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New Horizons in Antiarrhythmic Therapy: Will Novel Agents Overcome Current Deficits?

  • Emily Conway
    Affiliations
    Division of Cardiovascular Diseases, Main Line Health Heart Center, Wynnewood, Pennsylvania, USA; and Jefferson Medical College, Philadelphia, Pennsylvania, USA
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  • Simone Musco
    Affiliations
    Division of Cardiovascular Diseases, Main Line Health Heart Center, Wynnewood, Pennsylvania, USA; and Jefferson Medical College, Philadelphia, Pennsylvania, USA
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  • Peter R. Kowey
    Correspondence
    Address for reprints: Peter R. Kowey, MD, Lankenau MOBE Suite 558, 100 Lancaster Avenue, Wynnewood, Pennsylvania 19096
    Affiliations
    Division of Cardiovascular Diseases, Main Line Health Heart Center, Wynnewood, Pennsylvania, USA; and Jefferson Medical College, Philadelphia, Pennsylvania, USA
    Search for articles by this author
      Pharmacologic antiarrhythmic therapy is the most commonly used treatment in most patients with atrial fibrillation (AF), but currently available agents are limited by risks that may offset the benefits of sinus rhythm. The development of antiarrhythmic agents with the potential for fewer adverse ventricular effects and less extracardiac toxicity is a primary aim of current investigations. At present, pharmacologic research is actively focused on developing antiarrhythmic agents with multiple or novel ion channel effects. There are 4 agents that act by simultaneously blocking multiple ion channels that are currently under regulatory review: azimilide dihydrochloride, tedisamil, dronedarone, and vernakalant (RSD-1235). In addition, agents with mechanisms of action that differ from those of existing agents (eg, gap junction modulators) are under review, as is the use of nonantiarrhythmic agents (eg, renin–angiotensin system antagonists, statins, n-3 polyunsaturated fatty acids) to alter the cardiac substrate and suppress AF in some patient subtypes.
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