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. 2022 Oct 10;43:101130. doi: 10.1016/j.ijcha.2022.101130

Table 3.

Time to event comparison of the reduced and full doses for each individual DOAC (Dabigatran, Rivaroxaban, and Apixaban).

Events D75
(n = 53)
D150
(n = 57)
Univariable p value (log rank test) Multivariable hazard ratio
(95 % CI) *
R15
(n = 224)
R20
(n = 74)
Univariable p value (log rank test) Multivariable hazard ratio
(95 % CI) *
A2.5
(n = 236)
A5
(n = 68)
Univariable p value (log rank test) Multivariable hazard ratio
(95 % CI) *
%/year %/year %/year %/year %/year %/year
SSE 1.1 0 N/A N/A 1.1 0 N/A N/A 0.8 0 N/A N/A
CNS bleed 2.2 0.5 N/A N/A 1.7 0.6 0.32 N/A 0.8 0 N/A N/A
Non-CNS bleed 12.1 1.6 < 0.001 0.343
(CI: 0.07 to 1.62)
12.4 7.2 0.18 1.16
(CI: 0.53 to 2.5)
8.3 3.7 0.18 1.091
(CI: 0.28 to 4.2)
All-cause mortality 5.5 3.8 0.41 N/A 4.2 0 < 0.001 N/A 9.5 0.9 0.005 0.083
(CI: 0.01 to 0.7)

SSE = Stroke and systemic embolization; CNS = Central nervous system; D150: Dabigatran 150 mg twice daily; D75: Dabigatran 75 mg twice daily; R20: Rivaroxaban 20 mg daily; R15: Rivaroxaban 15 mg daily; A5: Apixaban 5 mg twice daily; A2.5: Apixaban 2.5 mg twice daily. *p values and CI adjusted for multivariable baseline differences using proportional hazards. The reduced group was the reference group. Some results were not available (N/A) either because the univariable analysis was not significant or because there were too few patients in one or both outcome groups for a meaningful analysis.