Table 1

Unmatched 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 219 69  159 60  
Age, y 73.0 (15.0-92.0) 73.0 (13.0-104.0) .94 73.0 (15.0-91.0) 76.5 (24.0-92.0) .02 
Sex, n (%)   .07   .06 
    Female 109 (49.7) 26 (37.7)  73 (45.9) 36 (60.0)  
    Male 110 (50.8) 43 (62.3) 86 (54.1) 24 (40.0) 
Weight, kg 69.0 (40.0-130.0) 69.0 (40.0-113.0) .92 69.0 (40.0-130.0) 69.2 (44.0-107.0) .70 
FVIII level, IU/dL 1.0 (0.0-40.0) 3.0 (0.0-34.0) .03 2.0 (0.0-32.0) 1.0 (0.0-40.0) .13 
Hb, g/dL 8.6 (3.0-15.2) 8.8 (3.3-14.4) .57 8.6 (3.0-15.2) 8.4 (4.6-14.8) .90 
Inhibitor titer, BU/mL 15.4 (0.1-2765.0) 8.0 (0.3-200.0) .0003 15.0 (1.0-2765.0) 17.0 (0.1-1700.0) .99 
Therapy delay, days 0.01 (0.0-0.5) 0.01 (0.00-0.11) .34 0.01 (0.00-0.27) 0.01 (0.00-0.54) .76 
Ancillary antifibrinolytic therapy, n (%) 30 (13.7) 20 (29.0) .0035 27 (17.0) 3 (5.0) .0215 
Cause of bleeding, n (%)  .715   .08 
    Unknown   
    Traumatic 46 (21.1) 16 (23.2) 38 (24.1) 8 (13.3) 
    Spontaneous 172 (78.9) 53 (76.8) 120 (75.9) 52 (86.7) 
Bleeding site, n (%)  .04   .12 
    CNS 5 (2.3) 0 (0.0)  5 (3.1) 0 (0.0)  
    Deep muscle 139 (63.4) 32 (46.4) 94 (59.1) 45 (75.0) 
    Hemarthrosis 6 (2.7) 3 (4.3) 5 (3.1) 1 (1.7) 
    Mucosa 34 (15.6) 21 (30.5) 30 (18.8) 4 (6.6) 
    Skin 34 (15.6) 13 (18.8) 24 (15.2) 10 (16.7) 
    Multiple sites 1 (0.4) 0 (0.0) 1 (0.7) 0 (0.0) 
Severity of bleeding, n (%)  .031   .31 
    Unknown   
    Severe 193 (88.5) 54 (78.2) 142 (89.8) 51 (85.0) 
    Nonsevere 25 (11.5) 15 (21.8) 16 (10.1) 9 (15.0) 
VariableBypassing agent, median (IQR)FVIII or DDAVP, median (IQR)P*rFVIIa, median (IQR)aPCC, median (IQR)P
Patients, n 219 69  159 60  
Age, y 73.0 (15.0-92.0) 73.0 (13.0-104.0) .94 73.0 (15.0-91.0) 76.5 (24.0-92.0) .02 
Sex, n (%)   .07   .06 
    Female 109 (49.7) 26 (37.7)  73 (45.9) 36 (60.0)  
    Male 110 (50.8) 43 (62.3) 86 (54.1) 24 (40.0) 
Weight, kg 69.0 (40.0-130.0) 69.0 (40.0-113.0) .92 69.0 (40.0-130.0) 69.2 (44.0-107.0) .70 
FVIII level, IU/dL 1.0 (0.0-40.0) 3.0 (0.0-34.0) .03 2.0 (0.0-32.0) 1.0 (0.0-40.0) .13 
Hb, g/dL 8.6 (3.0-15.2) 8.8 (3.3-14.4) .57 8.6 (3.0-15.2) 8.4 (4.6-14.8) .90 
Inhibitor titer, BU/mL 15.4 (0.1-2765.0) 8.0 (0.3-200.0) .0003 15.0 (1.0-2765.0) 17.0 (0.1-1700.0) .99 
Therapy delay, days 0.01 (0.0-0.5) 0.01 (0.00-0.11) .34 0.01 (0.00-0.27) 0.01 (0.00-0.54) .76 
Ancillary antifibrinolytic therapy, n (%) 30 (13.7) 20 (29.0) .0035 27 (17.0) 3 (5.0) .0215 
Cause of bleeding, n (%)  .715   .08 
    Unknown   
    Traumatic 46 (21.1) 16 (23.2) 38 (24.1) 8 (13.3) 
    Spontaneous 172 (78.9) 53 (76.8) 120 (75.9) 52 (86.7) 
Bleeding site, n (%)  .04   .12 
    CNS 5 (2.3) 0 (0.0)  5 (3.1) 0 (0.0)  
    Deep muscle 139 (63.4) 32 (46.4) 94 (59.1) 45 (75.0) 
    Hemarthrosis 6 (2.7) 3 (4.3) 5 (3.1) 1 (1.7) 
    Mucosa 34 (15.6) 21 (30.5) 30 (18.8) 4 (6.6) 
    Skin 34 (15.6) 13 (18.8) 24 (15.2) 10 (16.7) 
    Multiple sites 1 (0.4) 0 (0.0) 1 (0.7) 0 (0.0) 
Severity of bleeding, n (%)  .031   .31 
    Unknown   
    Severe 193 (88.5) 54 (78.2) 142 (89.8) 51 (85.0) 
    Nonsevere 25 (11.5) 15 (21.8) 16 (10.1) 9 (15.0) 
*

P values refer to Pearson χ2 or Mann-Whitney U test for the comparison between bypassing agent and FVIII or DDAVP.

P values refer to Pearson χ2 or Mann-Whitney U test for the comparison between rFVIIa and aPCC.

A total of 13 of 55 patients (23.6%) treated with FVIII received ancillary antifibrinolytic treatment; 7 of 14 (50%) of patients treated with DDAVP also received antifibrinolytics.

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