Antiarrhythmic drug

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Antiarrhythmic drugs are a group of pharmaceuticals that are used to suppress abnormal rhythms of the heart, such as atrial fibrillation, atrial flutter, ventricular tachycardia, and ventricular fibrillation.

Classification[edit | edit source]

Antiarrhythmic drugs are classified into four main classes (I, II, III, IV) based on the Vaughan Williams classification system. This system was designed by Miles Vaughan Williams in 1970.

Class I[edit | edit source]

Class I antiarrhythmic drugs interfere with the sodium (Na+) channel. They are subdivided into three categories: Ia, Ib, and Ic, which have different effects on the action potential.

Class II[edit | edit source]

Class II antiarrhythmic drugs are anti-sympathetic nervous system agents. Most agents in this class are beta blockers.

Class III[edit | edit source]

Class III antiarrhythmic drugs affect potassium (K+) efflux. They prolong repolarization and increase the duration of action potentials.

Class IV[edit | edit source]

Class IV antiarrhythmic drugs affect calcium channels and the AV node. Most agents in this class are calcium channel blockers.

Mechanism of action[edit | edit source]

Antiarrhythmic drugs work by altering the conduction of electrical impulses in the heart. They achieve this by blocking ion channels, inhibiting sympathetic stimulation of the heart, and prolonging repolarization.

Side effects[edit | edit source]

Like all drugs, antiarrhythmic drugs can have side effects. These can include dizziness, nausea, shortness of breath, and heart failure. It is important for patients to discuss these potential side effects with their healthcare provider before starting treatment.

See also[edit | edit source]

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