Sotalol hydrochloride
Sotalol has both beta adrenergic receptor blockade and antiarrhythmic properties. It is a non-selective beta adrenergic blocking agent affecting both beta1 and beta2 receptors.
Dose and administration
IV
0.5 to 1.5mg/kg/dose 8-hourly by slow IV infusion over 10 minutes³
Oral
1 to 2mg /kg/dose 8-hourly. Increase to 4mg/kg/dose if required³,⁶
Needs to be individualised
Indications
Supraventricular tachycardia
Hyperthyroidism
Contraindications
Cardiogenic shock.
Severe sinus bradycardia.
Congenital or acquired long QT syndromes.
Hypokalaemia and hypomagnesaemia.
Precautions
Tendency to bronchoconstriction.
Greater than first degree heart block
Heart failure
Renal failure - decrease the dose in renal impairment, and discontinue if renal impairment severe³
Metabolic acidosis.
Drug interactions
Amiodarone: Bradycardia and hypotension (mechanism not established). Monitor for haemodynamic depression
Diuretics: May induce hypokalaemia or hypomagnesemia therefore increasing the risk of Torsades de Pointes
Flecainide: Bradycardia, AV block, cardiac arrest (allow a gap of several days before starting flecainide)
Chlorpromazine: Hypotension
Clinical pharmacology
Sotalol has both beta adrenergic receptor blockade and antiarrhythmic properties. It is a non-selective beta adrenergic blocking agent affecting both beta1 and beta2 receptors. It has no intrinsic sympathomimetic activity or membrane stabilising activity. It inhibits renin release. Its beta adrenergic activity causes a reduction in heart rate (negative chronotropic effect) and a limited reduction in the force of contraction (negative inotropic effect). This leads to a decrease in myocardial oxygen consumption and cardiac work. Sotalol's antiarrhythmic activity causes a prolongation of the action potential in cardiac tissue by delaying the repolarisation phase.
When given orally its absorption is minimally affected by food. Sotalol undergoes very little first pass hepatic metabolism and, in adults, exhibits almost 100% bioavailability after oral dosing. It is not protein bound, and is hydrophilic with a low incidence of severe CNS adverse effects. Elimination is primarily by the kidneys with 75% of a dose excreted unchanged in the urine.
Possible adverse effects
Can worsen existing arrhythmias or cause new arrhythmias
Bradycardia, heart failure, hypotension, dyspnoea
Rash
Vomiting, diarrhoea
Special considerations
Have atropine on hand for excessive bradycardia
Monitor:
Electrolytes, especially potassium and magnesium
QT interval. Caution if QT becomes prolonged especially with increased dosage
Therapeutic drug monitoring is possible
Titrate dose of Sotalol when discontinuing treatment.
Management of Sotolol administration
Description
IV preparation: Clear, colourless solution 10mg/ml in 4ml ampoules. No antibacterial agent.
Oral preparation: During Pharmacy hours scan drug chart to Pharmacy for dispensing. Outside Pharmacy hours, contact Ward 23B (Starship Hospital) for their stock bottle of oral Sotalol liquid.
Prescription
Individual doses are charted on stat page of prescription chart in mg/dose.
Maintenance doses are charted on the prescription chart in mg/dose.
Administration
Slow IV Infusion
Dilute immediately prior to use to 1mg/ml by adding to sodium chloride 0.9% or glucose 5% .
Filter prior to administration through a 5 micron filter needle.
Administer by slow IV infusion over 10 minutes using a syringe pump.
Compatible with sodium chloride 0.9% or glucose 5%. Do not mix with other drugs or IV solutions
Flush line with sodium chloride 0.9% before and after infusion of Sotalol.
Oral
Follow instructions on bottle.
Is preferable to administer before food⁶. Be consistent when administering with or without food.
Do not administer with calcium containing products.
Observation and documentation
Assess for signs of adverse reactions.
Cardiorespiratory monitoring during acute usage. Report and record changes in heart rate and rhythm.
Monitor blood pressure.
Document vital signs.
Document baby's response to medication.
Storage
IV preparation: Unopened. Store at room temperature <25°C.