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Table 3 Efficacy and safety outcomes of clinical trials with NOACs for the treatment of VTE

From: The diagnosis and treatment of venous thromboembolism in Asian patients

All Patients

Asian Patients

Trial

N

VTE recurrencea

Major or CRNM bleedinga

Trial

N

VTE recurrencea

Major or CRNM bleedinga

Dabigatran

   

Dabigatran

   

RE-COVER [114]

2539

1.10 (0.65–1.84)

0.63 (0.47–0.84)

RE-COVER

RE-COVER II Asian subanalysisb

557

2.55 (0.66–9.90)

0.63 (0.33–1.19)

RE-COVER II [115]

2568

1.08 (0.64–1.80)

0.62 (0.45–0.84)

    

Rivaroxaban

   

Rivaroxaban

   

EINSTEIN-DVT [116]

3449

0.68 (0.44–1.04)

0.97 (0.76–1.22)

EINSTEIN-DVT and PE Asian subanalysis [111]

439

1.04 (0.36–3.0)

0.63 (0.31–1.26)

EINSTEIN-PE [117]

4832

1.12 (0.75–1.68)

0.90 (0.76–1.07)

J-EINSTEIN DVT and PE [73]

100

3.9% (−3.4 to 23.8)c

Rivaroxaban 7.8%

UFH/warfarin 5.3%d

Apixaban

   

Apixaban

   

AMPLIFY [119]

5395

0.84 (0.60–1.18)

0.44 (0.36–0.55)

AMPLIFY-J [112]

80

Apixaban 0/40

UFH/warfarin 1/40e

Apixaban 7.5%

UFH/warfarin 28.2%f

Edoxaban

   

Edoxaban

   

Hokusai-VTE [120]

8240

0.89 (0.70–1.13)

0.81 (0.71–0.94)

Hokusai-VTE Asian subanalysis [110]

1109

0.64 (0.34–1.19)

0.56 (0.40–0.78)

  1. aValues are hazard ratio (95% confidence interval) unless otherwise indicated
  2. bData on file
  3. cAbsolute risk difference (95% confidence interval)
  4. dPercentage of patients with CRNM bleeding
  5. eNumber of patients
  6. fPercentage of patients
  7. CRNM clinically relevant nonmajor, DVT deep vein thrombosis, NOAC non-vitamin K antagonist oral anticoagulant, PE pulmonary embolism, UFH unfractionated heparin, VTE venous thromboembolism