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. 2022 Dec 14;9:1009748. doi: 10.3389/fmed.2022.1009748

TABLE 1.

Relevant demographic, medical and drug therapy data of the study population.

n = 101
Age (years) 69 ± 13
Gender, male (n, %) 59 (58)
Weight (kg) 74 ± 18
Race (n, %)
Caucasian 61 (60)
Black African 14 (14)
Northern African 24 (24)
Asian 2 (2)
ESKD etiology (n, %)
Diabetes mellitus 17 (17)
Hypertensive nephrosclerosis 22 (22)
Combination of diabetic and vascular kidney failure 23 (23)
Glomerulonephritis 7 (7)
Tubulointerstitial nephropathy 7 (7)
Genetic disease 9 (9)
Other 16 (16)
Dialysis vintage (months) 33 (6–71)
Vascular access type (n, %)
AV fistula 41 (41)
AV graft 4 (4)
Catheter 56 (55)
History of HD vascular access dysfunction (n, %) 33 (33)
Treated diabetes mellitus (n, %) 47 (47)
Use of antiplatelets (n, %)
None 36 (36)
Acetylsalicylic acid 52 (51)
Clopidogrel 1 (1)
Combination 12 (12)
Use of anticoagulants (n, %)
None 85 (84)
Anti-vitamin K 14 (14)
LMWH 2 (2)

Data are given as mean ± SD, proportions (%) or median (IQR) when appropriate. ESKD, end-stage kidney disease; AV, arteriovenous; HD, hemodialysis; LMWH, low molecular weight heparin.

History of HD vascular access dysfunction was defined as arteriovenous fistula thrombosis ever, catheter replacement for thrombotic dysfunction ever, or urokinase use because of access thrombosis during the last 3 months.