Adenosine
Antiarrhythmics
AntiarrhythmicsHigh alert
An error with this medicine can cause serious harm: double checks and protocols are used.
A rapid intravenous push that blocks the AV node for a few seconds and stops most re-entrant supraventricular tachycardias.
Quick facts
- Group
- Antiarrhythmics
- Target
- Adenosine A1 receptor (AV node)
- Used for
- PSVT that uses an accessory pathway
- Key effects
- Facial flushing · Chest pressure or pain
- Monitor
- Continuous ECG recording during the push
- ATC
- C01EB10
No doses: the clinician sets them by the current guideline.
Mechanism of action
The figure shows adenosine bound to the human adenosine A1 receptor coupled to its Gi protein; the structure also holds an allosteric modulator at a separate site.
Adenosine stimulates A1 receptors in the AV node and sinus node. Through Gi proteins it opens acetylcholine/adenosine-sensitive potassium channels and lowers cAMP and calcium entry, so the cells hyperpolarise and AV conduction is briefly blocked. Re-entry circuits that use the AV node (AVNRT, AVRT) are broken; atrial fibrillation, flutter and VT are not converted, though the ventricular rate may slow for a moment and unmask flutter waves.
- Adenosine activates A1 receptors in the AV node
- Potassium channels open and the nodal cells hyperpolarise
- AV conduction stops for seconds, breaking the re-entry circuit
- Red cells and endothelium take it up within seconds
Indications
- Conversion of paroxysmal supraventricular tachycardia to sinus rhythm, after vagal manoeuvres Supraventricular tachycardia (AVNRT, AVRT) →
- PSVT that uses an accessory pathway (Wolff-Parkinson-White), when the complex is regular and narrow Wolff-Parkinson-White syndrome →
Adverse effects
Common
- Facial flushing
- Chest pressure or pain and breathlessness
- Headache and a sense of doom
- Brief pauses or new rhythms at conversion
Contraindications
- Second- or third-degree AV block without a working pacemaker
- Sick sinus syndrome or symptomatic bradycardia without a pacemaker
- Hypersensitivity to adenosine
Key interactions
- Caffeine and theophylline (methylxanthines)
- Block adenosine receptors: larger doses may be needed or it may fail
- Dipyridamole
- Blocks adenosine uptake and strengthens its effect; smaller doses may be enough
- Carbamazepine
- Can deepen heart block
- Digoxin, with or without verapamil
- Rare reports of ventricular fibrillation
What is monitored
- Continuous ECG recording during the push
- Blood pressure and heart rate
- Breathing and wheeze in patients with asthma
Administration and safety
- Given as a rapid intravenous push directly into a peripheral vein, followed at once by a rapid saline flush, because it is cleared in seconds.
- If given through a line, it is injected at the port closest to the patient.
- A defibrillator and resuscitation equipment are at hand.
- Not refrigerated, because crystals can form; the solution must be clear.
Pregnancy and breastfeeding
Adenosine is a natural body molecule with a very short half-life, so no fetal effects are expected, but human data are lacking and it is used in pregnancy only if clearly needed.
Nursing care
- Warn the patient that flushing, chest pressure and a brief feeling of doom are expected and pass in seconds.
- Run an ECG strip during the push to document the response and any pause.
- Ask about asthma, caffeine intake, theophylline and dipyridamole beforehand.
- After conversion, watch rhythm and blood pressure for recurrence.
Pharmacokinetics
- Distribution
- Cleared from blood within seconds by uptake into red cells and vascular endothelium
- Metabolism
- Phosphorylated to AMP or deaminated to inosine inside cells
- Half-life
- Less than ten seconds
- Onset and duration
- Seconds after a rapid push; adverse effects are brief
Test yourself
Think of the answer, then tap the question to see it.
Why is adenosine followed immediately by a rapid saline flush?
Its half-life is under ten seconds; the flush pushes it to the heart before red cells and endothelium take it up.
Which rhythms does adenosine convert and which does it not?
It converts re-entrant SVT that uses the AV node (AVNRT, AVRT); it does not convert atrial fibrillation, flutter or ventricular tachycardia.
How do theophylline and dipyridamole change the response to adenosine?
Theophylline (and caffeine) block its receptors and weaken it; dipyridamole blocks its uptake and strengthens it.
Which receptor in the AV node mediates adenosine's effect?
The A1 adenosine receptor, coupled to Gi, which opens potassium channels.
Connections
← Back to the class: Antiarrhythmics
Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.
Sources: DailyMed - ADENOSINE injection (DailyMed (U.S. National Library of Medicine), 2026); ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026); 7LD3: Cryo-EM structure of the human adenosine A1 receptor-Gi2-protein complex bound to its endogenous agonist and an allosteric ligand (RCSB Protein Data Bank, 2021).
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Representative model, for educational purposes only.
