When should adenosine be given to a patient with supraventricular tachycardia (SVT)?

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Adenosine Administration for Supraventricular Tachycardia

Adenosine should be administered for SVT after vagal maneuvers have failed in hemodynamically stable patients, with an initial dose of 6 mg IV push followed by a 20 mL saline flush, and if necessary, up to two additional 12 mg doses at 1-2 minute intervals. 1

Indications for Adenosine

  • Adenosine is indicated as first-line pharmacological therapy for regular, narrow-complex SVT after vagal maneuvers have failed, with success rates of 78-96% in terminating AVNRT and AVRT 1
  • Adenosine is particularly effective for SVTs that involve the AV node in the reentrant circuit, including AV nodal reentrant tachycardia (AVNRT) and AV reciprocating tachycardia (AVRT) 2
  • For hemodynamically unstable SVT, synchronized cardioversion is the primary treatment, though adenosine may be considered first if the tachycardia is regular with narrow QRS complexes 1

Administration Protocol

  • Administer adenosine via a large proximal vein (e.g., antecubital) as a rapid IV push followed immediately by a 20 mL saline flush 3
  • Initial dose: 6 mg IV push 3, 1
  • If rhythm does not convert within 1-2 minutes, administer 12 mg IV push 3
  • A third dose of 12 mg may be given if necessary after another 1-2 minutes 1
  • Continuous ECG recording during administration helps diagnostically and distinguishes between drug failure and successful termination with immediate reinitiation 1

Diagnostic Value

  • Adenosine serves as both a therapeutic and diagnostic agent for narrow-complex tachyarrhythmias 1
  • For arrhythmias not involving the AV node (atrial flutter, atrial fibrillation), adenosine produces transient AV block without terminating the arrhythmia, which can help unmask the underlying atrial activity 2
  • A defibrillator should be available when administering adenosine to any patient in whom Wolff-Parkinson-White syndrome is a consideration, due to the possibility of initiating atrial fibrillation with rapid ventricular rates 3

Special Considerations

  • Larger doses may be required for patients with significant blood levels of theophylline, caffeine, or theobromine 3
  • Reduce the initial dose to 3 mg in patients taking dipyridamole or carbamazepine, those with transplanted hearts, or if given by central venous access 3
  • Adenosine is safe and effective during pregnancy 3, 1
  • Adenosine should not be given to patients with asthma due to risk of bronchospasm 3
  • Patients with impaired venous return to the right heart (e.g., pulmonary hypertension with right heart failure) may require higher-than-recommended doses of adenosine 4

Post-Conversion Management

  • Monitor the patient for recurrence after conversion 3, 5
  • Maintain continuous cardiac monitoring for at least 1-2 hours after successful conversion 5
  • Treat any recurrence with adenosine or consider a longer-acting AV nodal blocking agent (e.g., diltiazem or β-blocker) 3, 5
  • If adenosine reveals another form of SVT (such as atrial fibrillation or flutter), consider treatment with a longer-acting AV nodal blocking agent 3

Common Side Effects

  • Side effects are common but transient due to adenosine's extremely short half-life (less than 10 seconds) 6
  • Most common side effects include flushing, dyspnea, and chest discomfort 3
  • Transient ventricular ectopy may occur but typically resolves within seconds 7

References

Guideline

Adenosine Therapy for Supraventricular Tachycardia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Manejo y Control Post Cardioversión Farmacológica de Taquicardia Supraventricular Estable

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Five paediatric case reports of the use of adenosine in supraventricular tachycardia.

Annals of the Academy of Medicine, Singapore, 1998

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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