Literature DB >> 27519494

Flecainide-induced Increase in QRS Duration and Proarrhythmia during Exercise.

P Bordier1, S Garrigue1, V Bernard1, M Haissaguerre1, H Douard1, J P Broustet1, J Clementy1.   

Abstract

In patients taking flecainide, exercise-induced arrhythmias are believed to be related to QRS widening at rest and during exercise. Our aim was to determine, retrospectively, predictive factors of flecainide-induced (a) QRS widening at rest and during exercise, and (b) proarrhythmia (PA) during exercise. Flecainide was administered to 119 patients for atrial and/or ventricular arrhythmias who performed a maximal treadmill test. A total of 63 patients had a normal heart (defined by the absence of structural heart disease and an ejection fraction ≥ 55% by echocardiography and/or cardiac catheterisation), 26 had coronaropathy, 18 valvulopathy and 3 had both, and 7 had dilated and 2 hypertrophic cardiomyopathy. The mean dosage of flecainide was 190 or 200 ± 10 mg/day. Previous myocardial infarction (MI) was a predictive variable of flecainide-induced QRS widening at rest (p = 0.04). During exercise, the risk factors of QRS widening were previous MI (p = 0.008), angina without previous MI (p = 0.009), structural heart disease (p = 0.001) and a bundle branch block at rest (p = 0.01). PA on exercise occurred in 7 patients. Structural heart disease (p = 0.04) and an impaired left ventricular ejection fraction (LVEF) [p = 0.02] were predictive variables of PA. All patients with left ventricular dysfunction and PA had a QRS widening with flecainide at rest ≥ 25%. The risk factors of QRS widening at rest and during exercise with flecainide were distinct from those of PA on exercise. In patients with an impaired LVEF, a flecainide-induced QRS widening of 25% at rest was the threshold value beyond which there was a high risk of PA during exercise. This study was retrospective and not a double-blind trial, therefore the results need to be corroborated in a prospectively designed trial.

Entities:  

Year:  1997        PMID: 27519494     DOI: 10.2165/00044011-199713060-00005

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  58 in total

1.  States and sites of actions of flecainide on guinea-pig cardiac sodium channels.

Authors:  J Nitta; A Sunami; F Marumo; M Hiraoka
Journal:  Eur J Pharmacol       Date:  1992-04-22       Impact factor: 4.432

2.  Experimental models of reentry, antiarrhythmic, and proarrhythmic actions of drugs. Complexities galore!

Authors:  N el-Sherif
Journal:  Circulation       Date:  1991-10       Impact factor: 29.690

3.  Is exercise testing safe in patients treated with flecainide for atrial arrhythmia?

Authors:  C M Blatt; S Lampert; T B Graboys
Journal:  Am Heart J       Date:  1993-07       Impact factor: 4.749

4.  Mechanisms of use-dependent block of sodium channels in excitable membranes by local anesthetics.

Authors:  C F Starmer; A O Grant; H C Strauss
Journal:  Biophys J       Date:  1984-07       Impact factor: 4.033

5.  Voltage- and time-dependent depression of maximum rate of depolarisation of guinea-pig ventricular action potentials by two new antiarrhythmic drugs, flecainide and lorcainide.

Authors:  T J Campbell; E M Vaughan Williams
Journal:  Cardiovasc Res       Date:  1983-05       Impact factor: 10.787

6.  Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction.

Authors: 
Journal:  N Engl J Med       Date:  1989-08-10       Impact factor: 91.245

7.  Mortality in patients treated with flecainide and encainide for supraventricular arrhythmias.

Authors:  E L Pritchett; W E Wilkinson
Journal:  Am J Cardiol       Date:  1991-05-01       Impact factor: 2.778

8.  Electrophysiologic mapping to determine the mechanism of experimental ventricular tachycardia initiated by premature impulses. Experimental approach and initial results demonstrating reentrant excitation.

Authors:  A L Wit; M A Allessie; F I Bonke; W Lammers; J Smeets; J J Fenoglio
Journal:  Am J Cardiol       Date:  1982-01       Impact factor: 2.778

9.  Safety and efficacy of oral flecainide therapy in patients with atrioventricular re-entrant tachycardia.

Authors:  J L Cockrell; M M Scheinman; C Titus; I Helmy; J J Langberg; M A Lee; J C Griffin
Journal:  Ann Intern Med       Date:  1991-02-01       Impact factor: 25.391

10.  Effects of flecainide on the electrophysiologic properties of isolated canine and rabbit myocardial fibers.

Authors:  N Ikeda; B N Singh; L D Davis; O Hauswirth
Journal:  J Am Coll Cardiol       Date:  1985-02       Impact factor: 24.094

View more
  4 in total

1.  Flecainide-Induced Left Bundle Branch Block.

Authors:  Swetha R Nuthulaganti; Yixin Zhang; Temitope Akinjogbin; Khadeeja Esmail
Journal:  Cureus       Date:  2022-04-22

2.  Initiation and outcomes with Class Ic antiarrhythmic drug therapy.

Authors:  Xu Gao; Avirup Guha; Benjamin Buck; Dilesh Patel; Melissa J Snider; Michael Boyd; Muhammad Afzal; Auroa Badin; Hemant Godara; Zhenguo Liu; Jaret Tyler; Raul Weiss; Steven Kalbfleisch; John Hummel; Ralph Augostini; Mahmoud Houmsse; Emile G Daoud
Journal:  Indian Pacing Electrophysiol J       Date:  2017-12-07

3.  Cardiac sodium channel inhibition by lamotrigine: In vitro characterization and clinical implications.

Authors:  Lindsey Ingleby-Talecki; Sven C van Dijkman; Sean P Oosterholt; Oscar Della Pasqua; Christina Winter; Marianne Cunnington; Linda Rebar; Sergio Forero-Schwanhaeuser; Vickas Patel; James A Cooper; Anthony Bahinski; Khuram W Chaudhary
Journal:  Clin Transl Sci       Date:  2022-05-31       Impact factor: 4.438

Review 4.  Atrial Fibrillation (AF) in Endurance Athletes: a Complicated Affair.

Authors:  Dimitrios Stergiou; Edward Duncan
Journal:  Curr Treat Options Cardiovasc Med       Date:  2018-10-26
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.