Table 2

Matched sample baseline characteristics according to treatment of the first bleeding episode (bypassing agent vs FVIII or DDAVP and rFVIIa vs aPCC)

VariableBypassing agent, median (IQR)FVIII or DDAVP, median (IQR)P*rFVIIa, median (IQR)aPCC, median (IQR)P*
Patients, n 60 60  57 57  
Age, y 74.0 (24.0-91.0) 72.5 (13.0-104.0) .95 72.00 (39.00-91.00) 77.00 (24.00-92.00) .41 
Sex, n (%)   .69   .41 
    Female 25 (41.7) 23 (38.3)  37 (64.91) 33 (57.89)  
    Male 35 (58.3) 37 (61.7) 20 (35.09) 24 (42.11) 
Weight, kg 70.0 (40.0-107.0) 68.0 (40.0-113.0) .49 70.00 (40.00-120.00) 70.00 (44.00-107.00) .66 
FVIII level, IU/dL 2.0 (0.0-40.0) 3.0 (0.0-34.0) .61 1.25 (0.00-32.00) 1.00 (0.00-40.00) .41 
Hb, g/dL 8.4 (3.0-14.2) 8.8 (3.3-14.4) .41 8.50 (3.00-14.00) 8.40 (4.60-14.80) .84 
Inhibitor titer, BU/mL 9.3 (1.0-2765.0) 8.0 (0.3-200.0) .52 16.00 (1.00-2765.00) 17.00 (0.10-1700.00) .52 
Therapy delay, d 0.01 (0.0-0.13) 0.01 (0.0-0.11) .46 0.01 (0.00-0.09) 0.01 (0.00-0.54) .64 
Cause of bleeding, n (%)  .51   .62 
    Traumatic 16 (26.7) 13 (21.7)  10 (17.54) 8 (14.04)  
    Spontaneous 44 (73.3) 47 (78.3) 47 (82.46) 49 (85.96) 
Bleeding site, n (%)  .99   .55 
    Deep 30 (50.0) 30 (50.0)  44 (77.19) 44 (77.19)  
    Hemarthrosis 3 (5.0) 2 (3.3) 0 (0.00) 1 (1.75) 
    Mucosa 15 (25.0) 16 (26.7) 5 (8.77) 4 (7.02) 
    Skin 12 (20.0) 12 (20.0) 8 (14.04) 8 (14.04) 
Severity of bleeding, n (%)  .63   .56 
    Severe 47 (78.3) 49 (81.7)  49 (85.96) 51 (89.47)  
    Nonsevere 13 (21.6) 11 (18.3) 8 (14.04) 6 (10.53) 
VariableBypassing agent, median (IQR)FVIII or DDAVP, median (IQR)P*rFVIIa, median (IQR)aPCC, median (IQR)P*
Patients, n 60 60  57 57  
Age, y 74.0 (24.0-91.0) 72.5 (13.0-104.0) .95 72.00 (39.00-91.00) 77.00 (24.00-92.00) .41 
Sex, n (%)   .69   .41 
    Female 25 (41.7) 23 (38.3)  37 (64.91) 33 (57.89)  
    Male 35 (58.3) 37 (61.7) 20 (35.09) 24 (42.11) 
Weight, kg 70.0 (40.0-107.0) 68.0 (40.0-113.0) .49 70.00 (40.00-120.00) 70.00 (44.00-107.00) .66 
FVIII level, IU/dL 2.0 (0.0-40.0) 3.0 (0.0-34.0) .61 1.25 (0.00-32.00) 1.00 (0.00-40.00) .41 
Hb, g/dL 8.4 (3.0-14.2) 8.8 (3.3-14.4) .41 8.50 (3.00-14.00) 8.40 (4.60-14.80) .84 
Inhibitor titer, BU/mL 9.3 (1.0-2765.0) 8.0 (0.3-200.0) .52 16.00 (1.00-2765.00) 17.00 (0.10-1700.00) .52 
Therapy delay, d 0.01 (0.0-0.13) 0.01 (0.0-0.11) .46 0.01 (0.00-0.09) 0.01 (0.00-0.54) .64 
Cause of bleeding, n (%)  .51   .62 
    Traumatic 16 (26.7) 13 (21.7)  10 (17.54) 8 (14.04)  
    Spontaneous 44 (73.3) 47 (78.3) 47 (82.46) 49 (85.96) 
Bleeding site, n (%)  .99   .55 
    Deep 30 (50.0) 30 (50.0)  44 (77.19) 44 (77.19)  
    Hemarthrosis 3 (5.0) 2 (3.3) 0 (0.00) 1 (1.75) 
    Mucosa 15 (25.0) 16 (26.7) 5 (8.77) 4 (7.02) 
    Skin 12 (20.0) 12 (20.0) 8 (14.04) 8 (14.04) 
Severity of bleeding, n (%)  .63   .56 
    Severe 47 (78.3) 49 (81.7)  49 (85.96) 51 (89.47)  
    Nonsevere 13 (21.6) 11 (18.3) 8 (14.04) 6 (10.53) 
*

P values refer to McNemar χ2 or Wilcoxon signed-rank test.

Two patients (3.5%) among the matched samples treated with rFVIIa also received ancillary immunoadsorption.

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