Electrophysiologic effects of the new class III antiarrhythmic drug dofetilide compared to the class IA antiarrhythmic drug quinidine in experimental canine atrial flutter: role of dispersion of refractoriness in antiarrhythmic efficacy
- PMID: 8884510
- DOI: 10.1111/j.1540-8167.1996.tb00594.x
Electrophysiologic effects of the new class III antiarrhythmic drug dofetilide compared to the class IA antiarrhythmic drug quinidine in experimental canine atrial flutter: role of dispersion of refractoriness in antiarrhythmic efficacy
Abstract
Introduction: Previous studies suggest that class III antiarrhythmic drugs are more effective in reentrant arrhythmias because they prolong refractoriness (ERP) and wavelength and reduce dispersion of refractoriness compared to Class IA antiarrhythmic drugs, which slow conduction velocity (CV) in addition to their effects on refractoriness.
Methods and results: To test this hypothesis, the Class III drug dofetilide and the Class IA drug quinidine were studied in the experimental canine crush-injury model of atrial flutter, utilizing right atrial multipoint programmed stimulation and activation mapping. In seven dogs dofetilide prolonged ERP by 23%, slowed CV by 9% at 200-msec cycle length (P < 0.001) and by 39% at 150-msec cycle length (P < 0.001), and increased wavelength by 11% (P < 0.02). Dofetilide reduced dispersion of ERP by 20% (P = 0.003) and adjacent electrodes with ERP difference > or = 20 msec by 76% (P < 0.001). Dofetilide slowed atrial flutter by 37% (P = 0.003) prior to terminating and suppressing it in all dogs. In eight dogs quinidine prolonged ERP by 14% (P < 0.001), slowed CV by 14% at 200-msec length cycle (P < 0.001) and by 19% at 150-msec cycle length (P < 0.001), and reduced wavelength by 2% (P = NS). Quinidine did not reduce dispersion of refractoriness. Quinidine slowed atrial flutter by 57% (P < 0.001), terminating and suppressing it in only three dogs. Efficacy of dofetilide was greater than quinidine (P = 0.026) and correlated with reduced dispersion of ERP (r = -0.653, P = 0.01), reduced adjacent electrodes with ERP difference > or = 20 msec (r = -0.637, P = 0.012), and prolonged wavelength (r = 0.61, P = 0.018). Dofetilide and quinidine terminated atrial flutter by similar mechanisms. Myocardial fiber orientation was nonuniform around the crush injury.
Conclusions: Antiarrhythmic efficacy of dofetilide was greater than that of quinidine and correlated with drug-induced prolongation of wavelength and reduction in dispersion of refractoriness, effects produced only by dofetilide.
Comment in
-
Dofetilide versus quinidine for atrial flutter: viva la difference!?J Cardiovasc Electrophysiol. 1996 Sep;7(9):828-32. doi: 10.1111/j.1540-8167.1996.tb00595.x. J Cardiovasc Electrophysiol. 1996. PMID: 8884511 Review.
Similar articles
-
Electrophysiologic Effects of the New Class III Antiarrhythmic Drug Dofetilide in an Experimental Canine Model of Pacing-induced Atrial Fibrillation.J Cardiovasc Pharmacol Ther. 1997 Jul;2(3):195-203. doi: 10.1177/107424849700200306. J Cardiovasc Pharmacol Ther. 1997. PMID: 10684458
-
Dofetilide versus quinidine for atrial flutter: viva la difference!?J Cardiovasc Electrophysiol. 1996 Sep;7(9):828-32. doi: 10.1111/j.1540-8167.1996.tb00595.x. J Cardiovasc Electrophysiol. 1996. PMID: 8884511 Review.
-
Electrophysiologic and antiarrhythmic effects of the new class III antiarrhythmic drug KCB-328 in experimental canine atrial flutter.J Cardiovasc Pharmacol Ther. 2001 Jul;6(3):297-306. doi: 10.1177/107424840100600310. J Cardiovasc Pharmacol Ther. 2001. PMID: 11584336
-
Pharmacologic conversion and suppression of experimental canine atrial flutter: differing effects of d-sotalol, quinidine, and lidocaine and significance of changes in refractoriness and conduction.Circulation. 1986 Jul;74(1):197-204. doi: 10.1161/01.cir.74.1.197. Circulation. 1986. PMID: 3708774
-
Dofetilide: a review of its use in atrial fibrillation and atrial flutter.Drugs. 1999 Dec;58(6):1043-59. doi: 10.2165/00003495-199958060-00007. Drugs. 1999. PMID: 10651390 Review.
Cited by
-
Chronic cyclic vagus nerve stimulation has beneficial electrophysiological effects on healthy hearts in the absence of autonomic imbalance.Physiol Rep. 2016 May;4(9):e12786. doi: 10.14814/phy2.12786. Physiol Rep. 2016. PMID: 27173672 Free PMC article.
-
Cardiac radiotherapy induces electrical conduction reprogramming in the absence of transmural fibrosis.Nat Commun. 2021 Sep 24;12(1):5558. doi: 10.1038/s41467-021-25730-0. Nat Commun. 2021. PMID: 34561429 Free PMC article. Clinical Trial.
-
Mechanisms of termination and prevention of atrial fibrillation by drug therapy.Pharmacol Ther. 2011 Aug;131(2):221-41. doi: 10.1016/j.pharmthera.2011.02.002. Epub 2011 Feb 18. Pharmacol Ther. 2011. PMID: 21334377 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous