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J Am Coll Cardiol, 2006; 48:471-477, doi:10.1016/j.jacc.2006.04.075 (Published online 11 July 2006).
© 2006 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: HEART RHYTHM DISORDER

Cumulative Experience of Azimilide-Associated Torsades de Pointes Ventricular Tachycardia in the 19 Clinical Studies Comprising the Azimilide Database

Craig M. Pratt, MD, FACC*,*, Hussein R. Al-Khalidi, PhD{dagger}, Jose M. Brum, MD{dagger}, Michael J. Holroyde, PhD{dagger}, Peter J. Schwartz, MD, FACC{ddagger}, Stephen R. Marcello, MD, FACC{dagger}, Martin Borggrefe, MD, FACC§, Paul Dorian, MD, FACC||, A. John Camm, MD, FACC on behalf of the Azimilide Trials Investigators

* Department of Cardiology, Methodist DeBakey Heart Center, Houston, Texas
{dagger} Procter & Gamble Pharmaceuticals, Cincinnati, Ohio
{ddagger} Department of Cardiology, Policlinico S. Matteo, IRRCS, and University of Pavia, Pavia, Italy
§ Klinikum Mannheim, Universtatsklinikum, Mannheim, Germany
|| Division of Cardiology, St. Michael’s Hospital, Toronto, Ontario, Canada
Department of Cardiology, St. George’s Hospital, London, England

Manuscript received November 23, 2005; revised manuscript received April 6, 2006, accepted April 11, 2006.

* Reprint requests and correspondence: Dr. Craig M. Pratt, The Methodist DeBakey Heart Center, 6565 Fannin Street, F1001, Houston, Texas 77030. (Email: cpratt{at}tmh.tmc.edu).

OBJECTIVES: The purpose of this study was to assess the incidence, temporal characteristics, and risk factors associated with azimilide-associated torsades de pointes (TdP) ventricular tachycardia.

BACKGROUND: Azimilide dihydrochloride is a class III antiarrhythmic drug possessing Ikr and Iks channel-blocking properties.

METHODS: Oral azimilide (75 to 125 mg/day) was taken by 5,375 patients in 19 clinical trials conducted at 775 international centers. Of 3,964 patients in double-blind studies, 1,427 had a history of atrial fibrillation or other supraventricular arrhythmia, 510 had an implantable cardioverter-defibrillator, and 2,027 were post-myocardial infarction patients with a left ventricular ejection fraction ≤35%.

RESULTS: The TdP occurred in 56 patients assigned to azimilide, was dose-related, and tended to occur earlier with an azimilide-loading regimen. Forty-three percent of TdP patients had a QT interval corrected by Bazett’s formula, for heart rate, (QTc) ≥500 ms at the time of or before the TdP occurrence. Significant risk factors using logistic regression were increasing age, female gender, diuretic use, and lack of aspirin use.

CONCLUSIONS: Azimilide-associated TdP has characteristics and risk factors similar to other Ikr blockers. However, there is a distinctive temporal profile. The TdP events are not concentrated in the first week. The azimilide-associated TdP rate is 1% (95% confidence interval 0.78 to 1.35) and is not increased in patients with low left ventricular ejection fraction, even in women.

Abbreviations and Acronyms
  AF = atrial fibrillation
  ALIVE = Azimilide Post-Infarct Survival Evaluation
  CI = confidence interval
  EC = event committee
  ECG = electrocardiogram
  ICD = implantable cardioverter-defibrillator
  JTc = JT interval corrected by Bazett’s formula, for heart rate
  LVEF = left ventricular ejection fraction
  MI = myocardial infarction
  QTc = QT interval corrected by Bazett’s formula, for heart rate
  SI = site investigator
  SVA = supraventricular arrhythmias




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