What is the role of adenosine in treating supraventricular tachycardia (SVT)?

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Last updated: December 13, 2025View editorial policy

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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

  • Attempt vagal maneuvers first 1
  • If vagal maneuvers fail, proceed to adenosine administration 1

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

References

Guideline

Adenosine Administration for Supraventricular Tachycardia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Adenosine Use for Supraventricular Tachycardia Post-Cardiac Arrest

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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