TY - JOUR
T1 - Antiarrhythmic drug use in patients <65 years with atrial fibrillation and without structural heart disease
AU - Allen LaPointe, Nancy M.
AU - Dai, Dadi
AU - Thomas, Laine
AU - Piccini, Jonathan P.
AU - Peterson, Eric D.
AU - Al-Khatib, Sana M.
N1 - Funding Information:
This work was funded in part through grant KM1 CA156687 from the National Institutes of Health and through co-operative agreement number 1U19 HS021092 from the Agency for Healthcare Research and Quality. Dr. Piccini reports funding from ARCA biopharma , Westminster, CO (> , Westminster, CO (>$10,000), 0,000), Boston Scientific , Marlborough, MA (> , Marlborough, MA (>$10,000), 0,000), Johnson & Johnson (New Brunswick, NJ)(> (New Brunswick, NJ)(>$10,000), 0,000), GE Healthcare, Piscataway, NJ (> (>$10,000), and 0,000), and ResMed, San Diego, CA (> (>$10,000) and consulting for Johnson & Johnson ($10,000) and consulting for Johnson & Johnson ($10,000) and consulting for Johnson & Johnson ($10,000) and consulting for Johnson & Johnson (<$10,000), Biosense Webster, Diamond Bar, CA (<$10,000), and Medtronic, Minneapolis, MN (<$10,000); Dr. Peterson reports research funding from the 0,000); Dr. Peterson reports research funding from the American College of Cardiology, Washington, DC , American Heart Association, Dallas, TX , Eli Lilly & Company, Indianapolis, IN , Janssen Pharmaceuticals, Titusville, NJ , and Society of Thoracic Surgeons , Chicago, IL (all significant) and consulting (including CME) for Merck & Co., Whitehouse Station, NJ (modest), Boehringer Ingelheim, Ridgefield, CT, Genentech, South San Francisco, CA, Janssen Pharmaceuticals, and Sanofi-Aventis, Bridgewater, NJ (all significant); Dr. Al-Khatib reports research funding from Bristol Myers Squibb, New York, NY (significant). Drs Allen LaPointe, Dai, and Thomas have no relevant disclosures to report. The authors are solely responsible for the design and conduct of this study, all study analyses, and the drafting and editing of the manuscript and its final contents.
Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Little is known in clinical practice about antiarrhythmic drug (AAD) use in patients with atrial fibrillation (AF) (particularly younger ones) who do not have structural heart disease. Using the MarketScan database, we identified patients <65 years without known coronary artery disease or heart failure who had an AAD prescription claim (class Ic drug, amiodarone, sotalol, or dronedarone) after their first AF encounter. A multinomial logistic regression model was created to assess factors associated with using each available AAD compared with using class Ic drugs before and after dronedarone was marketed in the United States. Additionally, we used the Kaplan-Meier method to determine the rates of change in AAD use and discontinuation during the year after AAD initiation. Of 8,562 patients with AF, 35% received class Ic drugs, 34% amiodarone, 24% sotalol, and 7% dronedarone. The median patient age was 56 (interquartile range 49 to 61), and 34% were women. Both before and after dronedarone was marketed, there was a statistically significant lower likelihood of class Ic drug use versus other AAD use with increasing age, inpatient index AF encounter, and previous or concomitant anticoagulation therapy. During the 1 year after AAD initiation, the AAD change rate was 14% for class Ic drugs, 8% for amiodarone, 17% for sotalol, and 18% for dronedarone (p <0.001); the AAD discontinuation rate was 40% for class Ic drugs, 52% for amiodarone, 40% for sotalol, and 69% for dronedarone (p <0.001). In conclusion, we found extensive use of amiodarone that may be inconsistent with guideline recommendations and unexpectedly high rates of AAD discontinuation.
AB - Little is known in clinical practice about antiarrhythmic drug (AAD) use in patients with atrial fibrillation (AF) (particularly younger ones) who do not have structural heart disease. Using the MarketScan database, we identified patients <65 years without known coronary artery disease or heart failure who had an AAD prescription claim (class Ic drug, amiodarone, sotalol, or dronedarone) after their first AF encounter. A multinomial logistic regression model was created to assess factors associated with using each available AAD compared with using class Ic drugs before and after dronedarone was marketed in the United States. Additionally, we used the Kaplan-Meier method to determine the rates of change in AAD use and discontinuation during the year after AAD initiation. Of 8,562 patients with AF, 35% received class Ic drugs, 34% amiodarone, 24% sotalol, and 7% dronedarone. The median patient age was 56 (interquartile range 49 to 61), and 34% were women. Both before and after dronedarone was marketed, there was a statistically significant lower likelihood of class Ic drug use versus other AAD use with increasing age, inpatient index AF encounter, and previous or concomitant anticoagulation therapy. During the 1 year after AAD initiation, the AAD change rate was 14% for class Ic drugs, 8% for amiodarone, 17% for sotalol, and 18% for dronedarone (p <0.001); the AAD discontinuation rate was 40% for class Ic drugs, 52% for amiodarone, 40% for sotalol, and 69% for dronedarone (p <0.001). In conclusion, we found extensive use of amiodarone that may be inconsistent with guideline recommendations and unexpectedly high rates of AAD discontinuation.
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U2 - 10.1016/j.amjcard.2014.11.005
DO - 10.1016/j.amjcard.2014.11.005
M3 - Article
C2 - 25491240
AN - SCOPUS:84920747994
SN - 0002-9149
VL - 115
SP - 316
EP - 322
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 3
ER -