Etripamil Nasal Spray for Rapid Conversion of Supraventricular Tachycardia to Sinus Rhythm

There is no nonparenteral medication for the rapid termination of paroxysmal supraventricular tachycardia. The purpose of this study was to assess the efficacy and safety of etripamil nasal spray, a short-acting calcium-channel blocker, for the rapid termination of paroxysmal supraventricular tachyc...

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Veröffentlicht in:Journal of the American College of Cardiology 2018-07, Vol.72 (5), p.489-497
Hauptverfasser: Stambler, Bruce S., Dorian, Paul, Sager, Philip T., Wight, Douglas, Douville, Philippe, Potvin, Diane, Shamszad, Pirouz, Haberman, Ronald J., Kuk, Richard S., Lakkireddy, Dhanunjaya R., Teixeira, Jose M., Bilchick, Kenneth C., Damle, Roger S., Bernstein, Robert C., Lam, Wilson W., O’Neill, Gearoid, Noseworthy, Peter A., Venkatachalam, Kalpathi L., Coutu, Benoit, Mondésert, Blandine, Plat, Francis
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Sprache:eng
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Zusammenfassung:There is no nonparenteral medication for the rapid termination of paroxysmal supraventricular tachycardia. The purpose of this study was to assess the efficacy and safety of etripamil nasal spray, a short-acting calcium-channel blocker, for the rapid termination of paroxysmal supraventricular tachycardia (SVT). This phase 2 study was performed during electrophysiological testing in patients with previously documented SVT who were induced into SVT prior to undergoing a catheter ablation. Patients in sustained SVT for 5 min received either placebo or 1 of 4 doses of active compound. The primary endpoint was the SVT conversion rate within 15 min of study drug administration. Secondary endpoints included time to conversion and adverse events. One hundred four patients were dosed. Conversion rates from SVT to sinus rhythm were between 65% and 95% in the etripamil nasal spray groups and 35% in the placebo group; the differences were statistically significant (Pearson chi-square test) in the 3 highest active compound dose groups versus placebo. In patients who converted, the median time to conversion with etripamil was 
ISSN:0735-1097
1558-3597
DOI:10.1016/j.jacc.2018.04.082