Table 4

ORs (95% CI) for the association between time since OAC discontinuation and the risk of IS among patients with AF

UK (IMRD-UK)Denmark (RSD)
Cases
n=615
Controls
n=3075
Crude OR
(95% CI)
Adjusted OR*
(95% CI)
Cases
n=643
Controls
n=6430
Crude OR
(95% CI)
Adjusted OR* (95% CI)
N%N%N%N%
Currently exposed to an OAC26743.4199464.81.0 (reference)1.0 (reference)33952.7423965.91.0 (reference)1.0 (reference)
OAC discontinuation at any time
 Any OAC13722.331310.23.25 (2.56 to 4.13)2.99 (2.31 to 3.86)13120.478312.22.18 (1.74 to 2.74)2.30 (1.79 to 2.95)
 VKA8413.72357.62.89 (2.13 to 3.92)2.38 (1.72 to 3.30)7511.75398.41.77 (1.34 to 2.33)1.83 (1.34 to 2.49)
 NOAC538.6782.54.83 (3.21 to 7.26)4.59 (2.97 to 7.08)568.72443.83.02 (2.14 to 4.25)3.37 (2.35 to 4.85)
OAC discontinuation
30–365 days before the index date
 Any OAC599.61254.13.54 (2.53 to 4.95)2.97 (2.09 to 4.23)517.92764.32.45 (1.74 to 3.45)2.39 (1.67 to 3.42)
 VKA264.2772.52.49 (1.57 to 3.94)2.08 (1.29 to 3.35)132.01352.11.20 (0.66 to 2.20)1.15 (0.62 to 2.15)
 NOAC335.4481.65.61 (3.46 to 9.08)4.78 (2.88 to 7.95)385.91412.23.84 (2.52 to 5.86)3.82 (2.44 to 5.97)
OAC discontinuation
>365 days before the index date
 Any OAC7812.71886.13.07 (2.29 to 4.13)3.03 (2.11 to 4.18)8012.45077.92.08 (1.58 to 2.73)2.48 (1.81 to 3.41)
 VKA589.41585.12.70 (1.95 to 3.75)2.72 (1.91 to 3.86)629.64046.31.95 (1.44 to 2.64)2.21 (1.55 to 3.15)
 NOAC203.3301.05.03 (2.70 to 9.07)4.98 (2.63 to 9.43)182.81031.62.07 (1.19 to 3.62)2.87 (1.60 to 5.15)
Intermediate use: discontinued 8–30 days before the index date
 Any OAC294.71173.81.84 (1.20 to 2.82)1.51 (0.97 to 2.36)223.41772.81.71 (1.05 to 2.78)1.41 (0.85 to 2.34)
 VKA162.6622.02.08 (1.17 to 3.70)1.59 (0.86 to 2.91)50.8661.01.17 (0.45 to 3.02)0.78 (0.29 to 2.10)
 NOAC132.1551.81.66 (0.88 to 3.12)1.50 (0.77 to 2.88)172.61111.71.97 (1.11 to 3.47)1.80 (1.00 to 3.24)
  • *Adjusted by number of referrals/outpatient visits in the year before the index date, the number of hospitalisations in the year before the index date, use of an antiplatelet medication 0–7 days before the index date, use of an antiarrhythmic medication 0–7 days before the index date (UK analysis only) and cerebrovascular disease before the start date.

  • AF, atrial fibrillation; IMRD-UK, IQVIA Medical Research Data-UK; IS, ischaemic stroke; NOAC, non-vitamin K antagonist oral anticoagulant; OAC, oral anticoagulant; RSD, Region of Southern Denmark; VKA, vitamin K antagonist.