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. 2021 May 25;8(2):214–227. doi: 10.1093/ehjqcco/qcab028

Table 3.

Wald χ2, P-values, and hazard ratios for components of the GARFIELD-AF non-haemorrhagic stroke/SE and major bleeding models

Model χ 2 P-value Hazard ratio (95% CI)
Non-haemorrhagic stroke/SE model
 Agea 132 <0.0001 1.22 (1.18–1.26)
 Prior stroke 84 <0.0001 2.23 (1.88–2.64)
 Treatment (ref.: no OAC) 49 <0.0001
  NOAC 0.56 (0.48–0.67)
  VKA 0.70 (0.61–0.81)
 Current smoker 22 <0.0001 1.61 (1.32–1.97)
 Diastolic blood pressure (80 mmHg or more)a 20 <0.0001 1.08 (1.05–1.12)
 Moderate-to-severe CKD 17 <0.0001 1.42 (1.20–1.67)
 Congestive heart failure 10 0.0015 1.26 (1.09–1.46)
 Dementia 9 0.0022 1.67 (1.20–2.32)
 Diabetes 8 0.0041 1.24 (1.07–1.43)
 Vascular disease 8 0.0057 1.22 (1.06–1.40)
 History of bleeding 3 0.0555 1.35 (0.99–1.83)
Major bleeding
 Agea 156 <0.0001 1.24 (1.20–1.29)
 Treatment (ref.: no OAC) 56 <0.0001
  NOAC 1.27 (1.05–1.55)
  VKA 1.84 (1.55–2.18)
 Moderate-to-severe CKD 36 <0.0001 1.65 (1.40–1.94)
 History of bleeding 31 <0.0001 2.19 (1.66–2.88)
 Pulse (b.p.m.)a 12 0.0005 1.02 (1.01–1.03)
 AP treatment (ref.: no AP treatment) 9 0.0021 1.27 (1.09–1.47)
 Diabetes 6 0.0176 1.19 (1.03–1.38)
 Vascular disease 5 0.0250 1.18 (1.02–1.37)
 Carotid occlusive disease 5 0.0281 1.37 (1.03–1.82)

AP, antiplatelet treatment; CI, confidence interval; CKD, chronic kidney disease; NOAC, non-VKA oral anticoagulant; OAC, oral anticoagulation; SE, systemic embolism; VKA, vitamin K antagonist.

a

Hazard ratios with 95% CIs are based on incremental units of ‘5’.