Non-selective β₁- and β₂-agonist without alpha effectNAMED-PATIENT LICENCE REQUIREDMONITORED CARE SETTING

Isoprenaline

Isoprenalin APL · Isuprel

Pharmacological pacemaker. Potent β₁-stimulation produces marked chronotropy and inotropy, while equally potent β₂-stimulation dilates the vessels — completely without alpha effect. The result is that heart rate rises while systemic vascular resistance and diastolic blood pressure fall, so the drug raises rate but not pressure. Used where rate itself is the problem: bradycardia while awaiting pacing, bradycardia-dependent torsades de pointes, and electrical storm in Brugada syndrome.

BOXED WARNING

Isoprenaline increases myocardial oxygen consumption while diastolic pressure and therefore coronary perfusion fall. In ischaemic heart disease it can trigger infarction and ventricular arrhythmias. Not given in tachyarrhythmia, digoxin toxicity, or marked hypovolaemia, and never without continuous telemetry and standby for transcutaneous or transvenous pacing.

Dosing in adults

By indicationuppdaterad 2026-08-22
IndicationRegimenComment
Symptomatic bradycardia or AV block II–III0,5–10 μg/min iv, titrate to heart rate and symptomsbridge to pacing, not definitive treatment
Bradycardia-dependent torsades de pointes0,5–10 μg/min iv targeting heart rate 90–110 per minuteafter magnesium; rate increase shortens QT and breaks the arrhythmia
Electrical storm in Brugada syndromeBolus 1–2 μg iv, then infusion 0,5–5 μg/minnormalises ST elevation in V₁–V₂ and suppresses arrhythmia burden
Beta-blocker intoxication (second choice)0,5–10 μg/min iv, often high dosesglucagon and high-dose insulin are the primary treatment
DiscontinuationTaper when pacing or causal treatment is in placeshort duration, effect wanes within minutes
Renal impairment

No established dose adjustment.

Hepatic impairment

No established dose adjustment.

Children

0,05–2 μg/kg/min on paediatric cardiology prescription; titrated to heart rate.

Pitfall

Avoid in ischaemic bradycardia in the acute phase of myocardial infarction: the increased rate and reduced diastolic coronary perfusion can extend the infarct, and pacing is the safer choice. Also avoid as a blood pressure agent — isoprenaline lowers mean arterial pressure and is the wrong tool in hypotension.

Pharmacokinetics

BIOAVAIL.
Intravenous only
ONSET
Immediate
2–5 minutes
DURATION
Under 10 minutes after the infusion stops
RECEPTORS
β₁ +++++, β₂ +++++, α 0
METABOLISM
COMT and sulfate conjugation
EXCRETION
Renal as metabolites
HAEMODYNAMICS
Raises heart rate and cardiac output, lowers diastolic pressure

Adverse effects by frequency

≥ 10 %
Tachycardia, palpitations, tremor, headache, hypotension with low diastolic pressure
1–10 %
Ventricular ectopics, angina, anxiety, sweating, hyperglycaemia, hypokalaemia
< 1 %
Ventricular tachycardia and ventricular fibrillation, myocardial infarction, pulmonary oedema