Have a personal or library account? Click to login
Safety and efficacy of non–vitamin K antagonist oral anticoagulants compared with well-controlled warfarin in Thai patients with atrial fibrillation Cover

Safety and efficacy of non–vitamin K antagonist oral anticoagulants compared with well-controlled warfarin in Thai patients with atrial fibrillation

Open Access
|Jun 2022

Figures & Tables

Figure 1

Comparison of total bleeding or thromboembolic events or both (A), thromboembolic events (B), major bleeding (C), and minor bleeding (D) between 90 patients with AF who received NOACs and 90 patients with AF who received well-controlled warfarin (TTR > 65%) treatment. Black bars indicate the presence of events, and gray bars indicate the absence of events. AF, atrial fibrillation; TTR, time in the therapeutic range; NOACs; non–vitamin K antagonist oral anticoagulants.
Comparison of total bleeding or thromboembolic events or both (A), thromboembolic events (B), major bleeding (C), and minor bleeding (D) between 90 patients with AF who received NOACs and 90 patients with AF who received well-controlled warfarin (TTR > 65%) treatment. Black bars indicate the presence of events, and gray bars indicate the absence of events. AF, atrial fibrillation; TTR, time in the therapeutic range; NOACs; non–vitamin K antagonist oral anticoagulants.

Primary and secondary outcomes of NOAC and well-controlled warfarin treatment in patients with AF

OutcomesWarfarin (n = 90) n (%)NOACs (n = 90) n (%)OR (95% CI)P
Primary outcome: total bleeding or thromboembolic events or both19 (21)7 (8)3.17 (2.27–4.07)0.01*
Secondary outcome
Thromboembolic events or major bleeding or both1 (1)1 (1)1.00 (−1.78 to 3.78)>0.99
Thromboembolic events0 (0)1 (1)
Major bleeding1 (1)0 (0)
Minor bleeding19 (21)6 (7)3.75 (2.79–4.71)0.01*
  Bleeding per gum2 (2)1 (1)2.02 (−0.40 to 4.44)>0.99
  Bruising12 (13)5 (6)2.61 (1.53–3.69)0.047
  Hematuria3 (3)2 (2)1.51 (−0.29 to 3.31)>0.99
  Epistaxis1 (1)0 (0)
  Subconjunctival hemorrhage2 (2)0 (0)
All-cause mortality0 (0)0 (0)

Baseline characteristics of Thai patients with AF

Demographic dataTotal (n = 180) n (%)Warfarin (n = 90) n (%)NOACs (n = 90) n (%)P
Age (years), mean ± SD72.8 ± 10.171.3 ± 10.274.3 ± 9.80.04*
Male sex107 (59)48 (53)59 (66)0.10
Medical welfare
  Affiliation reimbursement122 (68)40 (44)82 (91)<0.01*
  Universal healthcare coverage43 (24)40 (44)3 (3)
  Social security scheme3 (2)3 (3)0 (0)
  Self-payment12 (7)7 (8)5 (6)
Medical history
  Diabetes50 (28)23 (26)27 (30)0.51
  Hypertension162 (90)79 (88)83 (92)0.32
  Dyslipidemia139 (77)69 (77)70 (78)0.86
  Coronary artery disease36 (20)14 (16)22 (24)0.14
  Peripheral artery disease0 (0)0 (0)0 (0)
  Previous myocardial infarction24 (13)13 (14)11 (12)0.66
  Previous ischemic stroke or TIA34 (19)14 (16)20 (22)0.25
  History of intracranial bleeding2 (1)0 (0)2 (2)0.50
  History of heart failure74 (41)43 (48)31 (34)0.07
  Cirrhosis1 (1)0 (0)1 (1)
  Chronic kidney disease54 (30)28 (31)26 (29)0.78
Smoking, n (%)48 (28)23 (26)25 (29)0.66
eGFR (mL/min/1.73 m2), median (IQR)70.75 (58.0, 85.8)70.72 (57.3, 85.1)70.75 (58.2, 87.0)0.87
CHA2 DS2-VASc score, median (IQR)4 (3, 5)4 (3, 5)4 (3, 5.3)0.30
HAS-BLED score, median (IQR)2 (1, 2)1 (1, 2)2 (1, 2)<0.01*
SAMeTT2 R2 score, median (IQR)4 (3, 4)4 (3, 4)4 (3, 4)0.70
  0–215 (9)7 (8)8 (9)0.75
  ≥3157 (91)80 (92)77 (91)
Time in the therapeutic range (%), mean ± SD 84.9 ± 9.8
Antiplatelets10 (6)7 (8)3 (3)
  Aspirin3 (2)2 (2)1 (1)
  P2Y12 inhibitors7 (4)5 (6)2 (2)0.44
OAC
  Warfarin 90 (100)
  Rivaroxaban 30 (33)
  Apixaban 26 (29)
  Dabigatran 17 (19)
  Edoxaban 17 (19)
NSAIDs6 (3)0 (0)6 (7)0.03*
Proton pump inhibitors51 (28)23 (26)28 (31)0.41
DOI: https://doi.org/10.2478/abm-2022-0016 | Journal eISSN: 1875-855X | Journal ISSN: 1905-7415
Language: English
Page range: 131 - 136
Published on: Jun 30, 2022
Published by: Chulalongkorn University
In partnership with: Paradigm Publishing Services
Publication frequency: 6 issues per year

© 2022 Janekij Yamkasikorn, Komsing Methavigul, published by Chulalongkorn University
This work is licensed under the Creative Commons Attribution 4.0 License.