Related Experiment Video
Updated: Jun 16, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
[New antiarrhythmic drugs for atrial fibrillation]
1Service de Pharmacologie-Toxicologie, Hôpital Pasteur, 30, Avenue de Voie Romaine, 06002 Nice cedex 01, France. drici.md@chu-nice.fr
Abstract:
The development of new antiarrhythmic drugs is mainly aimed to treat atrial fibrillation, because of its prevalence and major consequences in terms cerebral vascular thrombosis. Specific blockade of I(Na) et I(K), even if efficacious, have previously shown to be proarrhythmogenic, with a global impairment of the cardiac patient's outcome. This lead to the development of new drugs, selectively targeting atrial currents such as I(Kur) ou I(KAch). The efficacy of amiodarone in treatment of atrial fibrillation has also yielded a whole array of new antiarrhythmic drugs targeting both these atrial currents but also sharing amiodarone pharmacodynamics properties. This renders the Vaughan-Williams classification ill-adapted for such drugs.
Insights
New antiarrhythmic drugs target atrial fibrillation, a common condition linked to stroke. Current drugs targeting sodium (Na) and potassium (K) channels can be proarrhythmic, necessitating novel approaches.
Area of Science:
- Cardiovascular pharmacology
- Cardiac electrophysiology
Context:
- Atrial fibrillation (AF) is prevalent and a major cause of cerebrovascular thrombosis.
- Traditional antiarrhythmic drugs targeting I(Na) and I(K) channels can be proarrhythmic, negatively impacting patient outcomes.
- Amiodarone's efficacy in AF has spurred the development of new drugs.
Purpose:
- To explore the development of novel antiarrhythmic drugs for atrial fibrillation.
- To address the limitations of traditional antiarrhythmic therapies.
- To investigate drugs targeting specific atrial currents like I(Kur) and I(KAch).
Summary:
- New antiarrhythmic drug development focuses on atrial fibrillation due to its prevalence and association with stroke.
- Drugs targeting specific atrial currents (I(Kur), I(KAch)) are being developed to overcome the proarrhythmic risks of non-selective I(Na) and I(K) blockade.
- These novel agents often share pharmacodynamic properties with amiodarone, challenging the existing Vaughan-Williams classification.
Impact:
- Development of safer and more effective antiarrhythmic treatments for atrial fibrillation.
- Improved patient outcomes by reducing the risk of proarrhythmia and stroke.
- Potential re-evaluation of antiarrhythmic drug classification systems.
Related Concept Videos
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Dysrhythmias VI: Management of Dysrhythmias
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...

