Key result
DOACs show similar bleeding and mortality risks to VKAs when used with antiplatelets in VTE.
Why the study?
Evidence on the effects of concomitant direct oral anticoagulant and antiplatelet use in patients with venous thromboembolism is scarce.
Does concomitant use of DOACs and antiplatelets reduce major bleeding and all-cause mortality in patients with VTE compared to VKAs and antiplatelets?
Cohort (n=4,971)
Yes
Does concomitant use of DOACs and antiplatelets reduce major bleeding and all-cause mortality in patients with VTE compared to VKAs and antiplatelets?
In patients with VTE requiring antiplatelet therapy, concomitant use of DOACs showed similar effectiveness and safety compared to VKAs.
Answers are grounded in this paper and cite their sources.
Comparable bleeding and mortality risks with DOACs plus antiplatelets in VTE; leaves open optimal choice pending randomized data.
BACKGROUND: Patients with venous thromboembolism (VTE) often have comorbidities that require use of antiplatelets. However, evidence on the effects of concomitant use of direct oral anticoagulants (DOACs) and antiplatelets in this high-risk population is scarce. Our international, multi-database cohort study assessed the real-world effectiveness and safety of concomitant use of DOACs and antiplatelets among patients with VTE. METHODS: We assembled two population-based cohorts using administrative health care databases from Québec and Germany. We included patients with incident VTE who initiated treatment with a DOAC or a vitamin K antagonist (VKA), while being exposed to antiplatelets (acetylsalicylic acid, clopidogrel, ticagrelor, prasugrel, dipyridamole). The study period spanned from 2012 to 2016 (Québec) or 2019 (Germany). Concomitant use of DOACs and antiplatelets was compared with concomitant use of VKAs and antiplatelets, using inverse probability of treatment weighting to balance exposure groups. Cox proportional hazards models estimated site-specific hazard ratios (HRs) and 95% confidence intervals (CIs) of major bleeding, all-cause mortality (primary outcomes), and recurrent VTE (secondary outcome). Site-specific estimates were meta-analyzed using random-effects models. RESULTS: Overall, 4971 patients with VTE initiated concomitant use of a DOAC (n = 2289) or a VKA (n = 2682) and antiplatelets. Compared with concomitant use of VKAs and antiplatelets, concomitant use of DOACs and antiplatelets was associated with similar risks of major bleeding (HR, 0.81; 95% CI, 0.46-1.45), all-cause mortality (HR, 1.25; 95% CI, 0.87-1.79), and recurrent VTE (HR, 0.96; 95% CI, 0.40-2.27). CONCLUSIONS: Among patients with VTE using antiplatelets, there were no major differences in effectiveness and safety between DOACs and VKAs.
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Douros et al. (2022) conducted a cohort in Venous thromboembolism (n=4,971). Direct oral anticoagulants (DOACs) + antiplatelet agents vs. Vitamin K antagonists (VKAs) + antiplatelet agents was evaluated on Major bleeding (HR 0.81, 95% CI 0.46-1.45). Concomitant use of DOACs and antiplatelet agents resulted in similar risks of major bleeding (HR 0.81) and all-cause mortality (HR 1.25) compared with VKAs and antiplatelets in patients with VTE.
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