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Table 4 Clinical outcomes and the association between nafamostat dose and outcomes. The association with each outcome was assessed using distinct generalised linear models, each adjusted for confounding factors appropriate to the respective outcome, as detailed in eTable 2

From: Dose of nafamostat mesylate during continuous kidney replacement therapy in critically ill patients: a two-centre observational study

Outcome

Overall (n = 269)

Adjusted OR

β

95%CI

p value

ICU mortality

61 (22.7%)

0.95

 

(0.90, 0.99)

0.04

Hospital mortality

94 (34.9%)

0.95

 

(0.91, 0.99)

0.03

ICU length of stay, day

14 ± 21.1

 

0.04

(-0.35, 0.44)

0.83

Hospital length of stay, day

66 ± 91.6

 

0.17

(-1.55, 1.89)

0.85

Mechanical ventilation days, day

8 ± 17.9

 

0.13

(-0.11, 0.37)

0.30

ΔC-reactive protein, mg/dL

1.49 ± 9.21

 

-0.03

(-0.15, 0.09)

0.67

Red blood cell over 48 h, ml

200.5 ± 377.8

 

-13.7

(-19.9, -7.5)

< 0.001

Fresh frozen plasma over 48 h, ml

241.1 ± 667.1

 

-22.9

(-34.1, -11.7)

< 0.001

Platelet over 48 h, ml

64.0 ± 162.5

 

-4.1

(-6.9, -1.2)

0.01

Dialysis dependence at discharge*

68 / 182 (37.4%)

0.95

 

(0.90, 1.00)

 0.05

  1. Values are presented as medians with interquartile range or means with standard deviations. OR denotes odds ratio; CI, confidence interval. *Among patients who had not been on chronic haemodialysis