TY - JOUR
T1 - Impact of polyvascular disease on patients with atrial fibrillation
T2 - Insights from ROCKET AF
AU - Chen, Sean T.
AU - Hellkamp, Anne S.
AU - Becker, Richard C.
AU - Berkowitz, Scott D.
AU - Breithardt, Günter
AU - Fox, Keith A.A.
AU - Hacke, Werner
AU - Halperin, Jonathan L.
AU - Hankey, Graeme J.
AU - Mahaffey, Kenneth W.
AU - Nessel, Christopher C.
AU - Piccini, Jonathan P.
AU - Singer, Daniel E.
AU - Patel, Manesh R.
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/6
Y1 - 2018/6
N2 - Background: We investigated the impact of polyvascular disease in patients enrolled in ROCKET AF. Methods: Cox regression models were used to assess clinical outcomes and treatment effects of rivaroxaban compared with warfarin in patients with atrial fibrillation and coronary, peripheral, or carotid artery disease, or any combination of the 3. Results: A total of 655 (4.6%) patients had polyvascular disease (≥2 disease locations), and 3,391 (23.8%) had single–arterial bed disease. Patients with polyvascular disease had similar rates of stroke/systemic embolism but higher rates of cardiovascular and bleeding events when compared with those without vascular disease. Use of rivaroxaban compared with warfarin was associated with higher rates of stroke in patients with polyvascular disease (hazard ratio [HR] 2.41, 95% CI 1.05-5.54); however, this was not seen in patients with single-bed (HR 0.90, 95% CI 0.64-1.28) or no vascular disease (HR 0.85, 95% CI 0.69-1.04; interaction P =.058). There was a significant interaction for major or nonmajor clinically relevant bleeding in patients with polyvascular (HR 1.23, 95% CI 0.91-1.65) and single-bed vascular disease (HR 1.30, 95% CI 1.13-1.49) treated with rivaroxaban compared with warfarin when compared with those without vascular disease (HR 0.95, 95% CI 0.87-1.04; interaction P =.0006). Additional antiplatelet therapy in this population did not improve stroke or cardiovascular outcomes. Conclusion: The use of rivaroxaban compared with warfarin was associated with a higher risk of stroke and bleeding in patients with polyvascular disease enrolled in ROCKET AF. Further studies are needed to understand the optimal management of this high-risk population.
AB - Background: We investigated the impact of polyvascular disease in patients enrolled in ROCKET AF. Methods: Cox regression models were used to assess clinical outcomes and treatment effects of rivaroxaban compared with warfarin in patients with atrial fibrillation and coronary, peripheral, or carotid artery disease, or any combination of the 3. Results: A total of 655 (4.6%) patients had polyvascular disease (≥2 disease locations), and 3,391 (23.8%) had single–arterial bed disease. Patients with polyvascular disease had similar rates of stroke/systemic embolism but higher rates of cardiovascular and bleeding events when compared with those without vascular disease. Use of rivaroxaban compared with warfarin was associated with higher rates of stroke in patients with polyvascular disease (hazard ratio [HR] 2.41, 95% CI 1.05-5.54); however, this was not seen in patients with single-bed (HR 0.90, 95% CI 0.64-1.28) or no vascular disease (HR 0.85, 95% CI 0.69-1.04; interaction P =.058). There was a significant interaction for major or nonmajor clinically relevant bleeding in patients with polyvascular (HR 1.23, 95% CI 0.91-1.65) and single-bed vascular disease (HR 1.30, 95% CI 1.13-1.49) treated with rivaroxaban compared with warfarin when compared with those without vascular disease (HR 0.95, 95% CI 0.87-1.04; interaction P =.0006). Additional antiplatelet therapy in this population did not improve stroke or cardiovascular outcomes. Conclusion: The use of rivaroxaban compared with warfarin was associated with a higher risk of stroke and bleeding in patients with polyvascular disease enrolled in ROCKET AF. Further studies are needed to understand the optimal management of this high-risk population.
UR - http://www.scopus.com/inward/record.url?scp=85045766830&partnerID=8YFLogxK
U2 - 10.1016/j.ahj.2018.02.013
DO - 10.1016/j.ahj.2018.02.013
M3 - Article
C2 - 29898836
AN - SCOPUS:85045766830
SN - 0002-8703
VL - 200
SP - 102
EP - 109
JO - American Heart Journal
JF - American Heart Journal
ER -