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Antiarrhythmic drugs treat dysrhythmias by restoring normal cardiac function. They are categorized based on their electrophysiological effects.
Class I antiarrhythmic drugs block open or inactivated voltage-sensitive Na+ channels in continuously depolarizing tissues. By reducing Na+ ion influx, they prevent auto-excitation and hinder action potential propagation.
Class I agents are subdivided based on their effects on the action potential duration and dissociation kinetics from the Na+ channel.
Class IA drugs feature intermediate dissociation kinetics and slow phase 0 depolarization. Additionally, they block K+ channels, prolonging the refractory period and action potential duration.
Class IB drugs exhibit fast dissociation kinetics. They do not affect phase 0 depolarization but shorten phase 3 depolarization and the action potential duration.
Class IC drugs possess slow dissociation kinetics, reducing phase 0 depolarization without affecting the action potential duration.
All class I drugs are proarrhythmic and show potential side effects like delayed conduction, tachycardia, and negative inotropy.