Whenever data are not available for complete group, number with available data is given (n).

anti-FH, factor H autoantibody; PLEX, plasma exchange; VUS, variant of uncertain significance.

*P < 0.05,

**

P < 0.01,

***

P < 0.001 for difference compared with prophylactic treatment group.