Table 7.
Author | Study design | Outcome | Inclusions/exclusions | Risk |
---|---|---|---|---|
Hart et al.59 | Meta-analysis adjusted-dose warfarin and aspirin | Stroke | 6 RCTs warfarin vs. placebo; n = 2900 | RR 64% reduction, 95% CI 49–74%; Absolute reduction: 1° prevention 2.7% per year, 2° prevention 8.48% per year |
7 RCTs aspirin vs. placebo or no Rx; n = 3900 | RR 19% reduction, 95% CI −1 to 35%; 1° prevention 0.8% per year, 2° prevention 2.5% per year | |||
8 RCTs warfarin vs. aspirin Rx; n = 3647 | RR 38% reduction, 95% CI 18–52%; 1° prevention 0.7% per year, 2° prevention 7.0% per year | |||
Ruff et al.60 | Meta-analysis phase 3 RCTs: | Stroke and systemic emboli | n = 29 312 NOAC; n = 29 272 warfarin | RR 0.81, 95% CI 0.73–0.91; P < 0.0001; I2 = 47%; P = 0.13 |
RE-LY, ROCKET AF, ARISTOTLE, ENGAGE AF–TIMI 48 | n = 41 257, no prior stroke; n = 17 269, prior stroke | RR 0.85, 95% CI 0.72–1.01 RR 0.89; 95% CI 0.77–1.02; Pinteraction = 0.30 | ||
Ischaemic stroke | n = 29 292 NOAC; n = 29 221 warfarin | RR 0.92, 95% CI 0.83–1.02; P = 0.10; I2 = 32%; P = 0.22 | ||
Haemorrhagic stroke | n = 29 292 NOAC; n = 29 221 warfarin | RR 0.49, 95% CI 0.38–0.64; P < 0.0001; I2 = 34%; P = 0.21 |
H/o, history of; NOAC, non-vitamin K antagonist oral anticoagulant; RCT, randomized clinical trial; RR, relative risk.