Clinical Study

Is Anticoagulation Discontinuation Achievable with Citrate Dialysate during HDF Sessions?

Table 3

Association of dialysis circuit coagulation with treatment characteristics.

ParametersUnivariate analysisMultivariate analysis
Estimation (±SD) valueEstimation (±SD) valueRR (95% CI)

Nadroparine quantity
 Baseline versus none−1.06 ± 0.640.098−1.63 ± 0.580.00480.20 (0.06–0.61)
 Reduced versus none−0.70 ± 0.430.11−1.04 ± 0.430.01460.35 (0.15–0.81)
Hemodiafilter
 FX versus ELISIO−0.37 ± 0.43ns
 TS versus ELISIO−0.38 ± 0.66ns
 VITAPES versus ELISIO−0.37 ± 0.52ns
Dialysis machine
 AK versus ARTIS0.83 ± 0.380.0271.97 ± 0.860.0227.15 (1.33–38.4)
Vitamin K antagonists
 Present versus Absent−4.01 ± 0.70<0.0001−3.12 ± 0.49<0.00010.04 (0.02–0.11)
Antiplatelet drugs
 Aspirin versus none0.06 ± 0.52ns
 Clopidogrel versus None0.73 ± 0.51ns
 Association versus none−0.62 ± 0.89ns
Iron sucrose (Venofer®)
 Present versus absent−0.68 ± 0.290.02−0.30 ± 0.310.33 (ns)
Total blood treated (RR/10 liters)−0.08 ± 0.020.0002−0.09 ± 0.040.01490.40 (0.19–0.84)
Ultrafiltration rate0.00 ± 0.00ns
Hemoglobin−0.21 ± 0.17ns
CRP0.002 ± 0.01ns

By univariate and multivariate analysis, the reduction and withdrawal of nadroparin are associated with increased risk for clots, as well as AK200 dialysis machine. VKA and high volume of blood treated during one session are protective. Antiplatelet drugs, venous iron, ultrafiltration rate, hemoglobin concentration, and CRP do not have significant impact on the risk of clots.