TY - JOUR
T1 - Cause of death and predictors of all-cause mortality in anticoagulated patients with nonvalvular atrial fibrillation
T2 - Data from ROCKET AF
AU - ROCKET AF Steering Committee and Investigators
AU - Pokorney, Sean D.
AU - Piccini, Jonathan P.
AU - Stevens, Susanna R.
AU - Patel, Manesh R.
AU - Pieper, Karen S.
AU - Halperin, Jonathan L.
AU - Breithardt, Günter
AU - Singer, Daniel E.
AU - Hankey, Graeme J.
AU - Hacke, Werner
AU - Becker, Richard C.
AU - Berkowitz, Scott D.
AU - Nessel, Christopher C.
AU - Mahaffey, Kenneth W.
AU - Fox, Keith A.A.
AU - Califf, Robert M.
AU - Anderson, J.
AU - Bedwell, N.
AU - Bilsker, M.
AU - Bruce, G.
AU - Agah, R.
AU - DeSantis, M.
AU - Eisenberg, S.
AU - Flores, A.
AU - Herzog, W.
AU - Klein, S.
AU - Snyder, H.
AU - Krueger, S.
AU - Almaguer, E.
AU - Lavie, E.
AU - Lee, C.
AU - Mallis, G.
AU - Modi, M.
AU - Woodworth, G.
AU - Niazi, I.
AU - Peart, B.
AU - Sundaram, S.
AU - Snoddy, B.
AU - Sotolongo, R.
AU - Moloney, J.
AU - Vijayaraghavan, K.
AU - Whittier, F.
AU - Yellen, L.
AU - Banerjee, S.
AU - Lustgarten, D.
AU - Suresh, D.
AU - Gelernt, M.
AU - Levinson, L.
AU - Ghanekar, R.
AU - Katz, A.
N1 - Publisher Copyright:
© 2016 The Authors.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intentionto- treat population. The median age was 73 years, and the mean CHADS2 score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P<0.0001) and age ≥75 years (hazard ratio 1.69, 95% CI 1.51-1.90, P<0.0001) were associated with higher all-cause mortality. Multiple additional characteristics were independently associated with higher mortality, with decreasing creatinine clearance, chronic obstructive pulmonary disease, male sex, peripheral vascular disease, and diabetes being among the most strongly associated (model C-index 0.677). Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, ≈7 in 10 deaths were cardiovascular, whereas <1 in 10 deaths were caused by nonhemorrhagic stroke or systemic embolism. Optimal prevention and treatment of heart failure, renal impairment, chronic obstructive pulmonary disease, and diabetes may improve survival.
AB - Background-Atrial fibrillation is associated with higher mortality. Identification of causes of death and contemporary risk factors for all-cause mortality may guide interventions. Methods and Results-In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF) study, patients with nonvalvular atrial fibrillation were randomized to rivaroxaban or dose-adjusted warfarin. Cox proportional hazards regression with backward elimination identified factors at randomization that were independently associated with all-cause mortality in the 14 171 participants in the intentionto- treat population. The median age was 73 years, and the mean CHADS2 score was 3.5. Over 1.9 years of median follow-up, 1214 (8.6%) patients died. Kaplan-Meier mortality rates were 4.2% at 1 year and 8.9% at 2 years. The majority of classified deaths (1081) were cardiovascular (72%), whereas only 6% were nonhemorrhagic stroke or systemic embolism. No significant difference in all-cause mortality was observed between the rivaroxaban and warfarin arms (P=0.15). Heart failure (hazard ratio 1.51, 95% CI 1.33-1.70, P<0.0001) and age ≥75 years (hazard ratio 1.69, 95% CI 1.51-1.90, P<0.0001) were associated with higher all-cause mortality. Multiple additional characteristics were independently associated with higher mortality, with decreasing creatinine clearance, chronic obstructive pulmonary disease, male sex, peripheral vascular disease, and diabetes being among the most strongly associated (model C-index 0.677). Conclusions-In a large population of patients anticoagulated for nonvalvular atrial fibrillation, ≈7 in 10 deaths were cardiovascular, whereas <1 in 10 deaths were caused by nonhemorrhagic stroke or systemic embolism. Optimal prevention and treatment of heart failure, renal impairment, chronic obstructive pulmonary disease, and diabetes may improve survival.
KW - Atrial fibrillation
KW - Mortality
KW - Rivaroxaban
KW - Stroke
KW - Warfarin
UR - http://www.scopus.com/inward/record.url?scp=85006208431&partnerID=8YFLogxK
U2 - 10.1161/JAHA.115.002197
DO - 10.1161/JAHA.115.002197
M3 - Article
C2 - 26955859
AN - SCOPUS:85006208431
SN - 2047-9980
VL - 5
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
IS - 3
M1 - e002197
ER -