A trial fibrillation (AF) is the most common cardiac arrhythmia.1 Guidelines strongly and uniformly recommend anticoagulation in patients with AF and risk factors for cardioembolic events to mitigate the likelihood of stroke or thromboembolism. [2][3][4][5] The benefits of oral anticoagulant therapy are directly proportional to the underlying stroke risk as measured by the congestive heart failure, hypertension, age, diabetes mellitus, prior stroke (CHADS 2 ) or congestive heart failure or left ventricular systolic dysfunction, hypertension, age, diabetes mellitus, prior stroke, vascular disease, and sex (CHA 2 DS 2 -VASc) scores.6 Despite the documented benefits of anticoagulation in high-risk patients, several prior studies have found that those with higher CHADS 2 scores are less likely to receive anticoagulation compared with healthier patients at lower risk for thromboembolism. This risk-treatment paradox with AF has been described in patients after acute ischemic stroke or transient ischemic attack, 7 in patients hospitalized for heart failure, 8 and in patients with acute coronary syndromes.
9,10The reasons for these patterns remain unclear. One hypothesis suggests that providers may withhold anticoagulation from Background-Patients with atrial fibrillation (AF) at the highest stroke risk derive the largest benefit from oral anticoagulation (OAC). Those with the highest stroke risk have been paradoxically less likely to receive OAC. This study assessed the association between stroke and bleeding risk on rates of OAC. Methods and Results-We analyzed OAC use among 10 098 patients with AF from 174 community-based outpatient practices enrolled in 2010-2011 in the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF). OAC was defined as warfarin or dabigatran use at study enrollment. Stroke and bleeding risk were calculated using congestive heart failure, hypertension, age, diabetes mellitus, prior stroke (CHADS 2 ), and anticoagulation and risk factors in AF (ATRIA) scores, respectively. The mean subject age was 73 years; 58% were men. Overall, 76% of patients received OAC (71% warfarin and 5% dabigatran). The use of OAC increased among those with higher CHADS 2 scores, from 53% for CHADS 2 =0 to 80% for CHADS 2 ≥2 (P<0.001). OAC use fell slightly with increasing ATRIA bleeding risk score, from 81% for ATRIA=3 to 73% for ATRIA≥5 (P<0.001