Vol.:(0123456789)
American Journal of Cardiovascular Drugs (2021) 21:563–572
https://doi.org/10.1007/s40256-021-00483-9
ORIGINAL RESEARCH ARTICLE
Use of Flecainide in Stable Coronary Artery Disease: An Analysis
of Its Safety in Both Nonobstructive and Obstructive Coronary Artery
Disease
Hasan Ashraf
1
· Nway Ko Ko
1
· Vatsal Ladia
1
· Pradyumna Agasthi
1
· Tadhg Prendiville
2
· Fergus O’Herlihy
2
·
Sai Harika Pujari
1
· Siva K. Mulpuru
3
· Luis Scott
1
· Dan Sorajja
1
Accepted: 3 May 2021 / Published online: 18 June 2021
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021
Abstract
Background Flecainide is a class IC antiarrhythmic drug that is contraindicated in patients who have a history of myocar-
dial infarction, but its efect on mortality and risk of proarrhythmia in patients with stable obstructive and nonobstructive
epicardial coronary artery disease (CAD) has not been assessed.
Objective We sought to compare the safety of fecainide administration in patients who had angiographic evidence of either
no or minimal CAD versus nonobstructive CAD, and those who underwent nuclear stress testing with perfusion defects
versus those without perfusion defects.
Methods We conducted a retrospective chart review of 348 patients who were treated with fecainide for at least 1 year dura-
tion and underwent evaluation for CAD with coronary angiography or myocardial perfusion imaging (MPI) stress testing
within 3 months of initiating fecainide. We compared overall mortality and proarrhythmia between varying levels of CAD
and perfusion defects.
Results There was a similar 10-year survival between those with no or minimal CAD, nonobstructive CAD, and obstructive
CAD (p = 0.6). Additionally, there was no diference in arrhythmia burden, including sustained ventricular tachycardias
or frequent premature ventricular contractions (> 5% daily burden; p = 0.25). There was also no increase in mortality
among those who had reversible perfusion defects >0% compared with those without, among subjects who underwent
MPI (p = 0.14). On subgroup analysis, there was no increased risk in all-cause mortality with any specifc coronary artery
involvement, or with obstructive multivessel CAD (p = 0.89).
Conclusion Flecainide use is not associated with an increase in either all-cause mortality or ventricular arrhythmias in low-
risk patients with stable nonobstructive CAD.
* Hasan Ashraf
ashraf.hasan@mayo.edu
Nway Ko Ko
koko.nway@mayo.edu
Vatsal Ladia
ladia.vatsal@mayo.edu
Tadhg Prendiville
tadhg.prendiville@ucdconnect.ie
Fergus O’Herlihy
oherlihy.fergus@mayo.edu
Sai Harika Pujari
pujari.saiharika@mayo.edu
Dan Sorajja
sorajja.dan@mayo.edu
1
Department of Cardiovascular Medicine, Mayo Clinic,
Phoenix, AZ, USA
2
Department of Internal Medicine, Mater Misericordiae
University Hospital, Dublin, Ireland
3
Department of Cardiovascular Medicine, Mayo Clinic,
Rochester, MN, USA