Adenosine for Supraventricular Tachycardia
Adenosine is the first-line pharmacologic agent for terminating hemodynamically stable supraventricular tachycardia (SVT) after vagal maneuvers fail, with success rates of 78-96% for AVNRT and AVRT. 1
Initial Management Algorithm
Step 1: Assess Hemodynamic Stability
- If hemodynamically unstable (hypotension, altered mental status, shock, chest pain, acute heart failure): proceed immediately to synchronized cardioversion 2
- Adenosine may be considered first only if the tachycardia is regular with narrow QRS complex, but defibrillator must be immediately available 2
Step 2: For Stable Patients
Administration Protocol
Dosing Regimen
- Initial dose: 6 mg IV push via large proximal vein, followed immediately by 20 mL saline flush 1
- If no conversion within 1-2 minutes: 12 mg IV push with saline flush 1
- If still no conversion: repeat 12 mg IV push one additional time 1
- Administer as rapid bolus—this is critical for efficacy 1
Dose Modifications Required
- Reduce initial dose to 3 mg in patients: 1
- Taking dipyridamole or carbamazepine
- With transplanted hearts
- Receiving central venous administration
- Increase dose in patients with significant blood levels of theophylline, caffeine, or theobromine 1
Mechanism and Effectiveness
Adenosine terminates approximately 95% of AVNRT cases and 78-96% of AVRT cases by causing transient AV nodal block. 1 The drug works by activating A1 receptors in the AV node, producing direct negative chronotropic and dromotropic effects 3. It has an extremely short half-life of less than 10 seconds, as it is rapidly taken up by erythrocytes and vascular endothelial cells 3.
Diagnostic Value
Beyond its therapeutic role, adenosine serves as a diagnostic tool: 1
- Continuous ECG recording during administration helps distinguish drug failure from successful termination with immediate reinitiation
- Can unmask underlying atrial flutter or atrial tachycardia by producing AV block
- Helps differentiate SVT from other narrow-complex tachyarrhythmias
Critical Safety Considerations and Contraindications
Absolute Contraindications
- Asthma or bronchospasm: adenosine can cause severe bronchospasm 1, 3
- High-grade AV block or sinus node dysfunction (unless functioning pacemaker present) 3
- Bronchoconstriction or bronchospastic lung disease 3
Serious Risks Requiring Immediate Defibrillator Availability
- Atrial fibrillation induction (1-15% incidence): can conduct rapidly in patients with accessory pathways (Wolff-Parkinson-White syndrome) and potentially trigger ventricular fibrillation 2, 3
- Fatal and nonfatal cardiac arrest, sustained ventricular tachycardia, and myocardial infarction have occurred 3
- AV block develops in approximately 6% of patients (first-degree 3%, second-degree 3%, third-degree 0.8%) 3
Use with Caution
- Pre-existing first-degree AV block or bundle branch block 3
- Obstructive lung disease without bronchoconstriction (emphysema, bronchitis) 3
- Autonomic dysfunction, hypovolemia, stenotic valvular disease, pericarditis, or stenotic carotid artery disease 3
- Acute myocardial ischemia or unstable angina 3
Common Side Effects
Most side effects are transient, lasting less than 60 seconds: 1
- Flushing (most common)
- Dyspnea
- Chest discomfort
- Headache
- These are dose-dependent and self-limiting
Post-Conversion Management
- Monitor for recurrence after successful conversion 1
- If SVT recurs: treat with adenosine again or consider longer-acting AV nodal blocking agent (diltiazem or β-blocker) 1
- If adenosine unmasks another form of SVT (atrial flutter, atrial tachycardia): consider longer-acting AV nodal blocking agent 1
Special Populations
Pregnancy
- Adenosine is safe and effective during pregnancy 1
Renal and Hepatic Impairment
- No dose adjustment needed—adenosine does not require renal or hepatic function for activation or inactivation 3
Common Pitfalls to Avoid
- Inadequate flush: must use 20 mL saline flush immediately after bolus to ensure drug reaches central circulation 1
- Slow administration: adenosine must be given as rapid IV push; slow administration results in peripheral metabolism before reaching the heart 1
- Wrong initial dose: starting with 12 mg instead of 6 mg increases unnecessary side effects, as 70% of patients convert with 6 mg or less 1
- Failure to have defibrillator available: particularly dangerous in patients with potential accessory pathways 2
- Use in asthmatic patients: absolute contraindication due to bronchospasm risk 1, 3