Coronary artery disease potentiates response to dofetilide for rhythm control of atrial fibrillation

Pankaj Manocha1, Venkata Bavikati, Jonathan Langberg

  • 1Department of Cardiac Electrophysiology, Emory University Hospital, Atlanta, Georgia 30322, USA.

Insights

Coronary artery disease (CAD) predicts success for dofetilide, an antiarrhythmic drug, in atrial fibrillation (AF) patients. This finding aids clinical decisions for initiating dofetilide treatment.

Area of Science:

  • Cardiology
  • Pharmacology

Background:

  • Dofetilide is a Class III antiarrhythmic agent used for atrial fibrillation (AF).
  • It serves as an alternative to amiodarone in patients with AF and heart failure or coronary artery disease (CAD).
  • Predictors of dofetilide response remain largely uncharacterized.

Purpose of the Study:

  • To identify clinical parameters associated with dofetilide treatment success.
  • To analyze the efficacy of dofetilide in a large cohort of AF patients.

Main Methods:

  • A retrospective analysis of 287 AF patients initiated on dofetilide between 2001 and 2008.
  • Dofetilide efficacy was defined as continuous use and absence of AF recurrence.
  • Clinical variables were analyzed for association with dofetilide efficacy using univariate and multivariate regression.

Main Results:

  • Dofetilide was completely effective in 26.8% of patients after a mean follow-up of 10.2 months.
  • A history of CAD was the sole significant univariate (OR 2.27) and multivariate (OR 2.01) predictor of dofetilide efficacy.
  • Efficacy was higher in patients with CAD (41.1%) compared to those without (23.5%).

Conclusions:

  • Underlying coronary artery disease is a significant predictor of dofetilide success in AF patients.
  • This finding can inform clinical decision-making regarding dofetilide initiation.
Abstract

Related Concept Videos

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of the heart's...
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which indirectly block calcium...