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. Author manuscript; available in PMC: 2024 Apr 24.
Published in final edited form as: Cardiovasc Drugs Ther. 2022 Jan 13;37(3):519–527. doi: 10.1007/s10557-021-07298-5

Table 2.

Baseline characteristics

DOAC (n = 48) Warfarin (n = 107) p value

CHA2DS2-VASc score
 0 11 (22.9) 16 (15.0) 0.25
 1 13 (27.1) 39 (36.4)
 2 12 (25.0) 23 (21.4)
 3 8 (16.7) 18 (16.8)
 4 2 ( 4.2) 6 (5.6)
 5 2 ( 4.2) 0
 N/A 0 5 (4.7)
NYHA classification
No CHF 18 (37.5) 61 (57.0) 0.15
 1 7 (14.6) 11 (10.3)
 2 17 (35.4) 28 (26.2)
 3 6 (12.5) 7 (6.5)
HASBLED score
 0 22 (45.8) 38 (35.5) 0.61
 1 15 (31.3) 33 (30.8)
 2 10 (20.8) 23 (21.5)
 3 1 ( 2.1) 5 (4.7)
 4 0 3 (2.8)
 N/A 0 5 (4.7)
Bleed Hx 2 (4.2) 5 (4.7) 1.00
TE Hx 11 (22.9) 27 (25.2)* 0.84
Diabetes mellitus 2 (4.2) 4 (3.7)* 1.00
Renal dysfunction 2 (4.2) 4 (3.7) 1.00
Liver disease 14 (29.2) 30 (28.0) 1.00
Labile INR 4 (8.3)* 7 (6.5) 0.74

Values are n (%). Bleed Hx, bleed history or predisposition; CHF, congestive heart failure; TE Hx, history of thrombotic/embolic complications; INR, international normalized ratio.

*

One patient converted to positive history during therapy re-initiation.

The number of warfarin patients with a bleed history/predisposition is underestimated because 7 patients initially did not have a bleed history/predisposition, and then had a bleeding event while on warfarin, and were ultimately restarted on warfarin because of high TE risk. Including these 7 patients who re-started warfarin after a bleeding event increases the proportion of warfarin patients with a bleed history/predisposition from 4.7 to 11.2%, although the p value is not statistically significant when compared to DOAC patients (p = 0.23)