A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation

Research output: Contribution to journalJournal articleResearchpeer-review

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A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation. / Camm, A John; Capucci, Alessandro; Hohnloser, Stefan H; Torp-Pedersen, Christian; Van Gelder, Isabelle C; Mangal, Brian; Beatch, Gregory; AVRO Investigators.

In: Journal of the American College of Cardiology, Vol. 57, No. 3, 18.01.2011, p. 313-21.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Camm, AJ, Capucci, A, Hohnloser, SH, Torp-Pedersen, C, Van Gelder, IC, Mangal, B, Beatch, G & AVRO Investigators 2011, 'A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation', Journal of the American College of Cardiology, vol. 57, no. 3, pp. 313-21. https://doi.org/10.1016/j.jacc.2010.07.046, https://doi.org/10.1016/j.jacc.2010.07.046

APA

Camm, A. J., Capucci, A., Hohnloser, S. H., Torp-Pedersen, C., Van Gelder, I. C., Mangal, B., Beatch, G., & AVRO Investigators (2011). A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation. Journal of the American College of Cardiology, 57(3), 313-21. https://doi.org/10.1016/j.jacc.2010.07.046, https://doi.org/10.1016/j.jacc.2010.07.046

Vancouver

Camm AJ, Capucci A, Hohnloser SH, Torp-Pedersen C, Van Gelder IC, Mangal B et al. A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation. Journal of the American College of Cardiology. 2011 Jan 18;57(3):313-21. https://doi.org/10.1016/j.jacc.2010.07.046, https://doi.org/10.1016/j.jacc.2010.07.046

Author

Camm, A John ; Capucci, Alessandro ; Hohnloser, Stefan H ; Torp-Pedersen, Christian ; Van Gelder, Isabelle C ; Mangal, Brian ; Beatch, Gregory ; AVRO Investigators. / A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation. In: Journal of the American College of Cardiology. 2011 ; Vol. 57, No. 3. pp. 313-21.

Bibtex

@article{c5cb83b5976d489e9bca94dc5fbeb767,
title = "A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation",
abstract = "Objectives This randomized double-blind study compared the efficacy and safety of intravenous vernakalant and amiodarone for the acute conversion of recent-onset atrial fibrillation (AF). Background Intravenous vernakalant has effectively converted recent-onset AF and was well tolerated in placebo-controlled studies. Methods A total of 254 adult patients with AF (3 to 48 h duration) eligible for cardioversion were enrolled in the study. Patients received either a 10-min infusion of vernakalant (3 mg/kg) followed by a 15-min observation period and a second 10-min infusion (2 mg/kg) if still in AF, plus a sham amiodarone infusion, or a 60-min infusion of amiodarone (5 mg/kg) followed by a maintenance infusion (50 mg) over an additional 60 min, plus a sham vernakalant infusion. Results Conversion from AF to sinus rhythm within the first 90 min (primary end point) was achieved in 60 of 116 (51.7%) vernakalant patients compared with 6 of 116 (5.2%) amiodarone patients (p < 0.0001). Vernakalant resulted in rapid conversion (median time of 11 min in responders) and was associated with a higher rate of symptom relief compared with amiodarone (53.4% of vernakalant patients reported no AF symptoms at 90 min compared with 32.8% of amiodarone patients; p = 0.0012). Serious adverse events or events leading to discontinuation of study drug were uncommon. There were no cases of torsades de pointes, ventricular fibrillation, or polymorphic or sustained ventricular tachycardia. Conclusions Vernakalant demonstrated efficacy superior to amiodarone for acute conversion of recent-onset AF. Both vernakalant and amiodarone were safe and well tolerated in this study. (A Phase III Superiority Study of Vernakalant vs Amiodarone in Subjects With Recent Onset Atrial Fibrillation ",
author = "Camm, {A John} and Alessandro Capucci and Hohnloser, {Stefan H} and Christian Torp-Pedersen and {Van Gelder}, {Isabelle C} and Brian Mangal and Gregory Beatch and Torp-Pedersen, {Christian Tobias}",
note = "Copyright {\^A}{\textcopyright} 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.",
year = "2011",
month = jan,
day = "18",
doi = "10.1016/j.jacc.2010.07.046",
language = "English",
volume = "57",
pages = "313--21",
journal = "Journal of the American College of Cardiology",
issn = "0735-1097",
publisher = "Elsevier",
number = "3",

}

RIS

TY - JOUR

T1 - A randomized active-controlled study comparing the efficacy and safety of vernakalant to amiodarone in recent-onset atrial fibrillation

AU - Camm, A John

AU - Capucci, Alessandro

AU - Hohnloser, Stefan H

AU - Torp-Pedersen, Christian

AU - Van Gelder, Isabelle C

AU - Mangal, Brian

AU - Beatch, Gregory

AU - AVRO Investigators

N1 - Copyright © 2011 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

PY - 2011/1/18

Y1 - 2011/1/18

N2 - Objectives This randomized double-blind study compared the efficacy and safety of intravenous vernakalant and amiodarone for the acute conversion of recent-onset atrial fibrillation (AF). Background Intravenous vernakalant has effectively converted recent-onset AF and was well tolerated in placebo-controlled studies. Methods A total of 254 adult patients with AF (3 to 48 h duration) eligible for cardioversion were enrolled in the study. Patients received either a 10-min infusion of vernakalant (3 mg/kg) followed by a 15-min observation period and a second 10-min infusion (2 mg/kg) if still in AF, plus a sham amiodarone infusion, or a 60-min infusion of amiodarone (5 mg/kg) followed by a maintenance infusion (50 mg) over an additional 60 min, plus a sham vernakalant infusion. Results Conversion from AF to sinus rhythm within the first 90 min (primary end point) was achieved in 60 of 116 (51.7%) vernakalant patients compared with 6 of 116 (5.2%) amiodarone patients (p < 0.0001). Vernakalant resulted in rapid conversion (median time of 11 min in responders) and was associated with a higher rate of symptom relief compared with amiodarone (53.4% of vernakalant patients reported no AF symptoms at 90 min compared with 32.8% of amiodarone patients; p = 0.0012). Serious adverse events or events leading to discontinuation of study drug were uncommon. There were no cases of torsades de pointes, ventricular fibrillation, or polymorphic or sustained ventricular tachycardia. Conclusions Vernakalant demonstrated efficacy superior to amiodarone for acute conversion of recent-onset AF. Both vernakalant and amiodarone were safe and well tolerated in this study. (A Phase III Superiority Study of Vernakalant vs Amiodarone in Subjects With Recent Onset Atrial Fibrillation

AB - Objectives This randomized double-blind study compared the efficacy and safety of intravenous vernakalant and amiodarone for the acute conversion of recent-onset atrial fibrillation (AF). Background Intravenous vernakalant has effectively converted recent-onset AF and was well tolerated in placebo-controlled studies. Methods A total of 254 adult patients with AF (3 to 48 h duration) eligible for cardioversion were enrolled in the study. Patients received either a 10-min infusion of vernakalant (3 mg/kg) followed by a 15-min observation period and a second 10-min infusion (2 mg/kg) if still in AF, plus a sham amiodarone infusion, or a 60-min infusion of amiodarone (5 mg/kg) followed by a maintenance infusion (50 mg) over an additional 60 min, plus a sham vernakalant infusion. Results Conversion from AF to sinus rhythm within the first 90 min (primary end point) was achieved in 60 of 116 (51.7%) vernakalant patients compared with 6 of 116 (5.2%) amiodarone patients (p < 0.0001). Vernakalant resulted in rapid conversion (median time of 11 min in responders) and was associated with a higher rate of symptom relief compared with amiodarone (53.4% of vernakalant patients reported no AF symptoms at 90 min compared with 32.8% of amiodarone patients; p = 0.0012). Serious adverse events or events leading to discontinuation of study drug were uncommon. There were no cases of torsades de pointes, ventricular fibrillation, or polymorphic or sustained ventricular tachycardia. Conclusions Vernakalant demonstrated efficacy superior to amiodarone for acute conversion of recent-onset AF. Both vernakalant and amiodarone were safe and well tolerated in this study. (A Phase III Superiority Study of Vernakalant vs Amiodarone in Subjects With Recent Onset Atrial Fibrillation

U2 - 10.1016/j.jacc.2010.07.046

DO - 10.1016/j.jacc.2010.07.046

M3 - Journal article

C2 - 21232669

VL - 57

SP - 313

EP - 321

JO - Journal of the American College of Cardiology

JF - Journal of the American College of Cardiology

SN - 0735-1097

IS - 3

ER -

ID: 34116249