Study note

Class II anti-arrhythmic drugs: β-blockers and sotalol

THE CONTEXT
Class II drugs are β-adrenoceptor antagonists with nodal effects that support rate control and arrhythmia prevention.

Actions and clinical benefits

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β-blockers reduce the rate of SA node depolarisation and cause relative AV nodal block, making them useful for rate control in atrial flutter and atrial fibrillation.
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They can prevent ventricular and supraventricular tachycardia.
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They reduce myocardial excitability and the risk of arrhythmic death in patients with coronary artery disease and heart failure.

Non-selective and cardioselective agents

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Non-selective β-blockers act on both β1 and β2 receptors. β2 blockade can cause bronchospasm and peripheral vasoconstriction.
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Propranolol is non-selective and undergoes extensive hepatic first-pass metabolism. Its effective oral dose is unpredictable, so treatment starts with a small dose and is subsequently titrated.
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Nadolol and carvedilol are other non-selective agents.
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Cardioselective β-blockers act mainly on myocardial β1 receptors and are relatively well tolerated. Examples are bisoprolol and metoprolol.

Sotalol

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Sotalol is a racemic mixture with non-selective β-blocker activity mainly attributable to l-sotalol and class III activity mainly attributable to d-sotalol.
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Sotalol may cause torsades de pointes.
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