Key result
Apixaban initiation for VTE was associated with a lower rate of hospitalised bleeding at 180 days compared to rivaroxaban (HR 0.58; 95% CI 0.41-0.80) and warfarin (HR 0.68; 95% CI 0.50-0.92).
Why the study?
Understanding of the comparative bleeding risks of oral anticoagulant therapies for the primary treatment of venous thromboembolism is limited.
Do different oral anticoagulants (apixaban, rivaroxaban, warfarin) have differing risks of hospitalised bleeding in anticoagulant-naïve VTE patients?
Cohort (n=83,985)
Do different oral anticoagulants (apixaban, rivaroxaban, warfarin) have differing risks of hospitalised bleeding in anticoagulant-naïve VTE patients?
Hazard Ratio: 0.58 (95% CI 0.41–0.8)
In a large real-world cohort of VTE patients, apixaban was associated with a significantly lower risk of hospitalised bleeding compared to both rivaroxaban and warfarin.
Apixaban was associated with lower hospitalized bleeding than rivaroxaban or warfarin in VTE; hypothesis-generating and requires prospective confirmation before practice change.
Understanding of the comparative bleeding risks of oral anticoagulant (OAC) therapies for the primary treatment of venous thromboembolism (VTE) is limited. Therefore, among anticoagulant-naïve VTE patients, we conducted comparisons of apixaban, rivaroxaban and warfarin on the rate of hospitalised bleeding within 180 days of OAC initation. MarketScan databases for the time-period from 2011 to 2016 were used and, for each OAC comparison, new users were matched with up to five initiators of a different OAC. The final analysis included 83 985 VTE patients, who experienced 1944 hospitalised bleeding events. In multivariable-adjusted Cox regression models, rate of hospitalised bleeding was lower among new users of apixaban when compared to new users of rivaroxaban [hazard ratio (95% confidence interval) 0·58 (0·41-0·80)] or warfarin [0·68 (0·50-0·92)]. Overall, the hospitalised bleeding rate was similar when comparing new users of rivaroxaban to new users of warfarin [0·98 (0·68-1·11)], though there was some suggestion that rivaroxaban was associated with lower bleeding risk among younger individuals. Findings from this large real-world population concur with results from the randomised trial which found lower bleeding risk with apixaban versus warfarin and, for the first time, reveal a lower risk of bleeding in a comparison of apixaban versus rivaroxaban.
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Lutsey et al. (2019) conducted a cohort in Venous thromboembolism (n=83,985). Apixaban vs. Rivaroxaban or warfarin was evaluated on Hospitalised bleeding within 180 days of OAC initiation (HR 0.58, 95% CI 0.41-0.80). Apixaban initiation for VTE was associated with a lower rate of hospitalised bleeding at 180 days compared to rivaroxaban (HR 0.58; 95% CI 0.41-0.80) and warfarin (HR 0.68; 95% CI 0.50-0.92).
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