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Arch. cardiol. Méx ; 77(supl.2): S2-59-S2-63, abr.-jun. 2007.
Article in Spanish | LILACS | ID: lil-568848

ABSTRACT

The convenience to count with a safe and effective pharmacological wealth for atrial fibrillation treatment had conduced, in a way, to a deep depuration of the vast array of antiarrhythmic drugs, keeping only a very restricted number of compounds with a widely proved anti-atrial activity. On the other hand, it had lead to the discovery of the pathophysiological concepts that point to novel therapeutic targets. Within these objectives is that new antiarrhythmic drugs with preferential, even selective, activity on myocardial atrium ion channels had been developed. Among these new antiarrhythmics, dofetilide, and AVE0118, are taken into account. In addition, new possibilities are opened based on the knowledge of the cardioprotective-antiarrhythmic qualities of the opioidergic system.


Subject(s)
Humans , Anti-Arrhythmia Agents , Atrial Fibrillation , Biphenyl Compounds , Phenethylamines , Potassium Channel Blockers , Sulfonamides , Administration, Oral , Anti-Arrhythmia Agents , Anti-Arrhythmia Agents/adverse effects , Anti-Arrhythmia Agents , Atrial Fibrillation , Biphenyl Compounds , Biphenyl Compounds , Electrophysiology , Heart Atria , Ion Channels , Phenethylamines , Phenethylamines , Potassium Channel Blockers , Potassium Channel Blockers , Randomized Controlled Trials as Topic , Receptors, Opioid , Sulfonamides , Sulfonamides , Time Factors
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