Antiarrhythmics
Antiarrhythmics are a group of pharmaceutical drugs used to treat arrhythmias or irregular heartbeats. These drugs work by modifying the electrical impulses in the heart that regulate the heartbeat, ensuring that the heart maintains a regular rhythm. Antiarrhythmics are categorized into different classes based on their mechanism of action and their effect on the cardiac action potential.
Classes of Antiarrhythmics[edit | edit source]
Antiarrhythmics are classified into five main classes, each targeting different aspects of cardiac electrophysiology:
Class I[edit | edit source]
Class I antiarrhythmics are sodium channel blockers, which inhibit the fast sodium channels in the cells of the heart. This action slows the rate of rise of the action potential, thereby slowing the propagation of the electrical impulse. Class I drugs are subdivided into three groups:
- Class IA (e.g., Quinidine, Procainamide, Disopyramide) - These drugs increase the action potential duration.
- Class IB (e.g., Lidocaine, Mexiletine) - These drugs decrease the action potential duration.
- Class IC (e.g., Flecainide, Propafenone) - These drugs have a minimal effect on the action potential duration but more significantly reduce the conduction velocity.
Class II[edit | edit source]
Class II antiarrhythmics are beta blockers. They work by blocking the beta-adrenergic receptors in the heart, which reduces the effects of adrenaline and noradrenaline. This results in a decrease in heart rate and contractility, which can be beneficial in treating arrhythmias that are caused by excessive sympathetic activity. Examples include Propranolol, Metoprolol, and Atenolol.
Class III[edit | edit source]
Class III antiarrhythmics are potassium channel blockers, which extend the duration of the action potential and the refractory period of the cardiac cells. This helps in preventing the reoccurrence of an abnormal rapid heartbeat. Common drugs in this class include Amiodarone, Sotalol, and Dofetilide.
Class IV[edit | edit source]
Class IV antiarrhythmics are calcium channel blockers. These drugs inhibit the slow calcium channels in the heart, which reduces the force of contraction and delays the conduction through the AV node. This class is particularly effective in treating arrhythmias that originate above the ventricles (supraventricular arrhythmias). Examples include Verapamil and Diltiazem.
Other Antiarrhythmics[edit | edit source]
Some antiarrhythmics do not fit neatly into the above classes and include drugs like Adenosine, which is primarily used in the emergency treatment of certain types of supraventricular tachycardias, and Digoxin, which increases vagal tone and decreases conduction through the AV node.
Indications[edit | edit source]
Antiarrhythmics are used to treat various types of arrhythmias, including atrial fibrillation, ventricular tachycardia, and supraventricular tachycardia. The choice of an antiarrhythmic drug depends on the type of arrhythmia, the presence of other medical conditions, and the patient's overall health.
Side Effects[edit | edit source]
The use of antiarrhythmics can be associated with significant side effects, some of which can be life-threatening. These include, but are not limited to, proarrhythmia (an increase in arrhythmia severity), systemic effects like dizziness, nausea, and effects on other organs such as the liver and lungs. Monitoring and management by a healthcare provider are crucial.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD