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July 1, 2017JAMA Cardiology170 citationsOpen Access

Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia

PKPrince J. KannankerilJMJeremy P. MooreMCMarina Cerrone

Key Result

Flecainide added to β-blocker therapy significantly reduced the median ventricular arrhythmia score during exercise compared with placebo (0 vs 2.5; P<.01).

Study Design

Type

RCT (n=14)

Blinding

Single-blind

Randomization

Crossover

Multicenter

Yes

Structured PICO

Does flecainide reduce exercise-induced ventricular arrhythmias in patients with CPVT receiving maximally tolerated β-blocker therapy?

P
Population
14 patients (median age 16) with CPVT and an ICD on maximally tolerated β-blocker therapy, evaluated in a 3-month crossover trial.
I
Intervention
Oral flecainide twice daily (dosage guided by trough serum levels) added to maximally tolerated β-blocker therapy for 3 months.
C
Comparator
Placebo twice daily added to maximally tolerated β-blocker therapy for 3 months.
O
Outcome
Ventricular arrhythmias during exercise, scored on an ordinal scale of worst ventricular arrhythmia observed (0 indicates no ectopy; 1, isolated premature ventricular beats; 2, bigeminy; 3, couplets; and 4, nonsustained ventricular tachycardia).surrogate

Flecainide added to beta-blocker therapy significantly reduces exercise-induced ventricular arrhythmias in patients with CPVT compared to beta-blocker therapy alone.

Main Result

Absolute Event Rate: 0% vs 2.5%

p-value: p=<.01

Abstract

Importance: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a potentially lethal genetic arrhythmia syndrome characterized by polymorphic ventricular tachycardia with physical or emotional stress, for which current therapy with β-blockers is incompletely effective. Flecainide acetate directly suppresses sarcoplasmic reticulum calcium release-the cellular mechanism responsible for triggering ventricular arrhythmias in CPVT-but has never been assessed prospectively. Objective: To determine whether flecainide dosed to therapeutic levels and added to β-blocker therapy is superior to β-blocker therapy alone for the prevention of exercise-induced arrhythmias in CPVT. Design, Setting, and Participants: This investigator-initiated, multicenter, single-blind, placebo-controlled crossover clinical trial was conducted from December 19, 2011, through December 29, 2015, with a midtrial protocol change at 10 US sites. Patients with a clinical diagnosis of CPVT and an implantable cardioverter-defibrillator underwent a baseline exercise test while receiving maximally tolerated β-blocker therapy that was continued throughout the trial. Patients were then randomized to treatment A (flecainide or placebo) for 3 months, followed by exercise testing. After a 1-week washout period, patients crossed over to treatment B (placebo or flecainide) for 3 months, followed by exercise testing. Interventions: Patients received oral flecainide or placebo twice daily, with the dosage guided by trough serum levels. Main Outcomes and Measures: The primary end point of ventricular arrhythmias during exercise was compared between the flecainide and placebo arms. Exercise tests were scored on an ordinal scale of worst ventricular arrhythmia observed (0 indicates no ectopy; 1, isolated premature ventricular beats; 2, bigeminy; 3, couplets; and 4, nonsustained ventricular tachycardia). Results: Of 14 patients (7 males and 7 females; median age, 16 years interquartile range, 15.0-22.5 years) randomized, 13 completed the study. The median baseline exercise test score was 3.0 (range, 0-4), with no difference noted between the baseline and placebo (median, 2.5; range, 0-4) exercise scores. The median ventricular arrhythmia score during exercise was significantly reduced by flecainide (0 range, 0-2 vs 2.5 range, 0-4 for placebo; P < .01), with complete suppression observed in 11 of 13 patients (85%). Overall and serious adverse events did not differ between the flecainide and placebo arms. Conclusions and Relevance: In this randomized clinical trial of patients with CPVT, flecainide plus β-blocker significantly reduced ventricular ectopy during exercise compared with placebo plus β-blocker and β-blocker alone. Trial Registration: clinicaltrials.gov Identifier: NCT01117454.

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Cite This Study

Kannankeril et al. (2017) conducted an RCT in Catecholaminergic polymorphic ventricular tachycardia (CPVT) (n=14). Flecainide vs. Placebo was evaluated on Ventricular arrhythmias during exercise (scored on an ordinal scale of 0 to 4) (p=<.01). Flecainide added to β-blocker therapy significantly reduced the median ventricular arrhythmia score during exercise compared with placebo (0 vs 2.5; P<.01).

synapsesocial.com/papers/6a46fdc28dd8ee62990509f6https://doi.org/10.1001/jamacardio.2017.1320
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