TY - JOUR
T1 - Comparison of safety of sotalol versus amiodarone in patients with Atrial fibrillation and coronary artery disease
AU - Piccini, Jonathan P.
AU - Al-Khatib, Sana M.
AU - Wojdyla, Daniel M.
AU - Shaw, Linda K.
AU - Horton, John R.
AU - Lokhnygina, Yuliya
AU - Anstrom, Kevin J.
AU - Dewald, Tracy
AU - Allen-Lapointe, Nancy
AU - Steinberg, Benjamin A.
AU - Thomas, Kevin
AU - Daubert, James P.
AU - Peterson, Eric D.
N1 - Funding Information:
Dr. Piccini receives grants for clinical research from ARCA Pharmaceuticals , Boston Scientific , GE Healthcare , Johnson & Johnson Services, Inc. , and ResMed Foundation and is a consultant to Biosense-Webster , Janssen Pharmaceuticals , Medtronic , and Spectranetics . Dr. Daubert receives research support from Boston Scientific , Gilead Sciences , Medtronic , ARCA Biopharma , and Biosense-Webster ; and honoraria for advisory board participation or lectures from Biosense-Webster , Boston Scientific , and Medtronic . Dr. Peterson reports research grant support from Eli Lilly and Company , Janssen Pharmaceuticals, Inc. , and the American Heart Association ; and consultancies to Boehringer Ingelheim , Bristol-Myers Squibb Foundation , Janssen Pharmaceuticals, Inc. , Pfizer , and Genentech . Dr. Thomas reports research support from American Heart Association , consulting for Boston Scientific , Janssen Pharmaceuticals , and Sanofi . Detailed online disclosures listing can be found for Drs. Piccini and Peterson at http://www.dcri.org/about-us/conflict-of-interest .
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Sotalol is a commonly prescribed antiarrhythmic drug (AAD) used for maintaining sinus rhythm in patients with atrial fibrillation (AF). Although randomized studies have found that sotalol can significantly delay time to AF recurrence, its association with mortality is less clear, particularly among those with coronary artery disease. We examined outcomes of 2,838 patients with coronary artery disease and AF. Using Cox proportional hazards modeling, landmark analysis, and time-dependent covariates for drug therapy, we compared cumulative survival among patients treated with sotalol (n = 226), amiodarone (n = 856), or no AAD (n = 1,756). Median follow-up was 4.2 years (interquartile range [IQR] 2.0-7.4). The median age was 68 years (IQR 60-75). Compared with those treated with amiodarone or no AAD, patients treated with sotalol were less likely to be black (6% vs 13% vs 13%) and have a previous myocardial infarction (35% vs 51% vs 48%) or a left ventricular ejection fraction <40% (13% vs 26% vs 21%). In follow-up, persistence of sotalol was limited; 97% of patients treated with sotalol were treated for <25% of the follow-up period. In adjusted analysis accounting for time on therapy, sotalol use was associated with an increased risk of all-cause death compared with no drug (hazard ratio 1.53, 95% confidence interval 1.19 to 1.96, p = 0.0009), but a decreased risk of death compared with amiodarone (hazard ratio 0.72, 95% confidence interval 0.55 to 0.91, p = 0.0141). In conclusion, sotalol therapy was more frequently used in patients with fewer co-morbidities, often discontinued early in follow-up, and was associated with increased mortality compared with no AAD but decreased mortality relative to amiodarone.
AB - Sotalol is a commonly prescribed antiarrhythmic drug (AAD) used for maintaining sinus rhythm in patients with atrial fibrillation (AF). Although randomized studies have found that sotalol can significantly delay time to AF recurrence, its association with mortality is less clear, particularly among those with coronary artery disease. We examined outcomes of 2,838 patients with coronary artery disease and AF. Using Cox proportional hazards modeling, landmark analysis, and time-dependent covariates for drug therapy, we compared cumulative survival among patients treated with sotalol (n = 226), amiodarone (n = 856), or no AAD (n = 1,756). Median follow-up was 4.2 years (interquartile range [IQR] 2.0-7.4). The median age was 68 years (IQR 60-75). Compared with those treated with amiodarone or no AAD, patients treated with sotalol were less likely to be black (6% vs 13% vs 13%) and have a previous myocardial infarction (35% vs 51% vs 48%) or a left ventricular ejection fraction <40% (13% vs 26% vs 21%). In follow-up, persistence of sotalol was limited; 97% of patients treated with sotalol were treated for <25% of the follow-up period. In adjusted analysis accounting for time on therapy, sotalol use was associated with an increased risk of all-cause death compared with no drug (hazard ratio 1.53, 95% confidence interval 1.19 to 1.96, p = 0.0009), but a decreased risk of death compared with amiodarone (hazard ratio 0.72, 95% confidence interval 0.55 to 0.91, p = 0.0141). In conclusion, sotalol therapy was more frequently used in patients with fewer co-morbidities, often discontinued early in follow-up, and was associated with increased mortality compared with no AAD but decreased mortality relative to amiodarone.
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UR - http://www.scopus.com/inward/citedby.url?scp=84908384387&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2014.06.004
DO - 10.1016/j.amjcard.2014.06.004
M3 - Article
C2 - 25129065
AN - SCOPUS:84908384387
SN - 0002-9149
VL - 114
SP - 716
EP - 722
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 5
ER -