Key result
Direct oral anticoagulants had similar all-cause mortality to Vitamin K antagonists overall (OR 0.69; CrI 0.40-1.06), but lower mortality when combined with antiplatelets (OR 0.13; CrI 0.02-0.65).
Why the study?
Patients undergoing TAVI commonly have comorbidities requiring anticoagulation, but the optimal post-procedural anticoagulation regimen is not well-established.
Do DOACs improve safety and efficacy outcomes compared to VKAs in post-TAVI patients with an indication for anticoagulation?
Meta-Analysis (n=6,359)
Do DOACs improve safety and efficacy outcomes compared to VKAs in post-TAVI patients with an indication for anticoagulation?
Odds Ratio: 0.69 (95% CI 0.4–1.06)
DOACs and VKAs have similar safety and efficacy profiles in post-TAVI patients requiring anticoagulation, though DOACs may offer a mortality benefit when concomitant antiplatelet therapy is required.
Similar all-cause mortality with DOACs versus VKAs overall; extends evidence on combined antiplatelet regimens.
Patients undergoing transcatheter aortic valve implantation (TAVI) commonly have co-morbidities requiring anticoagulation. However, the optimal post-procedural anticoagulation regimen is not well-established. This meta-analysis investigates safety and efficacy outcomes of direct oral anticoagulants (DOACs) and Vitamin K Antagonist (VKA), with or without concomitant antiplatelet therapy. We searched EMBASE and MEDLINE for appropriate studies. Subgroup analyses were performed for anticoagulant monotherapy and combined therapy with antiplatelet agents. Eleven studies (6359 patients) were included. Overall, there were no differences between DOACs and VKA for all-cause mortality (Odds Ratio [OR]: .69; Credible Interval [CrI]: .40-1.06), cardiovascular-related mortality (OR: .76; Crl: .13-3.47), bleeding (OR: .95; CrI: .75-1.17), stroke (OR: 1.04; CrI: .65-1.63), myocardial infarction (OR: 1.51; CrI: .55-3.84), and valve thrombosis (OR: .29; CrI: .01-3.54). For DOACs vs VKA monotherapy subgroup, there were no differences in outcomes. For the combined therapy subgroup, there was decreased odds of all-cause mortality in the DOACs group compared with the VKA group (OR: .13; CrI: .02-.65), but no differences for bleeding and stroke. DOACs and VKA have similar safety and efficacy profiles for post-TAVI patients with anticoagulation indication. However, if concomitant antiplatelet therapy is required, DOACs were more favorable than VKA for all-cause mortality.
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Lee et al. (2022) conducted a meta-analysis in Post-TAVI with anticoagulation indication (n=6,359). Direct oral anticoagulants (DOACs) vs. Vitamin K Antagonist (VKA) was evaluated on all-cause mortality (OR 0.69, 95% CI 0.40-1.06). Direct oral anticoagulants had similar all-cause mortality to Vitamin K antagonists overall (OR 0.69; CrI 0.40-1.06), but lower mortality when combined with antiplatelets (OR 0.13; CrI 0.02-0.65).
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