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March 28, 2019British Journal of Haematology49 citationsOpen Access

Risk of hospitalised bleeding in comparisons of oral anticoagulant options for the primary treatment of venous thromboembolism

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PLPamela L. LutseyNZNeil A. ZakaiRMRichard F. MacLehose

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).

Study Design

Type

Cohort (n=83,985)

Structured PICO

Do different oral anticoagulants (apixaban, rivaroxaban, warfarin) have differing risks of hospitalised bleeding in anticoagulant-naïve VTE patients?

P
Population
83,985 anticoagulant-naïve patients with venous thromboembolism initiating oral anticoagulants, followed for up to 180 days.
E
Exposure
Apixaban, rivaroxaban, or warfarin
C
Comparator
Active comparator (initiators of a different oral anticoagulant, matched up to 1:5)
O
Outcome
Rate of hospitalised bleeding within 180 days of oral anticoagulant initiationsafety

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.

Main Result

Hazard Ratio: 0.58 (95% CI 0.41–0.8)

Abstract

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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Cite This Study

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).

synapsesocial.com/papers/6a629d632e602d4c8b02a99chttps://doi.org/10.1111/bjh.15857
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