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. 2020 Dec 3;3(1):54–59.e1. doi: 10.1016/j.xkme.2020.09.010

Table 1.

Clinical Characteristics of Study Patients Assessed by LFIA

Variable HD Patients (N = 39) Transplant Recipients (N = 19) P
Time of IgG+ test post PCR diagnosis, d 17 [13-26] 18 [14-23] 0.43
Age, y 64 [58-76] 55 [47-62] 0.004a
Men 24 (61.5%) 12 (63.2%) 0.91
Ethnicity
 White 9 (23.7%) 3 (16.7%) 0.52
 BAME 30 (76.9%) 16 (84.2%)
Cause of ESKD
 APKD 1 (2.6%) 2 (10.5%) 0.02a
 Diabetes mellitusb 19 (48.7%) 3 (15.8%)
 Glomerulonephritis 5 (12.8%) 3 (15.8%)
 Unknown 8 (20.5%) 8 (42.1%)
 Other 6 (15.4%) 3 (15.8%)
Baseline immunosuppression
 Nob 35 (89.7%) 0 (0%) <0.001a
 Prednisolone 1 (2.6%)
 FK only 1 (2.6%) 3 (16.7%)
 Predisolone, FK 1 (2.6%)
 Prednisolone, FK, MMF 1 (2.6%) 6 (33.3%)
 FK, MMF 7 (38.9%)
 Sirolimus, prednisolone, MMF 2 (11.1%)
Historic cytotoxic, B- or T-cell monoclonal antibody use
 Nob 34 (89.7%) 0 (0%) <0.001a
 CyP 1 (2.6%)
 CyP/Ritux 1 (2.6%)
 Alemtuzumab 2 (5.1%) 16 (84.2%)
 IL-2R blocker 1 (5.3%)
 CyP/bortezomib 1 (2.6%)
 Alemtuzumab/Ritux 1 (5.3%)
 Unknown 1 (5.3%)
Disease severity
 Mildb 6 (15.4%) 12 (63.2%) <0.001a
 Moderate 19 (48.7%) 6 (31.6%)
 Severe 11 (28.2%) 1 (5.3%)
 Critical 3 (7.7%)
Care level
 Outpatientb 5 (12.8%) 15 (78.9%) <0.001a
 Inpatient ward 31 (79.5%) 3 (15.8%)
 Intensive care unit 3 (7.7%) 1 (5.3%)
Current patient status
 Alive 36 (92.3%) 19 (100%) 0.22
 Died 3 (7.7%)

Note: Values expressed as median [interquartile range] or number (percent).

Abbreviations: APKD, adult polycystic kidney disease; BAME, Black, Asian, and minority ethnic; CyP, cyclophosphamide; FK, tacrolimus; HD, hemodialysis; IgG, immunoglobulin G; IL-2R, interleukin 2 receptor; LFIA, lateral flow immunoassay; MMF, mycophenolate mofetil; PCR, polymerase chain reaction; Ritux, rituximab.

a

Statistically significant.

b

Comparator.